Room temperature deposition of homogeneous, highly transparent and conductive Al-doped ZnO films by reactive high power impulse magnetron sputtering

被引:75
作者
Mickan, Martin [1 ,2 ]
Helmersson, Ulf [2 ]
Rinnert, Herve [1 ]
Ghanbaja, Jaafar [1 ]
Muller, Dominique [3 ]
Horwat, David [1 ]
机构
[1] Univ Lorraine, Inst Jean Lamour, UMR7198, F-54011 Nancy, France
[2] Linkoping Univ, IFM Mat Phys, Plasma & Coatings Phys Div, SE-58183 Linkoping, Sweden
[3] Univ Strasbourg, CNRS UMR 7357, Lab ICube, F-67037 Strasbourg 2, France
关键词
Transparent conducting oxide; AZO; Thin films; Electronic properties; HiPIMS; THIN-FILMS; ELECTRONIC-STRUCTURE; OXIDE-FILMS; HYSTERESIS;
D O I
10.1016/j.solmat.2016.07.020
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
Aluminum doped zinc oxide (AZO) films have been deposited using reactive high power impulse magnetron sputtering (HiPIMS) and reactive direct current (DC) magnetron sputtering from an alloyed target without thermal assistance. These films have been compared in terms of their optical, electrical and structural properties. While both DC and HiPIMS deposited films show comparable transmittance, their electrical properties are significantly improved by the HiPIMS process. The HiPIMS deposited films show a low resistivity down to the order of 10(-4) Omega cm with a good homogeneity across the substrate, making them potential candidates for electrodes in solar cells. The density of electrons reached up to 11 x 10(20) cm(-3), making ionized impurities the main scattering defects. This improvement of the film properties can be related to the specific plasma/target interactions in a HiPIMS discharge. This allows the process to take place in the transition mode and to deposit highly conductive, transparent AZO films on large surfaces at low temperature. While the overall oxygen content is above that of stoichiometric ZnO, higher localization of oxygen is found at the interfaces between crystalline domains with substoichiometric composition. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:742 / 749
页数:8
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