Electrodeposited metal nanowires as transparent conductive electrodes: Their release conditions, electrical conductivity, optical transparency and chemical stability

被引:19
作者
Arefpour, M. [1 ]
Kashi, M. Almasi [1 ,2 ]
Barzoki, F. Khansari [1 ]
Noormohammadi, M. [2 ]
Ramazani, A. [1 ,2 ]
机构
[1] Univ Kashan, Inst Nanosci & Nanotechnol, Kashan 8731751167, Iran
[2] Univ Kashan, Dept Phys, Kashan 8731751167, Iran
基金
美国国家科学基金会;
关键词
Transparent conductive electrodes; Metal nanowires; Ag-based nanowires; Electrodeposition; Anodic aluminum oxide template; Sulfurization environment; LARGE-SCALE SYNTHESIS; SILVER NANOWIRES; COPPER NANOWIRES; FILMS; FABRICATION; ARRAYS; RESISTANCE; OXIDATION; NETWORK; DIAMETER;
D O I
10.1016/j.matdes.2018.07.048
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Metal nanowires (MNWs) have gained considerable attention from research groups as they can be effectively applied in new transparent conductive electrodes (TCEs), replacing indium tin oxide (ITO) materials. However, using conventional synthetic methods including the chemical solution, Ag and Cu NW-based TCEs have been found to be non-uniform and unstable in reactive environments. Here, we present an innovative high-throughput method in the fabrication of Ni, AgNi, AgCu and AgNiCu NW-based TCEs using the electrodeposition of metal ions into anodic aluminum oxide (AAO) templates, followed by drop-coating of highly uniform MNWs on glass substrates. After the complete release of 60 mu m long MNWs with high crystallinity from the templates, the resulting TCEs show enhanced electrical, optical and chemical stability properties compared to those of ITOs and Ag NW-based TCEs. Notably, in the case of Ag98Ni1Cu1NW-based TCEs, we obtain a low sheet resistance of 36 Omega sq.(-1) together with a high transparency of 88%, thereby evidencing the fabrication of high-quality TCEs without byproducts and difficult post-treatments. These MNW-based TCEs are also exposed to sulfurization environment, showing chemical stability with no precedent in the literature. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:326 / 336
页数:11
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