Oxygen reduction has been studied in alkaline solution on a ruthenium electrode modified by thallium and lead adsorbates. A partially oxidized ruthenium electrode is inactive for oxygen reduction. Thallium and lead adsorbates cause pronounced changes on the ruthenium surface giving rise to a four electron-reduction of oxygen. Disc-ring electrode measurements show a predominant direct four electron-reduction, with a first charge-transfer rate determining step. Mass fractions of various reaction pathways have been calculated and the model explaining a direct four electron-reduction discussed. Once activated, ruthenium retains its activity even in the absence of thallium and lead ions in solution phase.
TY - JOUR
AU - Anastasijević, Nikola A.
AU - Dimitrijević, Z. M.
AU - Adžić, Radoslav R.
PY - 1992
UR - https://cer.ihtm.bg.ac.rs/handle/123456789/4733
AB - Oxygen reduction has been studied in alkaline solution on a ruthenium electrode modified by thallium and lead adsorbates. A partially oxidized ruthenium electrode is inactive for oxygen reduction. Thallium and lead adsorbates cause pronounced changes on the ruthenium surface giving rise to a four electron-reduction of oxygen. Disc-ring electrode measurements show a predominant direct four electron-reduction, with a first charge-transfer rate determining step. Mass fractions of various reaction pathways have been calculated and the model explaining a direct four electron-reduction discussed. Once activated, ruthenium retains its activity even in the absence of thallium and lead ions in solution phase.
PB - Elsevier
T2 - Electrochimica Acta
T1 - Oxygen reduction on a modified ruthenium electrode
VL - 37
IS - 3
SP - 457
EP - 464
DO - 10.1016/0013-4686(92)87036-Y
ER -
@article{
author = "Anastasijević, Nikola A. and Dimitrijević, Z. M. and Adžić, Radoslav R.",
year = "1992",
url = "https://cer.ihtm.bg.ac.rs/handle/123456789/4733",
abstract = "Oxygen reduction has been studied in alkaline solution on a ruthenium electrode modified by thallium and lead adsorbates. A partially oxidized ruthenium electrode is inactive for oxygen reduction. Thallium and lead adsorbates cause pronounced changes on the ruthenium surface giving rise to a four electron-reduction of oxygen. Disc-ring electrode measurements show a predominant direct four electron-reduction, with a first charge-transfer rate determining step. Mass fractions of various reaction pathways have been calculated and the model explaining a direct four electron-reduction discussed. Once activated, ruthenium retains its activity even in the absence of thallium and lead ions in solution phase.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Oxygen reduction on a modified ruthenium electrode",
volume = "37",
number = "3",
pages = "457-464",
doi = "10.1016/0013-4686(92)87036-Y"
}
Anastasijević, N. A., Dimitrijević, Z. M.,& Adžić, R. R. (1992). Oxygen reduction on a modified ruthenium electrode.
Electrochimica Acta
Elsevier., 37(3), 457-464.
https://doi.org/10.1016/0013-4686(92)87036-Y
Anastasijević NA, Dimitrijević ZM, Adžić RR. Oxygen reduction on a modified ruthenium electrode. Electrochimica Acta. 1992;37(3):457-464
Anastasijević Nikola A., Dimitrijević Z. M., Adžić Radoslav R., "Oxygen reduction on a modified ruthenium electrode" Electrochimica Acta, 37, no. 3 (1992):457-464,
https://doi.org/10.1016/0013-4686(92)87036-Y .
