Self-supporting Nickel Phosphide/Hydroxides Hybrid Nanosheet Array as Superior Bifunctional Electrode for Urea-Assisted Hydrogen Production

被引:5
|
作者
Li, Kaixun [1 ]
Tong, Yun [1 ]
机构
[1] Zhejiang Sci Tech Univ, Key Lab Surface & Interface Sci Polymer Mat Zheji, Dept Chem, Hangzhou 310018, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni-based materials; nanosheet array; heterostructure; bifunctional activity; urea-assisted water electrolysis; HIGHLY-EFFICIENT; NI(OH)(2);
D O I
10.1002/cctc.202201047
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Urea oxidation reaction (UOR) is an important strategy to synergistically realize energy-saving hydrogen evolution reaction (HER) and urea-rich wastewater purification by replacing water oxidation in water electrolysis. However, the efficient realization of integral urea electrolysis remains challenging. Herein, a self-supporting Ni2P-Ni(OH)(2) hybrid nanosheet array on nickel foam (Ni2P@Ni(OH)(2)/NF) is designed by a simple hydrothermal accompanied by electrodeposition strategy, representing a new class of bifunctional electrodes for urea-assisted water electrolysis. The Ni2P@Ni(OH)(2)/NF reaches the current density of 100 mA cm(-2) at potentials of -0.16 V and 1.388 V, along with small Tafel slopes of 69 mV dec(-1) and 33 mV dec(-1) for HER/UOR, respectively. For the HER||UOR coupled system, the constructed electrolyzer only needs 1.38 V to realize the current density of 100 mA cm(-2) under 80 degrees C. The superior bifunctional activity of the Ni2P@Ni(OH)(2)/NF electrode is ascribed to the combined merits of the Ni2P@Ni(OH)(2) heterostructure, enriching the catalytic active sites and offering a faster charge transfer process for electrolysis. Our work provides important insights into the design of highly active bifunctional catalysts from the perspective of overall water electrolysis.
引用
收藏
页数:10
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