Abstract

An exceptional approach of appending tris(1,10-phenanthroline)cobalt(II)/(III)bis/tris(hexafluorophosphate) and synthesized tetramethyl benzidine-based thiourea derivatives as novel additives with hydroxypropyl cellulose are used to construct a gel polymer electrolyte for DSSC. The thiourea derivatives are synthesized using the cost-effective method. The synthesized derivatives are confirmed by 1H, 13C NMR and mass spectroscopy. The conductivity, surface and redox potential of thiourea derivatives doped Co2+/Co3+ redox electrolytes are scrutinized by impedance spectra, FTIR, UV, XRD. A density functional theory method with full geometry optimization is used to elucidate the adsorption of the symmetrical thiocarbamides on TiO2 (101) surface progressing with electron donating/accepting groups. All the organic compounds display a negative shift on the TiO2 Fermi level simultaneously by adsorption and rebutted as an escalated additive in stable Co(II/III)phen redox electrolyte of the dye-sensitized TiO2 solar cell. This impulse effect influences the sorbate dipole moment component normal to TiO2 surface plane; further, the stable redox mediator and hydroxypropyl cellulose deliver a good performance in a dye-sensitized solar cell. The newly synthesized thiourea derivatives doped Co2+/Co3+ with hydroxypropyl cellulose reports high solar to electric conversion, particularly 1,1'-(3,3′,5,5′-tetramethyl-[1,1′-biphenyl]-4,4′-diyl)bis(3-(3,4,5-trimethoxy phenyl)thiourea) (additive-6) doped redox electrolyte shows an outstanding efficiency (ŋ) of 9.1% under the sunlight irradiation of about 70 mW/cm2.

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