Dynamic Lattice Oxygen Participation on Perovskite LaNiO3 during Oxygen Evolution Reaction

被引:65
|
作者
Liu, Jishan [1 ,4 ,5 ]
Jia, Endong [1 ,6 ]
Stoerzinger, Kelsey A. [1 ,2 ]
Wang, Le [1 ]
Wang, Yining [1 ]
Yang, Zhenzhong [1 ]
Shen, Dawei [4 ,5 ]
Engelhard, Mark H. [3 ]
Bowden, Mark E. [3 ]
Zhu, Zihua [3 ]
Chambers, Scott A. [1 ]
Du, Yingge [1 ]
机构
[1] Pacific Northwest Natl Lab, Phys & Computat Sci Directorate, Richland, WA 99354 USA
[2] Oregon State Univ, Sch Chem Biol & Environm Engn, Corvallis, OR 97331 USA
[3] Pacific Northwest Natl Lab, Environm Mol Sci Lab, Richland, WA 99354 USA
[4] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Funct Mat Informat, Shanghai 200050, Peoples R China
[5] Chinese Acad Sci, Ctr Excellence Superconducting Elect, Shanghai 200050, Peoples R China
[6] Chinese Acad Sci, Key Lab Solar Thermal Energy & Photovolta Syst, Inst Elect Engn, Beijing 100190, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2020年 / 124卷 / 28期
关键词
WATER OXIDATION; CATALYSIS; ELECTROCATALYSTS; SURFACE; OXIDES; REDOX;
D O I
10.1021/acs.jpcc.0c04808
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
Determining the role of lattice oxygen in the oxygen evolution reaction (OER) is pivotal to understanding reaction mechanisms and predictive design of electrocatalysts based on transition metal oxides. Here, using well-defined, isotope (O-18) enriched, epitaxial LaNiO3 thin films as a model system, we show that dynamic lattice oxygen exchange occurs during OER Time-of-flight secondary ion mass spectrometry studies reveal that lattice oxygen exchange can affect the top 2 nm of the LaNiO3 films, but the surface largely remains crystalline and in the perovskite phase after OER, In addition, cyclic voltammetry and potentiostatic measurements show that OER kinetics are strongly pH-dependent, which is different from what is expected from the typical four concerted proton-electron transfer steps, most likely due to the involvement of lattice oxygen. Our findings suggest that the roles of lattice oxygen during OER and the mechanism of charge transfer in such systems need to be further studied in order to design more efficient and stable electrocatalysts.
引用
收藏
页码:15386 / 15390
页数:5
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