Activating self-supported NiPd electrodes by laser-direct-writing for efficient hydrogen evolution reaction

被引:1
|
作者
Zhou, Zihan [1 ]
Xiao, Liyang [1 ]
Zhao, Jun [1 ]
Zhou, Miao [1 ]
Zhang, Jingtong [1 ]
Du, Xiwen [1 ]
Yang, Jing [1 ]
机构
[1] Tianjin Univ, Inst New Energy Mat, Sch Mat Sci & Engn, Key Lab Adv Ceram & Machining Technol,Minist Educ, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCATALYST; NANOSTRUCTURES; CATALYSTS; DENSITY;
D O I
10.1039/d3qm00439b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pd-based catalytic electrodes for the hydrogen evolution reaction (HER) are promising as a replacement of Pt-based catalysts, but their strong hydrogen adsorption hinders hydrogen desorption and thus limits HER catalytic activity. Here, we report a function-structure integrated D-Ni3.5Pd/NF catalytic electrode with a very low Pd loading (0.19 mg(Pd) cm(-2)) and a large number of edge dislocations, which was prepared by millisecond laser direct writing in liquid nitrogen. The plentiful dislocations induce a strain effect leading to reduced hydrogen adsorption energies of Pd sites and enhanced water dissociation ability of Ni sites. Thereby, the dense dislocations improve the alkaline HER intrinsic activity and electrochemical stability of D-Ni3.5Pd/NF under high current densities. The as-prepared electrodes can achieve fairly low overpotentials of 35 and 352 mV at 10 mA cm(-2) and 1 A cm(-2) in a 1 M KOH electrolyte, respectively, while the Tafel slope is only 62.3 mV dec(-1). In addition, its overpotential only increases by 4.2% after 100 h of the chronoamperometric test at 500 mA cm(-2), showing an outstanding electrochemical stability at high current densities.
引用
收藏
页码:4508 / 4517
页数:10
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