共轭体系
共价键
催化作用
材料科学
电催化剂
Atom(片上系统)
共价有机骨架
纳米技术
密度泛函理论
电化学
组合化学
化学
聚合物
计算化学
有机化学
物理化学
电极
计算机科学
复合材料
嵌入式系统
作者
Kai Chi,Yangjiang Wu,Xuejun Wang,Qingsong Zhang,Wenqiang Gao,Longfei Yang,Xin Chen,Dongdong Chang,Yu Zhang,Tao Shen,Xuefeng Lu,Yan Zhao,Yunqi Liu
出处
期刊:Small
[Wiley]
日期:2022-09-22
卷期号:18 (44)
被引量:21
标识
DOI:10.1002/smll.202203966
摘要
Adjusting the local coordination environment of single-atom electrocatalysts is a viable way to improve catalytic performance. The diversity of coordination geometric structures is limited to the traditional in-plane configuration, with only a little consideration paid to out-of-plane configurations due to the lack of suitable carriers and fabrication methods. This study reports out-of-plane coordination of Co-based single-atom catalysts mediated by the conjugated bipyridine-rich covalent organic framework (COF). The bipyridine nitrogen on the COF layer backbone of these catalysts serves as the linker center for cobalt sites anchoring, while the complementary moieties are coordinated at the other side of the Co metal and reside beyond the COF backbone plane, thus yielding out-of-plane coordination. The electrochemical experiments and density functional theory calculations reveal that catalysts with multiple out-of-plane coordinations exhibit different electrocatalytic oxygen evolution activities and catalytic pathways. The out-of-plane coordination enabled by COFs provides a strategy for designing single-atom electrocatalysts, expanding the application of COFs in the field of electrocatalysis.
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