A cobalt hydroxide coated metal-organic framework for enhanced water oxidation electrocatalysis

被引:45
|
作者
Yao, Na [1 ]
Fan, Zhengyin [1 ]
Meng, Ran [1 ]
Jia, Hongnan [1 ]
Luo, Wei [1 ,2 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Hubei, Peoples R China
[2] Wuhan Univ, Suzhou Inst, Suzhou 215123, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MOFs; Oxygen evolution reaction; DFT; Adsorption of *OH; In situ cathodic electro-transformation; OXYGEN EVOLUTION; EFFICIENT; NANOSHEETS; HYDROGEN; TRANSFORMATION; NANOPARTICLES; PHOSPHIDE; SELENIDE;
D O I
10.1016/j.cej.2020.127319
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Although metal-organic frameworks (MOFs) with coordinatively unsaturated metal centers have been regarded as promising electrocatalysts towards oxygen evolution reaction (OER), few reports focus on MOFs with inactive coordinative-saturated metal centers. Herein, we report a universal strategy to generate a layer of Co(OH)(2) coating on the surface of Co-MOFs (Co(OH)(2)/Co-MOF) through an in situ cathodic electro- transformation approach. Experimental analysis and density functional theory (DFT) calculations reveal that electrons transfer from Co(OH)(2) to Co-MOF could synergistically tailor the adsorption free energy of oxygenic intermediates in the OER pathways, which together with the unique structure of Co-MOF, contribute to the outstanding OER performance and long-term stability, with overpotential of 196 mV to achieve the current density of 10 mA cm(-2).
引用
收藏
页数:6
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