Ni-Zn nanosheet anchored on rGO as bifunctional electrocatalyst for efficient alkaline water-to-hydrogen conversion via hydrazine electrolysis

被引:38
作者
Feng, Zhongbao [1 ,2 ]
Zhang, Han [1 ]
Gao, Bo [1 ]
Lu, Pai [1 ]
Li, Dagang [1 ]
Xing, Pengfei [1 ]
机构
[1] Northeastern Univ, Sch Met, Shenyang 110819, Liaoning, Peoples R China
[2] Northeastern Univ, State Key Lab Rolling & Automat, Shenyang 110819, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Electrodeposition; Ni-Zn/rGO nanosheet; Hydrogen evolution reaction; Hydrazine oxidation; Electrocatalysis; HIGHLY EFFICIENT; STABLE ELECTROCATALYST; METAL SULFIDES; EVOLUTION; CATALYSTS; ALLOYS; ARRAYS; SHELL; FUEL;
D O I
10.1016/j.ijhydene.2020.05.120
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
Bifunctional Ni-15 at.% Zn/rGO catalyst was fabricated by a two-step electrodeposition to be used for efficient alkaline water-to-hydrogen conversion via hydrazine electrolysis. Experiments show that the as-deposited Ni-15 at.% Zn/rGO nanosheet arrays with porous structure possesses excellent catalytic activity and stability towards both hydrogen evolution reaction (HER) and hydrazine oxidation reaction (HzOR). A small overpotential of 49 mV at 10 mA cm(-2) with a low Tafel slope of 26.3 mV dec(-1), and a retention rate of 91.4% after 12 h at 10 mA cm(-2) are observed for Ni-15 at.% Zn/rGO towards HER. Moreover, Ni-15 at.% Zn/rGO also shows an extra-high current density of 1097 mA cm(-2) at 0.6 V vs RHE with a low Tafel slope of 33.5 mV dec(-1), and a high durability of 90.5% after 5000 s towards HzOR. Moreover, two-electrode cell was constructed using Ni-15 at.% Zn/rGO as both cathode and anode for HER and HzOR, achieving 100 mA cm(-2) at an ultralow cell voltage of 0.418 V. The above outstanding bifunctional catalytic performance should be attributed to its large ECSA, high electrical conductivity and most importantly, its superaerophobic surface induced by the porous structure with nanosheet arrays. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:19335 / 19343
页数:9
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