N-enriched porous carbon doped with co, ni, and Mo as efficient electrocatalyst for hydrogen evolution reaction

被引:17
|
作者
Yang, Xiaobing [1 ]
Yang, Weisen [1 ]
Fu, Xingping [2 ]
Hu, Jiapeng [2 ]
Chen, Juan [2 ,3 ,4 ]
机构
[1] Wuyi Univ, Coll Ecol & Resource Engn, Wuyishan 354300, Fujian, Peoples R China
[2] Wuyi Univ, Fujian Prov Key Lab Ecoinductrial Green Technol, Wuyishan 354300, Fujian, Peoples R China
[3] Xiamen Univ, Dept Pharm, Zhongshan Hosp, Wuyishan 361004, Fujian, Peoples R China
[4] Xiamen Univ, Fujian Key Lab Adv Mat, Xiamen 361005, Fujian, Peoples R China
关键词
CoNiMo/NPC; ZIF-67; Hydrogen evolution reaction activity; Durability; METAL; CATALYSTS; MEMBRANE; CELL;
D O I
10.1016/j.ijhydene.2021.03.002
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
Splitting water for hydrogen production is still a promising technique to meet the energy requirements of society and overcome many environmental problems. However, the development of carbon-based transition electrocatalysts with superior activity for hydrogen evolution reaction (HER) is still challenging. In this study, a CoNiMo/NPC electrocatalyst was successfully fabricated using ZIF-67 as a precursor via facile absorption, pyrolysis and annealing processes. The fabricated CoNiMo/NPC was used as an electrocatalyst for hydrogen production. The results revealed that the doping of Ni and Mo increase the number of active sites and enhance the conductivity of electrocatalysts. CoNiMo/NPC exhibits excellent HER activity in alkaline solutions and only requires an overpotential of 182 mV to reach a current density of 10 mA/cm(2). Furthermore, long-term measurements demonstrated that CoNiMo/NPC has superior durability in alkaline solutions. The excellent HER performance of CoNiMo/NPC can be attributed to the doping of Co, Ni, and Mo on porous carbon. In addition, the high specific surface area and high graphitisation degree of the electrocatalyst are beneficial for rapid charge transport and collection. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:18318 / 18325
页数:8
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