过电位
二茂铁
催化作用
电子转移
金属有机骨架
镍
析氧
无机化学
化学
分解水
密度泛函理论
材料科学
化学工程
光化学
电化学
有机化学
吸附
物理化学
光催化
计算化学
工程类
电极
作者
Jing Liang,Xutao Gao,Biao Guo,Yu Ding,Jiawei Yan,Zhengxiao Guo,Edmund C. M. Tse,Jinxuan Liu
标识
DOI:10.1002/ange.202101878
摘要
We report the synthesis of two-dimensional metal–organic frameworks (MOFs) on nickel foam (NF) by assembling nickel chloride hexahydrate and 1,1′-ferrocenedicarboxylic acid (NiFc-MOF/NF). The NiFc-MOF/NF exhibits superior oxygen evolution reaction (OER) performance with an overpotential of 195 mV and 241 mV at 10 and 100 mA cm−2, respectively under alkaline conditions. Electrochemical results demonstrate that the superb OER performance originates from the ferrocene units that serve as efficient electron transfer intermediates. Density functional theory calculations reveal that the ferrocene units within the MOF crystalline structure enhance the overall electron transfer capacity, thereby leading to a theoretical overpotential of 0.52 eV, which is lower than that (0.81 eV) of the state-of-the-art NiFe double hydroxides.
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