Influence of Fe Substitution into LaCoO3 Electrocatalysts on Oxygen-Reduction Activity

被引:63
作者
Wang, Maoyu [1 ]
Han, Binghong [2 ]
Deng, Junjing [3 ]
Jiang, Yi [3 ]
Zhou, Mingyue [4 ]
Lucero, Marcos [1 ]
Wang, Yan [1 ]
Chen, Yubo [5 ]
Yang, Zhenzhen [2 ]
N'Diaye, Alpha T. [6 ]
Wang, Qing [4 ]
Xu, Zhichuan J. [5 ]
Feng, Zhenxing [1 ]
机构
[1] Oregon State Univ, Dept Chem Biol & Environm Engn, Corvallis, OR 97331 USA
[2] Argonne Natl Lab, Chem Sci & Engn Div, 9700 S Cass Ave, Argonne, IL 60439 USA
[3] Argonne Natl Lab, Adv Photon Source, 9700 S Cass Ave, Argonne, IL 60439 USA
[4] Natl Univ Singapore, Dept Mat Sci & Engn, Fac Engn, Singapore 117576, Singapore
[5] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[6] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
关键词
oxygen reduction reaction; X-ray absorption spectroscopy; electronic structure; perovskite; electrocatalyst; X-RAY-ABSORPTION; PEROVSKITE OXIDES; METAL; HYBRIDIZATION; SPECTROSCOPY; TRANSITION; COVALENCY;
D O I
10.1021/acsami.8b20780
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of commercially friendly and stable catalysts for oxygen reduction reaction (ORR) is critical for many energy conversion systems such as fuel cells and metal-air batteries. Many Co-based perovskite oxides such as LaCoO3 have been discovered as the stable and active ORR catalysts, which can be good candidates to replace platinum (Pt). Although researchers have tried substituting various transition metals into the Co-based perovskite catalysts to improve the ORR performance, the influence of substitution on the ORR. mechanism is rarely studied. In this paper, we explore the evolution of ORR mechanism after substituting Fe into LaCoO3, using the combination of X-ray photoelectron spectroscopy, high-resolution X-ray microscopy, X-ray diffraction, surface-sensitive soft X-ray absorption spectroscopy characterization, and electrochemical tests. We observed enhanced catalytic activities and increased electron transfer numbers during the ORR in Co-rich perovskite, which are attributed to the optimized e(g) filling numbers and the stronger hybridization of transition metal 3d and oxygen 2p bands. The discoveries in this paper provide deep insights into the ORR catalysis mechanism on metal oxides and new guidelines for the design of Pt-free ORR catalysts.
引用
收藏
页码:5682 / 5686
页数:5
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