Ethylene Glycol Electrochemical Reforming Using Ruthenium Nanoparticle-Decorated Nickel Phosphide Ultrathin Nanosheets

被引:18
|
作者
Ma, Ge [1 ,2 ]
Yang, Na [1 ,2 ]
Xue, Yafei [1 ,2 ]
Zhou, Guofu [1 ,2 ]
Wang, Xin [1 ,2 ]
机构
[1] South China Normal Univ, South China Acad Adv Optoelect, Guangzhou 510631, Guangdong, Peoples R China
[2] South China Normal Univ, Int Acad Optoelect Zhaoqing, Guangzhou 510631, Guangdong, Peoples R China
关键词
Ni2P nanosheets; Ru nanoparticles; synergistic effect; hydrogen evolution reaction; ethylene glycol electro-oxidation reaction; WATER ELECTROLYSIS; HYDROGEN EVOLUTION; EFFICIENT; ELECTROCATALYSTS; NANOTUBES; PLATINUM; COBALT; IRON; FOAM;
D O I
10.1021/acsami.1c10971
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this work, ruthenium nanoparticle-decorated ultrathin nickel phosphide nanosheets on nickel foam substrate (Ru/Ni2P/NF) nanocomposites are synthesized conveniently by a cyanogel-NaBH4 method and a subsequent phosphating process, which displays excellent electroactivity for both the hydrogen evolution reaction (HER) and ethylene glycol electro-oxidation reaction (EGEOR) in an alkaline solution. Concretely, at Ru/Ni2P/NF nanocomposites, only 1.37 and -0.13 V potentials are required to obtain a current density of 100 mA cm(-2) for EGEOR and HER, respectively. Meanwhile, Ru/Ni2P/NF nanocomposites also exhibit pre-eminent electrocatalytic performance of the long-running process for both EGEOR and HER. Density functional theory calculations demonstrate that the introduction of Ru nanoparticles results in an optimization of the surface adsorption energy and construction of a synergistic catalysis interface, which improve the electrocatalytic performance of nickel phosphide nanosheets. Notably, a symmetric Ru/Ni2P/NF parallel to Ru/Ni2P/NF ethylene glycol electrolyzer needs only 1.14 V electrolysis voltage to obtain 10 mA cm(-2) for hydrogen production, which effectively eliminates the H-2/O-2 explosion risk and highlights an energy-saving mode for electrochemical hydrogen production.
引用
收藏
页码:42763 / 42772
页数:10
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