TY  - CONF
AU  - Nikolić, Nenad
AU  - Senćanski, Jelena
AU  - Blagojević, Stevan
AU  - Pagnacco, Maja
AU  - Stojković Simatović, Ivana
PY  - 2023
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6966
AB  - Due to Li-ion batteries having become the main power source of most portable electronic devices, their waste has also become a significant environmental problem. To find batteries that would be environmentally friendly, this work examines Zn-ion batteries in an aqueous solution of ZnCl2. The ZnMnO4 was synthesized by glycine nitrate combustion of Zn(NO3)2, Mn(NO3)2 and glycine as a chelating agent [1]. The structure of the material obtained was characterized by X-ray powder diffraction (XRPD) showing a spinel structure; the morphology was characterized by scanning
electron microscopy (SEM) showing that nano-particles were obtained. The electrochemical characterization was done by cyclic voltammetry in an aqueous solution of ZnCl2. The mixture pasted on the glossy carbon electrode was prepared by mixing the cathode material, graphite and polyvinyl diene difluoride (PVDF) in a ratio 85:10:5 [2]. Due to the low discharge capacity obtained of ~14 mAh g-1 for 5 mV s-1 , further examination was done by adding 1 ml of 1M Mn(NO3)2 into 10ml of a saturated aqueous solution of ZnCl2. After adding the Mn(NO3)2 , the discharge
capacity increased from ~14 mAh g-1 to ~65 mAh g-1 at the same polarization rate, making this additive a promising one for aqueous Zn-ion batteries. Further investigation needs to be directed to adding the same additive in larger amounts compared to 1ml to the same volume of the electrolyte. The results obtained suggest the aqueous Zn-ion battery described in this work to be a potentially promising “green” battery that may replace harmful commercial organic Li-ion batteries.
PB  - Institut za multidisciplinarna istraživanja
C3  - Programme and book of abstracts - 7th Conference of the Serbian Society for Ceramic Materials, 7CSCS-2023, June 14-16. 2023, Belgrade, Serbia
T1  - ZnMn2O4 as a Cathode Material in an Aqueous Solution of ZnCl2 and Mn(NO3)2 for Zn-ion Batteries
SP  - 103
EP  - 103
UR  - https://hdl.handle.net/21.15107/rcub_cer_6966
ER  - 

@conference{
author = "Nikolić, Nenad and Senćanski, Jelena and Blagojević, Stevan and Pagnacco, Maja and Stojković Simatović, Ivana",
year = "2023",
abstract = "Due to Li-ion batteries having become the main power source of most portable electronic devices, their waste has also become a significant environmental problem. To find batteries that would be environmentally friendly, this work examines Zn-ion batteries in an aqueous solution of ZnCl2. The ZnMnO4 was synthesized by glycine nitrate combustion of Zn(NO3)2, Mn(NO3)2 and glycine as a chelating agent [1]. The structure of the material obtained was characterized by X-ray powder diffraction (XRPD) showing a spinel structure; the morphology was characterized by scanning
electron microscopy (SEM) showing that nano-particles were obtained. The electrochemical characterization was done by cyclic voltammetry in an aqueous solution of ZnCl2. The mixture pasted on the glossy carbon electrode was prepared by mixing the cathode material, graphite and polyvinyl diene difluoride (PVDF) in a ratio 85:10:5 [2]. Due to the low discharge capacity obtained of ~14 mAh g-1 for 5 mV s-1 , further examination was done by adding 1 ml of 1M Mn(NO3)2 into 10ml of a saturated aqueous solution of ZnCl2. After adding the Mn(NO3)2 , the discharge
capacity increased from ~14 mAh g-1 to ~65 mAh g-1 at the same polarization rate, making this additive a promising one for aqueous Zn-ion batteries. Further investigation needs to be directed to adding the same additive in larger amounts compared to 1ml to the same volume of the electrolyte. The results obtained suggest the aqueous Zn-ion battery described in this work to be a potentially promising “green” battery that may replace harmful commercial organic Li-ion batteries.",
publisher = "Institut za multidisciplinarna istraživanja",
journal = "Programme and book of abstracts - 7th Conference of the Serbian Society for Ceramic Materials, 7CSCS-2023, June 14-16. 2023, Belgrade, Serbia",
title = "ZnMn2O4 as a Cathode Material in an Aqueous Solution of ZnCl2 and Mn(NO3)2 for Zn-ion Batteries",
pages = "103-103",
url = "https://hdl.handle.net/21.15107/rcub_cer_6966"
}

Nikolić, N., Senćanski, J., Blagojević, S., Pagnacco, M.,& Stojković Simatović, I.. (2023). ZnMn2O4 as a Cathode Material in an Aqueous Solution of ZnCl2 and Mn(NO3)2 for Zn-ion Batteries. in Programme and book of abstracts - 7th Conference of the Serbian Society for Ceramic Materials, 7CSCS-2023, June 14-16. 2023, Belgrade, Serbia
Institut za multidisciplinarna istraživanja., 103-103.
https://hdl.handle.net/21.15107/rcub_cer_6966

Nikolić N, Senćanski J, Blagojević S, Pagnacco M, Stojković Simatović I. ZnMn2O4 as a Cathode Material in an Aqueous Solution of ZnCl2 and Mn(NO3)2 for Zn-ion Batteries. in Programme and book of abstracts - 7th Conference of the Serbian Society for Ceramic Materials, 7CSCS-2023, June 14-16. 2023, Belgrade, Serbia. 2023;:103-103.
https://hdl.handle.net/21.15107/rcub_cer_6966 .

Nikolić, Nenad, Senćanski, Jelena, Blagojević, Stevan, Pagnacco, Maja, Stojković Simatović, Ivana, "ZnMn2O4 as a Cathode Material in an Aqueous Solution of ZnCl2 and Mn(NO3)2 for Zn-ion Batteries" in Programme and book of abstracts - 7th Conference of the Serbian Society for Ceramic Materials, 7CSCS-2023, June 14-16. 2023, Belgrade, Serbia (2023):103-103,
https://hdl.handle.net/21.15107/rcub_cer_6966 .

TY  - JOUR
AU  - Rakočević, Lazar
AU  - Stojković Simatović, Ivana
AU  - Maksić, Aleksandar
AU  - Rajić, Vladimir
AU  - Štrbac, Svetlana
AU  - Srejić, Irina
PY  - 2022
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5292
AB  - PtAu nanoparticles spontaneously deposited on graphene support, PtAu/rGO, have shown
remarkably high catalytic activity for hydrogen evolution reaction (HER) in sulfuric acid solution.
SEM images of the PtAu/rGO electrode surface showed that Pt nanoparticles that are non-uniform
in size occupy both the edges of previously deposited uniform Au nanoparticles and the edges of
graphene support. XPS analysis showed that the atomic percentages of Au and Pt in PtAu/rGO were
0.6% and 0.3%, respectively. The atomic percentage of Au alone on previously prepared Au/rGO
was 0.7%. Outstanding HER activity was achieved for the PtAu/rGO electrode, showing the initial
potential close to the equilibrium potential for HER and a low Tafel slope of −38 mV/dec. This
was confirmed by electrochemical impedance spectroscopy. The chronoamperometric measurement
performed for 40 min for hydrogen evolution at a constant potential indicated good stability and
durability of the PtAu/rGO electrode.
T2  - Catalysis
T1  - PtAu Nanoparticles Supported by Reduced Graphene Oxide as a Highly Active Catalyst for Hydrogen Evolution
VL  - 12
IS  - 43
SP  - 2
EP  - 13
DO  - 10.3390/catal12010043
ER  - 

@article{
author = "Rakočević, Lazar and Stojković Simatović, Ivana and Maksić, Aleksandar and Rajić, Vladimir and Štrbac, Svetlana and Srejić, Irina",
year = "2022",
abstract = "PtAu nanoparticles spontaneously deposited on graphene support, PtAu/rGO, have shown
remarkably high catalytic activity for hydrogen evolution reaction (HER) in sulfuric acid solution.
SEM images of the PtAu/rGO electrode surface showed that Pt nanoparticles that are non-uniform
in size occupy both the edges of previously deposited uniform Au nanoparticles and the edges of
graphene support. XPS analysis showed that the atomic percentages of Au and Pt in PtAu/rGO were
0.6% and 0.3%, respectively. The atomic percentage of Au alone on previously prepared Au/rGO
was 0.7%. Outstanding HER activity was achieved for the PtAu/rGO electrode, showing the initial
potential close to the equilibrium potential for HER and a low Tafel slope of −38 mV/dec. This
was confirmed by electrochemical impedance spectroscopy. The chronoamperometric measurement
performed for 40 min for hydrogen evolution at a constant potential indicated good stability and
durability of the PtAu/rGO electrode.",
journal = "Catalysis",
title = "PtAu Nanoparticles Supported by Reduced Graphene Oxide as a Highly Active Catalyst for Hydrogen Evolution",
volume = "12",
number = "43",
pages = "2-13",
doi = "10.3390/catal12010043"
}

Rakočević, L., Stojković Simatović, I., Maksić, A., Rajić, V., Štrbac, S.,& Srejić, I.. (2022). PtAu Nanoparticles Supported by Reduced Graphene Oxide as a Highly Active Catalyst for Hydrogen Evolution. in Catalysis, 12(43), 2-13.
https://doi.org/10.3390/catal12010043

Rakočević L, Stojković Simatović I, Maksić A, Rajić V, Štrbac S, Srejić I. PtAu Nanoparticles Supported by Reduced Graphene Oxide as a Highly Active Catalyst for Hydrogen Evolution. in Catalysis. 2022;12(43):2-13.
doi:10.3390/catal12010043 .

Rakočević, Lazar, Stojković Simatović, Ivana, Maksić, Aleksandar, Rajić, Vladimir, Štrbac, Svetlana, Srejić, Irina, "PtAu Nanoparticles Supported by Reduced Graphene Oxide as a Highly Active Catalyst for Hydrogen Evolution" in Catalysis, 12, no. 43 (2022):2-13,
https://doi.org/10.3390/catal12010043 . .

TY  - JOUR
AU  - Rakočević, Lazar
AU  - Štrbac, Svetlana
AU  - Potočnik, Jelena
AU  - Popović, Maja
AU  - Jugović, Dragana
AU  - Stojković Šimatović, Ivana
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4235
AB  - Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.
PB  - Elsevier
T2  - Ceramics International
T1  - The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries
VL  - 47
IS  - 4
SP  - 4595
EP  - 4603
DO  - 10.1016/j.ceramint.2020.10.025
ER  - 

@article{
author = "Rakočević, Lazar and Štrbac, Svetlana and Potočnik, Jelena and Popović, Maja and Jugović, Dragana and Stojković Šimatović, Ivana",
year = "2021",
abstract = "Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries",
volume = "47",
number = "4",
pages = "4595-4603",
doi = "10.1016/j.ceramint.2020.10.025"
}

Rakočević, L., Štrbac, S., Potočnik, J., Popović, M., Jugović, D.,& Stojković Šimatović, I.. (2021). The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International
Elsevier., 47(4), 4595-4603.
https://doi.org/10.1016/j.ceramint.2020.10.025

Rakočević L, Štrbac S, Potočnik J, Popović M, Jugović D, Stojković Šimatović I. The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International. 2021;47(4):4595-4603.
doi:10.1016/j.ceramint.2020.10.025 .

Rakočević, Lazar, Štrbac, Svetlana, Potočnik, Jelena, Popović, Maja, Jugović, Dragana, Stojković Šimatović, Ivana, "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries" in Ceramics International, 47, no. 4 (2021):4595-4603,
https://doi.org/10.1016/j.ceramint.2020.10.025 . .

TY  - JOUR
AU  - Rakočević, Lazar
AU  - Štrbac, Svetlana
AU  - Potočnik, Jelena
AU  - Popović, Maja
AU  - Jugović, Dragana
AU  - Stojković Šimatović, Ivana
PY  - 2021
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/5542
AB  - Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.
PB  - Elsevier
T2  - Ceramics International
T1  - The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries
VL  - 47
IS  - 4
SP  - 4595
EP  - 4603
DO  - 10.1016/j.ceramint.2020.10.025
ER  - 

@article{
author = "Rakočević, Lazar and Štrbac, Svetlana and Potočnik, Jelena and Popović, Maja and Jugović, Dragana and Stojković Šimatović, Ivana",
year = "2021",
abstract = "Cathodic material for sodium-ion rechargeable batteries based on NaxMnO2 were synthesized by glycine nitrate method and subsequent annealing at high temperatures. Different crystal structures with different morphologies were obtained depending on the annealing temperature: hexagonal layeredα-Na0.7MnO2.05 nanoplates were obtained at 850 ◦C, while 3-D tunnel structured Na0⋅4MnO2 and Na0⋅44MnO2, both with rod-like morphology, were obtained at 800 ◦C and 900 ◦C, respectively. The investigations of the electrochemical behavior of obtained cathodic materials in aqueous NaNO3 solution have shown that Na0⋅44MnO2 obtained at 900 ◦C has shown the best battery performance. Its initial discharge capacities are 123.5 mA h/g, 113.2 mA h/g, and 102.0 mA h/g at the high current densities of 1000, 2000 and 5000 mA/g, respectively.",
publisher = "Elsevier",
journal = "Ceramics International",
title = "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries",
volume = "47",
number = "4",
pages = "4595-4603",
doi = "10.1016/j.ceramint.2020.10.025"
}

Rakočević, L., Štrbac, S., Potočnik, J., Popović, M., Jugović, D.,& Stojković Šimatović, I.. (2021). The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International
Elsevier., 47(4), 4595-4603.
https://doi.org/10.1016/j.ceramint.2020.10.025

Rakočević L, Štrbac S, Potočnik J, Popović M, Jugović D, Stojković Šimatović I. The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries. in Ceramics International. 2021;47(4):4595-4603.
doi:10.1016/j.ceramint.2020.10.025 .

Rakočević, Lazar, Štrbac, Svetlana, Potočnik, Jelena, Popović, Maja, Jugović, Dragana, Stojković Šimatović, Ivana, "The NaxMnO2 materials prepared by a glycine-nitrate method as advanced cathode materials for aqueous sodium-ion rechargeable batteries" in Ceramics International, 47, no. 4 (2021):4595-4603,
https://doi.org/10.1016/j.ceramint.2020.10.025 . .