Base-catalyzed synthesis of superhydrophobic and antireflective films for enhanced photoelectronic applications

被引:25
|
作者
Shefiu, Kareem [1 ]
Yi, Xie [1 ]
Tan, Li [1 ]
Yanxi, Ding [1 ]
Tsiwah, Emmanuel Acheampong [1 ]
Ahmed, Abdelaal S. A. [1 ]
Junwu Chen [2 ]
Fen Qiao [3 ]
Zhi Chen [4 ]
Xiujian Zhao [1 ]
机构
[1] Wuhan Univ Technol WUT, State Key Lab Silicate Mat Architectures, 122 Luoshi Rd, Wuhan 430070, Peoples R China
[2] Huazhong Univ Sci & Technol, State Key Lab Adv Elect Engn & Technol, 1037 Luoyu Rd, Wuhan, Peoples R China
[3] Jiangsu Univ, Sch Energy & Power Engn, Xuefu Rd 301, Zhenjiang, Jiangsu, Peoples R China
[4] Wuhan Shuneng New Mat Co Ltd, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
Transparent film; NaOH; Antireflective film; Superhydrophobic film; Photovoltaics; COATINGS; SOL; PERFORMANCE; SURFACES;
D O I
10.1016/j.jmrt.2020.02.022
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
In this work, a facile, cost-effective and environmentally friendly approach is developed to synthesize transparent silica sol for fabricating antireflective (AR) and superhydrophobic (SH) films on soda-lime glass. The transparent silica sol is prepared at room temperature by modification of hexamethyl disilazane (HMDS) on colloidal silica nanoparticles (NPs) which are synthesized via base-catalyzed hydrolysis of tetraethoxysilane (TEOS) in the presence of ammonia-free alkaline solution (i.e., NaOH). The AR and SH silica films are then achieved by dip-coating. The average transmittance, water static contact angle (CA) and sliding angle (SA) of the resulting film can reach 93.1%, 169.7 degrees and 3.0 degrees , respectively, exhibiting both AR and SH properties. In particular, the excellent SH and AR properties of the resulting film facilitate not only the excellent self-cleaning performance but also the increasing light transmittance and thus an enhanced power conversion efficiency (PCE) in photovoltaic module. (C) 2020 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:3958 / 3966
页数:9
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