Porous carbon air-electrodes activated by CoPC, FePHP, PdPC, PtPC and metal-free PC were studied in 2 mol dm-3 NaCl electrolyte. The activity of heat-treated carbon activated by CoPC was compared to carbon activated by in situ formed Co oxide. All the results show that the main catalytic activity of the catalyst used comes from the central metal atom used, while the chelate or oxide structures serve predominantly to keep the metal in the stable form at the carbon surface. Metal-free phthalocyanine does not show any catalytic activity for oxygen reduction.
TY - JOUR
AU - Dražić, Dragutin M.
AU - Ledinski, Z. V.
AU - Zečević, Strahinja K.
PY - 1983
UR - https://cer.ihtm.bg.ac.rs/handle/123456789/4427
AB - Porous carbon air-electrodes activated by CoPC, FePHP, PdPC, PtPC and metal-free PC were studied in 2 mol dm-3 NaCl electrolyte. The activity of heat-treated carbon activated by CoPC was compared to carbon activated by in situ formed Co oxide. All the results show that the main catalytic activity of the catalyst used comes from the central metal atom used, while the chelate or oxide structures serve predominantly to keep the metal in the stable form at the carbon surface. Metal-free phthalocyanine does not show any catalytic activity for oxygen reduction.
PB - Springer Nature
T2 - Journal of Applied Electrochemistry
T1 - Transition metal catalysts for porous carbon air-electrodes in neutral chloride electrolytes
VL - 13
IS - 3
SP - 337
EP - 340
DO - 10.1007/BF00941605
ER -
@article{
author = "Dražić, Dragutin M. and Ledinski, Z. V. and Zečević, Strahinja K.",
year = "1983",
abstract = "Porous carbon air-electrodes activated by CoPC, FePHP, PdPC, PtPC and metal-free PC were studied in 2 mol dm-3 NaCl electrolyte. The activity of heat-treated carbon activated by CoPC was compared to carbon activated by in situ formed Co oxide. All the results show that the main catalytic activity of the catalyst used comes from the central metal atom used, while the chelate or oxide structures serve predominantly to keep the metal in the stable form at the carbon surface. Metal-free phthalocyanine does not show any catalytic activity for oxygen reduction.",
publisher = "Springer Nature",
journal = "Journal of Applied Electrochemistry",
title = "Transition metal catalysts for porous carbon air-electrodes in neutral chloride electrolytes",
volume = "13",
number = "3",
pages = "337-340",
doi = "10.1007/BF00941605"
}
Dražić, D. M., Ledinski, Z. V.,& Zečević, S. K.. (1983). Transition metal catalysts for porous carbon air-electrodes in neutral chloride electrolytes. in Journal of Applied Electrochemistry
Springer Nature., 13(3), 337-340.
https://doi.org/10.1007/BF00941605
Dražić DM, Ledinski ZV, Zečević SK. Transition metal catalysts for porous carbon air-electrodes in neutral chloride electrolytes. in Journal of Applied Electrochemistry. 1983;13(3):337-340.
doi:10.1007/BF00941605 .
Dražić, Dragutin M., Ledinski, Z. V., Zečević, Strahinja K., "Transition metal catalysts for porous carbon air-electrodes in neutral chloride electrolytes" in Journal of Applied Electrochemistry, 13, no. 3 (1983):337-340,
https://doi.org/10.1007/BF00941605 . .
