Modulating adsorption energy on nickel nitride-supported ruthenium nanoparticles through in-situ electrochemical activation for urea-assisted alkaline hydrogen production

被引:3
|
作者
Luo, Yuan Hao [1 ]
Fu, Hong Chuan [1 ]
Chen, Xiao Hui [1 ]
Wang, Bing Jie [1 ]
Yang, Bo [1 ]
Li, Nian Bing [1 ]
Luo, Hong Qun [1 ]
机构
[1] Southwest Univ, Sch Chem & Chem Engn, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金;
关键词
Ni; 3; N; Ru; In-situ activation; Hydrogen evolution reaction; Urea-assisted hydrogen production; EFFICIENT BIFUNCTIONAL ELECTROCATALYSTS; EVOLUTION; NANOSHEETS; UNIVERSAL; ARRAYS;
D O I
10.1016/j.jcis.2023.08.154
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
The rational design of electrocatalysts with exceptional performance and durability for hydrogen production in alkaline medium is a formidable challenge. In this study, we have developed in-situ activated ruthenium nanoparticles dispersed on Ni3N nanosheets, forming a bifunctional electrocatalyst for hydrogen evolution and urea oxidation. The results of experimental analysis and theoretical calculations reveal that the enhanced hydrogen evolution reaction (HER) performance of O-Ru-Ni3N stems primarily from the optimized hydrogen adsorption and hydroxyl adsorption on Ru sites. The O-Ru-Ni3N on nickel foam (NF) electrode exhibits excellent HER performance, requiring only 29 mV to reach 10 mA cm-2 in an alkaline medium. Notably, when this O-Ru-Ni3N/ NF catalyst is employed for both HER and urea oxidation reaction (UOR) to create an integrated H2 production system, a current density of 50 mA cm-2 can be generated at the cell voltage of 1.41 V. This report introduces an energy-efficient catalyst for hydrogen production and proposes a viable strategy for anodic activation in energy chemistry.
引用
收藏
页码:1665 / 1672
页数:8
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