Abstract

Network hybrid gel prepared with tetraethyl orthosilicate, 3-aminopropyltrimethoxysilane (APS) and poly(ethylene glycol) was used as an electrolyte matrix in a quasi-solid state dye-sensitized solar cell (DSSC). Change in pH of this hybrid gel by varying the composition of APS was found to have remarkable effects on the photoelectrochemical performance of the cell. The hybrid gel matrix, having silane polymer backbones with free amine functionality, was characterized by FT-IR spectra and FE-SEM images, and the assembled DSSC by photocurrent-voltage and incident photon to current conversion efficiency curves. The unsealed, quasi-solid state DSSC with the hybrid gel has shown an increase in the open-circuit voltage ( V oc) and a steady decrease in the short-circuit photocurrent ( J sc), with increase in the content of APS. A maximum conversion efficiency of 4.5% was obtained for a DSSC by using 20% of APS in its hybrid gel at a light intensity of 100 mW cm −2. Upon replacing the amino group of APS by bulkier aniline and benzophenoaniline groups, conversion efficiencies of the corresponding DSSCs were reduced. Variations in the V oc and J sc are explained in terms of shift of the flat band potential of TiO 2 and a complex formation between I 3 − and −NH 2 of APS of the electrolyte.

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