TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Vasilic, Rastko
PY  - 2023
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6315
AB  - Ta2O5 coatings were created using micro-arc discharges (MDs) during anodization on a tantalum substrate in a sodium phosphate electrolyte (10 g/L Na3PO4·10H2O). During the process, the size of MDs increases while the number of MDs decreases. The elements and their ionization states present in MDs were identified using optical emission spectroscopy. The hydrogen Balmer line Hβ shape analysis revealed the presence of two types of MDs, with estimated electron number densities of around 1.1 × 1021 m−3 and 7.3 × 1021 m−3. The effect of MDs duration on surface morphology, phase and chemical composition, optical absorption, and photoluminescent, properties of Ta2O5 coatings, as well as their applications in photocatalytic degradation of methyl orange, were investigated. The created coatings were crystalline and were primarily composed of Ta2O5 orthorhombic phase. Since Ta2O5 coatings feature strong absorption in the ultraviolet light region below 320 nm, their photocatalytic activity is very high and increases with the time of the MDs process. This was associated with an increase of oxygen vacancy defects in coatings formed during the MDs, which was confirmed by photoluminescent measurements. The photocatalytic activity after 8 h of irradiation was around 69%, 74%, 80%, and 88% for Ta2O5 coatings created after 3 min, 5 min, 10 min, and 15 min, respectively.
PB  - MDPI
T2  - Micromachines
T1  - Application of Micro-Arc Discharges during Anodization of Tantalum for Synthesis of Photocatalytic Active Ta2O5 Coatings
VL  - 14
IS  - 3
SP  - 701
DO  - https://doi.org/10.3390/mi14030701
ER  - 

@article{
author = "Stojadinović, Stevan and Radić, Nenad and Vasilic, Rastko",
year = "2023",
abstract = "Ta2O5 coatings were created using micro-arc discharges (MDs) during anodization on a tantalum substrate in a sodium phosphate electrolyte (10 g/L Na3PO4·10H2O). During the process, the size of MDs increases while the number of MDs decreases. The elements and their ionization states present in MDs were identified using optical emission spectroscopy. The hydrogen Balmer line Hβ shape analysis revealed the presence of two types of MDs, with estimated electron number densities of around 1.1 × 1021 m−3 and 7.3 × 1021 m−3. The effect of MDs duration on surface morphology, phase and chemical composition, optical absorption, and photoluminescent, properties of Ta2O5 coatings, as well as their applications in photocatalytic degradation of methyl orange, were investigated. The created coatings were crystalline and were primarily composed of Ta2O5 orthorhombic phase. Since Ta2O5 coatings feature strong absorption in the ultraviolet light region below 320 nm, their photocatalytic activity is very high and increases with the time of the MDs process. This was associated with an increase of oxygen vacancy defects in coatings formed during the MDs, which was confirmed by photoluminescent measurements. The photocatalytic activity after 8 h of irradiation was around 69%, 74%, 80%, and 88% for Ta2O5 coatings created after 3 min, 5 min, 10 min, and 15 min, respectively.",
publisher = "MDPI",
journal = "Micromachines",
title = "Application of Micro-Arc Discharges during Anodization of Tantalum for Synthesis of Photocatalytic Active Ta2O5 Coatings",
volume = "14",
number = "3",
pages = "701",
doi = "https://doi.org/10.3390/mi14030701"
}

Stojadinović, S., Radić, N.,& Vasilic, R.. (2023). Application of Micro-Arc Discharges during Anodization of Tantalum for Synthesis of Photocatalytic Active Ta2O5 Coatings. in Micromachines
MDPI., 14(3), 701.
https://doi.org/https://doi.org/10.3390/mi14030701

Stojadinović S, Radić N, Vasilic R. Application of Micro-Arc Discharges during Anodization of Tantalum for Synthesis of Photocatalytic Active Ta2O5 Coatings. in Micromachines. 2023;14(3):701.
doi:https://doi.org/10.3390/mi14030701 .

Stojadinović, Stevan, Radić, Nenad, Vasilic, Rastko, "Application of Micro-Arc Discharges during Anodization of Tantalum for Synthesis of Photocatalytic Active Ta2O5 Coatings" in Micromachines, 14, no. 3 (2023):701,
https://doi.org/https://doi.org/10.3390/mi14030701 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Vasilic, Rastko
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6293
AB  - The synthesis of Eu3+-doped MgAl oxide coatings containing MgO and MgAl2O4 was accomplished through plasma electrolytic oxidation of AZ31 magnesium alloy in aluminate electrolyte with the addition of Eu2O3 particles in various concentrations. Their morphological, structural, and above all, photoluminescent (PL) and photocatalytic activity (PA) were thoroughly investigated. PL emission spectra of MgAl oxide coatings feature characteristic emission peaks, which are ascribed to f–f transitions of Eu3+ ions from excited level 5D0 to lower levels 7FJ. The charge transfer state of Eu3+ or direct excitation of the Eu3+ ground state 7F0 into higher levels of the 4f-manifold are both attributed to the PL peaks that appear in the excitation PL spectra of the obtained coatings. The fact that the transition 5D0 → 7F2 (electrical dipole transition) in Eu3+-doped MgAl oxide coatings is considerably stronger than the transition 5D0 → 7F1 (magnetic dipole transition) indicates that Eu3+ ions occupied sites with non-inversion symmetry. Because of oxygen vacancy formation, the Eu3+-doped MgAl oxide coatings had a higher PA in the degradation of methyl orange than the pure MgAl oxide coating. The highest PA was found in Eu3+-doped MgAl oxide coating formed in an aluminate electrolyte with 4 g/L of Eu2O3 particles. The PA, morphology, and phase of Eu3+-doped MgAl oxide coatings did not change after several consecutive runs, indicating outstanding stability of these photocatalysts.
PB  - MDPI
T2  - Coatings
T1  - Photoluminescent and Photocatalytic Properties of Eu3+-Doped MgAl Oxide Coatings Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy
VL  - 12
IS  - 12
SP  - 1830
DO  - 10.3390/coatings12121830
ER  - 

@article{
author = "Stojadinović, Stevan and Radić, Nenad and Vasilic, Rastko",
year = "2022",
abstract = "The synthesis of Eu3+-doped MgAl oxide coatings containing MgO and MgAl2O4 was accomplished through plasma electrolytic oxidation of AZ31 magnesium alloy in aluminate electrolyte with the addition of Eu2O3 particles in various concentrations. Their morphological, structural, and above all, photoluminescent (PL) and photocatalytic activity (PA) were thoroughly investigated. PL emission spectra of MgAl oxide coatings feature characteristic emission peaks, which are ascribed to f–f transitions of Eu3+ ions from excited level 5D0 to lower levels 7FJ. The charge transfer state of Eu3+ or direct excitation of the Eu3+ ground state 7F0 into higher levels of the 4f-manifold are both attributed to the PL peaks that appear in the excitation PL spectra of the obtained coatings. The fact that the transition 5D0 → 7F2 (electrical dipole transition) in Eu3+-doped MgAl oxide coatings is considerably stronger than the transition 5D0 → 7F1 (magnetic dipole transition) indicates that Eu3+ ions occupied sites with non-inversion symmetry. Because of oxygen vacancy formation, the Eu3+-doped MgAl oxide coatings had a higher PA in the degradation of methyl orange than the pure MgAl oxide coating. The highest PA was found in Eu3+-doped MgAl oxide coating formed in an aluminate electrolyte with 4 g/L of Eu2O3 particles. The PA, morphology, and phase of Eu3+-doped MgAl oxide coatings did not change after several consecutive runs, indicating outstanding stability of these photocatalysts.",
publisher = "MDPI",
journal = "Coatings",
title = "Photoluminescent and Photocatalytic Properties of Eu3+-Doped MgAl Oxide Coatings Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy",
volume = "12",
number = "12",
pages = "1830",
doi = "10.3390/coatings12121830"
}

Stojadinović, S., Radić, N.,& Vasilic, R.. (2022). Photoluminescent and Photocatalytic Properties of Eu3+-Doped MgAl Oxide Coatings Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy. in Coatings
MDPI., 12(12), 1830.
https://doi.org/10.3390/coatings12121830

Stojadinović S, Radić N, Vasilic R. Photoluminescent and Photocatalytic Properties of Eu3+-Doped MgAl Oxide Coatings Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy. in Coatings. 2022;12(12):1830.
doi:10.3390/coatings12121830 .

Stojadinović, Stevan, Radić, Nenad, Vasilic, Rastko, "Photoluminescent and Photocatalytic Properties of Eu3+-Doped MgAl Oxide Coatings Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy" in Coatings, 12, no. 12 (2022):1830,
https://doi.org/10.3390/coatings12121830 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Vasilic, Rastko
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6292
AB  - MgAl and MgAl/ZnO coatings were prepared by plasma electrolytic oxidation (PEO) of AZ31 magnesium alloy in aluminate electrolyte (5 g/L NaAlO2) without and with addition of ZnO particles in various concentrations. The MgAl coating was partially crystallized and contained MgO and MgAl2O4 phases. The addition of ZnO particles to aluminate electrolyte had no significant effect on the surface morphology of formed coatings, while the Zn content increased with ZnO particle concentrations. X-ray diffraction confirmed the incorporation of ZnO particles in the coatings. The photodegradation of methyl orange (10 cm3 of 8 mg/L) was used to measure the photocatalytic activity (PA) of MgAl and MgAl/ZnO coatings. The PA of MgAl coating after 8 h of irradiation was around 58%, while the PA of MgAl/ZnO coatings formed in aluminate electrolyte with the addition of ZnO particles in concentrations of 4 g/L, 8 g/L, and 12 g/L were around 69%, 86%, and 97%, respectively.
PB  - MDPI
T2  - Catalysts
T1  - ZnO Particles Modified MgAl Coatings with Improved Photocatalytic Activity Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy in Aluminate Electrolyte
VL  - 12
IS  - 12
SP  - 1503
DO  - 10.3390/catal12121503
ER  - 

@article{
author = "Stojadinović, Stevan and Radić, Nenad and Vasilic, Rastko",
year = "2022",
abstract = "MgAl and MgAl/ZnO coatings were prepared by plasma electrolytic oxidation (PEO) of AZ31 magnesium alloy in aluminate electrolyte (5 g/L NaAlO2) without and with addition of ZnO particles in various concentrations. The MgAl coating was partially crystallized and contained MgO and MgAl2O4 phases. The addition of ZnO particles to aluminate electrolyte had no significant effect on the surface morphology of formed coatings, while the Zn content increased with ZnO particle concentrations. X-ray diffraction confirmed the incorporation of ZnO particles in the coatings. The photodegradation of methyl orange (10 cm3 of 8 mg/L) was used to measure the photocatalytic activity (PA) of MgAl and MgAl/ZnO coatings. The PA of MgAl coating after 8 h of irradiation was around 58%, while the PA of MgAl/ZnO coatings formed in aluminate electrolyte with the addition of ZnO particles in concentrations of 4 g/L, 8 g/L, and 12 g/L were around 69%, 86%, and 97%, respectively.",
publisher = "MDPI",
journal = "Catalysts",
title = "ZnO Particles Modified MgAl Coatings with Improved Photocatalytic Activity Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy in Aluminate Electrolyte",
volume = "12",
number = "12",
pages = "1503",
doi = "10.3390/catal12121503"
}

Stojadinović, S., Radić, N.,& Vasilic, R.. (2022). ZnO Particles Modified MgAl Coatings with Improved Photocatalytic Activity Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy in Aluminate Electrolyte. in Catalysts
MDPI., 12(12), 1503.
https://doi.org/10.3390/catal12121503

Stojadinović S, Radić N, Vasilic R. ZnO Particles Modified MgAl Coatings with Improved Photocatalytic Activity Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy in Aluminate Electrolyte. in Catalysts. 2022;12(12):1503.
doi:10.3390/catal12121503 .

Stojadinović, Stevan, Radić, Nenad, Vasilic, Rastko, "ZnO Particles Modified MgAl Coatings with Improved Photocatalytic Activity Formed by Plasma Electrolytic Oxidation of AZ31 Magnesium Alloy in Aluminate Electrolyte" in Catalysts, 12, no. 12 (2022):1503,
https://doi.org/10.3390/catal12121503 . .

TY  - JOUR
AU  - Mladenović, Ivana
AU  - Lamovec, Jelena
AU  - Vasiljević-Radović, Dana
AU  - Vasilić, Rastko
AU  - Radojević, Vesna
AU  - Nikolić, Nebojša D.
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4840
AB  - The influence of various electrolysis parameters, such as the type of cathode, composition of the electrolyte and electrolysis time, on the morphology, structure and hardness of copper coatings has been investigated. Morphology and structure of the coatings were analyzed by scanning electron microscope (SEM), atomic force microscope (AFM) and X-ray diffraction (XRD), while coating hardness was examined by Vickers microindentation test applying the Chicot–Lesage (C–L) composite hardness model. Depending on the conditions of electrolysis, two types of Cu coatings were obtained: fine-grained mat coatings with a strong (220) preferred orientation from the sulfate electrolyte and smooth mirror bright coatings with a strong (200) preferred orientation from the electrolyte with added leveling/brightening additives. The mat coatings showed larger both measured composite and calculated coating hardness than the mirror bright coatings, that can be explained by the phenomena on boundary among grains. Independent of electrolysis conditions, the critical relative indentation depth (RID) of 0.14 was established for all types of the Cu coatings, separating the zone in which the composite hardness can be equaled with the coating hardness and the zone requiring an application of the C–L model for a determination of the absolute hardness of the Cu coatings.
PB  - MDPI
T2  - Metals
T1  - Implementation of the Chicot–Lesage Composite Hardness Model in a Determination of Absolute Hardness of Copper Coatings Obtained by the Electrodeposition Processes
VL  - 11
IS  - 11
SP  - 1807
DO  - 10.3390/met11111807
ER  - 

@article{
author = "Mladenović, Ivana and Lamovec, Jelena and Vasiljević-Radović, Dana and Vasilić, Rastko and Radojević, Vesna and Nikolić, Nebojša D.",
year = "2021",
abstract = "The influence of various electrolysis parameters, such as the type of cathode, composition of the electrolyte and electrolysis time, on the morphology, structure and hardness of copper coatings has been investigated. Morphology and structure of the coatings were analyzed by scanning electron microscope (SEM), atomic force microscope (AFM) and X-ray diffraction (XRD), while coating hardness was examined by Vickers microindentation test applying the Chicot–Lesage (C–L) composite hardness model. Depending on the conditions of electrolysis, two types of Cu coatings were obtained: fine-grained mat coatings with a strong (220) preferred orientation from the sulfate electrolyte and smooth mirror bright coatings with a strong (200) preferred orientation from the electrolyte with added leveling/brightening additives. The mat coatings showed larger both measured composite and calculated coating hardness than the mirror bright coatings, that can be explained by the phenomena on boundary among grains. Independent of electrolysis conditions, the critical relative indentation depth (RID) of 0.14 was established for all types of the Cu coatings, separating the zone in which the composite hardness can be equaled with the coating hardness and the zone requiring an application of the C–L model for a determination of the absolute hardness of the Cu coatings.",
publisher = "MDPI",
journal = "Metals",
title = "Implementation of the Chicot–Lesage Composite Hardness Model in a Determination of Absolute Hardness of Copper Coatings Obtained by the Electrodeposition Processes",
volume = "11",
number = "11",
pages = "1807",
doi = "10.3390/met11111807"
}

Mladenović, I., Lamovec, J., Vasiljević-Radović, D., Vasilić, R., Radojević, V.,& Nikolić, N. D.. (2021). Implementation of the Chicot–Lesage Composite Hardness Model in a Determination of Absolute Hardness of Copper Coatings Obtained by the Electrodeposition Processes. in Metals
MDPI., 11(11), 1807.
https://doi.org/10.3390/met11111807

Mladenović I, Lamovec J, Vasiljević-Radović D, Vasilić R, Radojević V, Nikolić ND. Implementation of the Chicot–Lesage Composite Hardness Model in a Determination of Absolute Hardness of Copper Coatings Obtained by the Electrodeposition Processes. in Metals. 2021;11(11):1807.
doi:10.3390/met11111807 .

Mladenović, Ivana, Lamovec, Jelena, Vasiljević-Radović, Dana, Vasilić, Rastko, Radojević, Vesna, Nikolić, Nebojša D., "Implementation of the Chicot–Lesage Composite Hardness Model in a Determination of Absolute Hardness of Copper Coatings Obtained by the Electrodeposition Processes" in Metals, 11, no. 11 (2021):1807,
https://doi.org/10.3390/met11111807 . .

TY  - JOUR
AU  - Mladenović, Ivana
AU  - Lamovec, Jelena
AU  - Vasiljević-Radović, Dana
AU  - Vasilić, Rastko
AU  - Radojević, Vesna
AU  - Nikolić, Nebojša D.
PY  - 2020
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3518
AB  - Copper electrodeposition on (111)-oriented Si substrate was performed by the pulsating current (PC) regime at various average current densities in the range of 15–70 mA·cm−2, obtained by varying either the frequency (30, 50, 80 and 100 Hz for the current density amplitude of 100 mA·cm−2) or the current density amplitude (120 and 140 mA·cm−2 at 100 Hz). The produced Cu coatings were examined by SEM, AFM and XRD techniques. The morphology of the coatings changed from those with large grains to fine-grained and globular, while the crystal structure changed from the strong (220) to the strong (111) preferred orientation by increasing the average current density. The mechanical characteristics of coatings were examined using Vickers micro-indentation tests, applying the Chicot–Lesage (C–L) composite hardness model for the analysis of microhardness. The maximum microhardness was obtained for the Cu coating produced at an average current density of 50 mA·cm−2, with a current density amplitude of 100 mA·cm−2 and a frequency of 100 Hz. This copper coating was fine-grained and showed the smallest roughness in relation to the other coatings, and it was obtained in the mixed activation–diffusion control between the end of the effect of the activation control and the beginning of the dominant effect of diffusion control.
PB  - MDPI
T2  - Metals
T1  - Morphology, Structure and Mechanical Properties of Copper Coatings Electrodeposited by Pulsating Current (PC) Regime on Si(111)
VL  - 10
IS  - 4
SP  - 488
DO  - 10.3390/met10040488
ER  - 

@article{
author = "Mladenović, Ivana and Lamovec, Jelena and Vasiljević-Radović, Dana and Vasilić, Rastko and Radojević, Vesna and Nikolić, Nebojša D.",
year = "2020",
abstract = "Copper electrodeposition on (111)-oriented Si substrate was performed by the pulsating current (PC) regime at various average current densities in the range of 15–70 mA·cm−2, obtained by varying either the frequency (30, 50, 80 and 100 Hz for the current density amplitude of 100 mA·cm−2) or the current density amplitude (120 and 140 mA·cm−2 at 100 Hz). The produced Cu coatings were examined by SEM, AFM and XRD techniques. The morphology of the coatings changed from those with large grains to fine-grained and globular, while the crystal structure changed from the strong (220) to the strong (111) preferred orientation by increasing the average current density. The mechanical characteristics of coatings were examined using Vickers micro-indentation tests, applying the Chicot–Lesage (C–L) composite hardness model for the analysis of microhardness. The maximum microhardness was obtained for the Cu coating produced at an average current density of 50 mA·cm−2, with a current density amplitude of 100 mA·cm−2 and a frequency of 100 Hz. This copper coating was fine-grained and showed the smallest roughness in relation to the other coatings, and it was obtained in the mixed activation–diffusion control between the end of the effect of the activation control and the beginning of the dominant effect of diffusion control.",
publisher = "MDPI",
journal = "Metals",
title = "Morphology, Structure and Mechanical Properties of Copper Coatings Electrodeposited by Pulsating Current (PC) Regime on Si(111)",
volume = "10",
number = "4",
pages = "488",
doi = "10.3390/met10040488"
}

Mladenović, I., Lamovec, J., Vasiljević-Radović, D., Vasilić, R., Radojević, V.,& Nikolić, N. D.. (2020). Morphology, Structure and Mechanical Properties of Copper Coatings Electrodeposited by Pulsating Current (PC) Regime on Si(111). in Metals
MDPI., 10(4), 488.
https://doi.org/10.3390/met10040488

Mladenović I, Lamovec J, Vasiljević-Radović D, Vasilić R, Radojević V, Nikolić ND. Morphology, Structure and Mechanical Properties of Copper Coatings Electrodeposited by Pulsating Current (PC) Regime on Si(111). in Metals. 2020;10(4):488.
doi:10.3390/met10040488 .

Mladenović, Ivana, Lamovec, Jelena, Vasiljević-Radović, Dana, Vasilić, Rastko, Radojević, Vesna, Nikolić, Nebojša D., "Morphology, Structure and Mechanical Properties of Copper Coatings Electrodeposited by Pulsating Current (PC) Regime on Si(111)" in Metals, 10, no. 4 (2020):488,
https://doi.org/10.3390/met10040488 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Tadić, Nenad
AU  - Vasilić, Rastko
AU  - Grbić, Boško
PY  - 2020
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/3761
AB  - This paper presents a new method for improvement of ultraviolet light driven photocatalytic activity of ZnO by immobilizing ZnO particles into Al2O3:Ce3+ coatings which emit intense radiation in the near ultraviolet region when excited by middle ultraviolet radiation. When Al2O3:Ce3+/ZnO coatings are illuminated by ultraviolet light in photocatalytic reactor, emitted ultraviolet radiation originating from Ce3+ ions synergistically participates in photocatalytic reactions on ZnO. Al2O3:Ce3+/ZnO coatings were formed by plasma electrolytic oxidation of
aluminum in electrolyte containing 2 g/L of ZnO particles and up to 8 g/L of CeO2 particles. Structural, optical, photoluminescent, and photocatalytic properties of formed surface coatings were examined. All formed coatings feature virtually the same thickness, morphology, phase composition, and absorption properties. Concentration of incorporated Ce3+ ions into Al2O3 host and concentration of immobilized ZnO particles are the only parameters by which the coatings differ from each other resulting in difference in photocatalytic activity. Al2O3:Ce3+/ZnO coatings show better photodegradation of methyl orange with respect to Al2O3/ZnO coatings. The best photocatalytic activity is observed for the coating formed in electrolyte containing 4 g/L of CeO2 particles.
PB  - Elsevier
T2  - Optical Materials
T1  - Enhanced ultraviolet light driven photocatalytic activity of ZnO particles incorporated by plasma electrolytic oxidation into Al2O3 coatings co-doped with Ce3+
VL  - 101
SP  - 109768
DO  - 10.1016/j.optmat.2020.109768
ER  - 

@article{
author = "Stojadinović, Stevan and Radić, Nenad and Tadić, Nenad and Vasilić, Rastko and Grbić, Boško",
year = "2020",
abstract = "This paper presents a new method for improvement of ultraviolet light driven photocatalytic activity of ZnO by immobilizing ZnO particles into Al2O3:Ce3+ coatings which emit intense radiation in the near ultraviolet region when excited by middle ultraviolet radiation. When Al2O3:Ce3+/ZnO coatings are illuminated by ultraviolet light in photocatalytic reactor, emitted ultraviolet radiation originating from Ce3+ ions synergistically participates in photocatalytic reactions on ZnO. Al2O3:Ce3+/ZnO coatings were formed by plasma electrolytic oxidation of
aluminum in electrolyte containing 2 g/L of ZnO particles and up to 8 g/L of CeO2 particles. Structural, optical, photoluminescent, and photocatalytic properties of formed surface coatings were examined. All formed coatings feature virtually the same thickness, morphology, phase composition, and absorption properties. Concentration of incorporated Ce3+ ions into Al2O3 host and concentration of immobilized ZnO particles are the only parameters by which the coatings differ from each other resulting in difference in photocatalytic activity. Al2O3:Ce3+/ZnO coatings show better photodegradation of methyl orange with respect to Al2O3/ZnO coatings. The best photocatalytic activity is observed for the coating formed in electrolyte containing 4 g/L of CeO2 particles.",
publisher = "Elsevier",
journal = "Optical Materials",
title = "Enhanced ultraviolet light driven photocatalytic activity of ZnO particles incorporated by plasma electrolytic oxidation into Al2O3 coatings co-doped with Ce3+",
volume = "101",
pages = "109768",
doi = "10.1016/j.optmat.2020.109768"
}

Stojadinović, S., Radić, N., Tadić, N., Vasilić, R.,& Grbić, B.. (2020). Enhanced ultraviolet light driven photocatalytic activity of ZnO particles incorporated by plasma electrolytic oxidation into Al2O3 coatings co-doped with Ce3+. in Optical Materials
Elsevier., 101, 109768.
https://doi.org/10.1016/j.optmat.2020.109768

Stojadinović S, Radić N, Tadić N, Vasilić R, Grbić B. Enhanced ultraviolet light driven photocatalytic activity of ZnO particles incorporated by plasma electrolytic oxidation into Al2O3 coatings co-doped with Ce3+. in Optical Materials. 2020;101:109768.
doi:10.1016/j.optmat.2020.109768 .

Stojadinović, Stevan, Radić, Nenad, Tadić, Nenad, Vasilić, Rastko, Grbić, Boško, "Enhanced ultraviolet light driven photocatalytic activity of ZnO particles incorporated by plasma electrolytic oxidation into Al2O3 coatings co-doped with Ce3+" in Optical Materials, 101 (2020):109768,
https://doi.org/10.1016/j.optmat.2020.109768 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Tadić, Nenad
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2292
AB  - Tb doped TiO2 coatings are formed by plasma electrolytic oxidation (PEO) of titanium in water solution of 10 g/L Na3PO4.12H(2)O with addition of Tb4O7 powder. Surface morphology, chemical, and phase composition of obtained PEO coatings are investigated utilizing scanning electron microscopy equipped with energy dispersive x-ray spectroscopy and X-ray diffraction. Uniformly distributed Ti, O, P, and Tb are identified as the main constituents of the coatings. Diffraction patterns of obtained coatings show well pronounced reflections inherent to anatase phase of TiO2. Performed photoluminescence measurements indicate that incorporated Tb is in trivalent oxidation state. Photoluminescence emission spectra feature two overlapping regions: the first region is related to band of TiO2 host and the second region which features several emission bands is ascribed to f-f transitions of Tb3+ from excited level D-5(4) to lower levels F-7(J) (J = 3,4,5, and 6). The photocatalytic activity (PA) of Tb3+ doped TiO2 coatings is probed by measuring the photodegradation of methyl orange under simulated sunlight conditions, suggesting that the main factor affecting PA is concentration of Tb3+ ions incorporated into coatings. Tb3+ doped TiO2 coatings formed for short time have better PA than pure TiO2 coatings formed under the same conditions; the highest PA is observed for the coating formed after 1 min of PEO process. Presence of Tb3+ ions into TiO2 coatings in small concentration improves PA through effective suppression of electron/hole recombination.
PB  - Elsevier
T2  - Surface and Coatings Technology
T1  - Effect of Tb3+ doping on the photocatalytic activity of TiO2 coatings formed by plasma electrolytic oxidation of titanium
VL  - 337
SP  - 279
EP  - 289
DO  - 10.1016/j.surfcoat.2018.01.033
ER  - 

@article{
author = "Stojadinović, Stevan and Tadić, Nenad and Radić, Nenad and Grbić, Boško and Vasilić, Rastko",
year = "2018",
abstract = "Tb doped TiO2 coatings are formed by plasma electrolytic oxidation (PEO) of titanium in water solution of 10 g/L Na3PO4.12H(2)O with addition of Tb4O7 powder. Surface morphology, chemical, and phase composition of obtained PEO coatings are investigated utilizing scanning electron microscopy equipped with energy dispersive x-ray spectroscopy and X-ray diffraction. Uniformly distributed Ti, O, P, and Tb are identified as the main constituents of the coatings. Diffraction patterns of obtained coatings show well pronounced reflections inherent to anatase phase of TiO2. Performed photoluminescence measurements indicate that incorporated Tb is in trivalent oxidation state. Photoluminescence emission spectra feature two overlapping regions: the first region is related to band of TiO2 host and the second region which features several emission bands is ascribed to f-f transitions of Tb3+ from excited level D-5(4) to lower levels F-7(J) (J = 3,4,5, and 6). The photocatalytic activity (PA) of Tb3+ doped TiO2 coatings is probed by measuring the photodegradation of methyl orange under simulated sunlight conditions, suggesting that the main factor affecting PA is concentration of Tb3+ ions incorporated into coatings. Tb3+ doped TiO2 coatings formed for short time have better PA than pure TiO2 coatings formed under the same conditions; the highest PA is observed for the coating formed after 1 min of PEO process. Presence of Tb3+ ions into TiO2 coatings in small concentration improves PA through effective suppression of electron/hole recombination.",
publisher = "Elsevier",
journal = "Surface and Coatings Technology",
title = "Effect of Tb3+ doping on the photocatalytic activity of TiO2 coatings formed by plasma electrolytic oxidation of titanium",
volume = "337",
pages = "279-289",
doi = "10.1016/j.surfcoat.2018.01.033"
}

Stojadinović, S., Tadić, N., Radić, N., Grbić, B.,& Vasilić, R.. (2018). Effect of Tb3+ doping on the photocatalytic activity of TiO2 coatings formed by plasma electrolytic oxidation of titanium. in Surface and Coatings Technology
Elsevier., 337, 279-289.
https://doi.org/10.1016/j.surfcoat.2018.01.033

Stojadinović S, Tadić N, Radić N, Grbić B, Vasilić R. Effect of Tb3+ doping on the photocatalytic activity of TiO2 coatings formed by plasma electrolytic oxidation of titanium. in Surface and Coatings Technology. 2018;337:279-289.
doi:10.1016/j.surfcoat.2018.01.033 .

Stojadinović, Stevan, Tadić, Nenad, Radić, Nenad, Grbić, Boško, Vasilić, Rastko, "Effect of Tb3+ doping on the photocatalytic activity of TiO2 coatings formed by plasma electrolytic oxidation of titanium" in Surface and Coatings Technology, 337 (2018):279-289,
https://doi.org/10.1016/j.surfcoat.2018.01.033 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Tadić, Nenad
AU  - Vasilić, Rastko
AU  - Stefanov, Plamen
AU  - Grbić, Boško
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2307
AB  - This paper presents the results of our recent investigation focused on the preparation and possible photocatalytic application of iron doped TiO2 coatings formed by plasma electrolytic oxidation of high purity titanium in electrolyte containing FeSO4. The morphology, phase and elemental composition, and absorption band of the coatings were characterized by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and diffuse reflectance spectroscopy. The photocatalytic activity of coatings was evaluated by measuring the degradation of methyl orange under simulated sunlight conditions. It was found that the addition of iron precursor to electrolyte solution improves the photocatalytic properties of obtained coatings with respect to pure TiO2 coating. The incorporation of iron in TiO2 lattice was identified as the main factor affecting the increase of photocatalytic activity. The highest photocatalytic activity was observed when coatings were processed for 2 min with addition of 1 g/L FeSO4 to electrolyte.
PB  - Springer, Dordrecht
T2  - Journal of Materials Science-Materials in Electronics
T1  - Influence of iron doping on photocatalytic activity of TiO2 coatings formed on titanium by plasma electrolytic oxidation
VL  - 29
IS  - 11
SP  - 9427
EP  - 9434
DO  - 10.1007/s10854-018-8975-6
ER  - 

@article{
author = "Stojadinović, Stevan and Radić, Nenad and Tadić, Nenad and Vasilić, Rastko and Stefanov, Plamen and Grbić, Boško",
year = "2018",
abstract = "This paper presents the results of our recent investigation focused on the preparation and possible photocatalytic application of iron doped TiO2 coatings formed by plasma electrolytic oxidation of high purity titanium in electrolyte containing FeSO4. The morphology, phase and elemental composition, and absorption band of the coatings were characterized by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and diffuse reflectance spectroscopy. The photocatalytic activity of coatings was evaluated by measuring the degradation of methyl orange under simulated sunlight conditions. It was found that the addition of iron precursor to electrolyte solution improves the photocatalytic properties of obtained coatings with respect to pure TiO2 coating. The incorporation of iron in TiO2 lattice was identified as the main factor affecting the increase of photocatalytic activity. The highest photocatalytic activity was observed when coatings were processed for 2 min with addition of 1 g/L FeSO4 to electrolyte.",
publisher = "Springer, Dordrecht",
journal = "Journal of Materials Science-Materials in Electronics",
title = "Influence of iron doping on photocatalytic activity of TiO2 coatings formed on titanium by plasma electrolytic oxidation",
volume = "29",
number = "11",
pages = "9427-9434",
doi = "10.1007/s10854-018-8975-6"
}

Stojadinović, S., Radić, N., Tadić, N., Vasilić, R., Stefanov, P.,& Grbić, B.. (2018). Influence of iron doping on photocatalytic activity of TiO2 coatings formed on titanium by plasma electrolytic oxidation. in Journal of Materials Science-Materials in Electronics
Springer, Dordrecht., 29(11), 9427-9434.
https://doi.org/10.1007/s10854-018-8975-6

Stojadinović S, Radić N, Tadić N, Vasilić R, Stefanov P, Grbić B. Influence of iron doping on photocatalytic activity of TiO2 coatings formed on titanium by plasma electrolytic oxidation. in Journal of Materials Science-Materials in Electronics. 2018;29(11):9427-9434.
doi:10.1007/s10854-018-8975-6 .

Stojadinović, Stevan, Radić, Nenad, Tadić, Nenad, Vasilić, Rastko, Stefanov, Plamen, Grbić, Boško, "Influence of iron doping on photocatalytic activity of TiO2 coatings formed on titanium by plasma electrolytic oxidation" in Journal of Materials Science-Materials in Electronics, 29, no. 11 (2018):9427-9434,
https://doi.org/10.1007/s10854-018-8975-6 . .

TY  - JOUR
AU  - Petrović, Srđan
AU  - Rožić, Ljiljana
AU  - Stojadinović, Stevan
AU  - Grbić, Boško
AU  - Vasilić, Rastko
AU  - Vuković, Zorica
AU  - Radić, Nenad
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2349
AB  - In this study, WO3 doped TiO2 powders were synthesized via sol-gel method combined with a hydrothermal process. The effect of sintering temperature on mesoporous structure and catalytic activities of these powders were investigated. The physical analysis via X-ray diffraction indicates that prepared samples are a mixture of anatase and rutile TiO2 phases. X-ray peak analysis is used to evaluate the crystallite size and lattice strain by the Williamson-Hall analysis. Considering all the reflections of the anatase phase the lattice strain ranging from c = 9.505 to c = 9.548 is calculated, suggesting that microstrain decreases when calcination temperature increases. N-2 adsorption-desorption analysis shows that the surface area and pore volume decrease with increasing temperature and that WOx-TiO2 powders primarily consist of mesopores. Sintering temperature induced a change in textural properties causing a systematic shift towards larger mesopores. Simultaneously, photoactivity in decolorization of methyl orange increases with increasing calcination temperature up to 700 degrees C, followed by significant decrease with its further increase.
PB  - International Institute for the Science of Sintering, Beograd
T2  - Science of Sintering
T1  - The Effect of Sintering Temperature on Mesoporous Structure of WO3 Doped Tio(2) Powders
VL  - 50
IS  - 1
SP  - 123
EP  - 132
DO  - 10.2298/SOS1801123P
ER  - 

@article{
author = "Petrović, Srđan and Rožić, Ljiljana and Stojadinović, Stevan and Grbić, Boško and Vasilić, Rastko and Vuković, Zorica and Radić, Nenad",
year = "2018",
abstract = "In this study, WO3 doped TiO2 powders were synthesized via sol-gel method combined with a hydrothermal process. The effect of sintering temperature on mesoporous structure and catalytic activities of these powders were investigated. The physical analysis via X-ray diffraction indicates that prepared samples are a mixture of anatase and rutile TiO2 phases. X-ray peak analysis is used to evaluate the crystallite size and lattice strain by the Williamson-Hall analysis. Considering all the reflections of the anatase phase the lattice strain ranging from c = 9.505 to c = 9.548 is calculated, suggesting that microstrain decreases when calcination temperature increases. N-2 adsorption-desorption analysis shows that the surface area and pore volume decrease with increasing temperature and that WOx-TiO2 powders primarily consist of mesopores. Sintering temperature induced a change in textural properties causing a systematic shift towards larger mesopores. Simultaneously, photoactivity in decolorization of methyl orange increases with increasing calcination temperature up to 700 degrees C, followed by significant decrease with its further increase.",
publisher = "International Institute for the Science of Sintering, Beograd",
journal = "Science of Sintering",
title = "The Effect of Sintering Temperature on Mesoporous Structure of WO3 Doped Tio(2) Powders",
volume = "50",
number = "1",
pages = "123-132",
doi = "10.2298/SOS1801123P"
}

Petrović, S., Rožić, L., Stojadinović, S., Grbić, B., Vasilić, R., Vuković, Z.,& Radić, N.. (2018). The Effect of Sintering Temperature on Mesoporous Structure of WO3 Doped Tio(2) Powders. in Science of Sintering
International Institute for the Science of Sintering, Beograd., 50(1), 123-132.
https://doi.org/10.2298/SOS1801123P

Petrović S, Rožić L, Stojadinović S, Grbić B, Vasilić R, Vuković Z, Radić N. The Effect of Sintering Temperature on Mesoporous Structure of WO3 Doped Tio(2) Powders. in Science of Sintering. 2018;50(1):123-132.
doi:10.2298/SOS1801123P .

Petrović, Srđan, Rožić, Ljiljana, Stojadinović, Stevan, Grbić, Boško, Vasilić, Rastko, Vuković, Zorica, Radić, Nenad, "The Effect of Sintering Temperature on Mesoporous Structure of WO3 Doped Tio(2) Powders" in Science of Sintering, 50, no. 1 (2018):123-132,
https://doi.org/10.2298/SOS1801123P . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Tadić, Nenad
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2445
AB  - CdS particles modified anatase TiO2 photocatalysts were formed on titanium substrate by plasma electrolytic oxidation for 2 min in supporting electrolyte (10 g/L Na-3 center dot PO4 center dot 12H(2)O) with addition of CdS particles in concentrations up to 8 g/L. Content of CdS particles incorporated into TiO2 coatings depends of CdS particles concentration in supporting electrolyte, while surface morphology, phase structure and absorption properties of formed coatings were not significantly influenced by the addition of CdS particles. In contrast to pure TiO2 coatings, TiO2/CdS coatings exhibit enhanced photocatalytic activity (PA) in the degradation of methyl orange, used as a model organic pollutant, under simulated solar irradiation. The highest PA was observed for TiO2/CdS coating formed in supporting electrolyte with addition of 0.4 g/L of CdS particles. Photoluminescence measurements indicate that enhanced PA is related to the reduction of the recombination rate of photogenerated electron/hole pairs as a result of TiO2 and CdS coupling.
PB  - Elsevier
T2  - Surface and Coatings Technology
T1  - CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity
VL  - 344
SP  - 528
EP  - 533
DO  - 10.1016/j.surfcoat.2018.03.080
ER  - 

@article{
author = "Stojadinović, Stevan and Tadić, Nenad and Radić, Nenad and Grbić, Boško and Vasilić, Rastko",
year = "2018",
abstract = "CdS particles modified anatase TiO2 photocatalysts were formed on titanium substrate by plasma electrolytic oxidation for 2 min in supporting electrolyte (10 g/L Na-3 center dot PO4 center dot 12H(2)O) with addition of CdS particles in concentrations up to 8 g/L. Content of CdS particles incorporated into TiO2 coatings depends of CdS particles concentration in supporting electrolyte, while surface morphology, phase structure and absorption properties of formed coatings were not significantly influenced by the addition of CdS particles. In contrast to pure TiO2 coatings, TiO2/CdS coatings exhibit enhanced photocatalytic activity (PA) in the degradation of methyl orange, used as a model organic pollutant, under simulated solar irradiation. The highest PA was observed for TiO2/CdS coating formed in supporting electrolyte with addition of 0.4 g/L of CdS particles. Photoluminescence measurements indicate that enhanced PA is related to the reduction of the recombination rate of photogenerated electron/hole pairs as a result of TiO2 and CdS coupling.",
publisher = "Elsevier",
journal = "Surface and Coatings Technology",
title = "CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity",
volume = "344",
pages = "528-533",
doi = "10.1016/j.surfcoat.2018.03.080"
}

Stojadinović, S., Tadić, N., Radić, N., Grbić, B.,& Vasilić, R.. (2018). CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity. in Surface and Coatings Technology
Elsevier., 344, 528-533.
https://doi.org/10.1016/j.surfcoat.2018.03.080

Stojadinović S, Tadić N, Radić N, Grbić B, Vasilić R. CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity. in Surface and Coatings Technology. 2018;344:528-533.
doi:10.1016/j.surfcoat.2018.03.080 .

Stojadinović, Stevan, Tadić, Nenad, Radić, Nenad, Grbić, Boško, Vasilić, Rastko, "CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity" in Surface and Coatings Technology, 344 (2018):528-533,
https://doi.org/10.1016/j.surfcoat.2018.03.080 . .

TY  - JOUR
AU  - Petrović, Srđan
AU  - Rožić, Ljiljana
AU  - Jović, Vesna
AU  - Stojadinović, Stevan
AU  - Grbić, Boško
AU  - Radić, Nenad
AU  - Lamovec, Jelena
AU  - Vasilić, Rastko
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2454
AB  - Nanocrystalline TiO2-CeO2 powders were synthesized from their TiO2 and CeO2 oxides using mechanical ball milling process. The response surface method is applied to identify optimal parameters for the synthesis of TiO2-CeO2 photocatalyst. Analysis of variance and main effect plot are used to determine the significant parameters and set the optimal level for each parameter. Regression analysis showed good agreement of experimental data with the second-order polynomial model with a coefficients of determination: R-2 = 0.991, R-Adj(2). = 0.940 and R-Pred(2). = 0.983. Under optimal experimental conditions of TiO2:CeO2 weight percentage ratio 71: 29, milling speed 200 rpm, and milling time 115 min the highest photodegradation efficiency was achieved. On the basis of the above statistical analysis, it was found that the band gap energy of TiO2-CeO2 nanoparticles decreases with the increase of the milling speed and milling time with constant TiO2:CeO2 weight percentage ratio. Obtained results suggest that mechanical ball milling process is a rapid, efficient and low energy consumption method to synthesize TiO2-CeO2 photocatalyst.
PB  - Elsevier
T2  - Advanced Powder Technology
T1  - Optimization of a nanoparticle ball milling process parameters using the response surface method
VL  - 29
IS  - 9
SP  - 2129
EP  - 2139
DO  - 10.1016/j.apt.2018.05.021
ER  - 

@article{
author = "Petrović, Srđan and Rožić, Ljiljana and Jović, Vesna and Stojadinović, Stevan and Grbić, Boško and Radić, Nenad and Lamovec, Jelena and Vasilić, Rastko",
year = "2018",
abstract = "Nanocrystalline TiO2-CeO2 powders were synthesized from their TiO2 and CeO2 oxides using mechanical ball milling process. The response surface method is applied to identify optimal parameters for the synthesis of TiO2-CeO2 photocatalyst. Analysis of variance and main effect plot are used to determine the significant parameters and set the optimal level for each parameter. Regression analysis showed good agreement of experimental data with the second-order polynomial model with a coefficients of determination: R-2 = 0.991, R-Adj(2). = 0.940 and R-Pred(2). = 0.983. Under optimal experimental conditions of TiO2:CeO2 weight percentage ratio 71: 29, milling speed 200 rpm, and milling time 115 min the highest photodegradation efficiency was achieved. On the basis of the above statistical analysis, it was found that the band gap energy of TiO2-CeO2 nanoparticles decreases with the increase of the milling speed and milling time with constant TiO2:CeO2 weight percentage ratio. Obtained results suggest that mechanical ball milling process is a rapid, efficient and low energy consumption method to synthesize TiO2-CeO2 photocatalyst.",
publisher = "Elsevier",
journal = "Advanced Powder Technology",
title = "Optimization of a nanoparticle ball milling process parameters using the response surface method",
volume = "29",
number = "9",
pages = "2129-2139",
doi = "10.1016/j.apt.2018.05.021"
}

Petrović, S., Rožić, L., Jović, V., Stojadinović, S., Grbić, B., Radić, N., Lamovec, J.,& Vasilić, R.. (2018). Optimization of a nanoparticle ball milling process parameters using the response surface method. in Advanced Powder Technology
Elsevier., 29(9), 2129-2139.
https://doi.org/10.1016/j.apt.2018.05.021

Petrović S, Rožić L, Jović V, Stojadinović S, Grbić B, Radić N, Lamovec J, Vasilić R. Optimization of a nanoparticle ball milling process parameters using the response surface method. in Advanced Powder Technology. 2018;29(9):2129-2139.
doi:10.1016/j.apt.2018.05.021 .

Petrović, Srđan, Rožić, Ljiljana, Jović, Vesna, Stojadinović, Stevan, Grbić, Boško, Radić, Nenad, Lamovec, Jelena, Vasilić, Rastko, "Optimization of a nanoparticle ball milling process parameters using the response surface method" in Advanced Powder Technology, 29, no. 9 (2018):2129-2139,
https://doi.org/10.1016/j.apt.2018.05.021 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Tadić, Nenad
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2018
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4292
AB  - CdS particles modified anatase TiO2 photocatalysts were formed on titanium substrate by plasma electrolytic oxidation for 2 min in supporting electrolyte (10 g/L Na-3 center dot PO4 center dot 12H(2)O) with addition of CdS particles in concentrations up to 8 g/L. Content of CdS particles incorporated into TiO2 coatings depends of CdS particles concentration in supporting electrolyte, while surface morphology, phase structure and absorption properties of formed coatings were not significantly influenced by the addition of CdS particles. In contrast to pure TiO2 coatings, TiO2/CdS coatings exhibit enhanced photocatalytic activity (PA) in the degradation of methyl orange, used as a model organic pollutant, under simulated solar irradiation. The highest PA was observed for TiO2/CdS coating formed in supporting electrolyte with addition of 0.4 g/L of CdS particles. Photoluminescence measurements indicate that enhanced PA is related to the reduction of the recombination rate of photogenerated electron/hole pairs as a result of TiO2 and CdS coupling.
PB  - Elsevier
T2  - Surface and Coatings Technology
T1  - CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity
VL  - 344
SP  - 528
EP  - 533
DO  - 10.1016/j.surfcoat.2018.03.080
ER  - 

@article{
author = "Stojadinović, Stevan and Tadić, Nenad and Radić, Nenad and Grbić, Boško and Vasilić, Rastko",
year = "2018",
abstract = "CdS particles modified anatase TiO2 photocatalysts were formed on titanium substrate by plasma electrolytic oxidation for 2 min in supporting electrolyte (10 g/L Na-3 center dot PO4 center dot 12H(2)O) with addition of CdS particles in concentrations up to 8 g/L. Content of CdS particles incorporated into TiO2 coatings depends of CdS particles concentration in supporting electrolyte, while surface morphology, phase structure and absorption properties of formed coatings were not significantly influenced by the addition of CdS particles. In contrast to pure TiO2 coatings, TiO2/CdS coatings exhibit enhanced photocatalytic activity (PA) in the degradation of methyl orange, used as a model organic pollutant, under simulated solar irradiation. The highest PA was observed for TiO2/CdS coating formed in supporting electrolyte with addition of 0.4 g/L of CdS particles. Photoluminescence measurements indicate that enhanced PA is related to the reduction of the recombination rate of photogenerated electron/hole pairs as a result of TiO2 and CdS coupling.",
publisher = "Elsevier",
journal = "Surface and Coatings Technology",
title = "CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity",
volume = "344",
pages = "528-533",
doi = "10.1016/j.surfcoat.2018.03.080"
}

Stojadinović, S., Tadić, N., Radić, N., Grbić, B.,& Vasilić, R.. (2018). CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity. in Surface and Coatings Technology
Elsevier., 344, 528-533.
https://doi.org/10.1016/j.surfcoat.2018.03.080

Stojadinović S, Tadić N, Radić N, Grbić B, Vasilić R. CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity. in Surface and Coatings Technology. 2018;344:528-533.
doi:10.1016/j.surfcoat.2018.03.080 .

Stojadinović, Stevan, Tadić, Nenad, Radić, Nenad, Grbić, Boško, Vasilić, Rastko, "CdS particles modified TiO2 coatings formed by plasma electrolytic oxidation with enhanced photocatalytic activity" in Surface and Coatings Technology, 344 (2018):528-533,
https://doi.org/10.1016/j.surfcoat.2018.03.080 . .

TY  - JOUR
AU  - Petrović, Srđan
AU  - Rožić, Ljiljana
AU  - Vuković, Zorica
AU  - Grbić, Boško
AU  - Radić, Nenad
AU  - Stojadinović, Stevan
AU  - Vasilić, Rastko
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2078
AB  - This article presents the comparison of structural and fractal properties of nanocrystalline titanium dioxide (TiO2) and TiO2 modified with tungstophosphoric acid (TiO2/HPW) and their impact on the photocatalytic degradation of hazardous water pollutants. TiO2 and TiO2/HPW samples were synthesized by a combined solgel and hydrothermal processing. The XRD analysis of pure TiO2 samples revealed that phase composition was mainly dependent on the calcination temperature, changing from amorphous TiO2 to crystalline anatase and rutile by increasing the temperature. On the other hand, the XRD of TiO2/HPW samples calcined at temperatures above 600 degrees C showed crystalline peaks associated to formation of WO3 and WO2.92 crystalline domains. The N-2 adsorption-desorption isotherm and pore size distribution of TiO2/HPW samples detected the existence of mesoporous characteristic with very narrow bimodal pores in the mesoporous region. The structural heterogeneity of samples was analyzed by means of pore size distribution functions, while the variation in fractal dimension were determined from the nitrogen adsorption isotherms, using the modified Frenkel-Halsey-Hill method. The results demonstrate that the approach is capable of characterizing complex textures such as those present in the TiO2 and TiO2/HPW photocatalysts. Besides, the effect of calcinations condition on photocatalytic properties of the samples was also investigated. The highest efficiency with respect to methyl orange photodecomposition was observed for TiO2/HPW photocatalysts calcined at 700 degrees C.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Journal of Physics and Chemistry of Solids
T1  - Structural and fractal characterization of tungstophosphoric acid modified titanium dioxide photocatalyst
VL  - 103
SP  - 95
EP  - 102
DO  - 10.1016/j.jpcs.2016.12.002
ER  - 

@article{
author = "Petrović, Srđan and Rožić, Ljiljana and Vuković, Zorica and Grbić, Boško and Radić, Nenad and Stojadinović, Stevan and Vasilić, Rastko",
year = "2017",
abstract = "This article presents the comparison of structural and fractal properties of nanocrystalline titanium dioxide (TiO2) and TiO2 modified with tungstophosphoric acid (TiO2/HPW) and their impact on the photocatalytic degradation of hazardous water pollutants. TiO2 and TiO2/HPW samples were synthesized by a combined solgel and hydrothermal processing. The XRD analysis of pure TiO2 samples revealed that phase composition was mainly dependent on the calcination temperature, changing from amorphous TiO2 to crystalline anatase and rutile by increasing the temperature. On the other hand, the XRD of TiO2/HPW samples calcined at temperatures above 600 degrees C showed crystalline peaks associated to formation of WO3 and WO2.92 crystalline domains. The N-2 adsorption-desorption isotherm and pore size distribution of TiO2/HPW samples detected the existence of mesoporous characteristic with very narrow bimodal pores in the mesoporous region. The structural heterogeneity of samples was analyzed by means of pore size distribution functions, while the variation in fractal dimension were determined from the nitrogen adsorption isotherms, using the modified Frenkel-Halsey-Hill method. The results demonstrate that the approach is capable of characterizing complex textures such as those present in the TiO2 and TiO2/HPW photocatalysts. Besides, the effect of calcinations condition on photocatalytic properties of the samples was also investigated. The highest efficiency with respect to methyl orange photodecomposition was observed for TiO2/HPW photocatalysts calcined at 700 degrees C.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Journal of Physics and Chemistry of Solids",
title = "Structural and fractal characterization of tungstophosphoric acid modified titanium dioxide photocatalyst",
volume = "103",
pages = "95-102",
doi = "10.1016/j.jpcs.2016.12.002"
}

Petrović, S., Rožić, L., Vuković, Z., Grbić, B., Radić, N., Stojadinović, S.,& Vasilić, R.. (2017). Structural and fractal characterization of tungstophosphoric acid modified titanium dioxide photocatalyst. in Journal of Physics and Chemistry of Solids
Oxford : Pergamon-Elsevier Science Ltd., 103, 95-102.
https://doi.org/10.1016/j.jpcs.2016.12.002

Petrović S, Rožić L, Vuković Z, Grbić B, Radić N, Stojadinović S, Vasilić R. Structural and fractal characterization of tungstophosphoric acid modified titanium dioxide photocatalyst. in Journal of Physics and Chemistry of Solids. 2017;103:95-102.
doi:10.1016/j.jpcs.2016.12.002 .

Petrović, Srđan, Rožić, Ljiljana, Vuković, Zorica, Grbić, Boško, Radić, Nenad, Stojadinović, Stevan, Vasilić, Rastko, "Structural and fractal characterization of tungstophosphoric acid modified titanium dioxide photocatalyst" in Journal of Physics and Chemistry of Solids, 103 (2017):95-102,
https://doi.org/10.1016/j.jpcs.2016.12.002 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Tadić, Nenad
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2178
AB  - TiO2/SnO2 coatings are formed by plasma electrolytic oxidation of titanium substrate in supporting electrolyte (10 g/L Na3PO4 center dot 12H(2)O) with addition of various concentrations of SnO2 particles. Photocatalytic activity (PA) of TiO2/SnO2 coatings was evaluated by measuring the degradation of methyl orange under simulated sunlight conditions. It was observed that PA of TiO2/SnO2 coatings strongly depends on the concentration of SnO2 particles in the electrolyte, i. e., the highest PA was observed with addition of 0.3 g/L of SnO2 particles to supporting electrolyte.
PB  - Elsevier
T2  - Materials Letters
T1  - TiO2/SnO2 photocatalyst formed by plasma electrolytic oxidation
VL  - 196
SP  - 292
EP  - 295
DO  - 10.1016/j.matlet.2017.03.115
ER  - 

@article{
author = "Stojadinović, Stevan and Tadić, Nenad and Radić, Nenad and Grbić, Boško and Vasilić, Rastko",
year = "2017",
abstract = "TiO2/SnO2 coatings are formed by plasma electrolytic oxidation of titanium substrate in supporting electrolyte (10 g/L Na3PO4 center dot 12H(2)O) with addition of various concentrations of SnO2 particles. Photocatalytic activity (PA) of TiO2/SnO2 coatings was evaluated by measuring the degradation of methyl orange under simulated sunlight conditions. It was observed that PA of TiO2/SnO2 coatings strongly depends on the concentration of SnO2 particles in the electrolyte, i. e., the highest PA was observed with addition of 0.3 g/L of SnO2 particles to supporting electrolyte.",
publisher = "Elsevier",
journal = "Materials Letters",
title = "TiO2/SnO2 photocatalyst formed by plasma electrolytic oxidation",
volume = "196",
pages = "292-295",
doi = "10.1016/j.matlet.2017.03.115"
}

Stojadinović, S., Tadić, N., Radić, N., Grbić, B.,& Vasilić, R.. (2017). TiO2/SnO2 photocatalyst formed by plasma electrolytic oxidation. in Materials Letters
Elsevier., 196, 292-295.
https://doi.org/10.1016/j.matlet.2017.03.115

Stojadinović S, Tadić N, Radić N, Grbić B, Vasilić R. TiO2/SnO2 photocatalyst formed by plasma electrolytic oxidation. in Materials Letters. 2017;196:292-295.
doi:10.1016/j.matlet.2017.03.115 .

Stojadinović, Stevan, Tadić, Nenad, Radić, Nenad, Grbić, Boško, Vasilić, Rastko, "TiO2/SnO2 photocatalyst formed by plasma electrolytic oxidation" in Materials Letters, 196 (2017):292-295,
https://doi.org/10.1016/j.matlet.2017.03.115 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Tadić, Nenad
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2198
AB  - This paper presents the results of our recent investigation of MgO/ZnO coatings formed on AZ31 magnesium alloy by plasma electrolytic oxidation in phosphate-based alkaline electrolyte with varying concentration of ZnO particles. Surface morphology of obtained coatings is not significantly influenced by the addition of ZnO particles to the supporting electrolyte, while processing time has considerable influence on the morphology of formed coatings. Elemental mapping showed that elements are distributed rather uniformly across the obtained oxide coatings. The content of Zn increases with ZnO particle concentration in the supporting electrolyte as well as with PEO processing time. Incorporation of ZnO particles in obtained coatings was confirmed by X-ray diffraction and Raman spectroscopy. Photoluminescent emission spectra of MgO/ZnO coatings featured sharp band centered at about 380 nm and broad band centered at about 535 nm, with the leading contribution coming from ZnO deposited on the surface. Diffuse reflectance spectra revealed that absorption edge of MgO/ZnO coatings is positioned at about 385 nm. Photoactivity of obtained coatings increases with processing time and ZnO concentration up to 6 g/L.
PB  - Elsevier
T2  - Surface and Coatings Technology
T1  - MgO/ZnO coatings formed on magnesium alloy AZ31 by plasma electrolytic oxidation: Structural, photoluminescence and photocatalytic investigation
VL  - 310
SP  - 98
EP  - 105
DO  - 10.1016/j.surfcoat.2016.12.073
ER  - 

@article{
author = "Stojadinović, Stevan and Tadić, Nenad and Radić, Nenad and Grbić, Boško and Vasilić, Rastko",
year = "2017",
abstract = "This paper presents the results of our recent investigation of MgO/ZnO coatings formed on AZ31 magnesium alloy by plasma electrolytic oxidation in phosphate-based alkaline electrolyte with varying concentration of ZnO particles. Surface morphology of obtained coatings is not significantly influenced by the addition of ZnO particles to the supporting electrolyte, while processing time has considerable influence on the morphology of formed coatings. Elemental mapping showed that elements are distributed rather uniformly across the obtained oxide coatings. The content of Zn increases with ZnO particle concentration in the supporting electrolyte as well as with PEO processing time. Incorporation of ZnO particles in obtained coatings was confirmed by X-ray diffraction and Raman spectroscopy. Photoluminescent emission spectra of MgO/ZnO coatings featured sharp band centered at about 380 nm and broad band centered at about 535 nm, with the leading contribution coming from ZnO deposited on the surface. Diffuse reflectance spectra revealed that absorption edge of MgO/ZnO coatings is positioned at about 385 nm. Photoactivity of obtained coatings increases with processing time and ZnO concentration up to 6 g/L.",
publisher = "Elsevier",
journal = "Surface and Coatings Technology",
title = "MgO/ZnO coatings formed on magnesium alloy AZ31 by plasma electrolytic oxidation: Structural, photoluminescence and photocatalytic investigation",
volume = "310",
pages = "98-105",
doi = "10.1016/j.surfcoat.2016.12.073"
}

Stojadinović, S., Tadić, N., Radić, N., Grbić, B.,& Vasilić, R.. (2017). MgO/ZnO coatings formed on magnesium alloy AZ31 by plasma electrolytic oxidation: Structural, photoluminescence and photocatalytic investigation. in Surface and Coatings Technology
Elsevier., 310, 98-105.
https://doi.org/10.1016/j.surfcoat.2016.12.073

Stojadinović S, Tadić N, Radić N, Grbić B, Vasilić R. MgO/ZnO coatings formed on magnesium alloy AZ31 by plasma electrolytic oxidation: Structural, photoluminescence and photocatalytic investigation. in Surface and Coatings Technology. 2017;310:98-105.
doi:10.1016/j.surfcoat.2016.12.073 .

Stojadinović, Stevan, Tadić, Nenad, Radić, Nenad, Grbić, Boško, Vasilić, Rastko, "MgO/ZnO coatings formed on magnesium alloy AZ31 by plasma electrolytic oxidation: Structural, photoluminescence and photocatalytic investigation" in Surface and Coatings Technology, 310 (2017):98-105,
https://doi.org/10.1016/j.surfcoat.2016.12.073 . .

TY  - JOUR
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Stojadinović, Stevan
AU  - Vasilić, Rastko
AU  - Petrović, Srđan
AU  - Rožić, Ljiljana
AU  - Stefanov, Plamen
PY  - 2017
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2259
AB  - Pt-Ba-Al2O3 coatings were obtained by spray pyrolysis deposition on stainless steel foil. The XRD results showed that the coatings consisted from Ba carbonate and Pt (fcc) phases. SEM micrographs demonstrated that the coatings are smooth and compact. The XPS data confirmed that Ba and Pt are in close contact. Pt crystallite size is only slightly influenced by the order of Pt and Ba deposition and the dispersion of Pt is in the narrow range from 28 to 33% for all samples. Catalyst component deposition order affects NOx storage capacity. Simultaneous deposition of Ba and Pt on already formed Al2O3 substrate produces the most efficient catalyst. Pt deposited on top of the Ba layer results in slightly reduced NOx storage capacity, while deposition of Pt on the separated layer with Ba layer on top significantly reduces the ability for NOx storage.
PB  - Elsevier Science Sa, Lausanne
T2  - Thin Solid Films
T1  - Preparation and characterization of Pt-Ba-Al2O3 coatings obtained by spray pyrolysis
VL  - 628
SP  - 7
EP  - 12
DO  - 10.1016/j.tsf.2017.03.007
ER  - 

@article{
author = "Radić, Nenad and Grbić, Boško and Stojadinović, Stevan and Vasilić, Rastko and Petrović, Srđan and Rožić, Ljiljana and Stefanov, Plamen",
year = "2017",
abstract = "Pt-Ba-Al2O3 coatings were obtained by spray pyrolysis deposition on stainless steel foil. The XRD results showed that the coatings consisted from Ba carbonate and Pt (fcc) phases. SEM micrographs demonstrated that the coatings are smooth and compact. The XPS data confirmed that Ba and Pt are in close contact. Pt crystallite size is only slightly influenced by the order of Pt and Ba deposition and the dispersion of Pt is in the narrow range from 28 to 33% for all samples. Catalyst component deposition order affects NOx storage capacity. Simultaneous deposition of Ba and Pt on already formed Al2O3 substrate produces the most efficient catalyst. Pt deposited on top of the Ba layer results in slightly reduced NOx storage capacity, while deposition of Pt on the separated layer with Ba layer on top significantly reduces the ability for NOx storage.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Thin Solid Films",
title = "Preparation and characterization of Pt-Ba-Al2O3 coatings obtained by spray pyrolysis",
volume = "628",
pages = "7-12",
doi = "10.1016/j.tsf.2017.03.007"
}

Radić, N., Grbić, B., Stojadinović, S., Vasilić, R., Petrović, S., Rožić, L.,& Stefanov, P.. (2017). Preparation and characterization of Pt-Ba-Al2O3 coatings obtained by spray pyrolysis. in Thin Solid Films
Elsevier Science Sa, Lausanne., 628, 7-12.
https://doi.org/10.1016/j.tsf.2017.03.007

Radić N, Grbić B, Stojadinović S, Vasilić R, Petrović S, Rožić L, Stefanov P. Preparation and characterization of Pt-Ba-Al2O3 coatings obtained by spray pyrolysis. in Thin Solid Films. 2017;628:7-12.
doi:10.1016/j.tsf.2017.03.007 .

Radić, Nenad, Grbić, Boško, Stojadinović, Stevan, Vasilić, Rastko, Petrović, Srđan, Rožić, Ljiljana, Stefanov, Plamen, "Preparation and characterization of Pt-Ba-Al2O3 coatings obtained by spray pyrolysis" in Thin Solid Films, 628 (2017):7-12,
https://doi.org/10.1016/j.tsf.2017.03.007 . .

TY  - JOUR
AU  - Tadić, Nenad
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1914
AB  - This paper presents a recent investigation of rapid deposition of TiO2 nanoparticles on aluminum by plasma electrolytic oxidation in Na2SiO3 center dot 5H(2)O water based electrolyte with addition of TiO2 nanoparticles and Na2WO4 center dot 2H(2)O. Oxide coatings were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy and grazing incidence X-ray diffraction. It was found that surface morphology, chemical and phase compositions of obtained coatings depend on electrolyte composition and processing time. The photocatalytic activity was tested by photodegrading methyl orange under simulated sunlight conditions. It was observed that photodegradation of methyl orange strongly depends on the concentration of TiO2 nanoparticles and sodium tungstate in the electrolyte and PEO treatment time. Coatings with the highest photoactivity were obtained in 4 g/L Na2SiO3 center dot 5H(2)O + 2 g/L Degussa P25 + 0.1 g/L Na2WO4 center dot 2H(2)O.
PB  - Elsevier
T2  - Surface and Coatings Technology
T1  - Characterization and photocatalytic properties of tungsten doped TiO2 coatings on aluminum obtained by plasma electrolytic oxidation
VL  - 305
SP  - 192
EP  - 199
DO  - 10.1016/j.surfcoat.2016.08.045
ER  - 

@article{
author = "Tadić, Nenad and Stojadinović, Stevan and Radić, Nenad and Grbić, Boško and Vasilić, Rastko",
year = "2016",
abstract = "This paper presents a recent investigation of rapid deposition of TiO2 nanoparticles on aluminum by plasma electrolytic oxidation in Na2SiO3 center dot 5H(2)O water based electrolyte with addition of TiO2 nanoparticles and Na2WO4 center dot 2H(2)O. Oxide coatings were characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy and grazing incidence X-ray diffraction. It was found that surface morphology, chemical and phase compositions of obtained coatings depend on electrolyte composition and processing time. The photocatalytic activity was tested by photodegrading methyl orange under simulated sunlight conditions. It was observed that photodegradation of methyl orange strongly depends on the concentration of TiO2 nanoparticles and sodium tungstate in the electrolyte and PEO treatment time. Coatings with the highest photoactivity were obtained in 4 g/L Na2SiO3 center dot 5H(2)O + 2 g/L Degussa P25 + 0.1 g/L Na2WO4 center dot 2H(2)O.",
publisher = "Elsevier",
journal = "Surface and Coatings Technology",
title = "Characterization and photocatalytic properties of tungsten doped TiO2 coatings on aluminum obtained by plasma electrolytic oxidation",
volume = "305",
pages = "192-199",
doi = "10.1016/j.surfcoat.2016.08.045"
}

Tadić, N., Stojadinović, S., Radić, N., Grbić, B.,& Vasilić, R.. (2016). Characterization and photocatalytic properties of tungsten doped TiO2 coatings on aluminum obtained by plasma electrolytic oxidation. in Surface and Coatings Technology
Elsevier., 305, 192-199.
https://doi.org/10.1016/j.surfcoat.2016.08.045

Tadić N, Stojadinović S, Radić N, Grbić B, Vasilić R. Characterization and photocatalytic properties of tungsten doped TiO2 coatings on aluminum obtained by plasma electrolytic oxidation. in Surface and Coatings Technology. 2016;305:192-199.
doi:10.1016/j.surfcoat.2016.08.045 .

Tadić, Nenad, Stojadinović, Stevan, Radić, Nenad, Grbić, Boško, Vasilić, Rastko, "Characterization and photocatalytic properties of tungsten doped TiO2 coatings on aluminum obtained by plasma electrolytic oxidation" in Surface and Coatings Technology, 305 (2016):192-199,
https://doi.org/10.1016/j.surfcoat.2016.08.045 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Vasilić, Rastko
AU  - Radić, Nenad
AU  - Tadić, Nenad
AU  - Stefanov, Plamen
AU  - Grbić, Boško
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1939
AB  - Tungsten doped Al2O3 /ZnO coatings are formed by plasma electrolytic oxidation of aluminum substrate in supporting electrolyte (0.1 M boric acid + 0.05 M borax + 2 g/L ZnO) with addition of different concentrations of Na2WO4 center dot 2H(2)O. The morphology, crystal structure, chemical composition, and light absorption characteristics of formed surface coatings are investigated. The X-ray diffraction and X-ray photoelectron spectroscopy results indicate that formed surface coatings consist of alpha and gamma phase of A(2)O(3), ZnO, metallic tungsten and WO3. Obtained results showed that incorporated tungsten does not have any influence on the absorption spectra of Al2O3/ZnO coatings, which showed invariable band edge at about 385 nm. The photocatalytic activity of undoped and tungsten doped Al2O3 /ZnO coatings is estimated by the photodegradation of methyl orange. The photocatalytic activity of tungsten doped A(2)O(3)/ZnO coatings is higher thanof undoped Al2O3 /ZnO coatings; the best photocatalytic activity is ascribed to coatings formed in supporting electrolyte with addition of 0.3 g/L Na2WO4 center dot 2H(2)O. Tungsten in A(2)O(3)/ZnO coatings acts as a charge trap, thus reducing the recombination rate of photogenerated electron-hole pairs. The results of PL measurements are in agreement with photocatalytic activity. Declining PL intensity corresponds to increasing photocatalytic activity of the coatings, indicating slower recombination of electron-hole pairs.
PB  - Elsevier
T2  - Applied Surface Science
T1  - The formation of tungsten doped Al2O3/ZnO coatings on aluminum by plasma electrolytic oxidation and their application in photocatalysis
VL  - 377
SP  - 37
EP  - 43
DO  - 10.1016/j.apsusc.2016.03.104
ER  - 

@article{
author = "Stojadinović, Stevan and Vasilić, Rastko and Radić, Nenad and Tadić, Nenad and Stefanov, Plamen and Grbić, Boško",
year = "2016",
abstract = "Tungsten doped Al2O3 /ZnO coatings are formed by plasma electrolytic oxidation of aluminum substrate in supporting electrolyte (0.1 M boric acid + 0.05 M borax + 2 g/L ZnO) with addition of different concentrations of Na2WO4 center dot 2H(2)O. The morphology, crystal structure, chemical composition, and light absorption characteristics of formed surface coatings are investigated. The X-ray diffraction and X-ray photoelectron spectroscopy results indicate that formed surface coatings consist of alpha and gamma phase of A(2)O(3), ZnO, metallic tungsten and WO3. Obtained results showed that incorporated tungsten does not have any influence on the absorption spectra of Al2O3/ZnO coatings, which showed invariable band edge at about 385 nm. The photocatalytic activity of undoped and tungsten doped Al2O3 /ZnO coatings is estimated by the photodegradation of methyl orange. The photocatalytic activity of tungsten doped A(2)O(3)/ZnO coatings is higher thanof undoped Al2O3 /ZnO coatings; the best photocatalytic activity is ascribed to coatings formed in supporting electrolyte with addition of 0.3 g/L Na2WO4 center dot 2H(2)O. Tungsten in A(2)O(3)/ZnO coatings acts as a charge trap, thus reducing the recombination rate of photogenerated electron-hole pairs. The results of PL measurements are in agreement with photocatalytic activity. Declining PL intensity corresponds to increasing photocatalytic activity of the coatings, indicating slower recombination of electron-hole pairs.",
publisher = "Elsevier",
journal = "Applied Surface Science",
title = "The formation of tungsten doped Al2O3/ZnO coatings on aluminum by plasma electrolytic oxidation and their application in photocatalysis",
volume = "377",
pages = "37-43",
doi = "10.1016/j.apsusc.2016.03.104"
}

Stojadinović, S., Vasilić, R., Radić, N., Tadić, N., Stefanov, P.,& Grbić, B.. (2016). The formation of tungsten doped Al2O3/ZnO coatings on aluminum by plasma electrolytic oxidation and their application in photocatalysis. in Applied Surface Science
Elsevier., 377, 37-43.
https://doi.org/10.1016/j.apsusc.2016.03.104

Stojadinović S, Vasilić R, Radić N, Tadić N, Stefanov P, Grbić B. The formation of tungsten doped Al2O3/ZnO coatings on aluminum by plasma electrolytic oxidation and their application in photocatalysis. in Applied Surface Science. 2016;377:37-43.
doi:10.1016/j.apsusc.2016.03.104 .

Stojadinović, Stevan, Vasilić, Rastko, Radić, Nenad, Tadić, Nenad, Stefanov, Plamen, Grbić, Boško, "The formation of tungsten doped Al2O3/ZnO coatings on aluminum by plasma electrolytic oxidation and their application in photocatalysis" in Applied Surface Science, 377 (2016):37-43,
https://doi.org/10.1016/j.apsusc.2016.03.104 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Maletić, Slavica
AU  - Stefanov, Plamen
AU  - Pacevski, Aleksandar
AU  - Vasilić, Rastko
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/2034
AB  - In this paper, we used plasma electrolytic oxidation (PEO) of titanium in water solution containing 10 g/L Na3PO4 center dot 12H(2)O + 2 g/L Eu2O3 powder for preparation of TiO2:Eu3+ coatings. The surfaces of obtained coatings exhibit a typical PEO porous structure. The energy dispersive X-ray spectroscopy analysis showed that the coatings are mainly composed of Ti, O, P, and Eu; it is observed that Eu content in the coatings increases with PEO time. The X-ray diffraction analysis indicated that the coatings are crystallized and composed of anatase and rutile TiO2 phases, with anatase being the dominant one. X-ray photoelectron spectroscopy revealed that Ti 2p spin-orbit components of TiO2:Eu3+ coatings are shifted towards higher binding energy, with respect to pure TiO2 coatings, suggesting that Eu3+ ions are incorporated into TiO2 lattice. Diffuse reflectance spectroscopy showed that TiO2:Eu3+ coatings exhibit evident red shift with respect to the pure TiO2 coatings. Photoluminescence (PL) emission spectra of TiO2:Eu3+ coatings are characterized by sharp emission bands in orange-red region ascribed to f-f transitions of Eu3+ ions from excited level D-5(0) to lower levels F-7(J) (J=0, 1, 2, 3, and 4). The excitation PL spectra of TiO2:Eu3+ coatings can be divided into two regions: the broad band region from 250 nm to 350 nm associated with charge transfer state of Eu3+ and the series of sharp peaks in the range from 350 nm to 550 rim corresponding to direct excitation of the Eu3+ ions. It is observed that the intensity of peaks in excitation and emission PL spectra increases with the concentration of Eu3+, but the peak positions remain practically unchanged. The ratio of PL emission for electric and magnetic dipole transitions indicates highly asymmetric environment around Eu3+ ions. The photocatalytic activity (PA) of TiO2:Eu3+ coatings is evaluated by measuring the photodegradation of methyl orange under simulated sunlight conditions. It is shown that PEO time, i.e., the amount of Eu3+ incorporated into coatings is an important factor affecting PA; TiO2:Eu3+ coating formed after 1 min of PEO time showed the highest PA.
PB  - Elsevier
T2  - Applied Surface Science
T1  - Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation
VL  - 370
SP  - 218
EP  - 228
DO  - 10.1016/j.apsusc.2016.02.131
ER  - 

@article{
author = "Stojadinović, Stevan and Radić, Nenad and Grbić, Boško and Maletić, Slavica and Stefanov, Plamen and Pacevski, Aleksandar and Vasilić, Rastko",
year = "2016",
abstract = "In this paper, we used plasma electrolytic oxidation (PEO) of titanium in water solution containing 10 g/L Na3PO4 center dot 12H(2)O + 2 g/L Eu2O3 powder for preparation of TiO2:Eu3+ coatings. The surfaces of obtained coatings exhibit a typical PEO porous structure. The energy dispersive X-ray spectroscopy analysis showed that the coatings are mainly composed of Ti, O, P, and Eu; it is observed that Eu content in the coatings increases with PEO time. The X-ray diffraction analysis indicated that the coatings are crystallized and composed of anatase and rutile TiO2 phases, with anatase being the dominant one. X-ray photoelectron spectroscopy revealed that Ti 2p spin-orbit components of TiO2:Eu3+ coatings are shifted towards higher binding energy, with respect to pure TiO2 coatings, suggesting that Eu3+ ions are incorporated into TiO2 lattice. Diffuse reflectance spectroscopy showed that TiO2:Eu3+ coatings exhibit evident red shift with respect to the pure TiO2 coatings. Photoluminescence (PL) emission spectra of TiO2:Eu3+ coatings are characterized by sharp emission bands in orange-red region ascribed to f-f transitions of Eu3+ ions from excited level D-5(0) to lower levels F-7(J) (J=0, 1, 2, 3, and 4). The excitation PL spectra of TiO2:Eu3+ coatings can be divided into two regions: the broad band region from 250 nm to 350 nm associated with charge transfer state of Eu3+ and the series of sharp peaks in the range from 350 nm to 550 rim corresponding to direct excitation of the Eu3+ ions. It is observed that the intensity of peaks in excitation and emission PL spectra increases with the concentration of Eu3+, but the peak positions remain practically unchanged. The ratio of PL emission for electric and magnetic dipole transitions indicates highly asymmetric environment around Eu3+ ions. The photocatalytic activity (PA) of TiO2:Eu3+ coatings is evaluated by measuring the photodegradation of methyl orange under simulated sunlight conditions. It is shown that PEO time, i.e., the amount of Eu3+ incorporated into coatings is an important factor affecting PA; TiO2:Eu3+ coating formed after 1 min of PEO time showed the highest PA.",
publisher = "Elsevier",
journal = "Applied Surface Science",
title = "Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation",
volume = "370",
pages = "218-228",
doi = "10.1016/j.apsusc.2016.02.131"
}

Stojadinović, S., Radić, N., Grbić, B., Maletić, S., Stefanov, P., Pacevski, A.,& Vasilić, R.. (2016). Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation. in Applied Surface Science
Elsevier., 370, 218-228.
https://doi.org/10.1016/j.apsusc.2016.02.131

Stojadinović S, Radić N, Grbić B, Maletić S, Stefanov P, Pacevski A, Vasilić R. Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation. in Applied Surface Science. 2016;370:218-228.
doi:10.1016/j.apsusc.2016.02.131 .

Stojadinović, Stevan, Radić, Nenad, Grbić, Boško, Maletić, Slavica, Stefanov, Plamen, Pacevski, Aleksandar, Vasilić, Rastko, "Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation" in Applied Surface Science, 370 (2016):218-228,
https://doi.org/10.1016/j.apsusc.2016.02.131 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Maletić, Slavica
AU  - Stefanov, Plamen
AU  - Pacevski, Aleksandar
AU  - Vasilić, Rastko
PY  - 2016
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4320
AB  - In this paper, we used plasma electrolytic oxidation (PEO) of titanium in water solution containing 10 g/L Na3PO4 center dot 12H(2)O + 2 g/L Eu2O3 powder for preparation of TiO2:Eu3+ coatings. The surfaces of obtained coatings exhibit a typical PEO porous structure. The energy dispersive X-ray spectroscopy analysis showed that the coatings are mainly composed of Ti, O, P, and Eu; it is observed that Eu content in the coatings increases with PEO time. The X-ray diffraction analysis indicated that the coatings are crystallized and composed of anatase and rutile TiO2 phases, with anatase being the dominant one. X-ray photoelectron spectroscopy revealed that Ti 2p spin-orbit components of TiO2:Eu3+ coatings are shifted towards higher binding energy, with respect to pure TiO2 coatings, suggesting that Eu3+ ions are incorporated into TiO2 lattice. Diffuse reflectance spectroscopy showed that TiO2:Eu3+ coatings exhibit evident red shift with respect to the pure TiO2 coatings. Photoluminescence (PL) emission spectra of TiO2:Eu3+ coatings are characterized by sharp emission bands in orange-red region ascribed to f-f transitions of Eu3+ ions from excited level D-5(0) to lower levels F-7(J) (J=0, 1, 2, 3, and 4). The excitation PL spectra of TiO2:Eu3+ coatings can be divided into two regions: the broad band region from 250 nm to 350 nm associated with charge transfer state of Eu3+ and the series of sharp peaks in the range from 350 nm to 550 rim corresponding to direct excitation of the Eu3+ ions. It is observed that the intensity of peaks in excitation and emission PL spectra increases with the concentration of Eu3+, but the peak positions remain practically unchanged. The ratio of PL emission for electric and magnetic dipole transitions indicates highly asymmetric environment around Eu3+ ions. The photocatalytic activity (PA) of TiO2:Eu3+ coatings is evaluated by measuring the photodegradation of methyl orange under simulated sunlight conditions. It is shown that PEO time, i.e., the amount of Eu3+ incorporated into coatings is an important factor affecting PA; TiO2:Eu3+ coating formed after 1 min of PEO time showed the highest PA.
PB  - Elsevier
T2  - Applied Surface Science
T1  - Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation
VL  - 370
SP  - 218
EP  - 228
DO  - 10.1016/j.apsusc.2016.02.131
ER  - 

@article{
author = "Stojadinović, Stevan and Radić, Nenad and Grbić, Boško and Maletić, Slavica and Stefanov, Plamen and Pacevski, Aleksandar and Vasilić, Rastko",
year = "2016",
abstract = "In this paper, we used plasma electrolytic oxidation (PEO) of titanium in water solution containing 10 g/L Na3PO4 center dot 12H(2)O + 2 g/L Eu2O3 powder for preparation of TiO2:Eu3+ coatings. The surfaces of obtained coatings exhibit a typical PEO porous structure. The energy dispersive X-ray spectroscopy analysis showed that the coatings are mainly composed of Ti, O, P, and Eu; it is observed that Eu content in the coatings increases with PEO time. The X-ray diffraction analysis indicated that the coatings are crystallized and composed of anatase and rutile TiO2 phases, with anatase being the dominant one. X-ray photoelectron spectroscopy revealed that Ti 2p spin-orbit components of TiO2:Eu3+ coatings are shifted towards higher binding energy, with respect to pure TiO2 coatings, suggesting that Eu3+ ions are incorporated into TiO2 lattice. Diffuse reflectance spectroscopy showed that TiO2:Eu3+ coatings exhibit evident red shift with respect to the pure TiO2 coatings. Photoluminescence (PL) emission spectra of TiO2:Eu3+ coatings are characterized by sharp emission bands in orange-red region ascribed to f-f transitions of Eu3+ ions from excited level D-5(0) to lower levels F-7(J) (J=0, 1, 2, 3, and 4). The excitation PL spectra of TiO2:Eu3+ coatings can be divided into two regions: the broad band region from 250 nm to 350 nm associated with charge transfer state of Eu3+ and the series of sharp peaks in the range from 350 nm to 550 rim corresponding to direct excitation of the Eu3+ ions. It is observed that the intensity of peaks in excitation and emission PL spectra increases with the concentration of Eu3+, but the peak positions remain practically unchanged. The ratio of PL emission for electric and magnetic dipole transitions indicates highly asymmetric environment around Eu3+ ions. The photocatalytic activity (PA) of TiO2:Eu3+ coatings is evaluated by measuring the photodegradation of methyl orange under simulated sunlight conditions. It is shown that PEO time, i.e., the amount of Eu3+ incorporated into coatings is an important factor affecting PA; TiO2:Eu3+ coating formed after 1 min of PEO time showed the highest PA.",
publisher = "Elsevier",
journal = "Applied Surface Science",
title = "Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation",
volume = "370",
pages = "218-228",
doi = "10.1016/j.apsusc.2016.02.131"
}

Stojadinović, S., Radić, N., Grbić, B., Maletić, S., Stefanov, P., Pacevski, A.,& Vasilić, R.. (2016). Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation. in Applied Surface Science
Elsevier., 370, 218-228.
https://doi.org/10.1016/j.apsusc.2016.02.131

Stojadinović S, Radić N, Grbić B, Maletić S, Stefanov P, Pacevski A, Vasilić R. Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation. in Applied Surface Science. 2016;370:218-228.
doi:10.1016/j.apsusc.2016.02.131 .

Stojadinović, Stevan, Radić, Nenad, Grbić, Boško, Maletić, Slavica, Stefanov, Plamen, Pacevski, Aleksandar, Vasilić, Rastko, "Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation" in Applied Surface Science, 370 (2016):218-228,
https://doi.org/10.1016/j.apsusc.2016.02.131 . .

TY  - JOUR
AU  - Stojadinović, Stevan D.J.
AU  - Tadić, Nenad
AU  - Radić, Nenad
AU  - Stojadinovic, B
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1722
AB  - Mixed Al2O3/ZnO coatings are prepared by conventional DC plasma electrolytic oxidation (PEO) of aluminum in boric acid and borax solution containing ZnO nanoparticles. Scanning electron microscopy equipped with energy dispersive x-ray spectroscopy, x-ray diffraction, and Raman spectroscopy were employed to monitor morphological, structural, and chemical changes of obtained oxide coatings. It was found that chemical and phase compositions strongly depend on PEO time. Photoluminescence and photodegradation of methyl orange served as a tool to estimate potential application of Al2O3/ZnO coatings. Photoluminescence measurements showed that clearly observable bands inherent to Al2O3 and ZnO are present in formed coatings, pointing at oxygen vacancies as the main source of photoluminescence. Longer PEO processing times proved beneficial for enhanced photocatalytic activity.
PB  - Elsevier
T2  - Surface and Coatings Technology
T1  - Synthesis and characterization of Al2O3/ZnO coatings formed by plasma electrolytic oxidation
VL  - 276
SP  - 573
EP  - 579
DO  - 10.1016/j.surfcoat.2015.06.013
ER  - 

@article{
author = "Stojadinović, Stevan D.J. and Tadić, Nenad and Radić, Nenad and Stojadinovic, B and Grbić, Boško and Vasilić, Rastko",
year = "2015",
abstract = "Mixed Al2O3/ZnO coatings are prepared by conventional DC plasma electrolytic oxidation (PEO) of aluminum in boric acid and borax solution containing ZnO nanoparticles. Scanning electron microscopy equipped with energy dispersive x-ray spectroscopy, x-ray diffraction, and Raman spectroscopy were employed to monitor morphological, structural, and chemical changes of obtained oxide coatings. It was found that chemical and phase compositions strongly depend on PEO time. Photoluminescence and photodegradation of methyl orange served as a tool to estimate potential application of Al2O3/ZnO coatings. Photoluminescence measurements showed that clearly observable bands inherent to Al2O3 and ZnO are present in formed coatings, pointing at oxygen vacancies as the main source of photoluminescence. Longer PEO processing times proved beneficial for enhanced photocatalytic activity.",
publisher = "Elsevier",
journal = "Surface and Coatings Technology",
title = "Synthesis and characterization of Al2O3/ZnO coatings formed by plasma electrolytic oxidation",
volume = "276",
pages = "573-579",
doi = "10.1016/j.surfcoat.2015.06.013"
}

Stojadinović, S. D.J., Tadić, N., Radić, N., Stojadinovic, B., Grbić, B.,& Vasilić, R.. (2015). Synthesis and characterization of Al2O3/ZnO coatings formed by plasma electrolytic oxidation. in Surface and Coatings Technology
Elsevier., 276, 573-579.
https://doi.org/10.1016/j.surfcoat.2015.06.013

Stojadinović SD, Tadić N, Radić N, Stojadinovic B, Grbić B, Vasilić R. Synthesis and characterization of Al2O3/ZnO coatings formed by plasma electrolytic oxidation. in Surface and Coatings Technology. 2015;276:573-579.
doi:10.1016/j.surfcoat.2015.06.013 .

Stojadinović, Stevan D.J., Tadić, Nenad, Radić, Nenad, Stojadinovic, B, Grbić, Boško, Vasilić, Rastko, "Synthesis and characterization of Al2O3/ZnO coatings formed by plasma electrolytic oxidation" in Surface and Coatings Technology, 276 (2015):573-579,
https://doi.org/10.1016/j.surfcoat.2015.06.013 . .

TY  - JOUR
AU  - Vasilić, Rastko
AU  - Stojadinović, Stevan D.J.
AU  - Radić, Nenad
AU  - Stefanov, P
AU  - Dohcevic-Mitrovic, Z
AU  - Grbić, Boško
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1744
AB  - In this paper, we have investigated one-step preparation of vanadium doped TiO2 coatings formed by plasma electrolytic oxidation (PEO) of titanium in electrolyte containing 10 g/L Na3PO4 center dot 12H(2)O + 0.5 g/L NH4VO3. The morphology, phase structure, and elemental composition of the formed coatings were characterized by atomic force microscopy (AFM), x-ray diffraction (XRD), and x-ray photoelectron spectroscopy (XPS) techniques. Ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS) was employed to evaluate the band gap energy of obtained coatings. Vanadium doped TiO2 coatings are partly crystallized and mainly composed of anatase phase TiO2, with up to about 2 wt% of vanadium present in the surface layer of the oxide. The valence band photoelectron spectra and UV-Vis DRS showed that vanadium doped TiO2 coatings exhibit notable red shift with respect to the pure TiO2 coatings. The photocatalytic activity was evaluated by monitoring the degradation of methyl orange under simulated sunlight conditions. Photocatalytic activity of vanadium doped TiO2 coatings increases with PEO time. Prolonged PEO times result in higher roughness of obtained coatings, thus increasing surface area available for methyl orange degradation. Vanadium doped TiO2 coatings obtained after 180 s of PEO time exhibit the best photocatalytic activity and about 67% of methyl orange is degraded after 12 h of irradiation under simulated sunlight.
PB  - Elsevier Science Sa, Lausanne
T2  - Materials Chemistry and Physics
T1  - One-step preparation and photocatalytic performance of vanadium doped TiO2 coatings
VL  - 151
SP  - 337
EP  - 344
DO  - 10.1016/j.matchemphys.2014.11.077
ER  - 

@article{
author = "Vasilić, Rastko and Stojadinović, Stevan D.J. and Radić, Nenad and Stefanov, P and Dohcevic-Mitrovic, Z and Grbić, Boško",
year = "2015",
abstract = "In this paper, we have investigated one-step preparation of vanadium doped TiO2 coatings formed by plasma electrolytic oxidation (PEO) of titanium in electrolyte containing 10 g/L Na3PO4 center dot 12H(2)O + 0.5 g/L NH4VO3. The morphology, phase structure, and elemental composition of the formed coatings were characterized by atomic force microscopy (AFM), x-ray diffraction (XRD), and x-ray photoelectron spectroscopy (XPS) techniques. Ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS) was employed to evaluate the band gap energy of obtained coatings. Vanadium doped TiO2 coatings are partly crystallized and mainly composed of anatase phase TiO2, with up to about 2 wt% of vanadium present in the surface layer of the oxide. The valence band photoelectron spectra and UV-Vis DRS showed that vanadium doped TiO2 coatings exhibit notable red shift with respect to the pure TiO2 coatings. The photocatalytic activity was evaluated by monitoring the degradation of methyl orange under simulated sunlight conditions. Photocatalytic activity of vanadium doped TiO2 coatings increases with PEO time. Prolonged PEO times result in higher roughness of obtained coatings, thus increasing surface area available for methyl orange degradation. Vanadium doped TiO2 coatings obtained after 180 s of PEO time exhibit the best photocatalytic activity and about 67% of methyl orange is degraded after 12 h of irradiation under simulated sunlight.",
publisher = "Elsevier Science Sa, Lausanne",
journal = "Materials Chemistry and Physics",
title = "One-step preparation and photocatalytic performance of vanadium doped TiO2 coatings",
volume = "151",
pages = "337-344",
doi = "10.1016/j.matchemphys.2014.11.077"
}

Vasilić, R., Stojadinović, S. D.J., Radić, N., Stefanov, P., Dohcevic-Mitrovic, Z.,& Grbić, B.. (2015). One-step preparation and photocatalytic performance of vanadium doped TiO2 coatings. in Materials Chemistry and Physics
Elsevier Science Sa, Lausanne., 151, 337-344.
https://doi.org/10.1016/j.matchemphys.2014.11.077

Vasilić R, Stojadinović SD, Radić N, Stefanov P, Dohcevic-Mitrovic Z, Grbić B. One-step preparation and photocatalytic performance of vanadium doped TiO2 coatings. in Materials Chemistry and Physics. 2015;151:337-344.
doi:10.1016/j.matchemphys.2014.11.077 .

Vasilić, Rastko, Stojadinović, Stevan D.J., Radić, Nenad, Stefanov, P, Dohcevic-Mitrovic, Z, Grbić, Boško, "One-step preparation and photocatalytic performance of vanadium doped TiO2 coatings" in Materials Chemistry and Physics, 151 (2015):337-344,
https://doi.org/10.1016/j.matchemphys.2014.11.077 . .

TY  - JOUR
AU  - Petrović, Srđan
AU  - Stojadinović, Stevan D.J.
AU  - Rožić, Ljiljana
AU  - Radić, Nenad
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1752
AB  - Plasma electrolytic oxidation of titanium in 12-tungstosilicic acid solution was investigated as a model reaction. The influence of the process parameters (concentration of 12-tungstosilicic acid solution, current density, and time) on the selected process response (efficiency of the methyl orange photodecolorization on the TiO2/WO3 coatings) was studied. A mathematical model was developed using a second-order response surface model with a central composite design incorporating the above-mentioned process parameters. The statistical analysis of experimental data indicates that a concentration of 12-tungstosilicic acid solution; process time, interaction between concentration and process time, and interaction between concentration and quadratic of process time have a significant effect on the methyl orange photodecolorization. Besides, the results show that obtained data were adequately fitted into the second-order polynomial model, since the calculated model F value (39.28) is higher than the critical F value. The values of coefficient of determination (R-2 = 0.960) and adjusted coefficient of determination (R-Adj.(2) = 0.937) are close to 1, indicating a high correlation between the observed and the predicted values. This model can also be useful for setting an optimum value of the process parameters for achieving the maximum efficiency of the methyl orange photodecolorization. Under the optimum conditions established in the region of experimentation (C = 1.14 . 10(-3) M, j = 153 mA/cm(2), and t = 58.9 s), a 38.6% (test duration of 8 h) efficiency of the methyl orange photodecolorization is obtained.
PB  - Elsevier
T2  - Surface and Coatings Technology
T1  - Process modelling and analysis of plasma electrolytic oxidation of titanium for TiO2/WO3 thin film photocatalysts by response surface methodology
VL  - 269
SP  - 250
EP  - 257
DO  - 10.1016/j.surfcoat.2014.12.026
ER  - 

@article{
author = "Petrović, Srđan and Stojadinović, Stevan D.J. and Rožić, Ljiljana and Radić, Nenad and Grbić, Boško and Vasilić, Rastko",
year = "2015",
abstract = "Plasma electrolytic oxidation of titanium in 12-tungstosilicic acid solution was investigated as a model reaction. The influence of the process parameters (concentration of 12-tungstosilicic acid solution, current density, and time) on the selected process response (efficiency of the methyl orange photodecolorization on the TiO2/WO3 coatings) was studied. A mathematical model was developed using a second-order response surface model with a central composite design incorporating the above-mentioned process parameters. The statistical analysis of experimental data indicates that a concentration of 12-tungstosilicic acid solution; process time, interaction between concentration and process time, and interaction between concentration and quadratic of process time have a significant effect on the methyl orange photodecolorization. Besides, the results show that obtained data were adequately fitted into the second-order polynomial model, since the calculated model F value (39.28) is higher than the critical F value. The values of coefficient of determination (R-2 = 0.960) and adjusted coefficient of determination (R-Adj.(2) = 0.937) are close to 1, indicating a high correlation between the observed and the predicted values. This model can also be useful for setting an optimum value of the process parameters for achieving the maximum efficiency of the methyl orange photodecolorization. Under the optimum conditions established in the region of experimentation (C = 1.14 . 10(-3) M, j = 153 mA/cm(2), and t = 58.9 s), a 38.6% (test duration of 8 h) efficiency of the methyl orange photodecolorization is obtained.",
publisher = "Elsevier",
journal = "Surface and Coatings Technology",
title = "Process modelling and analysis of plasma electrolytic oxidation of titanium for TiO2/WO3 thin film photocatalysts by response surface methodology",
volume = "269",
pages = "250-257",
doi = "10.1016/j.surfcoat.2014.12.026"
}

Petrović, S., Stojadinović, S. D.J., Rožić, L., Radić, N., Grbić, B.,& Vasilić, R.. (2015). Process modelling and analysis of plasma electrolytic oxidation of titanium for TiO2/WO3 thin film photocatalysts by response surface methodology. in Surface and Coatings Technology
Elsevier., 269, 250-257.
https://doi.org/10.1016/j.surfcoat.2014.12.026

Petrović S, Stojadinović SD, Rožić L, Radić N, Grbić B, Vasilić R. Process modelling and analysis of plasma electrolytic oxidation of titanium for TiO2/WO3 thin film photocatalysts by response surface methodology. in Surface and Coatings Technology. 2015;269:250-257.
doi:10.1016/j.surfcoat.2014.12.026 .

Petrović, Srđan, Stojadinović, Stevan D.J., Rožić, Ljiljana, Radić, Nenad, Grbić, Boško, Vasilić, Rastko, "Process modelling and analysis of plasma electrolytic oxidation of titanium for TiO2/WO3 thin film photocatalysts by response surface methodology" in Surface and Coatings Technology, 269 (2015):250-257,
https://doi.org/10.1016/j.surfcoat.2014.12.026 . .

TY  - JOUR
AU  - Stojadinović, Stevan D.J.
AU  - Vasilić, Rastko
AU  - Radić, Nenad
AU  - Grbić, Boško
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1802
AB  - In this paper, we have investigated photoluminescence and photocatalytic properties of zirconia films formed by plasma electrolytic oxidation (PEO) of zirconium foil in 0.1 M water solution of citric acid. Zirconia films with diverse morphology and phase structure are formed varying the time of PEO process. Characterization by atomic force microscopy and X-ray diffraction shows that obtained zirconia films mostly consist of monoclinic ZrO2 phase, while corresponding roughness and crystallite size increases with PEO time. Diffuse reflectance spectroscopy has shown that zirconia films have a broad absorption band in the range from 200 nm to 330 nm, indicating that zirconia films could be used as a photocatalyst using ultraviolet radiation. Strong photoluminescence bands are present in spectra featuring four distinct peaks in the 300-600 nm range. The peaks are centered at about 418 nm, 440 nm, 464 nm, and 495 nm. Apparent increase of photoluminescence intensity with PEO time is related to an increase of oxygen vacancy defects in zirconia films formed during the process. Also, higher concentration of oxygen vacancy defects in zirconia films result in higher photocatalytic activity.
PB  - Elsevier
T2  - Optical Materials
T1  - Zirconia films formed by plasma electrolytic oxidation: Photo luminescent and photocatalytic properties
VL  - 40
SP  - 20
EP  - 25
DO  - 10.1016/j.optmat.2014.11.041
ER  - 

@article{
author = "Stojadinović, Stevan D.J. and Vasilić, Rastko and Radić, Nenad and Grbić, Boško",
year = "2015",
abstract = "In this paper, we have investigated photoluminescence and photocatalytic properties of zirconia films formed by plasma electrolytic oxidation (PEO) of zirconium foil in 0.1 M water solution of citric acid. Zirconia films with diverse morphology and phase structure are formed varying the time of PEO process. Characterization by atomic force microscopy and X-ray diffraction shows that obtained zirconia films mostly consist of monoclinic ZrO2 phase, while corresponding roughness and crystallite size increases with PEO time. Diffuse reflectance spectroscopy has shown that zirconia films have a broad absorption band in the range from 200 nm to 330 nm, indicating that zirconia films could be used as a photocatalyst using ultraviolet radiation. Strong photoluminescence bands are present in spectra featuring four distinct peaks in the 300-600 nm range. The peaks are centered at about 418 nm, 440 nm, 464 nm, and 495 nm. Apparent increase of photoluminescence intensity with PEO time is related to an increase of oxygen vacancy defects in zirconia films formed during the process. Also, higher concentration of oxygen vacancy defects in zirconia films result in higher photocatalytic activity.",
publisher = "Elsevier",
journal = "Optical Materials",
title = "Zirconia films formed by plasma electrolytic oxidation: Photo luminescent and photocatalytic properties",
volume = "40",
pages = "20-25",
doi = "10.1016/j.optmat.2014.11.041"
}

Stojadinović, S. D.J., Vasilić, R., Radić, N.,& Grbić, B.. (2015). Zirconia films formed by plasma electrolytic oxidation: Photo luminescent and photocatalytic properties. in Optical Materials
Elsevier., 40, 20-25.
https://doi.org/10.1016/j.optmat.2014.11.041

Stojadinović SD, Vasilić R, Radić N, Grbić B. Zirconia films formed by plasma electrolytic oxidation: Photo luminescent and photocatalytic properties. in Optical Materials. 2015;40:20-25.
doi:10.1016/j.optmat.2014.11.041 .

Stojadinović, Stevan D.J., Vasilić, Rastko, Radić, Nenad, Grbić, Boško, "Zirconia films formed by plasma electrolytic oxidation: Photo luminescent and photocatalytic properties" in Optical Materials, 40 (2015):20-25,
https://doi.org/10.1016/j.optmat.2014.11.041 . .

TY  - JOUR
AU  - Stojadinović, Stevan
AU  - Tadić, Nenad
AU  - Radić, Nenad
AU  - Stefanov, Plamen
AU  - Grbić, Boško
AU  - Vasilić, Rastko
PY  - 2015
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1817
AB  - This article reports on properties of oxide films obtained by anodization of niobium in phosphoric acid before and after the dielectric breakdown. Weak anodic luminescence of barrier oxide films formed during the anodization of niobium is correlated to the existence of morphological defects in the oxide layer. Small sized sparks generated by dielectric breakdown of formed oxide film cause rapid increase of luminescence intensity. The luminescence spectrum of obtained films on niobium under spark discharging is composed of continuum radiation and spectral lines caused by electronic spark discharging transitions in oxygen and hydrogen atoms. Oxide films formed before the breakdown are amorphous, while after the breakdown oxide films are partly crystalline and mainly composed of Nb2O5 hexagonal phase. The photocatalytic activity of obtained oxide films after the breakdown was investigated by monitoring the degradation of methyl orange. Increase of the photocatalytic activity with time is related to an increase of oxygen vacancy defects in oxide films formed during the process. Also, higher concentration of oxygen vacancy defects in oxide films results in higher photoluminescence intensity.
PB  - Elsevier
T2  - Applied Surface Science
T1  - Anodic luminescence, structural, photoluminescent, and photocatalytic properties of anodic oxide films grown on niobium in phosphoric acid
VL  - 355
SP  - 912
EP  - 920
DO  - 10.1016/j.apsusc.2015.07.174
ER  - 

@article{
author = "Stojadinović, Stevan and Tadić, Nenad and Radić, Nenad and Stefanov, Plamen and Grbić, Boško and Vasilić, Rastko",
year = "2015",
abstract = "This article reports on properties of oxide films obtained by anodization of niobium in phosphoric acid before and after the dielectric breakdown. Weak anodic luminescence of barrier oxide films formed during the anodization of niobium is correlated to the existence of morphological defects in the oxide layer. Small sized sparks generated by dielectric breakdown of formed oxide film cause rapid increase of luminescence intensity. The luminescence spectrum of obtained films on niobium under spark discharging is composed of continuum radiation and spectral lines caused by electronic spark discharging transitions in oxygen and hydrogen atoms. Oxide films formed before the breakdown are amorphous, while after the breakdown oxide films are partly crystalline and mainly composed of Nb2O5 hexagonal phase. The photocatalytic activity of obtained oxide films after the breakdown was investigated by monitoring the degradation of methyl orange. Increase of the photocatalytic activity with time is related to an increase of oxygen vacancy defects in oxide films formed during the process. Also, higher concentration of oxygen vacancy defects in oxide films results in higher photoluminescence intensity.",
publisher = "Elsevier",
journal = "Applied Surface Science",
title = "Anodic luminescence, structural, photoluminescent, and photocatalytic properties of anodic oxide films grown on niobium in phosphoric acid",
volume = "355",
pages = "912-920",
doi = "10.1016/j.apsusc.2015.07.174"
}

Stojadinović, S., Tadić, N., Radić, N., Stefanov, P., Grbić, B.,& Vasilić, R.. (2015). Anodic luminescence, structural, photoluminescent, and photocatalytic properties of anodic oxide films grown on niobium in phosphoric acid. in Applied Surface Science
Elsevier., 355, 912-920.
https://doi.org/10.1016/j.apsusc.2015.07.174

Stojadinović S, Tadić N, Radić N, Stefanov P, Grbić B, Vasilić R. Anodic luminescence, structural, photoluminescent, and photocatalytic properties of anodic oxide films grown on niobium in phosphoric acid. in Applied Surface Science. 2015;355:912-920.
doi:10.1016/j.apsusc.2015.07.174 .

Stojadinović, Stevan, Tadić, Nenad, Radić, Nenad, Stefanov, Plamen, Grbić, Boško, Vasilić, Rastko, "Anodic luminescence, structural, photoluminescent, and photocatalytic properties of anodic oxide films grown on niobium in phosphoric acid" in Applied Surface Science, 355 (2015):912-920,
https://doi.org/10.1016/j.apsusc.2015.07.174 . .