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Engineering anion defect in LaFeO2.85Cl0.15 perovskite for boosting oxygen evolution reaction
被引:25
|作者:
Zhang, Jing
[1
,2
]
Cui, Yuexiao
[1
]
Jia, Lichao
[3
]
He, Beibei
[1
,2
]
Zhang, Kun
[4
,5
]
Zhao, Ling
[1
,2
]
机构:
[1] China Univ Geosci, Dept Mat Sci & Chem, Wuhan 430074, Hubei, Peoples R China
[2] China Univ Geosci Wuhan, Zhejiang Inst, Hangzhou 311305, Zhejiang, Peoples R China
[3] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Mat Proc & & Mould Technol, Ctr Fuel Cell Innovat, Wuhan 430074, Hubei, Peoples R China
[4] Huizhou Univ, Sch Chem & Mat Engn, Huizhou 516007, Peoples R China
[5] Shenzhen Technol Univ, Coll New Mat & New Energies, Shenzhen 518118, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Oxygen evolution reaction;
Perovskite;
Anion defect;
Catalyst;
CATION DEFICIENCY;
WATER OXIDATION;
EFFICIENT;
OXIDE;
ELECTROCATALYST;
REDUCTION;
CATALYST;
SURFACE;
D O I:
10.1016/j.ijhydene.2019.07.162
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Development of cost-effective, highly-active and durable catalysts for oxygen evolution reaction (OER) is critical to sustainable energy conversion and storage devices. Perovskite oxides are exploited as a research frontier on OER, however, their activity and stability are still far from desirable. Herein, we highlight a paradigm shift in the design of highly efficient perovskite-type catalysts for OER by engineering anion defect. The Cl-doped LaFeO2.85Cl0.15 perovskite demonstrates an enhanced OER activity, which is attributed to the abundant surface oxygen vacancies and low adsorption energy of H2O molecule after Cl doping. Moreover, the LaFeO2.85Cl0.15 catalyst also delivers an improved electrocatalytic durability, in contrast to the pristine LaFeO3 catalyst. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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页码:24077 / 24085
页数:9
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