Catalytic and photoelectrochemical performances of Cu-Zn-Sn-Se thin films prepared using selenization of electrodeposited Cu-Zn-Sn metal precursors

被引:12
|
作者
Shao, Pin-Wen [1 ]
Li, Chun-Ting [2 ]
Ho, Kuo-Chuan [2 ]
Cheng, Kong-Wei [1 ]
机构
[1] Chang Gung Univ, Dept Chem & Mat Engn, Taoyuan, Taiwan
[2] Natl Taiwan Univ, Dept Chem Engn, Taipei 10764, Taiwan
关键词
Electrodeposition; Photoelectrochemical; Dye-sensitized solar cell; Counter electrode; COUNTER-ELECTRODE; SOLAR-CELLS; ELECTRICAL-PROPERTIES; CU2ZNSNSE4; WATER; GROWTH; PHOTOCATALYST; REDUCTION; SULFIDE; ALLOYS;
D O I
10.1016/j.jpowsour.2015.03.101
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
In this study, Cu2ZnSnSe4 (CZTSe) films are deposited onto the fluorine-doped-tin-oxide-coated glass substrate via the selenization of electrodeposited Cu-Zn-Sn metal precursors in an acidic solution with the applied potential of -0.9 V vs. an Ag/AgCl electrode. X-ray diffraction patterns reveal that the samples are the quaternary tetragonal CZTSe phase. The thicknesses and direct band gaps of the samples are in the ranges of 2.3 to 2.7 mu m and 0.95 to 1.02 eV, respectively. All samples are p-type semiconductors with carrier density, mobility and flat-band potential in the ranges of 3.88 x 10(17) to 1.37 x 10(18) cm(-3), 10.31 to 12.6 cm(2) v(-1) s(-1) and -0.01 V to -0.08 V vs. Ag/AgCl reference electrode, respectively. The sample with [Cu]/[Zn + Sn] and [Zn]/[Sn] molar ratios of 0.87 and 0.66, respectively, has a maximum photo-enhanced current density of 0.41 mA cm(-2) at an applied bias of -0.5 V vs. an Ag/AgCl electrode in 0.5 M H2SO4 solution under illumination. The best photo-conversion efficiency of dye-sensitized solar cells using CZTSe with [Cu]/[Zn Sn] and [Zn]/[Sn] molar ratios of 0.87 and 0.66, respectively, as the counter electrode was 7.98%. The results show the high quality CZTSe films have potentials in applications of photoelectrochemical water splitting and dye-sensitized solar cells. Crown Copyright (C) 2015 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 57
页数:11
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