双功能
联氨(抗抑郁剂)
催化作用
脱氢
钴
材料科学
氢
电化学
双功能催化剂
化学工程
化学
电极
冶金
物理化学
有机化学
工程类
色谱法
作者
Xiaotong Wei,Shucong Zhang,Xingshuai Lv,Shuixing Dai,Huanlei Wang,Minghua Huang
标识
DOI:10.1016/j.apcatb.2023.123661
摘要
Coupling hydrazine electrooxidation with hydrogen evolution reaction (HER) attracts ever-growing attention for energy-saving H2 production. However, the performance of hydrazine-assisted HER unit is restricted by the bifunctional catalysts with un-fully activated sites. Herein, a surface local-reconstruction strategy is proposed to integrate amorphous Co(OH)2 and P vacant CoP into the CoH-CoPV@CFP catalyst. The inherent electron-deficient Co sites in Co(OH)2 show strong N-Co interaction to accelerate the N2H4 dehydrogenation kinetics, while the as-formed P vacancies in CoP play a crucial role in moderating the H* adsorption energy, the excellent bifunctionality thus being obtained. Specifically, it achieves the low overpotentials of − 77 and − 61 mV at 10 mA cm−2 for HER and HzOR in alkaline media, respectively. A lab-scale electrolyzer can deliver the industrial-grade current density of 500 mA cm−2 under ultralow cell voltage of 0.23 V. This local-reconstruction strategy may pave new avenue to design efficient catalysts for hydrazine-assisted H2 generation.
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