Selective dissolution of A-site cations of La0.6Sr0.4Co0.8Fe0.2O3 perovskite catalysts to enhance the oxygen evolution reaction

被引:59
作者
Guo, Wei [1 ]
Cui, Lan [2 ]
Xu, Hanwen [1 ]
Gong, Cairong [1 ]
机构
[1] Tianjin Univ, Inst New Energy, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Ctr Anal, Tianjin 300072, Peoples R China
关键词
Oxygen evolution reaction; Interface modification; Perovskite; Transition-metal oxide catalysts; ELECTROCATALYST; VACANCIES; OXIDES; NANOSHEETS; LACOO3; NANOCOMPOSITES; NANOPARTICLES; ELECTROLYTE; DEFICIENCY; NANORODS;
D O I
10.1016/j.apsusc.2020.147165
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
Perovskite oxide is a potential alternative to precious metal oxides like IrO2 and RuO2 as electrocatalysts in the oxygen evolution reaction (OER), mostly for its cost-effectiveness and adequate stability. However, the low catalytic activity in the OER limits its practical application. This paper deals with the preparation of perovskite oxides (by the sol-gel method) with enhanced electrocatalytic activity through selective dissolution of A-site cations of La0.6Sr0.4Co0.8Fe0.2O3 (LSCF) in order to tune the A-site cation deficiency. Additionally, a thorough investigation of the catalysts' OER performance was performed in a 0.1 mol.L-1 KOH solution. Based on the results of XRD, SEM, TEM, XPS and ICP-AES, it can be concluded that selective dissolution of Sr cations on A-sites can be achieved using a HNO3 etching remaining the perovskite structure. The OER catalytic activity of LSCF can be effectively promoted after acid etching for 6 h, which can be attributed to the higher surface area (BET result) and ratio of the high oxidative oxygen species (O-2(-)/O-) and surface oxygen species (OH-/O-2). Moreover, the LSCF catalysts maintains an appropriate electrochemical stability after acid etching. Our work offers a simple but effective way to modify the perovskite surface so as to boost the OER performance.
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页数:9
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