过电位
钌
双金属片
钴
磷化物
析氧
分解水
材料科学
纳米技术
化学工程
无机化学
化学
催化作用
物理化学
电化学
光催化
电极
工程类
生物化学
作者
Shuo Chen,Zhicheng Zheng,Fenglin Wang,Hao Wan,Gen Chen,Ning Zhang,Xiaohe Liu,Renzhi Ma
标识
DOI:10.1021/acssuschemeng.2c05177
摘要
Rationally tuning the electronic structure and morphology of catalysts is a vital strategy to boost the catalytic activity. Herein, flower-like cobalt–ruthenium phosphide nanosheets (CoRuP NS) are reported for efficient electrocatalytic overall water splitting. A general principle for precisely modulating the electronic structure of bimetallic phosphate catalysts is developed. The competitive effect between Co and Ru atoms combining with the P atoms is revealed. Hydrogen evolution reaction (HER) activity of CoRuP NS shows a strong interaction with the electron redistribution of the P–metal structure. Benefiting from fully exposed active sites, hierarchical nanostructure, and optimum electron configuration, the CoRuP NS exhibit outstanding HER activity with an overpotential of 54.2 mV at 10 mA cm–2 comparable to that of 20% Pt/C. In addition, the catalysts possess appreciable oxygen evolution reaction (OER) activity with an overpotential of 282.9 mV at 10 mA cm–2. As a result, the CoRuP NS (+) || CoRuP NS (−) cell was constructed, requiring a small voltage of 1.55 V for efficient overall water splitting at 20 mA cm–2. This work provides an innovative strategy for designing bimetallic phosphating phosphate catalysts.
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