On the deactivation mechanism of RuO2–TiO2/Ti anodes prepared by the sol–gel procedure
Само за регистроване кориснике
2005
Аутори
Panić, VladimirDekanski, Aleksandar
Mišković-Stanković, Vesna
Milonjić, Slobodan
Nikolić, Branislav
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
The deactivation process that leads to the end of titanium supported RuO2-TiO2 coating service life, for anodes prepared from RuO2 and TiO2 sols, as well as by the conventional thermal decomposition of RuCl3 and TiCl3, was investigated. The loss of electrocatalytic activity was registered by an accelerated stability test in 0.50 mol dm-3 NaCl electrolyte, while the changes in the electrochemical properties were monitored during the stability test by cyclic voltammetry, polarization measurements and electrochemical impedance spectroscopy in 1.0 mol dm-3 HClO 4 and in 0.50 mol dm-3 NaCl. The changes in anode behavior suggest that the essential cause for the deactivation of the anode prepared by the sol-gel procedure is the formation of an insulating TiO 2-rich layer at the coating surface due to the continuous dissolution of the Ru active species. However, the growth of the insulating TiO2 layer in the coating/Ti substrate interphase mainly causes deactivation of the thermally prepared a...node. The deactivation mechanism appeared to be the consequence of the different morphology of the coatings prepared by two different procedures.
Кључне речи:
RuO2–TiO2 coating / Oxide sols / Sol–gel procedure / Deactivation mechanism / A.c. impedanceИзвор:
Journal of Electroanalytical Chemistry, 2005, 579, 1, 67-76Издавач:
- Elsevier
Финансирање / пројекти:
- The Ministry of Science and Environment Protection, Republic of Serbia, Contract No. 1230.
DOI: 10.1016/j.jelechem.2005.01.026
ISSN: 1572-6657; 1873-2569
WoS: 000228880400008
Scopus: 2-s2.0-17544363698
Институција/група
IHTMTY - JOUR AU - Panić, Vladimir AU - Dekanski, Aleksandar AU - Mišković-Stanković, Vesna AU - Milonjić, Slobodan AU - Nikolić, Branislav PY - 2005 UR - https://cer.ihtm.bg.ac.rs/handle/123456789/4134 AB - The deactivation process that leads to the end of titanium supported RuO2-TiO2 coating service life, for anodes prepared from RuO2 and TiO2 sols, as well as by the conventional thermal decomposition of RuCl3 and TiCl3, was investigated. The loss of electrocatalytic activity was registered by an accelerated stability test in 0.50 mol dm-3 NaCl electrolyte, while the changes in the electrochemical properties were monitored during the stability test by cyclic voltammetry, polarization measurements and electrochemical impedance spectroscopy in 1.0 mol dm-3 HClO 4 and in 0.50 mol dm-3 NaCl. The changes in anode behavior suggest that the essential cause for the deactivation of the anode prepared by the sol-gel procedure is the formation of an insulating TiO 2-rich layer at the coating surface due to the continuous dissolution of the Ru active species. However, the growth of the insulating TiO2 layer in the coating/Ti substrate interphase mainly causes deactivation of the thermally prepared anode. The deactivation mechanism appeared to be the consequence of the different morphology of the coatings prepared by two different procedures. PB - Elsevier T2 - Journal of Electroanalytical Chemistry T1 - On the deactivation mechanism of RuO2–TiO2/Ti anodes prepared by the sol–gel procedure VL - 579 IS - 1 SP - 67 EP - 76 DO - 10.1016/j.jelechem.2005.01.026 ER -
@article{ author = "Panić, Vladimir and Dekanski, Aleksandar and Mišković-Stanković, Vesna and Milonjić, Slobodan and Nikolić, Branislav", year = "2005", abstract = "The deactivation process that leads to the end of titanium supported RuO2-TiO2 coating service life, for anodes prepared from RuO2 and TiO2 sols, as well as by the conventional thermal decomposition of RuCl3 and TiCl3, was investigated. The loss of electrocatalytic activity was registered by an accelerated stability test in 0.50 mol dm-3 NaCl electrolyte, while the changes in the electrochemical properties were monitored during the stability test by cyclic voltammetry, polarization measurements and electrochemical impedance spectroscopy in 1.0 mol dm-3 HClO 4 and in 0.50 mol dm-3 NaCl. The changes in anode behavior suggest that the essential cause for the deactivation of the anode prepared by the sol-gel procedure is the formation of an insulating TiO 2-rich layer at the coating surface due to the continuous dissolution of the Ru active species. However, the growth of the insulating TiO2 layer in the coating/Ti substrate interphase mainly causes deactivation of the thermally prepared anode. The deactivation mechanism appeared to be the consequence of the different morphology of the coatings prepared by two different procedures.", publisher = "Elsevier", journal = "Journal of Electroanalytical Chemistry", title = "On the deactivation mechanism of RuO2–TiO2/Ti anodes prepared by the sol–gel procedure", volume = "579", number = "1", pages = "67-76", doi = "10.1016/j.jelechem.2005.01.026" }
Panić, V., Dekanski, A., Mišković-Stanković, V., Milonjić, S.,& Nikolić, B.. (2005). On the deactivation mechanism of RuO2–TiO2/Ti anodes prepared by the sol–gel procedure. in Journal of Electroanalytical Chemistry Elsevier., 579(1), 67-76. https://doi.org/10.1016/j.jelechem.2005.01.026
Panić V, Dekanski A, Mišković-Stanković V, Milonjić S, Nikolić B. On the deactivation mechanism of RuO2–TiO2/Ti anodes prepared by the sol–gel procedure. in Journal of Electroanalytical Chemistry. 2005;579(1):67-76. doi:10.1016/j.jelechem.2005.01.026 .
Panić, Vladimir, Dekanski, Aleksandar, Mišković-Stanković, Vesna, Milonjić, Slobodan, Nikolić, Branislav, "On the deactivation mechanism of RuO2–TiO2/Ti anodes prepared by the sol–gel procedure" in Journal of Electroanalytical Chemistry, 579, no. 1 (2005):67-76, https://doi.org/10.1016/j.jelechem.2005.01.026 . .