Preparation of Zn-In-S film electrodes using chemical bath deposition for photoelectrochemical applications

被引:36
作者
Cheng, Kong-Wei [1 ,2 ]
Liang, Chia-Jui [1 ]
机构
[1] Chang Gung Univ, Dept Chem & Mat Engn, Tao Yuan 333, Taiwan
[2] Chang Gung Univ, Solar Cell Grp, Technol Res Ctr, Tao Yuan 333, Taiwan
关键词
Chemical synthesis; Photoelectrode; Optical property; Photocurrent density; THIN-FILMS; PHYSICAL-PROPERTIES; WATER OXIDATION; ZNIN2S4; PHOTOCATALYST; PHOTORESPONSE; PHOTOANODES; REDUCTION; EVOLUTION; GROWTH;
D O I
10.1016/j.solmat.2010.02.049
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
Ternary zinc-indium-sulfide film electrodes were fabricated on fluorine doped tin oxide coated glass substrates using chemical bath deposition. New procedures for the growth of Zn-In-S films are presented. The physical and photoelectrochemical properties of the samples were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM). UV-vis spectroscopy, and a potentiostat. The XRD patterns and SEM images of samples reveal that the samples changed from the cubic ZnIn2S4 phase with lamellar microstructures to the cubic In2S3 phase with irregular platelet microstructures when the [Zn]/[In] molar ratio was decreased in precursor solutions. The thicknesses, direct and indirect band gaps of the samples, determined from the surface profile measurement and transmittance and reflectance spectra, are in the ranges of 1135-1714 nm, 2.47-2.74 eV and 1.88-2.11 eV, respectively. All samples were n-type semiconductors. The flat band potentials of the samples in 0.6 M K2SO3 solution (pH = 9.5), determined from Mott-Schottky plots, lie in the range of -0.58 to -0.45 V vs. the normal hydrogen electrode (NHE). The maximum photocurrent density of samples obtained in this study was 0.67 mA/cm(2) at an external potential of +0.5 V vs. an Ag/AgCl electrode in contact with 0.6 M K2SO3 solution under illumination using a 300W Xe lamp system with the light intensity set at 100 mW/cm(2). Crown Copyright (C) 2010 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1137 / 1145
页数:9
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