Evaluation of photovoltaic efficiency of dye‐sensitized solar cells fabricated with electrospun PVDF‐PAN‐Fe2O3 composite membrane

Poly(vinylidene fluoride)‐polyacrylonitrile‐based membranes containing Fe₂O₃ nanoparticles were prepared by electrospinning technique and characterized by HR‐SEM, FTIR, and XRD analysis. The effect of electrolyte in the electrospun nanofibers on electrolyte uptake, ionic conductivity and porosity were studied. The electrospun membranes containing Fe₂O₃ showed an enhanced ionic conductivity than that of without Fe₂O₃. Among the prepared membranes, the membrane with 7 wt % Fe₂O₃ has the highest liquid electrolyte uptake of 562% and ionic conductivity of 6.81 × 10^?2 S cm^?1. The photovoltaic performance for open circuit voltage (V_oc), Short‐circuit current density (J_sc), Fill factor (FF), and η of the DSSC fabricated with 7 wt % Fe₂O₃ are 0.77 V, 10.4 mA/cm², 0.62 and 4.9%, respectively. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41107.     

Exploration on polypropylene carbonate polymer for gel polymer electrolyte preparation and dye‐sensitized solar cell application

Gel polymer electrolytes (GPEs) with incorporation of polypropylene carbonate (PPC) polymer and different weight percentages of sodium iodide (NaI) salt are prepared. Ethylene carbonate and propylene carbonate are used as plasticizers. The maximum ionic conductivity of 2.01 mS cm^?1 is achieved at room temperature. Temperature‐dependent ionic conductivity study is performed. The GPEs are studied for structural properties using Fourier transform infrared (FTIR). The FTIR analysis confirms that complexation between PPC and NaI has occurred. By using GPEs, dye‐sensitized solar cells (DSSC) are fabricated under the one Sun light intensity. The highest energy conversion efficiency of 6.38% is achieved with incorporation of 60 wt % of NaI. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45091.     

Gel Polymer Electrolyte with Anion‐Trapping Boron Moieties via One‐Step Synthesis for Symmetrical Supercapacitors

A novel gel polymer electrolyte (GPE) which is based on new synthesized boron‐containing monomer, benzyl methacrylate, 1 m LiClO₄/N,N‐dimethylformamidel liquid electrolyte solution is prepared through a one‐step synthesis method. The boron‐containing GPE (B‐GPE) not only displays excellent mechanical behavior, favorable thermal stability, but also exhibits an outstanding ionic conductivity of 2.33 mS cm^?1 at room temperature owing to the presence of anion‐trapping boron sites. The lithium ion transference in this gel polymer film at ambient temperature is 0.60. Furthermore, the symmetrical supercapacitor which is fabricated with B‐GPE as electrolyte and reduced graphene oxide as electrode demonstrates a broad potential window of 2.3 V. The specific capacitance of symmetrical B‐GPE supercapacitors retains 90% after 3000 charge–discharge cycles at current density of 1 A g^?1.     

Development of quasi‐solid‐state dye‐sensitized solar cell based on an electrospun polyvinylidene fluoride–polyacrylonitrile membrane electrolyte

Dye sensitized solar cell (DSSC) has been magnetizing more awareness in current research due to more efficiency. The foremost drawback of the solar cell is the evaporation of organic electrolyte. In order to address this problem, the polyvinylidene fluoride–polyacrylonitrile–Electrospinning Fibrous Membranes were prepared by electrospinning method and the photovoltaic performances were evaluated. The polyvinylidene fluoride and polyacrylonitrile were mixed in N,N′‐dimethylformamide and acetone at an applied potential of 15 kV. The surface morphology of membrane is interconnected with network structure and a large number of voids were observed from Field Emission Scanning Electron Microscopy images. The electrolyte uptakes up to 310% were observed and it shows an increase in the ionic conductivity up to 6.12 × 10^?2 S cm^?1 at 25°C. The fabricated DSSCs show open circuit voltage (V_oc) of 0.74 V, fill factor (FF) of 0.65 and short circuit current (J_sc) of 6.20 mA cm^?2 at an incident light intensity of 100 mW cm^?2. The photovoltaic efficiency also reached up to 3.09%. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 40022.     

Effect of 1‐butyl‐3‐methylimidazolium iodide containing electrospun poly(vinylidene fluoride‐co‐hexafluoropropylene) membrane electrolyte on the photovoltaic performance of dye‐sensitized solar cells

Electrospun poly(vinylidene fluoride‐co‐hexafluoropropylene) (PVdF‐HFP) membrane was prepared from a solution of 16 wt % of PVdF‐HFP containing acetone/N,N‐dimethyl acetamide (7:3 wt %). The prepared electrospun PVdF‐HFP membrane (esPM) was then soaked in ionic liquid electrolyte containing 0.5M LiI, 0.05M I₂ , and 0.5M 4‐tert butylpyridine, 0.5M 1‐butyl‐3‐methylimidazolium iodide (BMImI) in acetonitrile to get electrospun PVdF‐HFP membrane electrolyte (esPME). The effect of various concentrations of BMImI containing esPME on ionic conductivity was studied by AC‐impedance measurements and the diffusion co‐efficients was determined by linear sweep voltammetry. The photovoltaic performance of a DSSC fabricated using 0.5M BMImI containing electrospun PVdF‐HFP membrane electrolyte (0.5M BMImI‐esPME) has power conversion efficiency (PCE) of 6.42%. But the stability of the DSSC fabricated using 0.5M BMImI‐esPME was considerably superior to that fabricated using 0.5M BMImI containing liquid electrolyte (0.5M BMImI‐LE). © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42032.     

Preparation of PAA‐g‐PEG/PANI polymer gel electrolyte and its application in quasi solid state dye‐sensitized solar cells

A microporous hybrid polymer of poly(acrylic acid)‐g‐poly(ethylene glycol)/polyaniline (PAA‐g‐PEG/PANI) is synthesized by a two‐step solution polymerization method. The influence of aniline concentration on the conductivity of PAA‐g‐PEG/PANI gel electrolyte is discussed, when the concentration of aniline is 0.66 wt%, the conductivity of PAA‐g‐PEG/PANI gel electrolyte is 11.50 mS cm^?1. Using this gel electrolyte as host, a quasi solid state dye‐sensitized solar cell (QS‐DSSC) is assembled. The QS‐DSSC based on this gel electrolyte achieves a power conversion efficiency of 6.38% under a simulated solar illumination of 100 mW cm^?2 (AM 1.5). POLYM. ENG. SCI., 55:322–326, 2015. © 2014 Society of Plastics Engineers     

Polyacrylonitrile–poly(1-vinyl pyrrolidone-co-vinyl acetate) blend based gel polymer electrolytes incorporated with sodium iodide salt for dye-sensitized solar cell applications

New gel polymer electrolytes (GPEs) were prepared via the blending of a polyacrylonitrile polymer and a poly(1-vinyl pyrrolidone-co-vinyl acetate) copolymer. The sodium iodide (NaI) salt concentration was varied for each GPE sample. From ionic conductivity (σ) studies, we observed that the sample with a 40 wt % NaI salt content (N40) showed the highest σ of 3.54 × 10⁻³ ± 0.05 S/cm at room temperature, and all of the GPE samples obeyed Arrhenius behavior. The dielectric properties of the GPE samples were also analyzed to study the electrical polarization of the materials. The developed GPE samples were also characterized with X-ray diffraction and Fourier transform infrared spectroscopy. We also then used the developed GPE samples for the fabrication of dye-sensitized solar cells by sandwiching them between a photoanode and Pt counter electrode for photovoltaic studies. The highest photovoltaic performance was achieved by N40, with an efficiency of 3.04%. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47810.     

Preparation and properties of gel‐filled PVDF separators for lithium ion cells

Polyether gel‐filled poly(vinylidene fluoride) separators (GF‐PVDF separators) were prepared by means of thermal crosslinking of poly(ethylene glycol) methyl ether acrylate (PEGMEA) and poly(ethylene glycol) diacrylate (PEGDA) as gel constituents. The intrinsic properties of GF‐PVDF and their corresponding gel polymer electrolyte (GPE) were characterized by SEM, DSC, and electrochemical methods. It was found a relatively better GPE could be got when the filled polyether content no more than 60 wt % and its ion conductivity could reach 1.3 × 10^?3 S cm^?1. The GPE is compatible with anode and cathode of lithium ion battery at high voltage and its electrochemical window is 4.6 V (vs. Li/Li⁺). The coulombic efficiency could reach 94% after 100 cycles for the cells using such GPE. The results reveal that the composite polymer electrolyte qualifies as a potential application in lithium cells. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44473.     

Application of thermosetting organic solvent free polymer gel electrolyte in quasi‐solid‐state dye‐sensitized solar cell

A kind of thermosetting organic solvent free polymer gel electrolyte with oligomer ethylene glycol as liquid phase was prepared and applied in quasi‐solid‐state dye‐sensitized solar cell (QS‐DSSC). The viscosity and the ionic conductivity of the polymer gel electrolyte are sensitive to the changed temperature. The photovoltaic performance of QS‐DSSC is also improved with the increased temperature due to the increased ionic conductivity and diffusion coefficient of iodide in polymer gel electrolyte. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Application of polymer gel electrolyte with graphite powder in quasi‐solid‐state dye‐sensitized solar cells

A polymer gel electrolyte with ionic conductivity of 5.11 mS cm⁻¹ was prepared by using poly (acrylonitrile‐co‐styrene) as polymer matrix, acetonitrile and tetrahydrofuran as binary organic mixture solvent, NaI + I₂ as electrolyte, graphite powder and 1‐methylimidazole as additives. The components ratio of the polymer gel electrolyte was optimized, and the influence of the components and temperature on the ionic conductivity of the polymer gel electrolyte and photoelectronic properties of dye sensitized solar cell were investigated. On the basis of the polymer gel electrolyte with the optimized conditions, a quasi‐solid‐state dye‐sensitized solar cell was fabricated and its light‐ to‐electricity energy conversion efficiency of 3.25% was achieved under irradiation of 100 mW cm⁻². POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

A redox‐mediator‐doped gel polymer electrolyte applied in quasi‐solid‐state supercapacitors

Methylene blue (MB) redox mediator was introduced into polyvinyl alcohol/polyvinyl pyrrolidone (PVA/PVP) blend host to prepare a gel polymer electrolyte (PVA‐PVP‐H₂SO₄‐MB) for a quasi‐solid‐state supercapacitor. The electrochemical properties of the supercapacitor with the prepared gel polymer electrolyte were evaluated by cyclic voltammetry, galvanostatic charge–discharge, electrochemical impedance spectroscopy, and self‐discharge measurements. With the addition of MB mediator, the ionic conductivity of gel polymer electrolyte increased by 56% up to 36.3 mS·cm^?1, and the series resistance reduced, because of the more efficient ionic conduction and higher charge transfer rate, respectively. The electrode specific capacitance of the supercapacitor with PVA‐PVP‐H₂SO₄‐MB electrolyte is 328 F·g^?1, increasing by 164% compared to that of MB‐undoped system at the same current density of 1 A·g^?1. Meanwhile, the energy density of the supercapacitor increases from 3.2 to 10.3 Wh·kg^?1. The quasi‐solid‐state supercapacitor showed excellent cyclability over 2000 charge/discharge cycles. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39784.     

The Effect of Incorporation of Multi-Walled Carbon Nanotube into Poly(Ethylene Oxide) Gel Electrolyte on the Photovoltaic Performance of Dye-Sensitized Solar Cell

Gel polymer electrolytes (GPEs) consist of poly(ethylene oxide) (PEO), sodium iodide (NaI) and different amount of multi-walled carbon nanotubes (MWCNT) were prepared. The conductivity study revealed that the highest ionic conductivity of GPE was 7.02 × 10^?3 S cm^?1. The structural and complexation between the materials are authenticated via X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. Under the exposure of AM 1.5, the fabricated DSSCs exhibited the highest photoenergy conversion efficiency of 7.23% with a short circuit current density (J_SC) of 18.64 mA cm^?2, open circuit voltage (V_OC) of 0.590 mV and fill factor (FF) of 65.7%.     

Blending poly(methyl methacrylate) and poly(styrene‐co‐acrylonitrile) as composite polymer electrolyte

A blend of poly(methyl methacrylate) (PMMA) and poly(styrene‐co‐acrylonitrile) (PSAN) has been evaluated as a composite polymer electrolyte by means of differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectroscopy, ac impedance measurements, and linear sweep voltammetry (LSV). The blends show an interaction with the Li⁺ ions when complexed with lithium perchlorate (LiClO₄), which results in an increase in the glass‐transition temperature (T_g) of the blends. The purpose of using PSAN as another component of the blend is to improve the poor mechanical properties of PMMA‐based plasticized electrolytes. The mechanical property is further improved by introducing fumed silica as inert filler, and hence the liquid electrolyte uptake and ionic conductivity of the composite systems are increased. Room‐temperature conductivity of the order of 10^?4 S/cm has been achieved for one of the composite electrolytes made from a 1/1 blend of PSAN and PMMA containing 120% liquid electrolyte [1M LiClO₄/propylene carbonate (PC)] and 10% fumed silica. These systems also showed good compatibility with Li electrodes and sufficient electrochemical stability for safe operation in Li batteries. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1319–1328, 2001     

Novel amphiphilic polymer gel electrolytes based on (PEG‐b‐GMA)‐co‐MMA

Amphiphilic conetwork–structured copolymers containing different lengths of ethylene oxide (EO) chains as ionophilic units and methyl methacrylate (MMA) chains as ionophobic units were prepared by free radical copolymerization and characterized by FTIR and thermal analysis. Polymer gel electrolytes based on the copolymers complexed with liquid lithium electrolytes (dimethyl carbonate (DMC) : diethyl carbonate (DEC) : ethylene carbonate (EC) = 1 : 1 : 1 (W/W/W), LiPF₆ 1.0M) were characterized by differential scanning calorimetry and impedance spectroscopy. A maximum ion conductivity of 4.27 × 10^?4 S/cm at 25^oC was found for the polymer electrolyte based on (PEG2000‐b‐GMA)‐co‐MMA with long EO groups. Moreover, the effect of temperature on conductivity of the amphiphilic polymer electrolytes obeys the Arrhenius equation. The good room temperature conductivity of the polymer electrolytes is proposed to relate to the enhancement in the amorphous domain of the copolymers due to their amphiphilic conetwork structure. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Improved stability in P3HT:PCBM photovoltaics by incorporation of well‐designed polythiophene/graphene compositions

Morphological and photovoltaic stabilities of poly(3‐hexylthiophene) (P3HT):phenyl‐C₆₁‐butyric acid methyl ester (PC₇₁BM) solar cells were investigated in pristine and modified states. To this end, four types of patterned/assembled nanostructures, namely reduced graphene oxide (rGO)‐g‐poly(3‐dodecylthiophene)/P3HT patched‐like pattern, rGO–polythiophene/P3HT/PC₇₁BM nanofiber, rGO‐g‐P3HT/P3HT cake‐like pattern and supra(polyaniline (PANI)‐g‐rGO/P3HT), were designed on the basis of rGO and various conjugated polymers. Intermediately covered rGO nanosheets by P3HT crystals (supra(PANI‐g‐rGO/P3HT)) performed better than sparsely (patched‐like pattern) and fully (cake‐like pattern) covered ones in P3HT:PC₇₁BM solar cell systems. Supra(PANI‐g‐rGO/P3HT) nanohybrids largely phase‐separated in active layers (root mean square = 0.88 nm) and also led to the highest performance (power conversion efficiency of 5.74%). The photovoltaic characteristics demonstrated decreasing trends during air aging for all devices, but with distinct slopes. The steepest decreasing plots were obtained for the unmodified P3HT:PC₇₁BM devices (from 1.77% to 0.28%). The two supramolecules with the most ordered structures, that is, cake‐like pattern (10.12 mA cm^?2, 51%, 0.58 V, 2.2 × 10^?6 cm² V^?1 s^?1, 4.3 × 10^?5 cm² V^?1 s^?1, 0.69 nm and 2.99%) and supra(PANI‐g‐rGO/P3HT) (12.51 mA cm^?2, 57%, 0.63 V, 1.2 × 10^?5 cm² V^?1 s^?1, 3.4 × 10^?4 cm² V^?1 s^?1, 0.82 nm and 4.49%), strongly retained morphological and photovoltaic stabilities in P3HT:PC₇₁BM devices after 1 month of air aging. According to the morphological, optical, photovoltaic and electrochemical results, the supra(PANI‐g‐rGO/P3HT) nanohybrid was the best candidate for stabilizing P3HT:PC₇₁BM solar cells. © 2020 Society of Chemical Industry     

Fabrication and properties of crosslinked poly(propylene carbonate maleate) gel polymer electrolyte for lithium‐ion battery

The poly(propylene carbonate maleate) (PPCMA) was synthesized by the terpolymerization of carbon dioxide, propylene oxide, and maleic anhydride. The PPCMA polymer can be readily crosslinked using dicumyl peroxide (DCP) as crosslinking agent and then actived by absorbing liquid electrolyte to fabricate a novel PPCMA gel polymer electrolyte for lithium‐ion battery. The thermal performance, electrolyte uptake, swelling ratio, ionic conductivity, and lithium ion transference number of the crosslinked PPCMA were then investigated. The results show that the T_g and the thermal stability increase, but the absorbing and swelling rates decrease with increasing DCP amount. The ionic conductivity of the PPCMA gel polymer electrolyte firstly increases and then decreases with increasing DCP ratio. The ionic conductivity of the PPCMA gel polymer electrolyte with 1.2 wt % of DCP reaches the maximum value of 8.43 × 10⁻³ S cm⁻¹ at room temperature and 1.42 × 10⁻² S cm⁻¹ at 50°C. The lithium ion transference number of PPCMA gel polymer electrolyte is 0.42. The charge/discharge tests of the Li/PPCMA GPE/LiNi_1/3Co_1/3Mn_1/3O₂ cell were evaluated at a current rate of 0.1C and in voltage range of 2.8–4.2 V at room temperature. The results show that the initial discharge capacity of Li/PPCMA GPE/LiNi_1/3Co_1/3Mn_1/3 O₂ cell is 115.3 mAh g⁻¹. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Well‐functioned photovoltaics based on nanofibers composed of PBDT‐TIPS‐DTNT‐DT and graphenic precursors thermally modified by polythiophene,polyaniline and polypyrrole

Reduced graphene oxide nanosheets modified by conductive polymers including polythiophene (GPTh), polyaniline (GPANI) and polypyrrole (GPPy) were prepared using the graphene oxide as both substrate and chemical oxidant. UV–visible and Raman analyses confirmed that the graphene oxide simultaneously produced the reduced graphene oxide and polymerized the conjugated polymers. The prepared nanostructures were subsequently electrospun in mixing with poly(3‐hexylthiophene) (P3HT)/phenyl‐C71‐butyric acid methyl ester (PC₇₁BM) and poly[bis(triisopropylsilylethynyl)benzodithiophene‐bis(decyltetradecylthien)naphthobisthiadiazole] (PBDT‐TIPS‐DTNT‐DT)/PC₇₁BM components and embedded in the active layers of photovoltaic devices to improve the charge mobility and efficiency. The GPTh/PBDT‐TIPS‐DTNT‐DT/PC₇₁BM devices demonstrated better photovoltaic features (J_sc = 11.72 mA cm^?2, FF = 61%, V_oc = 0.68 V, PCE = 4.86%, μ_h = 8.7 × 10^?3 cm² V^–1 s^?1 and μ_e = 1.3 × 10^?2 cm² V^–1 s^?1) than the GPPy/PBDT‐TIPS‐DTNT‐DT/PC₇₁BM (J_sc = 10.30 mA cm^?2, FF = 60%, V_oc = 0.66 V, PCE = 4.08%, μ_h = 1.4 × 10^?3 cm² V^–1 s^?1 and μ_e = 8.9 × 10^?3 cm² V^–1 s^?1) and GPANI/PBDT‐TIPS‐DTNT‐DT/PC₇₁BM (J_sc = 10.48 mA cm^?2, FF = 59%, V_oc = 0.65 V, PCE = 4.02%, μ_h = 8.6 × 10^?4 cm² V^–1 s^?1 and μ_e = 7.8 × 10^?3 cm² V^–1 s^?1) systems, assigned to the greater compatibility of PTh in the nano‐hybrids and the thiophenic conjugated polymers in the bulk of the nanofibers and active thin films. Furthermore, the PBDT‐TIPS‐DTNT‐DT polymer chains (3.35%–5.04%) acted better than the P3HT chains (2.01%–3.76%) because of more complicated conductive structures. © 2019 Society of Chemical Industry     

Preparation and performance study on P(St‐MMA)‐SiO2 doped P(VDF‐HFP) based composite polymer electrolyte

The organic–inorganic hybrid material poly(styrene‐methyl methacrylate)‐silica (P(St‐MMA )‐SiO₂) was successfully prepared by in situ polymerization confirmed by Fourier transform infrared spectroscopy and was employed to fabricate poly(vinylidene fluoride‐hexafluoropropylene) (P(VDF‐HFP )) based composite polymer electrolyte (CPE ) membrane. Desirable CPEs can be obtained by immersing the CPE membranes into 1.0 mol L^?1 LiPF₆‐EC /DMC /EMC (LiPF₆ ethylene carbonate + dimethyl carbonate + ethylmethyl carbonate) liquid electrolyte for about 0.5 h for activation. The corresponding physicochemical properties were characterized by SEM , XRD , electrochemical impedance spectroscopy and charge–discharge cycle testing measurements. The results indicate that the as‐prepared CPEs have excellent properties when the mass ratio of the hybrid P(St‐MMA )‐SiO ₂ particles to polymer matrix P(VDF‐HFP ) reaches 1:10, at which point the SEM analyses show that the as‐prepared P(St‐MMA )‐SiO ₂ particles are uniformly dispersed in the membrane and the CPE membrane presents a homogeneous surface with abundant interconnected micropores. The XRD results show that there may exist interaction forces between the P(St‐MMA )‐SiO ₂ particles and the polymer matrix, which can obviously decrease the crystallinity of the composite membrane. Moreover, the ionic conductivity at room temperature and the electrochemical working window of the CPE membrane can reach 3.146 mS cm^?1 and 4.7 V, respectively. The assembled LiCoO₂/CPE /Li coin cell with the CPE presents excellent charge–discharge and C ‐rate performance, which indicates that P(St‐MMA )‐SiO ₂ hybrid material is a promising additive for the P(VDF‐HFP ) based CPE of the lithium ion battery. © 2016 Society of Chemical Industry     

Synthesis of a novel alkylimidazolium iodide containing an amide group for electrolyte of dye-sensitized solar cells

A novel alkylimidazolium iodide containing an amide group, 1-(2-hexanamidoethyl)-3-methylimidazol-3-ium iodide (amido-ImI), was synthesized to act as the quasi-solid-state electrolyte of dye-sensitized solar cells (DSSCs). The DSSC with the amido-ImI electrolyte exhibited short-circuit photocurrent density (J_sc) and overall energy conversion efficiency (η) that were improved by 7.2% and 10.2%, respectively, compared to those obtained with the cell containing 1-hexyl-2,3-dimethylimidazolium iodide, a commonly used liquid electrolyte, at 100 mW cm⁻². Furthermore, the stability of the DSSC was enhanced by the presence of amido-ImI.     

Highly efficient dye-sensitized solar cells: A comparative study with two different system of solvent-free binary room-temperature ionic liquid-based electrolytes

In this work, novel redox electrolytes based on poly (ethylene oxide) (PEO) were prepared using binary ionic liquid 1-methyl-3-propylimidazolium iodide (MPII) with 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIMTFSI) or 1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF₄) to reduce the high viscosity of MPII. The addition of low viscosity ionic liquids is to overcome the low mass transportation of redox mediator faced by the single ionic liquid. Therefore, different ratios of ionic liquids were added, and their effect on the electrical properties of the ionic liquid-based gel polymer electrolytes (GPE) was observed. It was confirmed that all the system dominant by ions rather than electron. The binary ionic liquid system containing 37.5 wt.% of BMIMBF₄ showed the highest ionic conductivity of 24.2 mS cm⁻¹. Fourier-transform infrared and X-ray diffraction studies confirmed that complexation occurred between all materials. The combination of two alkyl side chain length has enhanced the efficiency of the DSSC with short-circuit current density (J_SC) of 26.81 mA cm⁻¹, open-circuit voltage (V_OC) of 0.67 V, fill factor of 44.5% and photovoltaic conversion efficiency (η) of 7.8%. This work has provided valuable insight for further stability of binary ionic liquid-based GPE compared to single ionic liquid electrolytes.