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Starch and cellulose have long been used in various industrial applications as gelating agents. In this work, the intrinsic adhesive properties of these biopolymers are exploited for application as electrolytes in DSSC. Firstly, potato starch was chemically modified into phthaloyl starch in a facile esterification process. Fabrication of polymer electrolyte with phthaloyl starch (PhSt) and hydroxyethyl cellulose (HEC) incorporated with dimethylformamide and tetrapropylammonium iodide produced homogeneous gels with diminished crystallinity. Infusion of different weight percentages of 1-butyl-3-methylimidazolium iodide (BMII) into the gels were revealed to further suppress polymer crystallinity and elevate ionic conductivity. Rheological analysis revealed that addition of up to 6 wt% of ionic liquid aid in elevating the rigidity, strength and tackiness of the gels. The improved adhesiveness of the gels can be correlated to effective reduction of interfacial resistance and restraining of recombination reactions based on electrochemical impedance spectroscopy. Quasi-solid DSSC fabricated with PhSt-HEC with 8 wt% of BMII exhibited enhanced short-circuit current density, JSC and fill factor, contributing to an optimized efficiency of 5.20%. [ABSTRACT FROM AUTHOR]

• Organosoluble starch derivative is employed as host in gel electrolyte. • Impact of rheological characters of gel on photovoltaic properties is analysed. • IPCE of 3% is recorded, highest among contemporary starch based polymer electrolyte. A novel blend of organosoluble phthaloyl starch (PhSt) and hydroxyethyl cellulose (HEC) was used as the polymer host to fabricate polymer gel electrolytes. Rheological analyses, such as amplitude sweep studies and tack tests, indicate that gels with good rigidity, strength and adhesiveness were attained upon inclusion of 20 wt% of HEC onwards. However, beyond 60 wt% of HEC, the mechanical properties and ionic conductivity of the gels were considerably compromised. Gels comprising 20–60 wt% of HEC were then fabricated into quasi-solid dye-sensitised solar cells (QSDSSC) with the addition of tetrapropylammonium iodide/iodine. The highest efficiency of 3.02% was recorded with gels comprising 70 wt% of PhSt and 30 wt% of HEC, which to the best of our knowledge is the highest ever efficiency in literature for starch-based electrolytes. Electrochemical impedance spectroscopy (EIS) of the QSDSSC revealed that the adhesive property of the gels plays a crucial role in charge transfer processes at the electrode/electrolyte interfaces. [ABSTRACT FROM AUTHOR]

Guar gum succinate (GGS) was chemically modified by reacting guar gum with succinic anhydride in the presence of 4-dimethylaminopyridine. Succination was confirmed by Fourier transform infrared (FTIR) spectroscopy with carbonyl bands at 1724 cm−1 and ester linkage at 1567 cm−1 of the succinate group. The resulting amorphous, GGS was used as a polymer host to prepare cost-effective solid polymer electrolyte (SPE) films via incorporating a blend of ethylene carbonate (EC), carboxymethyl cellulose (CMC), lithium triflate (LiTf) and lithium iodide (LiI). SPE system for GGS:EC (1.0:0.6) with 30 wt% LiTf showed highest conductivity of 6.29 × 10−5 S cm−1 and GGS:CMC:EC (0.5:0.5:0.6) with 25 wt% LiI showed highest conductivity of 2.10 × 10−4 S cm−1. FTIR revealed multiple complexation sites for ion mobility indicating that GGS possesses high prospects as a conductive SPE. [ABSTRACT FROM AUTHOR]

A first-of-its-kind, eco-friendly quasi-solid bioelectrolyte derived from potato starch was prepared. Starch was chemically modified via phthaloylation to synthesize amorphous, hydrophobic starch derivative and the attachment of the phthaloyl group was confirmed via FTIR which showed phthalate ester peak at 1715 cm −1 ; and 1 H NMR peaks between 7.30–7.90 ppm attributed to the aromatic protons of the phthaloyl group. The resulting starch derivative was then infused with ternary natural deep eutectic solvent (NADES) made from different molar ratios of choline chloride, urea and glycerol. Electrochemical Impedance Spectroscopy (EIS) revealed that the highest ionic conductivity was obtained by the system consisting of NADES with choline chloride:urea:glycerol in molar ratios of 4:6:2, with a magnitude of 2.86 mS cm −1 , hence validating the prospects of the materials to be further experimented as an alternative electrolyte in various electrochemical devices. [ABSTRACT FROM AUTHOR]

A gel polymer electrolyte system based on phthaloylchitosan was prepared. The effects of process variables, such as lithium iodide, caesium iodide, and 1-butyl-3-methylimidazolium iodide were investigated using a distance-based ternary mixture experimental design. A comparative approach was made between response surface methodology (RSM) and artificial neural network (ANN) to predict the ionic conductivity. The predictive capabilities of the two methodologies were compared in terms of coefficient of determination R2 based on the validation data set. It was shown that the developed ANN model had better predictive outcome as compared to the RSM model. [ABSTRACT FROM AUTHOR]

This study explores the possibility of transforming lignocellulose-rich agricultural waste materials into value-added products. Cellulose was extracted from an empty fruit bunch of oil palm and further modified into carboxymethyl cellulose (CMC), a water-soluble cellulose derivative. The CMC was then employed as the polymeric content in fabrication of solid polymer electrolyte (SPE) films incorporated with lithium iodide. To enhance the ionic conductivity of the solid polymer electrolytes, the compositions were optimized with different amounts of glycerol as a plasticizing agent. The chemical and physical effects of plasticizer content on the film composition were studied by Fourier transform infrared (FTIR) and X-ray diffraction (XRD) analysis. FTIR and XRD analysis confirmed the interaction plasticizer with the polymer matrix and the amorphous nature of fabricated SPEs. The highest ionic conductivity of 6.26 × 10−2 S/cm was obtained with the addition of 25 wt % of glycerol. By fabricating solid polymer electrolytes from oil palm waste-derived cellulose, the sustainability of the materials can be retained while reducing the dependence on fossil fuel-derived materials in electrochemical devices. [ABSTRACT FROM AUTHOR]

A starch-resorcinol-formaldehyde (RF)-lithium triflate (LiTf) based biodegradable polymer electrolyte membrane was synthesized via the solution casting technique. The formation of RF crosslinks in the starch matrix was found to repress the starch's crystallinity as indicated by the XRD data. Incorporation of the RF plasticizer improved the conductivity greatly, with the highest room-temperature conductivity recorded being 4.29 × 10−4 S cm−1 achieved by the starch:LiTf:RF (20 wt.%:20 wt.%:60 wt.%) composition. The enhancement in ionic conductivity was an implication of the increase in the polymeric amorphous region concurrent with the suppression of the starch's crystallinity. Chemical complexation between the plasticizer, starch, and lithium salt components in the electrolyte was confirmed by FTIR spectra. [ABSTRACT FROM AUTHOR]