Observation of oxygen evolution over a {Ni12}-cluster-based metal-organic framework

被引:0
|
作者
Zongsu Han
Zheng Yan
Kunyu Wang
Xinchen Kang
Kai Lv
Xiaoping Zhang
Zhen Zhou
Sihai Yang
Wei Shi
Peng Cheng
机构
[1] Nankai University,Department of Chemistry, Key Laboratory of Advanced Energy Materials Chemistry (MOE), Renewable Energy Conversion and Storage Center (RECAST), College of Chemistry
[2] Jiaxing University,College of Biological, Chemical Sciences and Engineering
[3] Chinese Academy of Sciences,Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry
[4] University of Manchester,Department of Chemistry
[5] Nankai University,School of Materials Science and Engineering, Institute of New Energy Material Chemistry
来源
Science China Chemistry | 2022年 / 65卷
关键词
metal-organic framework; oxygen evolution reaction; secondary coordination sphere; X-ray diffraction; binding site;
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学科分类号
摘要
The development of efficient electrocatalysts based on non-noble metals for oxygen evolution reaction (OER) remains an important and challenging task. Multinuclear transition-metal clusters with high structural stability are promising OER catalysts but their catalytic role is poorly understood. Here we report the crystallographic observation of OER activity over robust {Ni12}-clusters immobilised in a porous metal-organic framework, NKU-100, by single-crystal X-ray diffraction as a function of external applied potential. We observed the aggregation of confined oxygen species around the {Ni12}-cluster as a function of applied potential during the electrocatalytic process. The refined occupancy of these oxygen species shows a strong correlation with the variation of current density. This study demonstrates that the enrichment of oxygen species in the secondary co-ordination sphere of multinuclear transition-metal clusters can promote the OER activity. [graphic not available: see fulltext]
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页码:1088 / 1093
页数:5
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