A dinuclear cobalt cluster as electrocatalyst for oxygen reduction reaction
Dinuclear metal clusters as metalloenzymes execute efficient catalytic activities in biological systems. Enlightened by this, a dinuclear {Co II 2 } cluster was selected to survey its ORR (Oxygen Reduction Reaction) catalytic activities. The crystalline {Co II 2 } possesses defined structure and pot...
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Published in | RSC advances Vol. 9; no. 72; pp. 42554 - 4256 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
23.12.2019
The Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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Summary: | Dinuclear metal clusters as metalloenzymes execute efficient catalytic activities in biological systems. Enlightened by this, a dinuclear {Co
II
2
} cluster was selected to survey its ORR (Oxygen Reduction Reaction) catalytic activities. The crystalline {Co
II
2
} possesses defined structure and potential catalytic active centers of {CoN
4
O
2
} sites, which was identified by X-ray single crystal diffraction, Raman and XPS. The appropriate supramolecular porosity combining abundant pyridinic-N and triazole-N sites of {Co
II
2
} catalyst synergistically benefit the ORR performance. As a result, this non-noble metal catalyst presents a nice ORR electrocatalytic activity and abides by a nearly 4-electron reduction pathway. Thus, this unpyrolyzed crystalline catalyst clearly provide precise active sites and the whole defined structural information, which can help researcher to design and fabricate efficient ORR catalysts to improve their activities. Considering the visible crystal structure, a single cobalt center-mediated catalytic mechanism was also proposed to elucidate the ORR process.
A Pt-free dinuclear {Co
II
2
} cluster was selected to research its ORR catalytic activities. The {Co
II
2
} possesses defined crystal structure and displays a nice ORR electrocatalytic performance by a nearly 4-electrons reduction pathway. |
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Bibliography: | 10.1039/c9ra08068f Electronic supplementary information (ESI) available. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c9ra08068f |