Surface protonation and oxygen evolution activity of epitaxial La1-xSrxCoO3 thin films

被引:0
|
作者
XiaoShuo Wang [1 ]
Liang Zhou [2 ]
MengXin Li [1 ]
Yi Luo [2 ]
TieYing Yang [3 ]
TianLi Wu [1 ]
XiaoLong Li [3 ]
Kui-Juan Jin [4 ]
Er-Jia Guo [4 ,5 ]
LiFen Wang [4 ]
XueDong Bai [4 ]
WeiFeng Zhang [1 ]
HaiZhong Guo [2 ,6 ]
机构
[1] Henan Key Laboratory of Photovoltaic Materials, School of Physics and Electronics, Henan University
[2] School of Physics and Microelectronics, Zhengzhou University
[3] Shanghai Synchrotron Radiation Facility (SSRF), Shanghai Institute of Applied Physics, Chinese Academy of Sciences
[4] Beijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences
[5] Center of Materials Science and Optoelectronics Engineering, University of Chinese Academy of Sciences
[6] Collaborative Innovation Center of Light Manipulations and Applications, Shandong Normal University
基金
中国国家自然科学基金;
关键词
oxygen evolution reaction; La1-xSrxCoO3 thin films; lattice oxygen protonation;
D O I
暂无
中图分类号
TB383.2 [];
学科分类号
070205 ; 080501 ; 1406 ;
摘要
As an alternative electrode material, transition metal oxides are promising candidates due to multivalent nature and oxygen vacancies present in the structure with facilitate redox reactions. The aim of this study is to explore the intrinsic mechanism of oxygen evolution reaction(OER) using two-dimensional thin film La1-xSrxCoO3electrode as a model. Herein, we report a planar two-dimensional model La1-xSrxCoO3electrode grown on a Nb-SrTiO3single-crystal substrate via pulsed laser deposition. The two-dimensional La1-xSrxCoO3films offer different oxygen evolution activities at different pH electrolyte solutions. The mechanisms behind the variations of the oxygen evolution activity were discussed after comparing the oxygen evolution activity before and after treatments of the electrodes and measurements by various test methods. The results of this study offer a promising, low-cost electrode material for the efficient OER and a sustainable production of hydrogen fuel.
引用
收藏
页码:81 / 86
页数:6
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