Improved photoelectrochemical water splitting performance of Sn-doped hematite photoanode with an amorphous cobalt oxide layer

被引:2
|
作者
Huang, Qiuyang [1 ,2 ]
Zhao, Yicheng [1 ,2 ]
Li, Yongdan [3 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin Key Lab Appl Catalysis Sci & Technol, State Key Lab Chem Engn, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[3] Aalto Univ, Dept Chem & Met Engn, Kemistintie 1, FI-00076 Aalto, Finland
基金
中国国家自然科学基金;
关键词
Photoelectrochemical water splitting; Hematite; Photoanode; Cobalt oxide; Oxygen evolution reaction; ELECTRON-HOLE RECOMBINATION; XPS SPECTRA; EFFICIENT; OXIDATION; CATALYSTS; FILMS;
D O I
10.1016/j.ijhydene.2023.11.033
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
Hematite with a suitable band gap is a promising candidate as the photoanode for photoelectrochemical water splitting, but it suffers from low catalytic activity and severe electron-hole recombination. Herein, a novel twostep solvothermal synthetic strategy is developed to fabricate a uniform CoOx amorphous layer with a thickness of 5 nm on Sn-doped Fe2O3 nanowire photoanode. The CoOx surface layer increases the roughness of the photoanode significantly, and thus enlarges the electrochemical active area. Furthermore, the CoOx layer brings Co2+/Co3+ redox couples, enhances the concentration of oxygen vacancies and increases the charge carrier density. The bulk and surface charge separation efficiencies are both improved. The surface charge transfer process and the oxygen evolution reaction are accelerated. The photocurrent density of the Sn-Fe2O3 photoanode at 1.23 V (vs. reversible hydrogen electrode) is improved from 0.83 to 1.40 mA cm-2 after the deposition of the CoOx surface layer.
引用
收藏
页码:1176 / 1183
页数:8
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