Perfluoro anion based binary and ternary ionic liquids as electrolytes for dye-sensitized solar cells

被引:18
|
作者
Lin, Hsi-Hsin [1 ]
Peng, Jia-De [1 ]
Suryanarayanan, V. [2 ]
Velayutham, D. [2 ]
Ho, Kuo-Chuan [1 ,3 ]
机构
[1] Natl Taiwan Univ, Dept Chem Engn, Taipei 10617, Taiwan
[2] CSIR Cent Electrochem Res Inst, Electroorgan Div, Karaikkudi 630006, Tamil Nadu, India
[3] Natl Taiwan Univ, Inst Polymer Sci & Engn, Taipei 10617, Taiwan
关键词
Ionic liquid; Dye-sensitized solar cell; Perfluoro carboxylate; Long-term stability; Gel electrolytes; PHYSICOCHEMICAL PROPERTIES; GEL ELECTROLYTES; TEMPERATURE; PERFORMANCE; SALTS; EFFICIENCY; COST;
D O I
10.1016/j.jpowsour.2016.02.029
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, eight new ionic liquids (ILs) based on triethylammonium (TEA) or n-methylpiperidinium (NMP) cations and perfluoro carboxylate (PFC) anions having different carbon chain lengths are synthesized and their physico-chemical properties such as density, decomposition temperature, viscosity and conductivity are determined. Photovoltaic characteristics of dye-sensitized solar cells (DSSCs) with binary ionic liquids electrolytes, containing the mixture of the synthesized ILs and 1-methyl-3-propyl imidazolium iodide (PMII) (v/v = 35/65), are evaluated. Among the different ILs, solar cells containing NMP based ILs show higher V-OC than that of TEA, whereas, higher J(SC) is noted for the DSSCs incorporated with the latter when compared to the former. Further, the photo-current of the DSSCs decreases with the increase of the carbon chain length of perfluoro carboxylate anionic group of ILs. The cell performance of the DSSC containing ternary ionic liquids-based electrolytes compose of NMP-2C/TEA-2C/PMII (v/v/v = 28/7/65) exhibits a J(SC) of 12.99 mA cm(-2), a V-OC of 639.0 mV, a FF of 0.72, and a cell efficiency of 6.01%. The extraordinary durability of the DSSC containing the above combination of electrolytes stored in dark at 50 degrees C is proved to be unfailing up to 1200 h. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:167 / 174
页数:8
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