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Amorphous nickel hydroxide shell tailors local chemical environment on platinum surface for alkaline hydrogen evolution reaction.

Authors :
Wan C
Zhang Z
Dong J
Xu M
Pu H
Baumann D
Lin Z
Wang S
Huang J
Shah AH
Pan X
Hu T
Alexandrova AN
Huang Y
Duan X
Source :
Nature materials [Nat Mater] 2023 Aug; Vol. 22 (8), pp. 1022-1029. Date of Electronic Publication: 2023 Jun 22.
Publication Year :
2023

Abstract

In analogy to natural enzymes, an elaborated design of catalytic systems with a specifically tailored local chemical environment could substantially improve reaction kinetics, effectively combat catalyst poisoning effect and boost catalyst lifetime under unfavourable reaction conditions. Here we report a unique design of 'Ni(OH) <subscript>2</subscript> -clothed Pt-tetrapods' with an amorphous Ni(OH) <subscript>2</subscript> shell as a water dissociation catalyst and a proton conductive encapsulation layer to isolate the Pt core from bulk alkaline electrolyte while ensuring efficient proton supply to the active Pt sites. This design creates a favourable local chemical environment to result in acidic-like hydrogen evolution reaction kinetics with a lowest Tafel slope of 27 mV per decade and a record-high specific activity and mass activity in alkaline electrolyte. The proton conductive Ni(OH) <subscript>2</subscript> shell can also effectively reject impurity ions and retard the Oswald ripening, endowing a high tolerance to solution impurities and exceptional long-term durability that is difficult to achieve in the naked Pt catalysts. The markedly improved hydrogen evolution reaction activity and durability in an alkaline medium promise an attractive catalyst material for alkaline water electrolysers and renewable chemical fuel generation.<br /> (© 2023. The Author(s), under exclusive licence to Springer Nature Limited.)

Details

Language :
English
ISSN :
1476-4660
Volume :
22
Issue :
8
Database :
MEDLINE
Journal :
Nature materials
Publication Type :
Academic Journal
Accession number :
37349398
Full Text :
https://doi.org/10.1038/s41563-023-01584-3