化学
析氧
催化作用
磷化物
碳化
电催化剂
碳纤维
过渡金属
化学工程
电解质
纳米技术
协同催化
分解水
复合数
电化学
材料科学
电极
物理化学
吸附
复合材料
生物化学
工程类
光催化
作者
Daorui Wang,Lin Gu,Xinruo Luo,Rui Su,Yuxiang Shang,Yuanyuan Wang,Shijie Hao,Ying Yang
标识
DOI:10.1016/j.jelechem.2022.116875
摘要
Exploring cost-effective electrocatalysts with robust oxygen evolution reaction (OER) activity is urgent for widespread application for many energy conversion technologies. However, the fundamental understanding on the source of highly active single atoms catalysts (SACs) at the atomic level is still lacking. Herein, an ultralow Ru SACs (0.2 wt%) anchored on transition metal phosphide composite with N-doped carbon matrix (Ru-Ni-Co-P/NC) is derived from RuNi-ZIF-67 via carbonization and subsequent phosphating, which effectively drives OER in the alkaline electrolyte. Abundant carbon defect sites and reorganized electronic structure of metal sites can collectively tailor the OER performance of Ru-Ni-Co-P/NC by structure and electron modulation. As expected, the resulting Ru-Ni-Co-P/NC catalyst delivers 318 mV overpotentials to afford 10 mA cm−2, and exhibits negligible performance degradation for OER. This finding elucidates a rational design of multisite nanomaterials as efficient electrocatalysts, illuminating a potential guide to meet high-performance electrocatalysts.
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