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Role of Water in the Lyotropic Liquid Crystalline Lithium Iodide-Iodine-Water-CE Mesophase as a Gel Electrolyte in a Dye-Sensitized Solar Cell.

作者信息

Topuzlu Ezgi Yılmaz, Ulgut Burak, Dag Ömer

机构信息

Department of Chemistry, Bilkent University, 06800 Ankara, Turkey.

UNAM-National Nanotechnology Research Center and Institute of Materials Science and Nanotechnology, Bilkent University, 06800 Ankara, Turkey.

出版信息

Langmuir. 2021 Jul 13;37(27):8305-8313. doi: 10.1021/acs.langmuir.1c01094. Epub 2021 Jun 29.

DOI:10.1021/acs.langmuir.1c01094
PMID:34185544
Abstract

By replacing volatile and flammable organic-based electrolytes with gel electrolytes, dye-sensitized solar cells (DSSCs) may be a viable and more practical alternative to other clean energy sources. Although they present a promising alternative, gel electrolytes still have some drawbacks for practical applications, such as low ionic conductivity and infusion difficulties into the pores of the working electrode. Here, we introduce a new one-step fabrication method that uses a lyotropic liquid crystalline (LLC) gel electrolyte (LiI:I:HO:CH(OCHCH)OH) and a dye (N719) to construct a DSSC that performs (7.32%) 2.2 times better compared with a traditional two-step production. Water plays a key role in the gel electrolyte, where the HO/LiI mole ratio is around 2.57 under ambient laboratory conditions (ALCs); however, this ratio linearly increases to 4.00 and then to 5.85 at 40 and 75% humidities, respectively, without affecting the two-dimensional (2D) hexagonal structure of the mesophase. The ionic conductivity of the gel electrolyte linearly increases accordingly, by 2.2 (4.8 × 10 to 10.6 × 10) and 13.1 times (63.0 × 10 S/cm) from ALC to 40 and ALC to 75% humidity, respectively. Increasing water in the gel phase improves the conductivity of the LLC mesophase and the short-circuit current () of the DSSC, but negatively influences the open-circuit voltage () of the cell, equilibrium reaction between the LiI and I, and the anchoring of the dye molecules over the titania surface.

摘要

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