Cost-effective centrifuge coating method for silver nanowire-based transparent conducting electrode

被引:13
|
作者
Shin, Hee Jeong [1 ]
Oytun, Faruk [2 ,3 ]
Kim, Jae Won [4 ]
Lee, Bo Ram [5 ]
Kim, Jin Young [4 ]
Basarir, Fevzihan [6 ]
Choi, Hyosung [1 ]
机构
[1] Hanyang Univ, INST, Res Inst Convergence Basic Sci, Dept Chem, Seoul 04763, South Korea
[2] Istanbul Tech Univ, Dept Chem, TR-34469 Maslak, Turkey
[3] VSY Biotechnol, TR-34959 Istanbul, Turkey
[4] Ulsan Natl Inst Sci & Technol, Dept Energy Engn, Ulsan 44919, South Korea
[5] Pukyong Natl Univ, Dept Phys, Busan 48513, South Korea
[6] NEXT Chem, TR-34490 Istanbul, Turkey
基金
新加坡国家研究基金会;
关键词
Centrifuge coating; Transparent conducting electrode; Silver nanowires; Organic photovoltaics; SOLAR-CELLS; NETWORK; FILMS;
D O I
10.1016/j.electacta.2020.135839
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The silver nanowire (Ag NW)-based electrode, a promising candidate for replacing the conventional indium tin oxide (ITO) electrode, is suitable for flexible device fabrication due to low cost production, high electrical conductivity, high transparency, and mechanical flexibility. Although many types of coating processes exist to produce Ag NW films, those methods require post-treatments and a Ag NW solution with a high concentration in excess of 0.5 mg/ml. In this work, we report a cost-effective method to produce a Ag NW electrode on a flexible polyethylene terephthalate (PET) substrate using centrifuge coating with a Ag NW solution with extremely low concentrations of 0.003-0.02 mg/ml without post-treatment. The optimized Ag NW electrode has a sheet resistance of 7.25 Omega/sq and optical transmittance of 73.62% in the visible wavelength region, resulting in a figure-of-merit value (FOM) of 157.13, which is better than that of a commercial ITO electrode. As a result, organic photovoltaic devices based on this Ag NW electrode on a PET substrate exhibited a power conversion efficiency of 7.61%, which is comparable to that of devices based on an ITO electrode. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页数:7
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