Photoelectrochemical properties of nitrogen-doped indium tin oxide thin films prepared by reactive DC magnetron sputtering

被引:12
|
作者
Wu, Kee-Rong [1 ]
Yeh, Chung-Wei [2 ]
Hung, Chung-Hsuang [3 ]
Cheng, Li-Hsun [1 ]
Chung, Chih-Yuan [1 ]
机构
[1] Natl Kaohsiung First Univ Sci & Technol, Natl Kaohsiung Marine Univ, Dept Marine Engn, Kaohsiung, Taiwan
[2] Natl Kaohsiung First Univ Sci & Technol, Kao Yuan Univ, Dept Informat Syst, Kaohsiung, Taiwan
[3] Natl Kaohsiung First Univ Sci & Technol, Dept Safety Hlth & Environm Engn, Kaohsiung, Taiwan
关键词
Visible light; Nitrogen-doped tin indium oxide; Photocurrent; Water splitting; WATER; TIO2; PHOTOCATALYSIS;
D O I
10.1016/j.tsf.2009.09.056
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nitrogen-doped indium tin oxide (N-ITO) thin films are deposited on unheated ITO glass substrates in this study. The structural properties of the N-ITO thin films, determined by X-ray diffraction (XRD) and Raman scattering, show that the indium nitride (InN) phase is liable to form in N-ITO films prepared in 20% N-2. A broad XRD peak around 2 theta = 33 degrees and Raman peak around 490 cm(-1) are assigned to the InN phase, but no such peak is observed from the ITO film. Hence, the bandgap is narrowed by N-doping for absorbing light of longer wavelengths of similar to 500 rim. However. under illumination by ultraviolet, the N-ITO film prepared in 20% N-2 exhibits the least photocurrent response, which is less than one third that of the N-ITO catalyst that was doped in 16.4% N-2. This result is attributed mostly to the fact that the valence and conduction band potentials are not positioned properly between the newly formed InN and host ITO phases, rendering inefficient inter-semiconductor electron transfer. Therefore, higher N-doped samples exhibit a lower photocurrent response. Interestingly, the N-ITO film prepared in 16.4% N-2 exhibits the highest photocurrent density of about 165.5 mu A/cm(2) at an applied bias of 1.2 V. This implies that the N-ITO films should be prepared at a low N-2 ratio to ensure a favorable photoelectrochemical activity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1581 / 1584
页数:4
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