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Overall electrochemical splitting of water at the heterogeneous interface of nickel and iron oxide
被引:580
|作者:
Suryanto, Bryan H. R.
[1
]
Wang, Yun
[2
]
Hocking, Rosalie K.
[3
]
Adamson, William
[1
]
Zhao, Chuan
[1
]
机构:
[1] Univ New South Wales, Sch Chem, Kensington, NSW 2052, Australia
[2] Griffith Univ, Sch Environm & Sci, Ctr Clean Environm & Energy, Gold Coast, Qld 4222, Australia
[3] Swinburne Univ Technol, Dept Chem & Biotechnol, Melbourne, Vic 3122, Australia
基金:
澳大利亚研究理事会;
关键词:
HYDROGEN-EVOLUTION CATALYSTS;
OXYGEN EVOLUTION;
EFFICIENT;
METAL;
ELECTROCATALYSTS;
SULFIDE;
FILMS;
ELECTROLYSIS;
IMPURITIES;
NANOSHEETS;
D O I:
10.1038/s41467-019-13415-8
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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 similar to 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.
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页数:10
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