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Dealloyed NiTiZrAg as an efficient electrocatalyst for hydrogen evolution in alkaline seawater.
- Source :
-
International Journal of Hydrogen Energy . Jan2024, Vol. 53, p318-324. 7p. - Publication Year :
- 2024
-
Abstract
- Seawater, one of nature's most bountiful resources, holds promise as a valuable and inexhaustible raw material for hydrogen production through water electrolysis. However, to combat chloride corrosion and maintain a stable operating state, it is essential to design strong and effective electrocatalysts appropriate for the hydrogen evolution reaction (HER). Herein, we demonstrate that Ni 40 Ti 20 Zr 38 Ag 2 alloy, after the successive arc-melting, melt-spinning, and dealloying treatments, generates a distinctive nanosheet structure. In alkaline seawater electrolyte (1 M KOH + natural seawater), this materials for HER not only could achieve a smaller overpotential of 69 mV driving 10 mA cm−2, but also possess excellent stability including the 10 mA cm−2 current density over 24 h and 3000 cycles measurement. This is mainly attributed to the array of cascading interconnected nanosheets and the incorporation of Ag, as well as the resulting electron transfer and changes in the chemical state of the elements on the catalyst surface. This work proposes a novel design strategy for alloy materials for preparing an efficient HER electrocatalyst in alkaline seawater. The dealloyed NiTiZrAg can be used as an efficient and stable electrocatalyst for hydrogen production in alkaline seawater. [Display omitted] • NiTiZrAg-20 electrocatalysts with nanosheet arrays were constructed by dealloying. • Ag promotes the electron transfer between components and changes in chemical states. • The NiTiZrAg-20 showed superior HER performance in alkaline seawater. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03603199
- Volume :
- 53
- Database :
- Academic Search Index
- Journal :
- International Journal of Hydrogen Energy
- Publication Type :
- Academic Journal
- Accession number :
- 174842147
- Full Text :
- https://doi.org/10.1016/j.ijhydene.2023.12.007