Abstract

Efficient generation of hydrogen from water-splitting is an underpinning chemistry to realize the hydrogen economy. Low cost, transition metals such as nickel and iron-based oxides/hydroxides have been regarded as promising catalysts for the oxygen evolution reaction in alkaline media with overpotentials as low as ~200 mV to achieve 10 mA cm−2, however, they are generally unsuitable for the hydrogen evolution reaction. Herein, we show a Janus nanoparticle catalyst with a nickel–iron oxide interface and multi-site functionality for a highly efficient hydrogen evolution reaction with a comparable performance to the benchmark platinum on carbon catalyst. Density functional theory calculations reveal that the hydrogen evolution reaction catalytic activity of the nanoparticle is induced by the strong electronic coupling effect between the iron oxide and the nickel at the interface. Remarkably, the catalyst also exhibits extraordinary oxygen evolution reaction activity, enabling an active and stable bi-functional catalyst for whole cell water-splitting with, to the best of our knowledge, the highest energy efficiency (83.7%) reported to date.

Details

Title
Overall electrochemical splitting of water at the heterogeneous interface of nickel and iron oxide
Author
Suryanto, Bryan H R 1   VIAFID ORCID Logo  ; Wang, Yun 2   VIAFID ORCID Logo  ; Hocking, Rosalie K 3   VIAFID ORCID Logo  ; Adamson, William 1 ; Zhao, Chuan 1 

 School of Chemistry, The University of New South Wales, Kensington, NSW, Australia 
 Centre for Clean Environment and Energy, School of Environment and Science, Griffith University, Gold Coast, QLD, Australia 
 Department of Chemistry and Biotechnology, Swinburne University of Technology, Melbourne, VIC, Australia 
Pages
1-10
Publication year
2019
Publication date
Dec 2019
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2322187777
Copyright
© 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.