Efficient flexible dye-sensitized solar cells from rear illumination based on different morphologies of titanium dioxide photoanode

The TiO_(2) with nanoparticles(NPs),nanowires(NWs),nanorods(NRs)and nanotubes(NTs)structures were prepared by using a in-situ hydrothermal technique,and then proposed as a photoanode for flexible dye-sensitized solar cell(FDSSC).The influences of the morphology of TiO_(2) on the photovoltaic performances of FDSSCs were investigated.Under rear illumination of 100 mW·cm^(−2),the power conversion efficiencies of FDSSCs achieved 6.96%,7.36%,7.65%,and 7.83%with the TiO_(2) photoanodes of NPs,NWs,NRs,and NTs and PEDOT counter electrode.The FDSSCs based on TiO_(2) NRs and NTs photoanodes have higher short circuit current densities and power conversion efficiencies than that of the others.The enhanced power conversion efficiency is responsible for their nanotubes and rod-shaped ordered structures,which are more beneficial to transmission of electron and hole in semiconductor compared to the TiO_(2) nanoparticles and nanowires disordered structure.

Synthesis and Characterization of Novel Schiff Base for Enhanced Dye-Sensitized Solar Cell Photo-Response Mechanism

The efficient photo-response mechanism is one of the key factors in the commercialization of dye-sensitized solar cells in a bid to satisfy renewable energy demands. Progress in green technology has put solar energy on the front burner as a provider of clean and affordable energy for a sustainable society. We report the synthesis of a novel Schiff base with optical transparency in the visible and near IR region of the solar spectrum that can find application in the DSSCs photo-response mechanism. The synthesized crystal exhibited features that could handle some of the shortcomings of dye-sensitized solar cells which include wide band solar spectrum absorption and capability for swift charge transfer within the photoelectrodes. The synthesized Schiff base was characterized using x-ray diffractometer, UV/Visible spectrometer, Frontier transmission infrared spectrometer and conductometer. XRD data revealed the grown crystal to have an average crystallite size of 2.08 nm with average microstrain value of about 269.43. The FT-IR recorded transmission wave ѵ (CO) at 1207.7 cm−1 while dominant wave occurred at ѵ1654.9 and ѵ1592.3 cm−1 relating to ѵ (CN) stretching and ѵ (NH) bending respectively were observed. The IR spectrum revealed the bonding species and a probable molecular structure of 2,6-bis(benzyloxy)pyridine. The UV/Visible spectra convoluted to maximum peak within the near IR region suggesting that 2,6-bis(benzyloxy)pyridine can absorb both the visible and near IR region while its electrical conductivity was determined to be 4.58 µS/cm. The obtained result of the present study revealed promising characteristics of a photosensitizer that can find application in the photo-response mechanism of DSSCs.

Selective synthesis of Sb2S3 nanostructures with different morphologies for high performance in dye-sensitized solar cells

In this work,we initially synthesized Sb2S3 with uniform flower-like structures via a facile hydrothermal method through the modification of the Sb source and pH value.Afterward,Sb2S3 with a nanosheet structure was successfully synthesized on reduced graphene oxide(Sb2S3@RGO).The flower-like Sb2S3 and the Sb2S3@RGO nanosheets were tested as the counter electrode(CE)of dye-sensitized solar cells,and the latter exhibited a higher electrocatalytic property than the former owing to the introduction of graphene.The results from electrochemical tests indicated that the as-prepared Sb2S3@RGO nanosheets possess higher catalytic activity,charge-transfer ability,and electrochemical stability than Sb2S3,RGO,and Pt CEs.More notably,the power conversion efficiency of Sb2S3@RGO reached 8.17%,which was higher than that of the standard Pt CE(7.75%).

Influence of Triarylamine and Indoline as Donor on Photovoltaic Performance of Dye-Sensitized Solar Cells Employing Cobalt Redox Shuttle

Two organic dyes XSS1 and XS52 derivated from triarylamine and indoline are synthesized for dye-sensitized solar ceils （DSCs） employing cobalt and iodine redox shuttles. The effects of dye structure upon the photophysical, electro-chemical characteristics and cell perfor- mance are investigated. XS51 with four hexyloxyl groups on triarylamine performs better steric hindrance and an improvement of photovoltage. X852 provides higher short-circuit photocurrent density due to the strong electron-donating capability of indoline unit. The results from the redox electrolyte on cell performances indicate that the synthesized dyes are more suitable for tris（1,10-phenanthroline）cobalt（II/III） redox couple than I-/I3- redox couple in assembling DSCs. Application of X852 in the cobalt electrolyte yields a DSC with an overall power conversion efficiency of 6.58% under AM 1.5 （100 mW/cm2） irradiation.

PREPARATION OF POLYANILINE/ACETYLENE BLACK COMPOSITE AS HOLE CONDUCTOR IN SOLID-STATE DYE-SENSITIZED SOLAR CELL

A clay-like conductive material comprising polyaniline（PANI）-acetylene black particles is fabricated as a hole conductor for dye sensitized solar cell（DSSC）.The results show that the introduction of acetylene black into the polymer electrolyte improves the photovoltaic behavior of solid-state DSSC,owing to the increase of the hole mobility of PANI electrolyte,the improvement of the wetting quality of the composite electrolyte,and the reinforcement of interface contact between electrode and the electrolyte.Finally,the overall energy conversion efficiency of DSSC with PANI-50%（in weight）acetylene black electrolyte is 48% of that of liquid DSSC.Therefore,the PANI-acetylene black composition is a credible alternative to hole conductor in application of solid DSSC.

PREPARATION AND PROPERTIES OF GEL POLYMER ELECTROLYTE BASED ON PVDF/ACRYLATE INTERPENETRATING POLYMER NETWORK FOR DYE-SENSITIZED SOLAR CELL

The gel polymer electrolytes（GPEs）based on poly（vinylidence fluoride）（PVDF）/acrylate interpenetrating polymer network（IPN）are prepared.The micro-phase separation type GPEs are characterized by Fourier transform infrared（FTIR）spectroscopy,scanning electron microscope（SEM）,respectively.Moreover,the conductivity and the voltage-current curves of the electrolytes are measured by electrochemical workstation.The higher porosity and electrolyte uptake are observed in the membranes prepared at lower crosslinker concentration.The suitable cross-linking acrylate monomer improves the porosity and the electrochemical behavior of GPE.A dye-sensitized solar cell（DSSC）employing PGE based on PVDF/poly（ethylene glycol dimethacrylate）（PEGDMA）IPN yields an open-circuit voltage of 0.674 V,short-circuit current of 8.476 mA·cm-2and the conversion efficiency of 2.710% under 100 mW·cm-2illumination.

采用Cell-SELEX技术的核酸适配体在肿瘤靶向治疗的研究进展

阐述细胞-配体指数富集系统进化(Cell-SELEX)技术特点,以及通过该技术筛选得到的核酸适配体在肿瘤靶向治疗中的应用进展和挑战,通过查阅近年的相关文献,综述核酸适配体作为药物及药物载体在肿瘤靶向治疗中的应用研究进展。结果表明:基于Cell-SELEX技术筛选得到的核酸适配体在肿瘤靶向治疗中的疗效显著,可开发成为肿瘤靶向治疗的潜力药物及良好的药物载体。

Influence of TiCl_4 treatment on performance of dye-sensitized solar cell assembled with nano-TiO_2 coating deposited by vacuum cold spraying

Titanium tetrachloride (TiCl4) treatment was employed to TiO2 coating deposited on fluoride-doped tin oxide (FTO) conducting glass and indium oxide doped tin oxide (ITO) conducting glass, respectively. The nano-crystalline TiO2 coating was deposited using a composite powder composed of polyethylene glycol (PEG) and 25 nm TiO2 particles by vacuum cold spraying (VCS) process. A commercial N-719 dye was used to adsorb on the surface of TiO2 coating to prepare TiO2 electrode, which was applied to assemble dye-sensitized solar cell (DSC). The cell performance was measured under simulated solar light at an intensity of 100 mW·cm-2. Results show that with an FTO substrate the DSC composed of a VCS TiO2 electrode untreated by TiCl4 gives a short-circuit current density of 13.1 mA·cm-2 and an open circuit voltage of 0.60 V corresponding to an overall conversion efficiency of 4.4%. It is found that after TiCl4 treatment to the VCS TiO2 electrode with an FTO substrate, the short circuit current density of the cell increases by 31%, the open-circuit voltage increases by 60 mV and a higher conversion yield of 6.5% was obtained. However, when an ITO substrate is used to deposit TiO2 coating by VCS, after TiCl4 treatment, the conversion efficiency of the assembled cell reduces slightly due to corrosion of the conducting layer on the ITO glass by TiCl4.

Dye-sensitized Solar Cells with Higher J_(sc) by Using Polyvinylidene Fluoride Membrane Counter Electrodes

A flexible counter electrode(CE) for dye-sensitized solar cells(DSCs) has been fabricated using a micro-porous polyvinylidene fluoride membrane as support media and sputtered Pt as the catalytic material.Non-conventional structure DSCs have been developed by the fabricated CEs. The Pt metal was sputtered onto one surface of the membrane as the catalytic material. DSCs were assembled by attaching the Ti O2 electrode to the membrane surface without Pt coating. The membrane was with cylindrical pore geometry. It served not only as a substrate for the CE but also as a spacer for the DSC. The fabricated DSC with the flexible membrane CE showed higher photocurrent density than the conventional sandwich devices based on chemically deposited Pt/FTO glass, achieving a photovoltaic conversion efficiency of 4.43%. The results provides useful information in investigation and development of stable, low-cost, simple-design, flexible and lightweight DSCs.

Novel micro-ring structured ZnO photoelectrode for dye-sensitized solar cell

The micro-ring like structured zinc oxide(ZnO) film was deposited on SnO_2: F coated glass substrate by sol-gel dip-coating technique with 1.0 g polyethylene glycol(PEG) content. The surface morphology of micro-ring structured ZnO film has been confirmed by the scanning electron microscope. This ZnO film is used to fabricate the solar cell with the help of ruthenium based dye and carbon counter electrode. The photoelectric and incident photon-to-current conversion efficiency was 1.17% and 48.4%, respectively. The DSC results have been compared with ZnO films prepared without PEG contents.

Recent Progress of Counter Electrodes in Nanocrystalline Dye-sensitized Solar Cells

Dye-sensitized solar cell （DSC） consists a combination of several different materials： photoanodes with nanoparticulated semiconductors, sensitizers, electrolytes and counter electrodes （CEs）. Each materials performs specific task for the conversion of solar energy into electricity. The main function of CE is to transfer electrons to the redox electrolyte and regenerate iodide ion. The work of CE is mainly focused on the studies of the kinetic performance and stability of the traditional CEs to improve the overall efficiency of DSC, seeking novel design concepts or new materials. In this review, the development and research progress of different CE materials and their electrochemical performance, and the problems are discussed.

Preparation and performance of dye-sensitized solar cells based on ZnO-modified TiO_2 electrodes

The ZnO-modified TiO2 electrode was prepared by adding Zn（CH3COO）2·2H2O to the TiO2 colloid during the sol-gel production process, and was used in dye-sensitized solar cells （DSCs）. The open circuit voltage （Voc） and fill factor （if） of the cells were improved sig- nificantly. The performances of the ZnO-modified TiO2 electrode such as dark current, transient photocurrent, impedance, absorption spectra, and fiat band potential （Vfb） were investigated. It is found that the interface charge recombination impedance increases and Vfb shifts about 200 mV toward the cathodic potential. The effect mechanism of ZnO modification on the performance of DSCs may be that ZnO occupies the surface states of the TiO2 film.

Unique ZnS nanobuns decorated with reduced graphene oxide as an efficient and low-cost counter electrode for dye-sensitized solar cells

Unique ZnS nanobuns decorated with reduced graphene oxide （ROO） was synthesized and found to exhibit a synergetic effect as a highly efficient and low-cost counter electrode （CE） in dye-sensitized solar cells （DSCs）. Using this ZnS-ROO CE, a power conversion efficiency （PCE） of 7.03% was achieved. This value was 53% and 41 % higher than those of pure ZnS and ROO CEs, respectively. The ZnS-ROO nanocomposite is indeed an efficient and cost-effective Pt-like alternative for iodine reduction reaction.

Recent advances in cobalt-, nickel-, and iron-based chalcogen compounds as counter electrodes in dye-sensitized solar cells

The electroactive materials used in the counter electrode(CE)are of great concern as they influence the photovoltaic performances of dye-sensitized solar cells.The main functions of CE materials are collecting electrons from the external circuit and transferring them to the electrolyte and realizing the catalytic reduction of the redox species(I3^– or Co^3+)present in the electrolyte.The research hotspot of CE materials is seeking functional materials that display high efficiency,low cost,and good electrochemical stability and can substitute the benchmark platinum electrode.Chalcogen compounds of cobalt,nickel,and iron have been widely applied as CE materials and exhibit excellent electrocatalytic performances owing to their unique electrical properties,similar energies of adsorption of I atoms as platinum,excellent catalytic activities,and good chemical stabilities.In this review,we trace the developments and performances of chalcogen compounds of iron,cobalt,and nickel as CE materials and present the latest research directions for improving the electrocatalytic performances.We then highlight the optimization strategies for further improving their performances,such as fabrication of architectures,regulation of the components,synthesis of composites containing carbon materials,and elemental doping.

A new D–D–π–A dye for efficient dye-sensitized solar cells

New metal-free organic dye sensitizers containing mono-triphenylamine or bis-triphenylamine as the electron donor, a thiophene as the π-conjugated system, and a cyanoacrylic acid moiety as the electron acceptor were synthesized. The optical and electrochemical properties of the dyes were investigated,and their performance as sensitizers in solar cells was evaluated. Dye-sensitized solar cells based on dye containing bis-triphenylamine as the electron donor produced a photon-to-current conversion efficiency of 6.06%（Jsc = 14.21 m A/cm;, Voc = 0.62 V, ff = 0.69） under 100 m W/cm;simulated AM 1.5 G solar irradiation（100 m W/cm;）.

High efficiency and stable solid-state fiber dye-sensitized solar cells obtained using TiO_(2) photoanodes enhanced with metal organic frameworks

Solid-state fiber dye-sensitized solar cells(SS-FDSSCs) have been the subject of intensive attention and development in recent years. Although this field is only in its infancy, metal–organic frameworks(MOFs) are one such material that has been utilized to further improve the power conversion efficiency of solar cells. In this study, MOF-integrated DSSCs were shown to have potential in the development of solar cell devices with efficiency comparable to or better than that of conventional solar cells. The power conversion efficiency(PCE) of SS-FDSSCs was improved by embedding MOF-801 into a mesoporous-TiO_(2)(mp-TiO_(2)) layer, which was used as a photoanode in SS-FDSSCs, which are inherently flexible. The PCE of the MOF-integrated SS-FDSSCs was 6.50%, which is comparable to that of the reference devices(4.19%).The MOF-801 enhanced SS-FDSSCs decreased the series resistance(R_(s)) value, resulting in effective electron extraction with improved short-circuit current density(J_(SC)), while also increasing the shunt resistance(R_(sh)) value to prevent the recombination of photo-induced electrons. The result is an improved fill factor and, consequently, a higher value for the PCE.

Effects of structure and electronic properties of D-π-A organic dyes on photovoltaic performance of dye-sensitized solar cells

Herein,we examine the performance of dye-sensitized solar cells containing five D-π-A organic dyes designed by systematic modification of π-bridge size and geometric structure.Each dye has a simple push-pull structure with a triarylamino group as an electron donor,bithiophene-4,4-dimethyl-4 H-cyclopenta 1,2-b:5,4-b’]dithiophene(M11),4,4-dimethyl-4 H-cyclopenta[1,2-b:5,4-b’]dithiophenethiophene(M12),thiophene-4,4-dimethyl-4 H-cyclopenta[1,2-b:5,4-b’]dithiophene(M13),4,4-dimethyl-4 H-cyclopenta[1,2-b:5,4-b’]dithiophene-benzene(M14),and 4,4-dimethyl-4 H-cyclopenta[1,2-b:5,4-b’]dithiophene(M15)units asπ-bridges,and cyanoacrylic acid as an electron acceptor/anchor.The extension of theπ-bridge linkage favors wide-range absorption but,because of the concomitant molecular volume increase,hinders the efficient adsorption of dyes on the TiO_(2) film surface.Hence,higher loadings are achieved for smaller dye molecules,resulting in(i)a shift of the TiO_(2) conduction band edge to more negative values,(ii)a greater photocurrent,and(iii)suppressed charge recombination between the photoanode and the redox couple in the electrolyte.Consequently,under one-sun equivalent illumination(AM 1.5 G,100 mW/cm^(2)),the highest photovoltage,photocurrent,and conversion efficiency(η=7.19%)are observed for M15,which has the smallest molecular volume among M series dyes.

New strategy to incorporate nano-particle sized water oxidation catalyst into dye-sensitized photoelectrochemical cell for water splitting

In order to develop a new strategy to deposit nano-particle sized water oxidation catalyst based on earth abundant element to the photoanode in a photoelectrochemical cell for water splitting, Co;O;as water oxidation catalyst was prepared and subsequently modified by 3-aminopropyltriethoxysilane. The amino functionalized Co;O;catalyst was carefully characterized and then integrated to the ruthenium dye sensitized photoelectrode through fast Schiff base reaction. Cyclic voltammetry experiments in the dark confirmed that the modified Co;O;catalyst was still active toward water oxidation, which could be initiated by oxidation of the ruthenium photosensitizer. Under visible light irradiation, incorporation of the modified Co;O;catalyst resulted in dramatic enhancement of the transient photocurrent density for the photoanode, which was 8 times higher than that of without Co;O;catalyst.

Gel electrolytes containing several kinds of particles used in quasi-solid-state dye-sensitized solar cells

Composite gel electrolytes containing several kinds of particles used as the quasi-solid-state electrolytes in dye-sensitized solar cells(DSSCs)were reported.Mesoporous particles(MCM-41)with unique structures composed of ordered nanochannels were served as a new kind of gelator for quasi-solid-state electrolytes.MCM-41,hydrophobic fumed silica Aerosil R972 and TiO_(2)nanopatricles P25 were dispersed into gel electrolytes respectively.The solar energy-to-electricity conversion efficiency of these cells is 4.65%,6.85%and 5.05%respectively under 30 mW·cm^(-2)illumination.The preparation methods and the particles sizes exert an influence on the performance of corresponding solar cells.Owing to unique pore structures and high specific BET surface area,mesoporous silica MCM-41 was expected to have the potential to afford conducting nanochannels for redox couple diffusion.

Enhanced Electrocatalytic Activity by RGO/MWCNTs/NiO Counter Electrode for Dye-sensitized Solar Cells

We applied the reduced graphene oxide/multi-walled carbon nanotubes/nickel oxide(RGO/MWCNTs/Ni O)nanocomposite as the counter electrode(CE) in dye-sensitized solar cells(DSSCs) on fluorine-doped tin oxide substrates by blade doctor method. Power conversion efficiency(PCE) of 8.13 % was achieved for this DSSCs device, which is higher than that of DSSCs devices using Ni O, RGO, and RGO/Ni O-CE(PCE = 2.71 %, PCE = 6.77 % and PCE = 7.63 %). Also, the fill factor of the DSSCs devices using the RGO/MWCNTs/Ni O-CE was better than that of other CEs. The electron transfer measurement of cyclic voltammetry and electrochemical impedance spectroscopy showed that RGO/MWCNTs/Ni O film could provide fast electron transfer between the CE and the electrolyte, and high electrocatalytic activity for the reduction of triiodide in a CE based on RGO/MWCNTs/Ni O in a DSSC.