析氧
原位
化学工程
分解水
电极
电解水
材料科学
电解
异质结
可逆氢电极
电化学
无机化学
化学
催化作用
工程类
物理化学
有机化学
电解质
工作电极
光电子学
光催化
生物化学
作者
Cheng Gong,Lei Zhao,Dongming Li,Xuan He,Hui Chen,Xing Du,Daheng Wang,Wei Fang,Xianghui Zeng,Weixin Li
标识
DOI:10.1016/j.cej.2023.143124
摘要
Rational design of bi-functional catalysts with desirable activity and stability remains a challenge for overall water splitting. Herein, two-dimensional Co(OH)2/Fe7Se8 nanosheets are prepared via self-transformation and in-situ selective selenization to construct rich heterogeneous interfaces. The in-situ interfaces induced by Fe7Se8 assist to regulate electronic structure of Co(OH)2/Fe7Se8 heterostructure. The incorporation of Fe species along with selective selenization offer strong interfacial coupling effect between Co(OH)2 and Fe7Se8. The in-situ formed interfaces contribute to optimized d-band center, lower energy barrier of intermediates and higher desorption capability of intermediates. Hence, the Co(OH)2/Fe7Se8 nanosheets exhibit superb electrocatalytic activity for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), requiring overpotentials of 183 and 278 mV at 10 mA cm−2 in 1.0 M KOH solution, respectively. In addition, the Co(OH)2/Fe7Se8 electrode requires only 1.62 V at 10 mA cm−2 in a two-electrode assembled electrolyzer, suggesting the promising application as overall water splitting electrocatalysts.
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