Ga-doped ZnO transparent electrodes with TiO<Subscript>2</Subscript> blocking layer/nanoparticles for dye-sensitized solar cells

Ga-doped ZnO [GZO] thin films were employed for the transparent electrodes in dye-sensitized solar cells [DSSCs]. The electrical property of the deposited GZO films was as good as that of commercially used fluorine-doped tin oxide [FTO]. In order to protect the GZO and enhance the photovoltaic properties, a TiO₂ blocking layer was deposited on the GZO surface. Then, TiO₂ nanoparticles were coated on the blocking layer, and dye was attached for the fabrication of DSSCs. The fabricated DSSCs with the GZO/TiO₂ glasses showed an enhanced conversion efficiency of 4.02% compared to the devices with the normal GZO glasses (3.36%). Furthermore, they showed better characteristics even than those using the FTO glasses, which can be attributed to the reduced charge recombination and series resistance.     

Electrodeposited nanoporous ZnO films exhibiting enhanced performance in dye-sensitized solar cells

Electrodeposition of nanoporous ZnO films and their applications to dye-sensitized solar cells (DSSCs) were investigated in the aim of developing cost-effective alternative synthetic methods and improving the ZnO-based DSSCs performance. ZnO films were grown by cathodic electrodeposition from an aqueous zinc nitrate solution containing polyvinylpyrrolidone (PVP) surfactant. PVP concentration had strong effects on the grain sizes and surface morphologies of ZnO films. Nanoporous ZnO film with grain size of 20-40 nm was obtained in the electrolyte containing 4 g/L PVP. The X-ray diffraction pattern showed that nanoporous ZnO films had a hexagonal wurtzite structure. Optical properties of such films were studied and the results indicated that the films had a band gap of 3.3 eV. DSSCs were fabricated from nanoporous ZnO films and the cell performance could be greatly improved with the increase of ZnO film thickness. The highest solar-to-electric energy conversion efficiency of 5.08% was obtained by using the electrodeposited double-layer ZnO films (8 μm thick nanoporous ZnO films on a 200 nm thick compact nanocrystalline ZnO film). The performance of such cell surpassed levels attained in previous studies on ZnO film-based DSSCs and was among the highest for DSSCs containing electrodeposited film components.     

Hydrothermal Growth and Application of ZnO Nanowire Films with ZnO and TiO2 Buffer Layers in Dye-Sensitized Solar Cells

This paper reports the effects of the seed layers prepared by spin-coating and dip-coating methods on the morphology and density of ZnO nanowire arrays, thus on the performance of ZnO nanowire-based dye-sensitized solar cells (DSSCs). The nanowire films with the thick ZnO buffer layer (~0.8–1 μm thick) can improve the open circuit voltage of the DSSCs through suppressing carrier recombination, however, and cause the decrease of dye loading absorbed on ZnO nanowires. In order to further investigate the effect of TiO₂ buffer layer on the performance of ZnO nanowire-based DSSCs, compared with the ZnO nanowire-based DSSCs without a compact TiO₂ buffer layer, the photovoltaic conversion efficiency and open circuit voltage of the ZnO DSSCs with the compact TiO₂ layer (~50 nm thick) were improved by 3.9–12.5 and 2.4–41.7%, respectively. This can be attributed to the introduction of the compact TiO₂ layer prepared by sputtering method, which effectively suppressed carrier recombination occurring across both the film–electrolyte interface and the substrate–electrolyte interface.     

Growth of Comb-like ZnO Nanostructures for Dye-sensitized Solar Cells Applications

Dye-sensitized solar cells (DSSCs) were fabricated by using well-crystallized ZnO nanocombs directly grown onto the fluorine-doped tin oxide (FTO) via noncatalytic thermal evaporation process. The thin films of as-grown ZnO nanocombs were used as photoanode materials to fabricate the DSSCs, which exhibited an overall light to electricity conversion efficiency of 0.68% with a fill factor of 34%, short-circuit current of 3.14 mA/cm², and open-circuit voltage of 0.671 V. To the best of our knowledge, this is first report in which thin film of ZnO nanocombs was used as photoanode materials to fabricate the DSSCs.     

Direct synthesis of vertically aligned ZnO nanowires on FTO substrates using a CVD method and the improvement of photovoltaic performance

In this work, we report a direct synthesis of vertically aligned ZnO nanowires on fluorine-doped tin oxide-coated substrates using the chemical vapor deposition (CVD) method. ZnO nanowires with a length of more than 30 μm were synthesized, and dye-sensitized solar cells (DSSCs) based on the as-grown nanowires were fabricated, which showed improvement of the device performance compared to those fabricated using transferred ZnO nanowires. Dependence of the cell performance on nanowire length and annealing temperature was also examined. This synthesis method provided a straightforward, one-step CVD process to grow relatively long ZnO nanowires and avoided subsequent nanowire transfer process, which simplified DSSC fabrication and improved cell performance.     

Enhancement of the photoelectric performance of dye-sensitized solar cells using Ag-doped TiO<Subscript>2</Subscript> nanofibers in a TiO<Subscript>2</Subscript> film as electrode

For high solar conversion efficiency of dye-sensitized solar cells [DSSCs], TiO₂ nanofiber [TN] and Ag-doped TiO₂ nanofiber [ATN] have been extended to be included in TiO₂ films to increase the amount of dye loading for a higher short-circuit current. The ATN was used on affected DSSCs to increase the open circuit voltage. This process had enhanced the exit in dye molecules which were rapidly split into electrons, and the DSSCs with ATN stop the recombination of the electronic process. The conversion efficiency of TiO₂ photoelectrode-based DSSCs was 4.74%; it was increased to 6.13% after adding 5 wt.% ATN into TiO₂ films. The electron lifetime of DSSCs with ATN increased from 0.29 to 0.34 s and that electron recombination was reduced.     

Solid-state dye-sensitized solar cells based on ZnO nanoparticle and nanorod array hybrid photoanodes

The effect of ZnO photoanode morphology on the performance of solid-state dye-sensitized solar cells (DSSCs) is reported. Four different structures of dye-loaded ZnO layers have been fabricated in conjunction with poly(3-hexylthiophene). A significant improvement in device efficiency with ZnO nanorod arrays as photoanodes has been achieved by filling the interstitial voids of the nanorod arrays with ZnO nanoparticles. The overall power conversion efficiency increases from 0.13% for a nanorod-only device to 0.34% for a device with combined nanoparticles and nanorod arrays. The higher device efficiency in solid-state DSSCs with hybrid nanorod/nanoparticle photoanodes is originated from both large surface area provided by nanoparticles for dye adsorption and efficient charge transport provided by the nanorod arrays to reduce the recombinations of photogenerated carriers.     

Photovoltaic property dependence of dye-sensitized solar cells on sheet resistance of FTO substrate deposited via spray pyrolysis

F-doped SnO₂ (FTO) glass substrate was successfully fabricated via spray-pyrolysis deposition for use as a transparent conducting substrate in dye-sensitized solar cells (DSSCs). To investigate the performance dependence of DSSCs on the sheet resistance of the FTO films, three types of FTO films with sheet resistance values of 2 Ω/□, 4 Ω/□, and 10 Ω/□ were fabricated. Commercial FTO films having a sheet resistance of 15 Ω/□ were prepared for comparison. The structural, electrical, and optical properties of FTO films were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), the four-point probe method, and UV–vis spectrometry. The photocurrent–voltage data show that DSSCs fabricated with a sheet resistance of 2 Ω/□ exhibit the best photoconversion effciency (～5.5%) among the four samples. The performance improvement of DSSCs is due to improved short-circuit current density (～13.7 mA/cm²) and fill factor (～62.3%).     

Fabrication and characterization of silicon wire solar cells having ZnO nanorod antireflection coating on Al-doped ZnO seed layer

In this study, we have fabricated and characterized the silicon [Si] wire solar cells with conformal ZnO nanorod antireflection coating [ARC] grown on a Al-doped ZnO [AZO] seed layer. Vertically aligned Si wire arrays were fabricated by electrochemical etching and, the p-n junction was prepared by spin-on dopant diffusion method. Hydrothermal growth of the ZnO nanorods was followed by AZO film deposition on high aspect ratio Si microwire arrays by atomic layer deposition [ALD]. The introduction of an ALD-deposited AZO film on Si wire arrays not only helps to create the ZnO nanorod arrays, but also has a strong impact on the reduction of surface recombination. The reflectance spectra show that ZnO nanorods were used as an efficient ARC to enhance light absorption by multiple scattering. Also, from the current-voltage results, we found that the combination of the AZO film and ZnO nanorods on Si wire solar cells leads to an increased power conversion efficiency by more than 27% compared to the cells without it.     

Microwave-assisted one-pot synthesis of Ag decorated flower-like ZnO composites photocatalysts for dye degradation and NO removal

A series of Ag nanoparticles decorated flower-like ZnO (Ag/ZnO) composites with varying Ag loadings were fabricated via a microwave-assisted one-pot method. The flower-like Ag/ZnO structure with a diameter of about 800 nm was assembled by Ag distribution on ZnO nanosheets. The decoration of Ag on ZnO can obviously improve the degradation rate of dye and NO under simulated solar-light. The optimal loading amount of Ag was 8 mol%, where it exhibited the highest photocatalytic activity with complete degradation of RhB and 4-NP in 20 and 60 min, respectively. And for NO, the oxidation ratio is 55% within 15 min irradiation. The enhanced photocatalytic performance can be attributed to the special architecture and the introduction of Ag nanoparticles, which largely improved the light-absorbing capability and electron separation efficiency in Ag/ZnO composites.     

Effect of carbonaceous counter electrodes on the performance of ZnO-graphene nanocomposites based dye sensitized solar cells

With many advantages like low-cost preparation, excellent electrical properties, and high catalytic activity; carbon allotropes are the most expected carbon materials to substitute the expensive Platinum (Pt) as counter electrodes (CEs) for dye-sensitized solar cells (DSSCs). In the present study, the photovoltaic behaviors of DSSCs fabricated with graphene, multiwalled carbon nanotubes (MWCNTs), and Pt films CEs, respectively, were compared. The graphene and MWCNTs CEs films were prepared by doctor blading the graphene and MWCNTs pastes on Indium tin oxides (ITOs) glass substrates. The structural, morphological, and compositional properties of these carbon CEs viz. graphene and MWCNTs were investigated by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), and energy dispersive X-ray (EDX), respectively. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were employed for the examination of electrochemical and catalytic properties of Pt as well as carbonaceous CEs. These low-cost graphene and MWCNTs CEs were employed in the sandwich-structured DSSCs having ZnO-graphene nanocomposite films as photoanodes. The photoconversion efficiency (η) values of as prepared DSSCs were measured under AM 1.5 illumination (100?mW?cm^?2). The DSSCs with graphene CE and MWCNTs CE performed with efficiency values of 2.26% and 2.04%, respectively. The performance of these carbonaceous CEs are comparative to that of Pt CE which indicates the practicability of carbon based nanomaterials in DSSCs as low cost alternatives to the expensive Pt.     

Multilayer photoactive nanocolloidal PPy:PSS as a novel substitute for Pt free counter electrode in DSSC

Water dispersible and highly processable, Polypyrrole (PPy) nanocolloidal particles were synthesized by chemical oxidation polymerization with 15 wt % of anionic polyelectrolyte poly(styrene sulfonate) (PSS) at 5°C has been reported in this work. This polymer composite (PPy:PSS) was competent with conventional Pt counter electrode (CE) when compared for dye sensitized solar cells (DSSCs). Morphological analysis revealed smooth and spherical shaped nanoparticles of PPy. Interaction between the SO₃H groups and Py units in PPy improved the thermal stability of PPy with higher doping levels of PSS. The nanocolloidal solution was spin coated at 4000 rpm. The layer by layer, self‐assembled multilayer thin films were used as CE in DSSCs. There was a linear dependence of DSSCs performance with film roughness for the self‐assembled multilayer PPy:PSS films. Single layer films showed better electrocatalytic behavior than multilayer films. All the PPy:PSS films had good electrochemical stability. The DSSC efficiency of 3.40% was observed for chemically oxidized PPy with 15 wt % PSS for single layer film, with a highest FF of 0.7154. The low cost, good performance, rapid and simple fabrication method of PPy:PSS composite modified CE could be a potential alternative for Pt in the DSSCs. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43114.     

Fabrication and characterization of solution cast MWNTs/PEI nanocomposites

Under mild conditions with the aid of ultrasonic, multi‐walled carbon nanotubes (MWNTs) have been functionalized by mixed acid treatment which was proved by FTIR and XPS. According to SEM, acid treatment on MWNTs decreased the thickness of the membrane. However, no devastating damage and fracture happened on MWNTs after acid treatment under mild conditions. Precipitation observation illustrated that the enhanced solubility of MWNTs in water, ethanol, and dimethylformaide (DMF). Further, MWNTs/polyetherimide (PEI) nanocomposite films have been prepared by the simple solution casting method. The dispersion of MWNTs in polyetherimide (PEI) matrix was observed by Atomic Force Microscopy (AFM) which illustrated the improved dispersion for acid treated MWNTs in PEI. The adding of MWNTs in PEI decreased the dispersive component of surface energy and increased the polar component of surface energy, which resulted in the decrement of film surface energy. Differential scanning calorimetry showed that the glass transition temperature of PEI increased by about 4°C after the introduction of MWNTs. This improvement was related to the better affinity between MWNTs and PEI matrix, which also resulted in the improvement of mechanical strength in MWNTs/PEI nanocomposites. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

导电玻璃对纳米二氧化钛薄膜太阳能电池性能的影响

在3种导电玻璃基材上烧结制备一层纳米TiO2薄膜,并用它们各自组装成N3染料敏化太阳能电池.用紫外可见光仪、场发射扫描电镜及四探针仪研究了导电玻璃的透光率和导电性能对染料敏化太阳能电池电流、电压输出性能的影响.结果表明:在100mW/cm2模拟太阳光强照射下,导电玻璃的面电阻减小时,光电池的短路电流会迅速增加,开路电压基本不变.导致这种现象的主要原因是导电玻璃上导电层的面电阻减小会使太阳能电池的内阻下降.由于太阳能电池的开路电压与短路电流的对数成正比.当导电玻璃的透光率大于80%时,导电玻璃的透光率对太阳光电池的电流电压输出性能基本没有影响.     

Mechanical reinforcement of chitosan using unzipped multiwalled carbon nanotube oxides

In this paper, unzipped multiwalled carbon nanotube oxides (UMCNOs), obtained by oxidation unzipping multiwalled carbon nanotubes (MWNTs) were used as novel nanofillers for mechanical reinforcement of chitosan (CS) matrix. The UMCNOs/CS nanocomposite films with different amounts of UMCNOs were fabricated by solution-casting the mixtures of UMCNOs and CS acetic acid aqueous dispersions. The structures and mechanical properties of the nanocomposite films were characterized by XRD, FT-IR, SEM, and tensile tests. The results demonstrated that UMCNOs could be homogeneously dispersed throughout the chitosan matrix. Compared to neat chitosan, the UMCNOs/CS nanocomposite films showed ～105.9% increase in tensile strength from 69.3 to 142.7 MPa, and ～165.3% increase in Young’s modulus from 2.6 to 6.9 Gpa with the incorporation of only 0.2 wt% of UMCNOs into the chitosan matrix.     

Fast-response photoconductive ultraviolet light detectors fabricated using high-quality ZnO films obtained by plasma-assisted molecular beam epitaxy

ZnO films form the core of numerous ultraviolet (UV) optoelectronic devices. Herein, a ZnO buffer layer produced by thermal plasma oxidation of metallic Zn was used to grow an active ZnO layer, with Zn film and active layer growth achieved by plasma-assisted molecular beam epitaxy. Although low-temperature ZnO buffer layer and Zn film growth was mainly three-dimensional (3D) due to a large lattice mismatch between ZnO/Zn and Si, the use of thermal plasma oxidation changed the growth mode from 3D to 2D, producing a smooth ZnO active layer. The thus fabricated ZnO active layer (sample 2) exhibited a lower tensile stress than that fabricated on a ZnO buffer layer using a conventional method (sample 1). Both samples were used to fabricate UV sensors, with that based on sample 2 exhibiting a faster photoresponse.     

Fabrication of nanostructured ZnO film as a hole-conducting layer of organic photovoltaic cell

We have investigated the effect of fibrous nanostructured ZnO film as a hole-conducting layer on the performance of polymer photovoltaic cells. By increasing the concentration of zinc acetate dihydrate, the changes of performance characteristics were evaluated. Fibrous nanostructured ZnO film was prepared by sol-gel process and annealed on a hot plate. As the concentration of zinc acetate dihydrate increased, ZnO fibrous nanostructure grew from 300 to 600 nm. The obtained ZnO nanostructured fibrous films have taken the shape of a maze-like structure and were characterized by UV-visible absorption, scanning electron microscopy, and X-ray diffraction techniques. The intensity of absorption bands in the ultraviolet region was increased with increasing precursor concentration. The X-ray diffraction studies show that the ZnO fibrous nanostructures became strongly (002)-oriented with increasing concentration of precursor. The bulk heterojunction photovoltaic cells were fabricated using poly(3-hexylthiophene-2,5-diyl) and indene-C60 bisadduct as active layer, and their electrical properties were investigated. The external quantum efficiency of the fabricated device increased with increasing precursor concentration.     

Preparation of TiO<Subscript>2</Subscript> nanotube/nanoparticle composite particles and their applications in dye-sensitized solar cells

Efficiency of dye-sensitized solar cells [DSSCs] was enhanced by combining the use of TiO₂ nanotubes [TNTs] and nanoparticles. TNTs were fabricated by a sol-gel method, and TiO₂ powders were produced through an alkali hydrothermal transformation. DSSCs were constructed using TNTs and TiO₂ nanoparticles at various weight percentages. TNTs and TiO₂ nanoparticles were coated onto FTO glass by the screen printing method. The DSSCs were fabricated using ruthenium(II) (N-719) and electrolyte (I₃/I₃ ^-) dyes. The crystalline structure and morphology were characterized by X-ray diffraction and using a scanning electron microscope. The absorption spectra were measured using an UV-Vis spectrometer. The incident photocurrent conversion efficiency was measured using a solar simulator (100 mW/cm²). The DSSCs based on TNT/TiO₂ nanoparticle hybrids showed better photovoltaic performance than cells made purely of TiO₂ nanoparticles.     

The influence of anatase-rutile mixed phase and ZnO blocking layer on dye-sensitized solar cells based on TiO2nanofiberphotoanodes

High performance is expected in dye-sensitized solar cells (DSSCs) that utilize one-dimensional (1-D) TiO₂ nanostructures owing to the effective electron transport. However, due to the low dye adsorption, mainly because of their smooth surfaces, 1-D TiO₂ DSSCs show relatively lower efficiencies than nanoparticle-based ones. Herein, we demonstrate a very simple approach using thick TiO₂ electrospun nanofiber films as photoanodes to obtain high conversion efficiency. To improve the performance of the DSCCs, anatase-rutile mixed-phase TiO₂ nanofibers are achieved by increasing sintering temperature above 500°C, and very thin ZnO films are deposited by atomic layer deposition (ALD) method as blocking layers. With approximately 40-μm-thick mixed-phase (approximately 15.6?wt.% rutile) TiO₂ nanofiber as photoanode and 15-nm-thick compact ZnO film as a blocking layer in DSSC, the photoelectric conversion efficiency and short-circuit current are measured as 8.01% and 17.3?mA?cm^?2, respectively. Intensity-modulated photocurrent spectroscopy and intensity-modulated photovoltage spectroscopy measurements reveal that extremely large electron diffusion length is the key point to support the usage of thick TiO₂ nanofibers as photoanodes with very thin ZnO blocking layers to obtain high photocurrents and high conversion efficiencies.     

In situ electrochemical synthesis of a poly(o‐anisidine) counter electrode for a dye‐sensitized solar cell

Poly(o‐anisidine) (POA) counter electrodes (CEs) were fabricated by potentiodynamic deposition and incorporated into platinum (Pt)‐free dye‐sensitized solar cells (DSSCs). A different sweep number had great impact on the morphology and electrocatalytic activity of the POA films. The POA film fabricated by 25 sweep cycles was observed to have a highly porous morphology, and this resulted in a lower charge‐transfer resistance of 57 cm² in comparison with the Pt CE. The DSSC assembled with the POA CE showed a higher photovoltaic conversion efficiency of 1.67% compared to 1.2% for the DSSC with the Pt CE under full sunlight illumination. Therefore, the high active surface area of the 25‐sweep‐segmented POA film could be considered a promising alternative CE for use in DSSCs because of its high electrocatalytic performance and electrochemical stability. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42041.