Liquid crystal based electrolyte with light trapping scheme for enhancing photovoltaic performance of quasi-solid-state dye-sensitized solar cells

In this study, nematic liquid crystal, 4-Cyano-4′-n-heptyloxybiphenyl, is introduced into the poly(vinylidenefluoride-co-hexafluoropropylene) (PVDF) based polymeric gel electrolyte for quasi-solid-state dye-sensitized solar cells (DSC), aiming to improve the photovoltaic performance of DSC. The effects of liquid crystal on the electrochemical behavior of I₃⁻/I⁻ and photovoltaic performance, dynamic response as well as long-term stability of DSC are studied in detail. It is found that although the addition of liquid crystal would hinder the charge transport in the electrolyte, it could still fulfill the requirements of the photocurrent for DSC. More important, a significant increase in the photocurrent density for DSC is observed when liquid crystal is introduced into PVDF based polymeric gel electrolyte, resulting in the higher photoelectric conversion efficiency. The large increase in short-circuit photocurrent density could be attributed to the higher light harvesting efficiency, which is caused by the effective formation of light trapping scheme in electrolyte due to the addition of liquid crystal. Besides, at-rest long-term stability shows that when liquid crystal is introduced into PVDF based polymeric gel electrolyte, DSC could retain over 92% of its initial photoelectric conversion efficiency value after 1000 h, exhibiting relatively better stability.     

Dye-sensitized, nano-porous TiO2 solar cell with poly(acrylonitrile): MgI2 plasticized electrolyte

Dye-sensitized solar cells are promising candidates as supplementary power sources; the dominance in the photovoltaic field of inorganic solid-state junction devices is in fact now being challenged by the third generation of solar cells based on dye-sensitized, nano-porous photo-electrodes and polymer electrolytes. Polymer electrolytes are actually very favorable for photo-electrochemical solar cells and in this study poly(acrylonitrile)-MgI₂ based complexes are used. As ambient temperature conductivity of poly(acrylonitrile)-salt complexes are in general low, a conductivity enhancement is attained by blending with the plasticizers ethylene carbonate and propylene carbonate. At 20 °C the optimum ionic conductivity of 1.9 × 10⁻³ S cm⁻¹ is obtained for the (PAN)₁₀(MgI₂)_n(I₂)_n/10(EC)₂₀(PC)₂₀ electrolyte where n = 1.5. The predominantly ionic nature of the electrolyte is seen from the DC polarization data. Differential scanning calorimetric thermograms of electrolyte samples with different MgI₂ concentrations were studied and glass transition temperatures were determined. Further, in this study, a dye-sensitized solar cell structure was fabricated with the configuration Glass/FTO/TiO₂/Dye/Electrolyte/Pt/FTO/Glass and an overall energy conversion efficiency of 2.5% was achieved under solar irradiation of 600 W m⁻². The I-V characteristics curves revealed that the short-circuit current, open-circuit voltage and fill factor of the cell are 3.87 mA, 659 mV and 59.0%, respectively.     

Ionic liquid electrolyte based on S-propyltetrahydrothiophenium iodide for dye-sensitized solar cells

A new ionic liquid S-propyltetrahydrothiophenium iodide (T₃I) was developed as the solvent and iodide ion source in electrolyte for dye-sensitized solar cells. The electrochemical behavior of the /I⁻ redox couple and effect of additives in this ionic liquid system was tested and the results showed that this ionic liquid electrolyte revealed good conducting abilities and potential application for solar devices. The effects of LiI and dark-current inhibitors were investigated. The dye-sensitized solar cell with the electrolyte (0.1 mol L⁻¹ LiI, 0.35 mol L⁻¹ I₂, 0.5 mol L⁻¹ NMBI in pure T₃I) gave short-circuit photocurrent density (J_sc) of 11.22 mA cm², open-circuit voltage (V_oc) of 0.61 V and fill factor (FF) of 0.51, corresponding to the photoelectric conversion efficiency (η) of 3.51% under one Sun (AM1.5).     

Enhanced performance of a quasi-solid-state dye-sensitized solar cell with aluminum nitride in its gel polymer electrolyte

The effects of incorporation of aluminum nitride (AlN) in the gel polymer electrolyte (GPE) of a quasi-solid-state dye-sensitized solar cell (DSSC) were studied in terms of performance of the cell. The electrolyte, consisting of lithium iodide (LiI), iodine (I₂), and 4-tert-butylpyridine (TBP) in 3-methoxypropionitrile (MPN), was solidified with poly(vinyidene fluoride-co-hexafluoro propylene) (PVDF-HFP). The 0.05, 0.1, 0.3, and 0.5 wt% of AlN were added to the electrolyte for this study. XRD analysis showed a reduction of crystallinity in the polymer PVDF-HFP for all the additions of AlN. The DSSC fabricated with a GPE containing 0.1 wt% AlN showed a short-circuit current density (J_SC) and power-conversion efficiency (η) of 12.92±0.54 mA/cm² and 5.27±0.23%, respectively, at 100 mW/cm² illumination, in contrast to the corresponding values of 11.52±0.21 mA/cm² and 4.75±0.08% for a cell without AlN. The increases both in J_SC and in η of the promoted DSSC are attributed to the higher apparent diffusion coefficient of I⁻ in its electrolyte (3.52×10⁻⁶ cm²/s), compared to that in the electrolyte without AlN of a DSSC (2.97×10⁻⁶ cm²/s). At-rest stability of the quasi-solid-state DSSC with 0.1 wt% of AlN was found to decrease hardly by 5% and 7% at room temperature and at 40 °C, respectively, after 1000 h duration. The DSSC with a liquid electrolyte showed a decrease of about 40% at room temperature, while it virtually lost its performance in about 150 h at 40 °C. Explanations are further substantiated by means of electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and by porosity measurements.     

An investigation on the performance of a silver ionic solid electrolyte system for a new detergent-based nanocrystalline dye-sensitized solar cell

A new dye-sensitized solar cell containing a detergent-based solid-state composite electrolyte has been investigated. The electrolyte is composed of Triton-X (C₁₆H₂₆O₂)n, with a powder mixture of surface-treated carbon powder, a fast ion-conducting material (FCM) 40(Cu_1−xAg_xI)−30(Ag₂O)−30(WO₃), (x=0.2), I⁻/I₃⁻ redox couple and an iodine complexing agent. The introduction of this detergent-based solid-state composite electrolyte forms a mosaic-like surface for the smooth transfer of photo-ejected electrons between electrodes. The current-voltage characteristics of TiO₂ nanocrystalline dye-sensitized solar cells based on the above solid-state composite electrolyte measured under simulated sunlight with AM 1.5 at 40 mW/cm² have revealed a short circuit current of 0.7 mA, open circuit voltage of 588 mV and fill-factor of 0.4, thus yielding an over-all conversion efficiency of 0.4%. These results have suggested the origin of appreciably, high charge transfer and the suppressed reverse reaction of electrons as due to the presence of the detergent dispersed with suspensions of electron- and ion-conducting phases.     

Thiocyanate ligand substitution kinetics of the solar cell dye Z-907 by 3-methoxypropionitrile and 4-tert-butylpyridine at elevated temperatures

The dye-sensitized solar cell dye Z-907, [RuLL′(NCS)₂] may loose a thiocyanate ligand at elevated temperatures (80-100 °C) by ligand exchange with the solar cell additive 4-tert-butylpyridine (4-TBP) or the electrolyte solvent 3-methoxypropionitrile (3-MPN). The mechanism in homogeneous solution proceeds via three equilibrium reactions Eqs. (1)-(3) with the solvent complex [RuLL′(NCS)(3-MPN)] as an intermediate:[RuLL′(NCS)₂]+3-MPN=[RuLL′(NCS)(3-MPN)]⁺+NCS⁻ (1)[RuLL′(NCS)(3-MPN)]⁺+4-TBP=[RuLL′(NCS)(4-TBP)]⁺+3-MPN (2)[RuLL′(NCS)₂]+4-TBP=[RuLL′(NCS)(4-TBP)]⁺+NCS⁻ (3)A similar mechanism describes the heterogeneous substitution reactions of Z-907 attached to the surface of TiO₂ particles with 3-MPN and 4-TBP. All the six homogeneous and heterogeneous rate constants were obtained at 100 °C by monitoring the decay of Z-907 and product formation in test-tube experiments by HPLC coupled to UV/vis and electrospray mass spectrometry.A half-lifetime t_1/2=150 h was obtained for the Z-907 dye bound to TiO₂ nanocrystalline particles at 85 °C in the presence of 4-TBP and 3-MPN. Dye-sensitized solar cells (DSC) with Z-907 as a sensitizer and application of the so-called “non-robust” electrolytes containing 4-TBP and 3-MPN is therefore not expected to be able to pass a 1000 h thermal stress test at 85 °C. Addition of thiocyanate to the cell electrolyte may however, eliminate or reduce the problems caused by dye thiocyanate ligand substitution in DSC cells.     

Carbon-nanofiber counter electrodes for quasi-solid state dye-sensitized solar cells

Carbon-nanofibers (CNFs) with antler and herringbone structures are studied as a tri-iodide (I₃⁻) reduction electrocatalyst in combination with the liquid electrolyte or an alternative stable quasi-solid state electrolyte. The catalytic properties of the counter electrode (CE) are characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The doctor bladed low temperature CNFs-CE has faster I₃⁻ reduction rate and low charge transfer resistance (R_CT) of ∼0.5 Ω cm² than platinum (Pt) (∼2.3 Ω cm²) due to the nanofiber stacking morphology. Its herringbone and antler structures with graphitic layers lead to defect rich edge planes and larger diameter of CNFs facilitate the electron transfer kinetics. The cells with CNF counter electrodes are showing promising energy conversion efficiency greater than 7.0% for the glass based devices and 5.0% for the flexible cells filled with the quasi-solid state electrolyte, which is similar to Pt performance. Application of CNFs-CE in flexible and quasi-solid state electrolyte increases the possibility of roll to roll process, low cost and stable dye-sensitized solar cells (DSCs).     

High performance quasi-solid-state dye-sensitized solar cells based on poly(lactic acid-co-glycolic acid)

A stable quasi-solid-state dye-sensitized solar cell (DSC) with a novel amphiphilic polymer gel electrolyte (APGE) based on poly(lactic acid-co-glycolic acid) (PLGA) is fabricated. The APGE could be readily prepared by a simple method at low temperature of 50 °C and exhibits a quasi-solid property, high conductivity, and long-term stability. The 20 and 40 wt% APGE-based DSCs show high photovoltaic conversion efficiency of 7.5 and 7.4%, respectively, under AM 1.5 simulated sunlight, which is comparable to the liquid electrolyte-based DSC with the efficiency of 7.6%. The 40 wt% APGE-based DSC maintains 95% of the initial performance after 60 days in practical conditions. It is also noteworthy that the APGE endows with higher short-circuit current density than the liquid electrolyte. Different natures of the APGE from the typical polymer gel electrolytes have been elucidated by the I-V measurements, electrochemical impedance spectroscopy, electrophoretic measurements, and transmission electron microscopy.     

Performance of a new polymer electrolyte incorporated with diphenylamine in nanocrystalline dye-sensitized solar cell

A new solvent-free composite polymer electrolyte consisting of poly(ethylene oxide) (PEO) incorporated into diphenyl amine (DPA) along with KI and I₂ has been developed. The current-voltage characteristics of this nanocrystalline dye-sensitized solar cell measured under simulated sunlight with 1.5 AM at 60 mW/cm² have indicated that this cell generates a photocurrent of 10.2 mA/cm², together with a photovoltage of 810 mV and fill factor of 0.47 yielding an overall energy conversion efficiency of 6.5%. This result suggests that the electron donicity of DPA influences the interaction of nanocrystalline TiO₂ electrode and I⁻/I₃⁻ electrolyte, leading to a high performance of the fabricated solar cell.     

Effect of molecular weight of oligomer on ionic diffusion in oligomer electrolytes and its implication for dye-sensitized solar cells

This study measures the diffusion coefficients of I⁻ and I₃⁻ in oligomer electrolytes as a function of the molecular weight of oligomers and investigates their effect on the performance of dye-sensitized solar cells (DSSCs). The high-diffusion coefficients of ions in an oligomer electrolyte with a lower molecular weight can help to promote the redox mechanism in DSSCs and thereby increase the short-circuit current density. They can also cause a decrease in the open-circuit voltage since a high-diffusion coefficient of I₃⁻ is capable of reducing the lifetime of electrons in TiO₂ electrodes. To offset these effects, N-methyl-benzimidazole is added to the oligomer electrolytes, thereby improving the open-circuit voltage and fill factor and, consequently, the overall energy-conversion efficiency, which increases to over 5%. A further test involving storage at a high temperature of 75 °C demonstrates that DSSCs employing the oligomer electrolytes show excellent thermal stability over 200 h.     

Study on calcium and samarium co-doped ceria based nanocomposite electrolytes

Calcium co-doped SDC-based nanocomposite electrolyte (Ce_0.8Sm_0.2−xCa_xO_2−δ-Na₂CO₃) was synthesized by a co-precipitation method. The microstructure and morphology of the composite electrolytes were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and transmission electron microscope (TEM), and thermal properties were determined with differential scanning calorimetry (DSC). The particle size, as shown by TEM imaging, was 5-20 nm, which is in a good agreement with the SEM and XRD results. The co-doping effect on both interfaces of the composite electrolyte and doped bulk effect inside the ceria was studied. The excellent performance of the fuel cell was about 1000 mW cm⁻² at 560 °C and at the very low temperature of 350 °C the power density was 200 mW cm⁻². This paper may give a new approach to develop functional nanocomposite electrolyte for low-temperature solid oxide fuel cell (LTSOFC).     

Solid oxide fuel cells with bi-layered electrolyte structure

In this work, we have developed solid oxide fuel cells with a bi-layered electrolyte of 2 μm SSZ and 4 μm SDC using tape casting, screen printing, and co-firing processes. The cell reached power densities of 0.54 W cm⁻² at 650 °C and 0.85 W cm⁻² at 700 °C, with open circuit voltage (OCV) values larger than 1.02 V. The electrical leaking between anode and cathode through an SDC electrolyte has been blocked in the bi-layered electrolyte structure. However, both the electrolyte resistance (R_el) and electrode polarization resistance (R_p,a+c) increased in comparison to cells with single-layered SDC electrolytes. The formation of a solid solution of (Ce, Zr)O_2−x during sintering process and the flaws in the bi-layered electrolyte structure seem to be the main causes for the increase in the R_el value (0.32 Ω cm²) at 650 °C, which is almost one order of magnitude higher than the calculated value.     

Quasi-solid-state dye-sensitized solar cells with a novel efficient absorbent for liquid electrolyte based on PAA–PEG hybrid

A novel efficient absorbent for liquid electrolyte based on poly(acrylic acid)–poly(ethylene glycol) (PAA–PEG) hybrid is prepared. The highest value of liquid electrolyte absorbency about 3.65 is achieved. The polymer gel electrolyte shows a moderate value of ionic conductivity about 3.24 mS cm⁻¹ and high chemical stability. Based on the polymer gel electrolyte, a quasi-solid-state dye-sensitized solar cell was fabricated and its overall energy conversion efficiency of 3.19% was obtained under irradiation of 100 mW cm⁻².     

Electrochemical performance of Ba0.5Sr0.5CoxFe1−xO3−δ (x = 0.2–0.8) cathode on a ScSZ electrolyte for intermediate temperature SOFCs

Intermediate temperature solid oxide fuel cell cathode materials (Ba, Sr)Co_xFe_1−xO_3−δ [x = 0.2–0.8] (BSCF), were synthesized by a glycine-nitrate process (GNP) using Ba(NO₃)₂, Sr(NO₃)₂, Co(NO₃)₂·6H₂O, and Fe(NO₃)₃·9H₂O as starting materials and glycine as an oxidizer and fuel. Electrolyte-supported symmetric BSCF/GDC/ScSZ/GDC/BSCF cells consisting of porous BSCF electrodes, a GDC buffer layer, and a ScSZ electrolyte were fabricated by a screen printing technique, and the electrochemical performance of the BSCF cathode was investigated at intermediate temperatures (500–700 °C) using AC impedance spectroscopy. Crystallization behavior was found to depend on the pH value of the precursor solution. A highly acidic precursor solution increased the single phase perovskite formation temperature. In the case of using a precursor solution with pH 2, a single perovskite phase was obtained at 1000 °C. The thermal expansion coefficient of BSCF was gradually increased from 24 × 10⁻⁶ K⁻¹ for BSCF (x = 0.2) to 31 × 10⁻⁶ K⁻¹ (400–1000 °C) for BSCF (x = 0.8), which resulted in peeling-off of the cathode from the GDC/ScSZ electrolyte. Only the BSCF (x = 0.2) cathode showed good adhesion to the GDC/ScSZ electrolyte and low polarization resistance. The area specific resistance (ASR) of the BSCF (x = 0.2) cathode was 0.183 Ω cm² at 600 °C. The ASR of other BSCF (x = 0.4, 0.6, and 0.8) cathodes, however, was much higher than that of BSCF (x = 0.2).     

Photovoltaic performance of solid-state solar cells based on ZnO nanosheets sensitized with low-cost metal-free organic dye

In this study, the fabrication of photoanode of dye-sensitized solar cell (DSSC) using two-dimensional ZnO nanosheets (ZnONSs) and low-cost metal-free photosensitizer, evans blue, and evaluation of its photovoltaic performance in the solid-state DSSC with TiO₂ nanotubes (TNTs) modified poly(ethylene oxide) (PEO) polymer electrolyte is described. The ZnONSs are synthesized via hydrothermal method and are characterized by high resolution scanning electron microscopy (HR-SEM), diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PLS) and X-ray diffraction (XRD) analysis. The photovoltaic performance of the cells is evaluated under standard air mass 1.5 global simulated illumination (100 mW cm⁻²). The current-voltage (I-V) and photocurrent-time (I-T) curves proved effective collection of electrons in the solid-state DSSCs with the ZnONSs photoanode. The solar to electrical energy conversion efficiency of the ZnONSs based DSSC with TNTs modified PEO electrolyte is 0.12%, which is about 1.5 times higher than that of the ZnO nanoparticles based DSSC, due to fast electron diffusion within the nanosheets.     

Ion transport and ion-filler-polymer interaction in poly(methyl methacrylate)-based, sodium ion conducting, gel polymer electrolytes dispersed with silica nanoparticles

Experimental studies are carried out on novel sodium ion conducting, gel polymer electrolyte nanocomposites based on poly(methyl methacrylate) (PMMA) and dispersed with silica nanoparticles. The nanocomposites are obtained in the form of free-standing transparent films.A gel electrolyte with ∼4 wt.% SiO₂ offers the maximum electrical conductivity of ∼3.4 × 10⁻³ S cm⁻¹ at ∼20 °C with good mechanical, thermal and electrochemical stability. Physical characterization by X-ray diffraction, Fourier transformed infra-red and scanning electron microscopy is performed to examine ion/filler-polymer interaction and the possible changes in the texture of the host polymer due to liquid electrolyte entrapment and the dispersion of SiO₂ nanoparticles. The temperature dependence of the electrical conductivity is consistent with an Arrhenius-type relationship in the temperature range from 25 to 75 °C. Sodium ion conduction in the gel electrolyte film is confirmed from cyclic voltammetry and transport number measurements. The value of the sodium ion transport number (tNa⁺) of the undispersed gel electrolyte is ∼0.23 and it is almost unaffected due to the dispersion of SiO₂ nanoparticles. The effect of SiO₂ dispersion on ionic conduction is described in terms of anion-filler surface interaction.     

Influence of polymer concentration and dyes on photovoltaic performance of dye-sensitized solar cell with P(VdF-HFP)-based gel polymer electrolyte

A series of gel polymer electrolytes (GPEs) is synthesized using Poly(vinylidenefluoride-hexafluoropropylene) P(VdF-HFP) as the host matrix and propylene carbonate (PC)–diethyl carbonate (DEC) as plasticizers to fabricate dye-sensitized solar cells. Equal amounts of PC and DEC are used to comprehend high dielectric constant and low viscosity of the electrolyte. The as-prepared GPEs are characterized by XRD, FTIR and SEM. Their thermal properties and ionic conductivities are investigated by TGA/DSC analyses and AC impedance measurements, respectively. The optimized gel polymer electrolyte gives a maximum ionic conductivity of 5.25 × 10⁻³ S cm⁻¹ at room temperature. The formation of porous structure in the electrolyte film supports the entrapment of large volumes of liquid electrolyte inside its cavities. The role of N3 and N719 dyes are also investigated for better photovoltaic performance of DSSC. The overall light-to-electrical-energy conversion efficiencies of 3.95% and 4.41% are obtained for N3 and N719 dyes, respectively, under 100 mW cm⁻² irradiation, which are comparable to those obtained from the corresponding liquid electrolyte cell.     

Novel agarose polymer electrolyte for quasi-solid state dye-sensitized solar cell

Quasi-solid state dye-sensitized solar cells (DSSCs) are fabricated with a novel polysaccharide gel electrolyte composed of agarose in 1-methyl-2-pyrrolidinone (NMP) as polymer matrix, lithium iodide (LiI)/iodine (I₂) as redox couple and titania nanoparticles as fillers. The polysaccharide electrolyte with different agarose concentrations (1-5 wt%) and various inorganic filler TiO₂ concentrations (0-10 wt%) are studied systematically by differential scanning calorimetry (DSC) and the AC impedance spectra. The electrochemical and photoelectric performances of DSSCs with these electrolytes are also investigated. It is found that increasing agarose and inorganic filler concentration leads to a decrease in T_g in the range of 1-2 wt% for agarose and 0-2.5 wt% for TiO₂ changed electrolytes, which results in high conductivity in these electrolytes. From the electrochemical analysis, it is observed that the electron lifetime in TiO₂ of DSSCs increases with agarose, while decreases with inorganic filler contents. The prolonged electron lifetime in DSSCs is advantageous to improve open-circuit voltage (V_oc). Based on these results, the cell with the electrolyte of 2 wt% agarose shows the optimized energy conversion efficiency of 4.14%. The optimized efficiency of the DSSC with added titania is 4.74% at 2.5 wt% titania concentration.     

A high-performance counter electrode based on poly(3,4-alkylenedioxythiophene) for dye-sensitized solar cells

A poly(3,3-diethyl-3,4-dihydro-2H-thieno-[3,4-b][1,4]dioxepine) (PProDOT-Et₂) counter electrode prepared by electrochemical polymerization on a fluorine-doped tin oxide (FTO) glass substrate was incorporated in a platinum-free dye-sensitized solar cell (DSSC). The surface roughness and I⁻/I₃⁻ redox reaction behaviors based on PProDOT-Et₂, poly(3,4-propylenedioxythiophene) (PProDOT), poly(3,4-ethylenedioxythiophene) (PEDOT), and sputtered-Pt electrodes were characterized, and their performances as counter electrodes in DSSCs were compared. Cells fabricated with a PProDOT-Et₂ counter electrode showed a higher conversion efficiency of 7.88% compared to cells fabricated with PEDOT (3.93%), PProDOT (7.08%), and sputtered-Pt (7.77%) electrodes. This enhancement was attributed to increases in the effective surface area and good catalytic properties for I₃⁻ reduction. In terms of the film thickness effect, the fill factor was strongly dependent on the deposition charge capacity of the PProDOT-Et₂ layer, but the aggregation of PProDOT-Et₂ in thicker layers (>80 mC cm⁻²) resulted in decreases in J_SC and the cell conversion efficiency. The charge transfer resistances (R_ct1) of the PProDOT-Et₂ counter electrodes had the lowest value of ∼18 Ω at a deposition charge capacity of 40 mC cm⁻². These results indicate that films with high conductivity, high active surface area, and good catalytic properties for I₃⁻ reduction can potentially be used as the counter electrode in a high-performance DSSC.     

Pyridinium molten salts as co-adsorbents in dye-sensitized solar cells

The influence of using pyridinium molten salts as co-adsorbents to modify the monolayer of a TiO₂ semiconductor on the performance of a dye-sensitized solar cell is studied. The current-voltage characteristics are measured under AM 1.5 (100 mW cm⁻²). The pyridinium molten salts significantly enhance the open-circuit photovoltage (V_oc), the short circuit photocurrent density (J_sc) as well as the solar energy conversion efficiency (η). 1-Ethyl-3-carboxypyridinium iodide ([ECP][I]) is applied successfully to prepare an insulating molecular layer with N719, and achieve high energy conversion efficiency as high as 4.49% at 100 mW cm⁻² and AM 1.5. The resulting efficiency is 20% higher than that of a non-additive device. This enhancement of conversion efficiency is attributed to the negative shift of the conduction band (CB) edge and the abundant concentration of I⁻ on the surface of the electrode when using [ECP][I] as the co-adsorbent.