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 inRSC advances Vol. 9; no. 72; pp. 42554 - 4256
Main Authors Li, Yun-Wu, Zhang, Wen-Jie, Li, Chun-Xia, Gu, Lin, Du, Hong-Mei, Ma, Hui-Yan, Wang, Su-Na, Zhao, Jin-Sheng
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 23.12.2019
The Royal Society of Chemistry
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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.
Bibliography:10.1039/c9ra08068f
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ISSN:2046-2069
2046-2069
DOI:10.1039/c9ra08068f