Improvement of performance of dye-sensitized solar cells based on electrodeposited-platinum counter electrode

Platinum nanoparticle was electrodeposited on FTO conducting glass substrate as counter electrode for application in dye-sensitized solar cells (DSSCs). Images of transmission electron microscope (TEM) and Scanning Electron Microscope (SEM) showed that platinum nanoparticle was with the mean size of 20-30 nm and was homogeneously distributed on the surface of the FTO conductive glass sheet. Using such a counter electrode, DSSC showed a 6.40% overall energy conversion efficiency under one sun illumination. It exhibited the same high-performance as the DSSC with a platinum counter electrode prepared by electroplating. Furthermore, the present preparation method for the platinum counter electrode has the advantage of low platinum loading and transparence.     

Eosin-G and ethyl eosin dye sensitized CdS nanowires towards dye sensitized solar cells applications

One dimensional (1-D) CdS nanowires have been grown through a low temperature chemical route and have been sensitized with eosin-G and ethyl eosin dyes to broaden the absorption spectrum of CdS and to enhance the photoelectrochemical (PEC) performance under illumination. The used method is advantageous due to its simplicity, low cost, scalability, and controllability. Interestingly, eosin-G and ethyl eosin dyes yield nearly four- and six-fold increase in device efficiency compared to bare CdS when tested in dye-sensitized solar cell assembly. Structural, surface morphological, optical, and surface wettability studies have been formulated for CdS, whereas identification of materials along with PEC investigations were conducted through current density–voltage (J-V), external quantum efficiency (EQE), characteristics under the illumination of 94.6 mW/cm² (AM 1.5G), and electrochemical impedance spectroscopy (EIS).     

High-performance and low platinum loading electrodeposited-Pt counter electrodes for dye-sensitized solar cells

This study demonstrates platinum (Pt) counter electrodes with low charge-transfer resistance (R_ct), low Pt loading and high active surface area can be obtained within 30 s by using the direct-current deposition in the presence of 3-(2-aminoethylamino)propyl-methyldimethoxysilane (Me-EDA-Si) as an additive. The addition of appropriate Me-EDA-Si can not only enhance the current efficiency but also inhibit the growth of semicircle-like grains, thus resulting in Pt electrode with high active surface area. Consequently, the dye-sensitized solar cells (DSSCs) fabricated with so-prepared Pt electrodes exhibited cell efficiency of 7.39% while 0.01 vol% Me-EDA-Si was added, which is much superior to that with sputtered-Pt electrodes under the same assembly conditions.     

Polyaniline nanofiber/carbon film as flexible counter electrodes in platinum-free dye-sensitized solar cells

Efficient transfer of charges from a counter electrode to an electrolyte is a key process during the operation of dye-sensitized solar cells. Here, we develop a flexible counter electrode by electrochemical deposition of polyaniline nanofibers on graphitized polyimide carbon films for use in a tri-iodide reduction. As determined by the electrochemical impedance spectroscopy, the flexible counter electrode exhibited very low charge transfer resistance and series resistance. These results are due to the high electrocatalytic activity of the polyaniline nanofibers and the high conductivity of the flexible graphitized polyimide film. In combination with a dye-sensitized TiO₂ photoelectrode and electrolyte, the photovoltaic device with the polyaniline counter electrode shows an energy conversion efficiency of 6.85% under 1 sun illumination. Short-term stability tests indicate that the photovoltaic device with the polyaniline counter electrode almost maintains its initial performance.     

染料敏化太阳能电池非铂对电极研究进展

对电极作为染料敏化太阳能电池（dye-sensitized solar cell,DSSC）的重要组成部分,对电极材料性能的好坏直接影响着染料敏化太阳能电池的光电转化效率。最常使用的对电极电催化材料是贵金属铂,而铂十分稀少而且价格昂贵,并且铂很容易被碘电解液腐蚀,不利于染料敏化太阳能电池的产业化发展。本文重点综述了2010年以来染料敏化太阳能电池非铂对电极的研究成果,简要说明了对电极在染料敏化太阳能电池中的作用,详细介绍了非铂金属、碳材料、导电聚合物和无机化合物等对电极材料,分析了各类非铂对电极材料的特点、制备工艺、发展前景、优缺点和改进措施。最后提出,继续开发各种成本低、原料易得以及稳定高效的新型非金属对电极材料仍是今后染料敏化太阳能电池研究的一个重要方向。     

Synthesis of graphene-CoS electro-catalytic electrodes for dye sensitized solar cells

A large CoS-implanted graphene (G-CoS) film electrode was prepared using chemical vapor deposition followed by successive ionic layer absorption and reaction. HRTEM and AFM show that CoS nanoparticles are uniformly implanted on the graphene film. Furthermore, the G-CoS electro-catalytic electrode is characterized in a dye sensitized solar cells (DSSC) and is found to be highly electro-catalytic towards iodine reduction with low charge transfer resistance (R_ct ～5.05 Ω cm²) and high exchange current density (J₀～2.50 mA cm^?2). The improved performance compared to the pristine graphene is attributed to the increased number of active catalytic sites of G-CoS and highly conducting path of graphene. The comprehensive G-CoS synthesis process is a simple and scalable process which can easily adapt for large scale electro-catalytic film fabrication for several other electro-chemical energy harvesting and storage applications.     

A novel high-performance counter electrode for dye-sensitized solar cells

A novel Pt counter electrode for dye-sensitized solar cells (DSC) was prepared by thermal decomposition of H₂PtCl₆ on NiP-plated glass substrate. The charge-transfer kinetic properties of the platinized NiP-plated glass electrode (Pt/NiP electrode) for triiodide reduction were studied by electrochemical impedance spectroscopy. Pt/NiP electrode has the advantage over the platinized FTO conducting glass electrode (Pt/FTO electrode) in increasing the light reflectance and reducing the sheet resistance leading to improve the light harvest efficiency and the fill factor of the dye-sensitized solar cells effectively. The photon-to-current efficiency and the overall conversion efficiency of DSC using Pt/NiP counter electrode is increased by 20% and 33%, respectively, compared to that of using Pt/FTO counter electrode. Examination of the anodic dissolution and the long-term test on the variation of charge-transfer resistance indicates the good stability of the Pt/NiP electrode in the electrolyte containing iodide/triiodide.     

Study of graphene nanoflake as counter electrode in dye sensitized solar cells

Graphene nanoflake (GNF) films have been fabricated on a fluorine doped tin oxide (FTO) glass using a doctor blade method and thermally annealed in air and argon ambient at various temperatures. The GNF/FTO thin films were employed as a counter electrode for dye sensitized solar cells (DSSCs). Results showed the GNF/FTO film could enhance the power conversion efficiency (PCE) of DSSC devices more effectively when annealed in argon ambient rather than in air and at annealing temperatures higher than 380 °C. The PCE enhancement was mainly due to the lowered oxygen concentration in the film and the elevated electrical conductance. A PCE of 6.08% or 88% of that with a Pt counter electrode has been achieved for DSSCs with a GNF counter electrode, suggesting that GNF is a highly potential candidate to replace Pt catalyst.     

Electrophoretic deposition of carbon nanotubes films as counter electrodes of dye-sensitized solar cells

Carbon nanotubes (CNTs) films have been successfully fabricated by electrophoretic deposition (EPD) technique and used as counter electrodes of dye-sensitized solar cells (DSSCs). The CNTs counter electrodes consisting of a large number of bamboo-like structures with defect-rich edge planes exhibit a highly interconnected network structure with high electrical conductivity and good catalytic activity. A high photovoltaic conversion efficiency of 7.03% is achieved for DSSCs based on the CNTs counter electrodes, which is comparable to the cell based on conventional Pt counter electrode at one sun (AM 1.5G, 100 mW cm⁻²). The results suggest that the present synthetic strategy provides a potential feasibility for the fabrication of low-cost flexible counter electrodes of DSSCs using a facile deposition technique from an environmentally “friendly” solution at low temperature.     

Wurtzite copper-zinc-tin sulfide as a superior counter electrode material for dye-sensitized solar cells

Wurtzite and kesterite Cu₂ZnSnS₄ (CZTS) nanocrystals were employed as counter electrode (CE) materials for dye-sensitized solar cells (DSSCs). Compared to kesterite CZTS, the wurtzite CZTS exhibited higher electrocatalytic activity for catalyzing reduction of iodide electrolyte and better conductivity. Accordingly, the DSSC with wurtzite CZTS CE generated higher power conversion efficiency (6.89%) than that of Pt (6.23%) and kesterite CZTS (4.89%) CEs.     

Low temperature preparation of a high performance Pt/SWCNT counter electrode for flexible dye-sensitized solar cells

A platinum/single-wall carbon nanotube (Pt/SWCNT) film was sprayed onto a flexible indium-doped tin oxide coated polyethylene naphthalate (ITO/PEN) substrate to form a counter electrode for use in a flexible dye-sensitized solar cell using a vacuum thermal decomposition method at low temperature (120 °C). The obtained Pt/SWCNT electrode showed good chemical stability and light transmittance and had lower charge transfer resistance and higher electrocatalytic activity for the I₃⁻/I⁻ redox reaction compared to the flexible Pt electrode or a commercial Pt/Ti electrode. The light-to-electric energy conversion efficiency of the flexible DSSC based on the Pt/SWCNT/ITO/PEN counter electrode and the TiO₂/Ti photoanode reached 5.96% under irradiation with a simulated solar light intensity of 100 mW cm⁻². The efficiency was increased by 25.74% compared to the flexible DSSC with an unmodified Pt counter electrode.     

Fabrication of high performance Pt counter electrodes on conductive plastic substrate for flexible dye-sensitized solar cells

Pt counter electrodes (CEs) with different platinum loading have been prepared using chemical reduced method on flexible indium-doped tin oxide coated polyethylene naphthalate (ITO-PEN) for dye-sensitized solar cells (DSSCs). H₂PtCl₆·6H₂O terpineol solutions were screen printed on the transparent ITO-PEN substrates. After drying, H₂PtCl₆ was reduced by treating it in NaBH₄ solution followed by the hydrothermal treatment at 100 °C. The obtained Pt CEs with different Pt-loading (2.4-7.7 μg/cm²) were characterized by SEM, XPS, electrochemical impedance and transmission spectrum measurement. The Pt CEs show high catalytic activity, low charge transfer resistance (0.26-1.38 Ω cm²) and good light transmittance (about 70% at 400-800 nm). The light-to-electricity conversion efficiency of the flexible DSSC fabricated with the prepared Pt CE and the TiO₂ photoanode prepared on Ti substrate by screen printing technique attains 5.41% under the simulated AM 1.5 sunlight, which is almost same as that based on the thermal decomposited Pt CE on FTO-glass. Compared with other methods to prepare Pt CEs, chemical reduced method is simple and suitable for flexible polymer substrates and the large scale preparation of DSSCs.     

染料敏化太阳电池介孔薄膜电极的研究进展

介绍了染料敏化太阳电池多孔二氧化钛薄膜电极的结构、工作原理及其制备方法,并进一步阐述了减小电荷复合速率、改进薄膜电极性能、提高器件的光电转化效率的方法,主要涉及多孔二氧化钛薄膜电极的复合、掺杂和表面包覆等表面改性处理技术。指出了基于有序二氧化钛薄膜电极、柔性二氧化钛薄膜电极的染料敏化太阳电池和叠层薄膜结构的太阳电池高效的转化效率和应用方便的特点,并在此基础上展望了未来的研究方向。     

Stability study of carbon-based counter electrodes in dye-sensitized solar cells

This study describes a systematic investigation of the stability of a carbon/TiO₂ counter electrode for use in dye-sensitized solar cells (DSSCs). In this system, nanoparticle additives were introduced by adding Ti-hydrogel. The additives then bound carbon particles and enhanced the adhesion of carbon materials to the conductive substrate. After introducing the Ti-hydrogel into the carbon paste, the carbon/Ti-hydrogel composited counter electrode (HC-CE) showed a better conductivity and stability compared with that of the carbon counter electrode (C-CE), while the catalytic activity was not influenced. The device based on the HC-CE showed superior power conversion efficiency (6.3%) and long-term stability over the device based on the C-CE (5.8%).     

Exploring the influence of Zn2SnO4/ZIF-8 nanocomposite photoelectrodes on boosting efficiency of dye sensitized solar cells

It is imperative to develop innovative efficient photoelectrode materials for high-performance dye-sensitized solar cells (DSSCs). In this work, cubic spinel Zn₂SnO₄ (ZTO)+(5, 10, 15, 20%) zeolite imidazole framework-8 (ZIF-8) nanoparticles were applied as photoanode materials of DSSC devices. The Zn₂SnO₄ was effectively synthesized in a simple and cost-effective manner by carefully controlling the hydrothermal conditions. The Zn₂SnO₄/ZIF-8 nanocomposite photoelectrodes were coated over the TiO₂ compact layer to decrease charge recombination at the transparent conductive oxide/mesoporous interface. The X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS), diffuse reflectance spectroscopy (DRS), photoluminescence (PL), Brunauer–Emmett–Teller (BET) isotherms, Fourier transform infrared spectroscopy (FT-IR) and electrochemical impedance spectroscopy (EIS) analysis methods were used to study the properties of all nanostructured photoanodes. In addition, the effects of Zn₂SnO₄/ZIF-8 nanocomposites were evaluated on DSSCs performances. The results clearly showed that adding ZIF-8 to Zn₂SnO₄ improved the photovoltaic performance of the fabricated DSSCs. Furthermore, compared to pure Zn₂SnO₄ NPs, Zn₂SnO₄+15% ZIF-8 increased open circuit voltage (V_OC) from 0.64 to 0.77 V and short current density (J_SC) from 6.89 to 11.27 mA/cm². The Zn₂SnO₄+15% ZIF-8 photoanodes increased the power conversion efficiency (PCE) of DSSC by about 195% (from 2.02 to 3.94%) relative to the pure ZTO photoanode. This was due to the fact that the Zn₂SnO₄+15% ZIF-8 nanocomposite had the quickest electron transport rate, the best electron collecting efficiency, and the greatest charge recombination resistance, all of which are extremely advantageous to improve device efficiency.     

Nanocomposites of Bi5FeTi3O15 with MoS2 as novel Pt-free counter electrode in dye-sensitized solar cells

Bi₅FeTi₃O₁₅ (BFTO) nanofibers with diameters in the range of 40–100 nm have been fabricated by sol-gel based electrospinning technique. The structure and morphology of the nanofibers were characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The MoS₂ nanoparticles are uniformly dispersed into the BFTO, forming nanocomposites. The optical bandgap of the nanocomposites decreases as MoS₂ content increases. The nanocomposites with different MoS₂ contents serve as low-cost counter electrodes (CEs) for dye-sensitized solar cells (DSSCs). Through photocurrent–voltage curves, electrochemical impedance spectroscopy and Tafel curves, the performance of the CEs indicates that the charge transfer resistance on the electrolyte-electrode interface lower and the catalytic activity for reduction of triiodide to iodide enhance with the increase of MoS₂ concentration. The DSSC with the CE exhibits a power conversion efficiency of 5.20% after the optimization of the content of MoS₂, which is almost 24 times larger than that of the pure BFTO CE.     

Micro–meso hierarchical porous carbon as low-cost counter electrode for dye-sensitized solar cells

A micro–meso hierarchical porous carbon with low crystallinity was prepared by a combination of self-assembly and post activation and explored as a counter electrode in dye-sensitized solar cells. Pore structure analysis showed that the pristine mesopores were basically preserved during activation and the micropores were mainly generated within the mesopore wall. Due to its low crystallinity and unique pore-structure including both mesopores and micropores, hierarchical porous carbon exhibited a relatively higher electrocatalytic activity for triiodide reduction, as compared with the pristine mesoporous carbon electrode. This enhanced electrocatalytic activity is beneficial for improving the photovoltaic performance of dye-sensitized solar cells. Under irradiation of 100 mW cm⁻², the dye-sensitized solar cell with hierarchical porous carbon counter electrode showed an overall conversion efficiency of 6.48%, which was 11.5% higher than that of the cell with pristine mesoporous carbon counter electrode.     

A study of TiO2/carbon black composition as counter electrode materials for dye-sensitized solar cells

This study describes a systematic approach of TiO₂/carbon black nanoparticles with respect to the loading amount in order to optimize the catalytic ability of triiodide reduction for dye-sensitized solar cells. In particular, the cell using an optimized TiO₂ and carbon black electrode presents an energy conversion efficiency of 7.4% with a 5:1 ratio of a 40-nm TiO₂ to carbon black. Based on the electrochemical analysis, the charge-transfer resistance of the carbon counter electrode changed based on the carbon black powder content. Electrochemical impedance spectroscopy and cyclic voltammetry study show lower resistance compared to the Pt counter electrode. The obtained nanostructures and photo electrochemical study were characterized.     

Nanostructured polyaniline counter electrode for dye-sensitised solar cells: Fabrication and investigation of its electrochemical formation mechanism

Nanostructured polyaniline films with controlled thickness have been successfully grown on fluorine-doped tin oxide (FTO) glass substrates using the cyclic voltammetry (CV) method at room temperature. The formation mechanism of the polyaniline film is monitored by CV techniques, alternating current (AC) impedance spectroscopy, scanning electron microscopy (SEM) and atomic force microscopy (AFM). It is found that the accumulation of nanostructured polyaniline (>70 nm) on both the scattered and compact layers simultaneously increased the reactive interface, which supports charge transfer at the interface and resistance that hinders electronic transport in the film. By optimising the preparation conditions, the short-circuit photocurrent density of a dye-sensitised solar cell (DSSC) with a PANI counter electrode (CE) increased by 11.6% in comparison to a DSSC with an electrodeposited platinum CE.