PVdF-HFP quasi-solid-state electrolyte for application in dye-sensitized solar cells

Farish Irfal Saaid, Tseung-Yuen Tseng, Tan Winie*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


A quasi-solid-state polymer electrolyte is prepared by incorporating poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) in a propylene carbonate (PC) / 1,2-dimethoxyethane (DME) / 1-methyl-3-propylimidazolium iodide (MPII) liquid electrolyte. The amount of PVdF-HFP in the liquid electrolyte is varied from 0.1 to 0.4 g. Incorporation of 0.1 g of PVdF-HFP decreases the conductivity of the DME/PC/MPII liquid electrolyte from 1.3 × 10-2 to 5.6 × 10-3 S cm-1. Conductivity decreases gradually with increasing PVdF-HFP. No-flow "jelly-like" electrolyte samples are obtained for PVdF-HFP ≥ 0.2 g. The decrease in conductivity is the result of the decrease in ion mobility. Ion mobility was calculated by impedance spectroscopy. The PVdF-HFP quasi-solid-state electrolytes were assembled into dye sensitized solar cells (DSSCs). The performance of the DSSCs was measured under illumination of a 100 mW cm-2 Xenon light source. The DSSC without PVdF-HFP polymer shows an efficiency of 4.88% with short-circuit current density, Jsc of 11.24 mA cm-2, fill factor, FF of 70% and open circuit voltage, Voc of 619 mV. The presence of PVdF-HFP deteriorates the performance of DSSCs, but problems such as electrolyte leakage and volatilization are eliminated. The performance of DSSCs was found to be correlated to the conductivity behaviour of the electrolyte.

Original languageEnglish
Pages (from-to)1187-1195
Number of pages9
JournalInternational Journal of Technology
Issue number6
StatePublished - 1 Dec 2018


  • Conductivity
  • Dye-sensitized solar cell
  • Ionic liquid
  • PVdF-HFP
  • Quasi-solid- state electrolyte

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