The study of carrier transfer mechanism for nanostructural hematite photoanode for solar water splitting

被引:29
|
作者
Chen, Yen-Jhih [1 ]
Chen, Liang-Yih [1 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Dept Chem Engn, 43,Sect 4,Keelung Rd, Taipei 106, Taiwan
关键词
Hematite; Nanocorals; Ti doping; Water splitting; Oxygen evolution reaction; ZNO NANOWIRE ARRAYS; ALPHA-FE2O3; PHOTOANODES; OXYGEN EVOLUTION; THIN-FILMS; OXIDATION; SEMICONDUCTOR; PERFORMANCE; TI; ENHANCEMENT; EFFICIENCY;
D O I
10.1016/j.apenergy.2015.08.105
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Due to the band gap of hematite (alpha-Fe2O3) (E-g = 2.1 eV) in visible light region, it is regarded as suitable n-type semiconductor material for solar water splitting. Although theoretical conversion efficiency can achieve 12.9%, the drawbacks of hematite, such as short hole diffusion length (similar to 10 nm), poor charge transport and slow oxygen evolution kinetic rate, cause the generated holes being trapped in photo anodes for low conversion efficiency. In this study, hematite nanorods photoanode was prepared via hydrothermal method and the grain sizes of hematite nanorods increased by adding absolute ethanol into growth aqueous solution. In addition, the morphologies observed by SEM showed that hematite nanorods transformed to nanocorals due to the addition of ethanol. To improve the electrical conductivity for reducing carrier recombination, Ti4+ ions were doped into hematite nanocorals photoanode. Herein, the photocurrent density of Ti-doped hematite nanocorals photoanode could achieve 1.72 mA/cm(2) at 1.23 V (vs. RHE). Finally, the surfaces of hematite nanocorals photoanode was decorated by ZnFe2O4 heterojunction layer and Co-Pi oxygen evolution catalysts (OECs) to improve the oxygen evolution reaction. The current density and power conversion efficiency could furthermore improve to 3.60 mA/cm(2) at 1.23 V and 0.33%, respectively. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:924 / 933
页数:10
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