In Situ Spectroscopic Identification of μ-OO Bridging on Spinel Co3O4 Water Oxidation Electrocatalyst

被引:163
作者
Wang, Hsin-Yi [1 ]
Hung, Sung-Fu [2 ]
Hsu, Ying-Ya [3 ]
Zhang, Lulu [4 ]
Miao, Jianwei [1 ]
Chan, Ting-Shan [3 ]
Xiong, Qihua [4 ]
Liu, Bin [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Block N1-2,62 Nanyang Dr, Singapore 637459, Singapore
[2] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
[4] Nanyang Technol Univ, Sch Phys & Math Sci, Div Phys & Appl Phys, Singapore 637371, Singapore
基金
新加坡国家研究基金会;
关键词
OXYGEN EVOLUTION; COBALT OXIDE; ELECTROCHEMICAL EVOLUTION; SOLID-SOLUTIONS; SURFACE; ELECTRODES; CATALYST; BEHAVIOR; FILMS; CO;
D O I
10.1021/acs.jpclett.6b02147
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
The formation of mu-OO peroxide (Co-OO-Co) moieties on spinel Co3O4 electrocatalyst prior to the rise of the electrochemical oxygen evolution reaction (OER) current was identified by in situ spectroscopic methods. Through a combination of independent in situ X-ray absorption, grazing-angle X-ray diffraction, and Raman analysis, we observed a clear coincidence between the formation of mu-OO peroxide moieties and the rise of the anodic peak during OER. This finding implies that a chemical reaction step could be generally ignored before the onset of OER current. More importantly, the tetrahedral Co2+ ions in the spinet Co3O4 could be the vital species to initiate the formation of the mu-OO peroxide moieties.
引用
收藏
页码:4847 / 4853
页数:7
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