Journal
DYES AND PIGMENTS
Volume 132, Issue -, Pages 72-78Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2016.04.028
Keywords
DSSC; Copper dye; I-3(-)/I- liquid electrolyte; Photoconversion efficiency; Solar cell
Funding
- Swiss National Science Foundation [200020_144500]
- European Research Council [267816]
- University of Basel
- Swiss National Science Foundation (SNF) [200020_144500] Funding Source: Swiss National Science Foundation (SNF)
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The performances of dye-sensitized solar cells (DSSCs) containing a heteroleptic bis(diimine)copper(I) dye and an I-3(-)/I- liquid electrolyte have been investigated as a function of the electrolyte composition. Starting from a standard electrolyte with LiI (0.1 M), I-2 (0.05 M), 1-butyl-3-methylimidazolium (BMII) ionic liquid (0.6 M), 1-methylimidazole additive (0.5 M) in 3-methoxypropionitrile (MPN), a series of ten electrolytes was initially screened; the solvent, additives, concentration of I-2, and sources (LiI and/or BMII) and concentrations of I- were varied. The highest short-circuit current densities (J(SC) = 7.85 and 7.60 mA cm(-2)) and photoconversion efficiencies (eta = 2.64 and 2.70% relative to 6.56 and 6.11% for two N719 references) were observed for DSSCs with an electrolyte comprising I-2 (0.03 M), BMII (0.6 M), 4-tert-butylpyridine (TBP, 0.4 M) and guanidinium thiocyanate (GNCS, 0.1 M) in MPN solvent; no LiI was added. This composition was further optimized by varying the amounts of TBP and GNCS. A low concentration of I-2 (0.015 M) is optimal. The presence or absence of GNCS has little effect on overall DSSC performance, but increasing the concentration of TBP is detrimental to DSSC performance, and an absence of TBP is beneficial. Open-circuit voltage decay (OCVD) measurements confirm that the addition of GNCS and/or TBP reduces recombination rates at the TiO2-dye interface. The best DSC parameters obtained for the copper(I)-based dye were J(sc) = 7.80 mA cm(-2), open-circuit voltage (V-OC) = 501 mV and eta = 2.76% (relative to 6.72% for N719). (C) 2016 Elsevier Ltd. All rights reserved.
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