电催化剂
分解水
材料科学
双功能
析氧
普鲁士蓝
过渡金属
制氢
电解质
催化作用
氢
镍
无机化学
化学工程
纳米技术
磷化物
电化学
物理化学
冶金
电极
化学
有机化学
工程类
生物化学
光催化
作者
Ding Chen,Zonghua Pu,Ruihu Lu,Pengxia Ji,Pengyan Wang,Jiawei Zhu,Can Lin,Haiwen Li,Xiangang Zhou,Zhi‐Yi Hu,Fanjie Xia,Jingsong Wu,Shichun Mu
标识
DOI:10.1002/aenm.202000814
摘要
Abstract Water splitting is a promising technology for sustainable conversion of hydrogen energy. The rational design of oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) bifunctional electrocatalysts with superior activity and stability in the same electrolyte is the key to promoting their large‐scale applications. Herein, an ultralow Ru (1.08 wt%) transition metal phosphide on nickel foam (Ru–MnFeP/NF) derived from Prussian blue analogue, that effectively drivies both the OER and the HER in 1 m KOH, is reported. To reach 20 mA cm −2 for OER and 10 mA cm −2 for HER, the Ru–MnFeP/NF electrode only requires overpotentials of 191 and 35 mV, respectively. Such high electrocatalytic activity exceeds most transition metal phosphides for the OER and the HER, and even reaches Pt‐like HER electrocatalytic levels. Accordingly, it significantly accelerates full water splitting at 10 mA cm −2 with 1.470 V, which outperforms that of the integrated RuO 2 and Pt/C couple electrode (1.560 V). In addition, the extremely long operational stability (50 h) and the successful demonstration of a solar‐to‐hydrogen generation system through full water splitting provide more flexibility for large‐scale applications of Ru–MnFeP/NF catalysts.
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