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Boosted Charge Separation in Core@Shell N-Ta2O5@α-Fe2O3 Heterojunctions via Band Structure Engineering for Enhanced Visible-Light-Driven Photoelectrocatalytic Water Oxidation ( EI收录)
文献类型:期刊文献
英文题名:Boosted Charge Separation in Core@Shell N-Ta2O5@α-Fe2O3 Heterojunctions via Band Structure Engineering for Enhanced Visible-Light-Driven Photoelectrocatalytic Water Oxidation
作者:Liu, Yaqiao[1]; Hu, Shuozhen[1]; Gao, Zhaoqun[1]; Zhang, Xinsheng[1]; Sun, Shigang[2]
机构:[1] State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai, 200237, China; [2] State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, China
年份:2023
卷号:6
期号:18
起止页码:9672
外文期刊名:ACS Applied Energy Materials
收录:EI(收录号:20234414984554)
语种:英文
外文关键词:Band structure - Chemical stability - Doping (additives) - Fermi level - Heat treatment - Hematite - Heterojunctions - Nanorods - Oxidation - Oxygen vacancies - Photoelectrochemical cells - Solar fuels - Tantalum oxides
摘要:Photoelectrochemical (PEC) water oxidation is considered to be a promising approach to converting solar energy into clean chemical fuels. α-Fe2O3 is a potential photoanode material for water oxidation with a high theoretical photocurrent density (12.6 mA cm-2) driven by visible light. Constructing α-Fe2O3-based heterojunction with other semiconductors is a promising strategy to improve the actual photoelectrocatalytic activity. In this work, nitrogen-doped Ta2O5 is introduced to synthesize N-Ta2O5-h@α-Fe2O3 nanorod heterojunction with different band structures. At the interface, electrons transfer from N-Ta2O5-h to α-Fe2O3, which forms a built-in electric field. The heterojunction structure contributes to inhibiting the severe recombination of photogenerated electron-hole pairs. By controlling the duration of mild heat treatment, the N-Ta2O5-h nanorods with different Fermi energy levels and contents of oxygen vacancies are obtained. A mild heat treatment in N2 is proved to enlarge the ΔE by leveling up the Fermi level and to promote the content of oxygen vacancies for the N-Ta2O5-h@α-Fe2O3 heterojunction as the heat-treatment time increases. The PEC water oxidation performance of the N-Ta2O5-h@α-Fe2O3 heterojunction increases when the mild-heat-treatment time is 2 h and decreases for 6 h treatment. Eventually, N-Ta2O5-2@α-Fe2O3 exhibits an enhanced photocurrent density of 3.10 mA cm-2 (4.4 times higher than that of bare α-Fe2O3), an efficiently boosted charge separation (2.0 times higher than bare α-Fe2O3), and a high chemical stability after a long-term test. ? 2023 American Chemical Society.
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