2008
DOI: 10.1016/j.jelechem.2008.04.017
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Electrocatalytic oxygen reduction by Co(III) porphyrins incorporated in aerogel carbon electrodes

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Cited by 40 publications
(41 citation statements)
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“…In the case of the Fe‐corrole, the first step reaches the limiting current at approximately 0.6 V and the second at 0.3 V versus RHE. The phenomenon of mixed reaction mechanisms, manifested by multiple catalytic waves, was observed in the past and explained by the presence of different catalytic sites on the electrode surface . This is possible if some of the macrocyclic complex interacts with surface moieties on the carbon support …”
Section: Resultsmentioning
confidence: 95%
“…In the case of the Fe‐corrole, the first step reaches the limiting current at approximately 0.6 V and the second at 0.3 V versus RHE. The phenomenon of mixed reaction mechanisms, manifested by multiple catalytic waves, was observed in the past and explained by the presence of different catalytic sites on the electrode surface . This is possible if some of the macrocyclic complex interacts with surface moieties on the carbon support …”
Section: Resultsmentioning
confidence: 95%
“…The surface area 382 m 2 /g (∼ 3.8 m 2 per 1 geometrical cm 2 ) and the surface pore distribution (128 m 2 /g for the micropores (≤ 2 nm) and 254 m 2 /g for the meso-and macropores) were obtained by the Brunauer, Emmet, and Teller (BET) technique, as described elsewhere. 17 Catalytic electrodes containing Pt or PtRu were obtained by filtering repeatedly the BmimBF 4 solutions containing the respective nanoparticles through the CAE sheets. These were then immersed in an alcohol Nafion (5%) solution for 24 h, followed by air drying.…”
Section: Methodsmentioning
confidence: 99%
“…[27] This has been explained as a statistical proximity effect, which allows cooperative catalysis by adjacent Mn-oxo porphyrins. [31] This paper describes the spectroscopic and electrochemical properties of self-assembled structures obtained by the interaction of negatively charged carboxylic-rich graphene oxide (CGO) and a positively charged Mn III porphyrin [manganese(III) tetrakis(N-methyl-4-pyridinio)porphyrin, MnTMPyP]. [31] This paper describes the spectroscopic and electrochemical properties of self-assembled structures obtained by the interaction of negatively charged carboxylic-rich graphene oxide (CGO) and a positively charged Mn III porphyrin [manganese(III) tetrakis(N-methyl-4-pyridinio)porphyrin, MnTMPyP].…”
Section: Introductionmentioning
confidence: 99%