A self-supported heterogeneous bimetallic phosphide array electrode enables efficient hydrogen evolution from saline water splitting

被引:30
|
作者
Li, Jingwen [1 ]
Song, Min [1 ]
Hu, Yezhou [2 ]
Zhang, Chang [1 ]
Liu, Wei [1 ]
Huang, Xiao [1 ]
Zhang, Jingjing [1 ]
Zhu, Ye [2 ]
Zhang, Jian [1 ]
Wang, Deli [1 ]
机构
[1] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Minist Educ, Hubei Key Lab Mat Chem & Serv Failure,Sch Chem &, Wuhan 430074, Peoples R China
[2] Hong Kong Polytech Univ, Res Inst Smart Energy, Dept Appl Phys, Kowloon, Hong Kong, Peoples R China
关键词
saline water splitting; hydrogen evolution reaction; bimetallic phosphides; chlorine-corrosion resistance; DOUBLE HYDROXIDE NANOSHEETS; BIFUNCTIONAL ELECTROCATALYSTS; CARBON NANOFIBERS; SEAWATER; ALKALINE; SUPERIOR; METAL;
D O I
10.1007/s12274-022-4608-8
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
Hydrogen generation from water splitting is of great prospect for the sustainable energy conversion. However, it is still challenging to explore stable and high-performance electrocatalysts toward hydrogen evolution reaction (HER) from saline water such as seawater due to the chloride corrosion. Herein, we developed a self-supported heterogeneous bimetallic phosphide (Ni2P-FeP) array electrode that possesses excellent HER performance in alkaline saline water with an overpotential of 89 mV at 10 mA.cm(-2) and long-term stability over 90 h at 200 mA.cm(-2). The analysis showed that the heterostructure between the interfaces of Ni2P-FeP plays a pivotal role in promoting the activity of catalyst. Moreover, the bimetallic phosphide nanoarrays can be employed as a shield for chlorine-corrosion resistance in the saline water, ensuring the long-term durability of hydrogen generation. When employed for alkaline saline water electrolysis, a current density of 100 mA.cm(-2) is achieved at cell voltage of 1.68 V. This work presents an effective approach for the fabrication of high-performance electrode for HER in alkaline saline environments.
引用
收藏
页码:3658 / 3664
页数:7
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