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Porous NiS@Ni2P nanoframe as a multi-functional catalyst for enhanced oxygen evolution and urea oxidation reactions.

Authors :
Huang, Yin
Pan, Yaoyao
Huang, Xiaoyu
Zhao, Jialu
Wang, Xiuhua
Source :
Journal of Industrial & Engineering Chemistry; Feb2023, Vol. 118, p239-246, 8p
Publication Year :
2023

Abstract

Successfully synthesize of porous NiS@Ni 2 P nanoframes via anion exchange and phosphating. They display high UOR and HER electrolysis performance. [Display omitted] During water electrolysis, multifunctional electrocatalysts with outstanding functionality and endurance must be thoughtfully constructed and designed. Below, we report a hollow NiS@Ni 2 P nanoframe heterostructure that works well as a substitute catalyst for the urea oxidation and general water splitting reactions. The hollow NiS@Ni 2 P nanoframe was synthesized by ion exchange, sulfurization and phosphating, which is favorable for achieving a heterostructure. The NiS@Ni 2 P catalyst exhibits excellent catalytic activity and strong long-term stability in 1.0 M KOH solutions for the hydrogen evolution reaction, which needs 121 mV to achieve 10 mA cm<superscript>−2</superscript>. And for the oxygen evolution reaction, the catalyst needs 311 mV to acquire 50 mA cm<superscript>−2</superscript>. These advantages come from the optimal electronic structural configuration, hierarchical hollow nanoframe structure, and large surface area. It could attain 10 mA cm<superscript>−2</superscript> at 1.41 V when utilized as a urea oxidation reaction anode, which is lower than the oxygen evolution reaction. For total water splitting and urea oxidation process, NiS@Ni 2 P as a bifunctional catalyst holds tremendous promise due to its strong electrocatalytic activity, ease of manufacture, and low cost of raw ingredients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1226086X
Volume :
118
Database :
Supplemental Index
Journal :
Journal of Industrial & Engineering Chemistry
Publication Type :
Periodical
Accession number :
160962528
Full Text :
https://doi.org/10.1016/j.jiec.2022.11.009