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