催化作用
材料科学
析氧
电化学
异质结
金属
化学工程
电子转移
金属有机骨架
吸附
氧气
化学
物理化学
电极
冶金
有机化学
光电子学
工程类
作者
Kang Ji,Yunlong Yue,Ping Yang
标识
DOI:10.1016/j.apsusc.2022.155184
摘要
The interface nature of composite catalysts affected drastically the oxygen evolution reaction (OER) behavior. In this paper, nanoarchitecture consisted of Fe-based metal–organic frameworks (MIL-53) and metal-phenolic networks were created. Metal (Mn2+, Co2+, and Ni2+) phenolic networks were assembled on the surface of MIL-53 to form heterostructures. Among them, MIL-53(Fe)/Ni-phenolic network nanoarchitectures revealed the best electrochemical performance. The existence of MIL-53 enhanced the adsorption ability for OH− in the nanoarchitectures. The electron transfer between MIL-53 and Ni-phenolic networks adjusted the filling degree of eg orbitals to optimize the bonding strength between Fe3+/Ni2+ and oxygen intermediate species. MIL-53/Ni-phenolic networks nanoarchitectures exhibited well OER performance with a potential of 282 mV at 10 mA cm−2. This work provided an efficient insight into the structure-properties relation of a promising heterostructure catalyst for water splitting.
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