Improved catalytic activity of Pt/rGO counter electrode in In2O3-based DSSC

A platinum/reduced graphene oxide (Pt/rGO) nanocomposite acting as a counter electrode (CE) was fabricated using a chemical bath deposition method for In₂O₃-based dye-sensitized solar cell (DSSC) via sol-gel technique. The report analyzes the morphological and electrochemical impedance spectroscopy of the annealing Pt/rGO films at 350, 400, and 450 °C. Micrograph images obtained from field emission scanning electron microscopy demonstrated the annealed films are highly porous. The energy-dispersive X-ray results show that the carbon atoms were homogeneously distributed on the film annealed at 400 °C. A good photovoltaic performance was exhibited with high photocurrent density of 8.1 mA cm⁻² and power conversion efficiency (η) of 1.68 % at the Pt/rGO CE annealed at 400 °C. The employed electrochemical impedance spectroscopy analysis quantifies that the Pt/rGO films annealed at 400 °C provide more efficient charge transfer with the lowest effective recombination rate and high electron life time, hence improving the performance of Pt/rGO CE.

     

Low resistance dye-sensitized solar cells based on all-titanium substrates using wires and sheets

Low resistance dye-sensitized solar cells (DSSCs) based on all-titanium substrates were proposed in this paper. To minimize the internal resistance of DSSCs, the titanium wires and titanium sheets were used as the substrates of the photoanode and the counter electrode, respectively. Compared with the FTO substrate, titanium wires could absorb much diffused light by back reflection since the reflectivity in the titanium sheet was highly increased up to 53.12%. Furthermore, the transmittance of the front cover was increased by 13.2% using the super white glass instead of FTO substrate. The thickness of TiO₂ thin film coated on titanium wire was optimized to achieve a high cell performance. The efficiency of 5.6% for the cell was obtained with a J_sc of 15.41 mA cm⁻², V_oc of 0.59 V, and FF of 0.62. The results showed that the titanium-based DSSCs had superiority for producing the large-scale DSSCs without metal grid line.     

Anodic TiO<Subscript>2</Subscript> nanotubes powder and its application in dye-sensitized solar cells

An increasing energy demand and environmental pollution create a pressing need for clean and sustainable energy solutions. TiO₂ semiconductor material is expected to play an important role in helping solve the energy crisis through effective utilization of solar energy based on photovoltaic devices. Dye-sensitized solar cells (DSSCs) are potentially lower cost alternative to inorganic silicon-based photovoltaic cells. In this study, we report on the fabrication of DSSCs from anodic TiO₂ nanotubes (NT) powder, produced by rapid breakdown potentiostatic anodization of Ti foil in 0.1 M HClO₄ electrolyte, as photoanode. TiO₂ NT powders with a typical NT outer diameter of approximately 40 nm, wall thickness of approximately 8–15 nm, and length of about 20–25 μm, have been synthesized. The counter electrode was made by electrodeposition of Pt from an aqueous solution of 5 mM H₂PtCl₆ onto fluorine-doped tin oxide (FTO) glass substrate. The above front-side illuminated DSSCs were compared with back-side illuminated DSSCs fabricated from anodic TiO₂ NTs that were grown on the top of Ti foil as photoanode. The highest cell efficiency was 3.54% under 100 mW/cm² light intensity (1 sun AM 1.5G light, Jsc = 14.3 mA/cm², Voc = 0.544 V, FF = 0.455). To the best of our knowledge, this is the first report on the fabrication of DSSC from anodic TiO₂ NTs powder. The TiO₂/FTO photoanodes were characterized by FE-SEM, XRD, and UV–Visible spectroscopy. The catalytic properties of Pt/FTO counter electrodes have been examined by cyclic voltammetry.     

二硒化铁/还原氧化石墨烯的制备及其在染料敏化太阳能电池中的应用

通过水热反应合成出二硒化铁/还原氧化石墨烯(FeSe₂/rGO)复合材料, 并将其作为对电极材料应用于染料敏化太阳能电池(DSSC). 利用X射线衍射、拉曼光谱、场发射扫描电子显微镜和高分辨透射电子显微镜对FeSe₂/rGO的结构和形貌进行了表征. 利用循环伏安法、电化学阻抗谱和Tafel曲线测试分析了FeSe₂/rGO对电极的电催化活性. 结果表明: FeSe₂呈纳米棒结构, 长度在100-200 nm之间, 且紧密地附着在rGO 的表面, FeSe₂/rGO对电极对I₃^-的还原具有很好的催化活性. 电池的J-V曲线测试显示: 基于FeSe₂/rGO对电极的DSSC的转换效率达到了8.90%, 相比基于单纯的FeSe₂对电极的DSSC(7.91%)和rGO对电极的DSSC(5.24%)都有了显著提高, 甚至优于铂对电极的DSSC(8.52%).     

Interface modification of MoS2 counter electrode/electrolyte in dye-sensitized solar cells by incorporating TiO2 nanoparticles

To achieve the high efficiency in dye-sensitized solar cells (DSSCs), the interface modification of MoS₂ counter electrode (CE)/electrolyte should be carried out. Making the modified MoS₂ CE by incorporating TiO₂ nanoparticles provides possibilities to enhance electrocatalytic activity. The DSSCs with the MoS₂/TiO₂ CE show enhanced performance compared with DSSCs with the MoS₂ CE. The experimental results revealed that the MoS₂/TiO₂ nanocomposite influences on the power conversion efficiency by enhancing electrocatalytic activity and increasing the active surface area that serve to increase the short circuit current. This understanding can provide guidance for the development of highly efficient DSSCs with platinum-free CEs.     

Graphene/carbon nanotubes composites as a counter electrode for dye-sensitized solar cells

As an alternative platinum counter electrode in dye-sensitized solar cells (DSSCs), carbon materials based counter electrode were prepared using multi-walled carbon nanotubes (MWNTs)/graphene nano-sheets (GNS) composite by simple doctor blade method. We found that the photovoltaic performance was strongly influenced by the concentration of GNS in composite electrode. The composite electrode with 60% MWNTs and 40% GNS based DSSCs showed the maximum power conversion efficiency of 4.0% while sputter deposited platinum counter electrode based DSSCs showed a power conversion efficiency of 5.0%.     

Zinc oxide nanostructures for applications as ethanol sensors and dye-sensitized solar cells

ZnO nanostructures were prepared by thermal oxidation technique for applying as ethanol sensors and dye-sensitized solar cells. To improve sensitivity of the sensor based on ZnO nanostructures, gold doping was performed in ZnO nanostructures. Gold-doped with 0%, 5%, and 10% by weight were investigated. The improvement of sensor sensitivity toward ethanol due to gold doping was observed at entire operating temperature and ethanol concentration. The sensitivity up to 145 was obtained for 10% Au-doped ZnO sensor. This can be explained by an increase of the quantity of oxygen ion due to catalytic effect of gold. Also, it was found that oxygen ion species at the surface of the Au-doped ZnO sensor remained O²⁻ as pure ZnO sensor. For dye-sensitized solar cell application, the dye-sensitized solar cell structure based on ZnO as a photoelectrode was FTO/ZnO/Eosin-Y/electrolyte/Pt counter electrode. ZnO with different morphologies of nanobelt, nano-tetrapod, and powder were investigated. It was found that DSSCs with ZnO powder showed higher photocurrent, photovoltage and overall energy conversion efficiencies than that of ZnO nanobelt and ZnO nano-tetrapod. The best results of DSSCs were the short circuit current (J_sc) of 1.25 mA/cm², the open circuit voltage (V_oc) of 0.45 V, the fill factor (FF) of 0.65 and the overall energy conversion efficiency (η) of 0.68%.     

Tailoring MoS2 Ultrathin Sheets Anchored on Graphene Flexible Supports for Superstable Lithium‐Ion Battery Anodes

2D MoS₂ has a significant capacity decay due to the stack of layers during the charge/discharge process, which has seriously restricted its practical application in lithium‐ion batteries. Herein, a simple preform‐in situ process to fabricate vertically grown MoS₂ nanosheets with 8–12 layers anchored on reduced graphene oxide (rGO) flexible supports is presented. As an anode in MoS₂/rGO//Li half‐cell, the MoS₂/rGO electrode shows a high initial coulomb efficiency (84.1%) and excellent capacity retention (84.7% after 100 cycles) at a current density of 100 mA g^?1. Moreover, the MoS₂/rGO electrode keeps capacity as high as 786 mAh g^?1 after 1000 cycles with minimum degradation of 54 µAh g^?1 cycle^?1 after being further tested at a high current density of 1000 mA g^?1. When evaluated in a MoS₂/rGO//LiCoO₂ full‐cell, it delivers an initial charge capacity of 153 mAh g^?1 at a current density of 100 mA g^?1 and achieves an energy density of 208 Wh kg^?1 under the power density of 220 W kg^?1.     

A simple dye-sensitized solar cell sealing technique using a CO2 laser beam excited by 60 Hz AC discharges

Dye-sensitized solar cells (DSSCs) use two glass substrates (photo electrode and counter electrode) coated with fluorine-doped tin oxide (FTO) to harvest light into the cell and to collect electrons. The space between the photo electrode and the counter electrode are filled with a liquid type electrolyte for electron transfer into the cell. Therefore, an appropriate sealing method is required to prevent the liquid electrolyte leaking out. In this paper, a simple CO₂ laser beam with TEM₀₀ mode excited by a 60 Hz AC discharge was used to seal two glass substrates coated with FTO for the fabrication of DSSCs. The sealing technique improved the durability and stability of the DSSCs. The optimal conditions for the sealing of the DSSCs are related to the pin-hole diameter, the discharge current and the moving velocity of the target. Especially, the CO₂ laser beam is used as a heat source that is precisely controlled by the pin-hole, which plays an important role in adjusting its spot size. From these results, the maximum laser power was found to be 40 W at 18 Torr and 35 mA. In order to achieve the best sealing quality, the following parameters are required: a pin-hole diameter of 4 mm, input voltage of 10.73 kV, discharge current of 9.31 mA, moving velocity of 1 mm/s and distance from the target surface of 26.5 cm. Scanning electron microscope images show that the sealing quality obtained using the CO₂ laser beam is superior to that obtained using a hot press or soldering iron.     

Synthesis of Li3V2(PO4)3/reduced graphene oxide cathode material with high-rate capability

The Li₃V₂(PO₄)₃/reduced graphene oxide (LVP/rGO) composite is successfully synthesized by a conventional solid-state reaction with a high yield of 10 g, which is suitable for large-scale production. Its structure and physicochemical properties are investigated using X-ray diffraction, Raman spectra, field-emission scanning electron microscopy, transmission electron microscopy, and electrochemical methods. The rGO content is as low as ~3 wt%, and LVP particles are strongly adhered to the surface of the rGO layer and/or enwrapped into the rGO sheets, which can facilitate the fast charge transfer within the whole electrode and to the current collector. The galvanostatic charge–discharge tests show that the LVP/rGO electrode delivers an initial discharge capacity of 177 mAh g^?1 at 0.5 C with capacity retention of 88 % during the 50th cycle in a wide voltage range of 3.0–4.8 V. A superior rate capability is also achieved, e.g., exhibiting discharge capacities of 137 and 117 mAh g^?1 during the 50th cycle at high C rates of 2 and 5 C, respectively.     

Effects of ZnO coating on the performance of TiO2 nanostructured thin films for dye-sensitized solar cells

ZnO-coated TiO₂ (ZTO) thin films were deposited on ITO substrates by a sol–gel method for application as the work electrode for dye-sensitized solar cells (DSSCs). The I–V curve and the incident photon-to-current conversion efficiency (IPCE) value of DSSCs for ZTO thin films were studied and compared with single TiO₂ films. The results show that the short-circuit photocurrent (J _sc) and open-circuit voltage (V _oc) values increased from 3.7 mA/cm² and 0.68 V for the DSSCs with a single TiO₂ film to 4.5 mA/cm² and 0.72 V, respectively, for the DSSCs with a ZTO thin film. It indicated that the DSSCs with a ZTO thin film contributed to provide an inherent energy barrier that suppressed charge recombination significantly. In addition, the higher IPCE value in the ZTO thin film is attributed to the better charge separation by a fast electron transfer process using two semiconductors with different conduction band edges and energy positions.     

Flexible TiO<Subscript>2</Subscript> nanotube-based dye-sensitized solar cells using laser-drilled microhole array electrodes

Here we report on the growth of TiO₂ nanotube arrays (TNAs) on Ti foil with laser-drilled microhole arrays (MHAs). The MHAs promoted the adhesion of the TNA film to Ti substrate, which is well suited for flexible dye-sensitized solar cells (DSSCs). The MHA photoanode and TNAs were characterized by SEM, 3D optical profiling, XRD and TEM. For such a flexible MHA photoanode, the TNA-based DSSC was assembled using a platinized conductive glass counter electrode, and a conversion efficiency of 3.45% was achieved under AM 1.5 condition. A flexible TNA-based DSSC was also fabricated using a flexible MHA photoanode combined with a platinized indium tin oxide-polyethylene naphthalate counter electrode, which achieved 2.67% photovoltaic conversion efficiency under simulated AM 1.5 sunlight.     

Facile synthesis of nitrogen-doped reduced graphene oxide as an efficient counter electrode for dye-sensitized solar cells

A nitrogen-doped reduced graphene oxide (N-RGO) nanosheet was synthesized by a simple hydrothermal method and characterized by X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning electrode microscopy. After being deposited as counter electrode film for dye-sensitized solar cells (DSSCs), it is found that the synthesized N-RGO nanosheet has smaller charge-transfer resistance and better electrocatalytic activity towards reduction of triiodide than the reduced graphene oxide (RGO) nanosheet. Consequently, the DSSCs based on the N-RGO counter electrode achieve an energy conversion efficiency of 4.26%, which is higher than that of the RGO counter electrode (2.85%) prepared under the same conditions, and comparable to the value (5.21%) obtained with the Pt counter electrode as a reference. This N-RGO counter electrode offers the advantages of not only saving the cost of Pt itself but also simplifying the process of counter electrode preparation. Therefore, an inexpensive N-RGO nanosheet is a promising counter electrode material to replace noble metal Pt.

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Graphical abstract A nitrogen-doped reduced graphene oxide nanosheet was synthesized by a simple hydrothermal method, which is a promising counter electrode material to replace noble metal Pt.

     

Solid state photoelectrochemical cells utilising graphite thin films counter electrode

This paper reports the use of graphite thin films as a counter electrode of a solid state photoelectrochemical cells of ITO/TiO₂/PVC-LiClO₄/graphite. The photoelectrochemical cells material was a screen-printed layer of titanium dioxide onto an ITO-covered glass substrate which was used as a working electrode of the device. The solid electrolyte used was PVC-LiClO₄ that was prepared by solution casting technique. The graphite films which serve as a counter electrode were prepared onto glass substrate by electron beam evaporation technique at substrate temperatures variation of 25, 50, 100, 150 and 200 °C. The dependence of sheet resistance and surface morphology of the graphite films on substrate temperature were studied. The films deposited at 25 °C shows the smoothest surface morphology and the smallest grain size. Bigger grain size, rougher surface morphology of graphite film counter electrode. The current-voltage characteristics of four devices utilising the graphite counter electrode with different substrate temperature in dark as well as under illumination of 100 mWcm⁻² light from a tungsten halogen lamp were recorded at room temperature and at 50 °C, respectively. It was found that the photovoltaic parameters of the device such as short-circuit current density, J_sc and open-circuit voltage, V_oc increases with the decreasing average grain size of the graphite counter electrode. The device whose graphite film counter electrode was deposited onto the glass substrate at 25 °C gave the highest J_sc of 0.32 μA/cm² and V_oc of 117 mV, respectively.     

三维多孔复合碳层对电极的制备及其光伏性能研究

基于TiO_2光阳极、Pt对电极的染料敏化太阳能电池(DSSC)因其优异的光电转换特性受到了广泛的关注,然而Pt昂贵的价格制约了其发展与应用.针对这一问题,本文设计、制备了一种由相对致密且高导电的石墨膜(PC层,底层)及多孔碳纳米颗粒膜(CC层,顶层)构成的低成本、高性能三维多孔复合碳层对电极.基于该CC/PC对电极的DSSC具有优异的光伏性能:在1.5标准太阳光照射下,其填充因子高达65.28%(较Pt对电极高4.1%)、光电转换效率高达5.9%(为Pt对电极的94.2%). CC/PC对电极的优异光伏性能主要归因于其独特的三维多孔导电结构,该结构有极高的比表面积和丰富的催化反应活性位,有利于电子的快速传输及离子的快速转移,在这些因素的协同作用下,其光电转换性能大大改善.     

有机金属化学气相沉积法制备的Ni/Al2O3纳米复合材料的氢吸附

研究了通过有机金属化学气相沉积技术及单源分子前躯体方法制备的Ni/Al₂O₃纳米复合材料的氢吸附(存储). 在冷壁的有机金属化学气相沉积反应器中,通过降解Ni(acac)₂粉末基底上的[H₂Al(OtBu)]₂制备的Ni/Al₂O₃纳米复合材料. 通过X射线粉末衍射、扫描电镜、透射电镜以及能量色散型X射线荧光光谱等技术表征该复合材料. 采用自制Sievert's设备研究该复合材料的氢吸附(存储),可以储存约2.9%(重量比)的氢.     

Reduced graphene oxide field-effect transistor with indium tin oxide extended gate for proton sensing

In this study, the reduced graphene oxide field-effect transistor (rGO FET) with indium tin oxide (ITO) extended gate electrode was demonstrated as a transducer for proton sensing application. In this structure, the proton sensing area of the ITO extended gate electrode is isolated from the active area of the rGO FET. The proton sensing properties based on the rGO FET transducer were analyzed. The rGO FET device with encapsulation by a tetratetracontane (TTC) layer showed good stability in electrolytic solutions. The device showed an ambipolar behavior with shifts in Dirac point as the pH of the electrolyte is varied. The pH sensitivity based on the Dirac point shift as a sensing parameter was about 43–50 mV/pH for a wide range of pH values from 2 to 12. The ITO extended gate rGO FET may be considered a potential transducer for sensing of H⁺ in electrolytes. Its sensing area can be modified further for various ions sensing applications.     

Natural dye-based photoelectrode for improvement of solar cell performance

In the present paper, photovoltaic studies of dye-sensitized solar cells (DSSCs) based on betacyanin/TiO₂ and betacyanin/WO₃–TiO₂ have been done. The cell performances were compared through I–V curves and wavelength dependant photocurrent measurements for the two new types of DSSCs. The TiO₂-coated DSSC showed the photovoltage and photocurrent of 300 mV and 4.96 mA/cm², whereas the cell employing WO₃–TiO₂ photoelectrode showed the values 435 mV and 9.86 mA/cm², respectively. The conversion efficiency of TiO₂ based dye-sensitized solar cell was found to be 0.69 %, while WO₃–TiO₂-based cell exhibited a higher conversion efficiency of 2.2 %. The better performance of the WO₃–TiO₂ dye-sensitized solar cell photoelectrode is thought to be due to an inherent energy barrier at the electrode/electrolyte interface leading to the reduced recombination of photoinduced electrons.     

Synthesis of NiCo2S4 nanospheres/reduced graphene oxide composite as electrode material for supercapacitor

The NiCo₂S₄ nanospheres arrayed on the surface of reduced graphene oxide (rGO) was fabricated via one-step hydrothermal method. The effect of initial feeding mass of Ni(NO₃)₂·6H₂O and Co(NO₃)₂·6H₂O to rGO on the microstructure and electrochemical performance of the as-prepared composites was studied. The results indicated that the specific capacitances of the composites were first increased and then reduced due to the aggregation of NiCo₂S₄ nanospheres. NiCo₂S₄ nanospheres/rGO composites exhibited a remarkable specific capacitance of 1406 F/g and excellent cyclic stability of 82.36% at the current density of 1 A/g, which were better than those of individual NiCo₂S₄ (792 F/g and 64.77%) counterpart. These results showed that the as-prepared NiCo₂S₄ nanospheres/rGO composites were outstanding candidate for electrode material of supercapacitors.     

Dependence of photovoltaic parameters on the size of cations adsorbed by TiO2 photoanode in dye-sensitized solar cells

The effects of “pre-adsorbed cations” in photoanodes on the performances of dye-sensitized solar cells (DSSCs) were studied using two different size cations (K⁺ and guanidine cation (G⁺)). While the DSSCs with optimized K⁺ ions pre-adsorbed photoanodes showed a maximum efficiency of 7.04%, the DSSCs with G⁺ ions pre-adsorbed photoanodes showed an efficiency of 6.73%. DSSCs fabricated with conventional photanodes (without pre-cation adsorption) showed an efficiency of 6.21%. Differences in efficiencies are very likely due to the cation pre-adsorption effects and could be due to a higher number of K⁺ cation adsorption per unit area of TiO₂ surface of the photoanode compared to a smaller number of G⁺ cation adsorption in TiO₂, due to their difference in sizes. This pre-cation adsorption technique can be used to improve the overall efficiency of a DSSC by about 14% fold over the conventional photoanodes use in DSSCs, specially using smaller cations.