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Nanoporous nonprecious multi-metal alloys as multisite electrocatalysts for efficient overall water splitting.

Authors :
Li, Lvrui
Xuan, Haicheng
Wang, Jie
Liang, Xiaohong
Li, Yuping
Han, Zhida
Cheng, Long
Source :
International Journal of Hydrogen Energy. Jan2025, Vol. 97, p38-45. 8p.
Publication Year :
2025

Abstract

Developing robust nonprecious metal-based electrocatalysts toward hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is essential for hydrogen production via electrochemical water splitting. Herein, the NiFeCoCuTi alloy is described as a multisite electrocatalyst for highly effective hydrogen and oxygen evolution in alkaline environments. This is achieved by utilizing heterogeneous atoms on the surface that exhibit distinct adsorption behaviors for hydrogen and hydroxyl, thereby accelerating the dissociation of water and mediating the adsorption of hydrogen intermediates required for molecule formation. The monolithic nanoporous multi-metal NiFeCoCuTi alloy electrode displays remarkable alkaline HER and OER electrocatalysis, exhibiting low overpotentials of 48.7 and 264.2 mV, respectively, to deliver a current density of 10 mA cm−2. Furthermore, it demonstrates exceptional stability for over 100 h in 1 M KOH electrolyte. The exceptional qualities of nanoporous NiFeCoCuTi alloy electrodes make them a highly desirable option for utilization as the cathode and anode material in water electrolysis, which produces hydrogen. They also imply that this is the optimal platform for the development of multisite electrocatalysts. [Display omitted] • The multi-metal NiFeCoCuTi alloys were synthesized by dealloying. • The precursor species and dealloying parameters were investigated. • The 4-NiFeCoCuTi catalyst exhibits excellent HER and OER catalytic properties. • Local structure engineering improves catalytic properties. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03603199
Volume :
97
Database :
Academic Search Index
Journal :
International Journal of Hydrogen Energy
Publication Type :
Academic Journal
Accession number :
181726131
Full Text :
https://doi.org/10.1016/j.ijhydene.2024.11.422