An enhancement of efficiency of a solid-state dye-sensitized solar cell due to cocktail effect of N719 and black dye

The solar cell performance of the black dye, N719 dye and the cocktail of two dyes on TiO₂ films were studied by mean of the utilization as light harvesting electrodes in solid-state FTO|TiO₂|dye|CuI|Cr–FTO cells. The power conversion efficiencies of 3.8% and 3.0% are obtained when N719 and black dye were used. When the mixture of 1:1 of two dyes was used, the conversion efficiency rises to 4.6%. In the mixture of N719 and black dye, the N719 dye acts as the aggregation preventer and a co-absorber on TiO₂ surfaces. The increased absorption of light by the two dyes results in increase of electron injection thus enhancing both the short-circuit current density and the open circuit voltage contributing to increased power conversion efficiency of the cell.     

Photophysical and enhanced daylight photocatalytic properties of N-doped TiO2/g-C3N4 composites

N-doped TiO₂/C₃N₄ composite samples were synthesized by heating the mixture of the hydrolysis product of TiCl₄ and C₃N₄ at different weight ratios. The samples were characterized by X-ray diffraction (XRD), Raman spectrum, UV–vis absorption spectrum, photoluminescence spectrum, X-ray photon electron spectrum (XPS) and surface photovoltage spectrum (SPS). The XRD and Raman results indicate that the introduction of C₃N₄ could inhibit the formation of rutile TiO₂. The composite samples show slight visible light absorption due to the introduction of C₃N₄. The XPS result reveals that some amount of nitrogen is doped into TiO₂, and C₃N₄ exists in the composite sample. The intensities of the SPS signal in the composite samples decrease with the rise in the amount of C₃N₄ in the samples. The photocatalytic activity was evaluated from the Rhodamine B (RhB) degradation under fluorescence light irradiation. The composite samples show significantly enhanced photocatalytic activities and the RhB self-sensitized photodegradation in this system was observed by measuring the photocurrent in the dye sensitized solar cell using the composite as the working electrode.     

Improving the visible light photocatalytic activity of mesoporous TiO2 via the synergetic effects of B doping and Ag loading

B-doped together with Ag-loaded mesoporous TiO₂ (Ag/B–TiO₂) was prepared by a two-step hydrothermal method in the presence of boric acid, triblock copolymer surfactant, and silver nitrate, followed by heat treatment. The obtained samples were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), UV–vis diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption–desorption. It was revealed that all samples consist of highly crystalline anatase with mesoporous structure. For Ag/B–TiO₂, B was doped into TiO₂ matrix in the form of both interstitial B and substitutional B while Ag was deposited on the surface of B–TiO₂ in the form of metallic silver. Compared with the single B-doped or Ag-loaded TiO₂ one, mesoporous Ag/B–TiO₂ exhibits much higher visible light photocatalytic activity for the degradation of Rhodamine 6G, which can be ascribed to the synergistic effects of B doping and Ag loading by narrowing the band gap of the photocatalyst and preventing the fast recombination of the photogenerated charge carriers, respectively.     

Applications of vertically oriented TiO2 micro-pillars array on the electrode of dye-sensitized solar cell

In this research, dye-sensitized solar cells based on TiO₂ micro-pillars fabricated by inductive couple plasma etcher were investigated by analyses of X-ray diffraction (XRD), scanning electron microscopy (SEM), contact angle, ultraviolet-visible absorption spectra (UV-vis), and current-voltage characteristics. X-ray diffraction patterns show that the TiO₂ anatase phase forms while sintering at 450 °C for 30 min. The SEM images reveal that the diameter and height of TiO₂ micro-pillars are about 3 and 0.8 μm, respectively. The measurements of contact angle between TiO₂ micro-pillars and deionized water (DI water) reveal that the TiO₂ micro-pillars is super-hydrophilic while annealed at 450 °C for 30 min.The absorption spectrum of TiO₂ micro-pillars is better than TiO₂ thin film and can be widely improved in visible region with N3 dye adsorbed. The results of current-voltage (I-V) characteristics analysis reveal that dye-sensitized solar cell with TiO₂ micro-pillars electrode has better I-V characteristics and efficiency than TiO₂ film electrodes. This result may be due to the annealed TiO₂ micro-pillars applied on the electrode of dye-sensitized solar cell can increase the contact area between TiO₂ and dye, resulting in the enhancement of I-V characteristics and efficiency for dye-sensitized solar cell.     

Synthesis and application of the solar cell of poly(3-hexylthiophene)/Fe N/titanium dioxide nanocomposite material

A series of nanocomposites of poly(3-hexylthiophene) with Fe N-doped TiO₂ (P3HT/Fe N/TiO₂) were synthesized by the chemical method in situ. The structure of the prepared composites was characterized using X-ray diffraction patterns (XRD), infrared spectroscopy (IR), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). Optical and electrochemical properties were determined using UV-vis spectroscopy, fluorescence spectroscopy, and cyclic voltammetry. These tests indicated that P3HT/Fe N/TiO₂ is a new p-n semiconductor. Two solar cells based on P3HT/Fe N/TiO₂ were manufactured and studied.     

Rapid microwave-assisted hydrothermal synthesis of Bi12TiO20 hierarchical architecture with enhanced visible-light photocatalytic activities

Flower-like Bi₁₂TiO₂₀ hierarchical nanostructures composed of numerous nanobelts were synthesized at 180 °C within 1 h by a microwave-assisted hydrothermal method in the presence of cetyltrimethylammonium bromide (CTAB) for the first time. The as-prepared products were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and ultraviolet–visible (UV–vis) absorption spectroscopy. Furthermore, the hierarchical Bi₁₂TiO₂₀ nanostructures exhibited higher photocatalytic activities in the degradation of Rhodamine B under visible-light irradiation than that of the samples prepared without CTAB. In addition, the role of CTAB cationic surfactant has been investigated thoroughly and a possible mechanism is proposed.     

Photo(electro)catalytic Activity of Cu-Modified TiO2 Nanorod Array Thin Films under Visible Light Irradiation

In the present study, a two-step method was applied to synthesise Cu²⁺-modified TiO₂ nanorod array thin films for photocatalytic processes. TiO₂ nanorod array thin films were synthesised by a hydrothermal method and then modified with an ultrasonic-assisted sequential cation adsorption method. The samples were characterised by X-ray diffraction (XRD), UV–vis diffuse reflectance spectra (DRS), scanning electron microscopy (SEM), photoluminescence (PL) spectroscopy and inductively coupled plasma mass spectroscopy (ICP-MS) analysis. The photoelectrochemical properties of the samples were evaluated by linear sweep voltammetry and Mott–Schottky analysis; photocatalytic activities were tested by methylene blue degradation under visible light. The photocurrent density of the TiO₂/FTO sample modified with 50 mM Cu²⁺ solution was 26 times higher than that of the unmodified TiO₂/FTO sample. Additionally, methylene blue degradation efficiency under visible light was increased 40% with respect to the efficiency of the unmodified sample. The mechanism of the photocatalytic activity enhancement of Cu²⁺-modified TiO₂ nanorod films was discussed.     

Analysis of adsorption properties of N719 dye molecules on nanoporous TiO2 surface for dye-sensitized solar cell

Ordered nanoporous TiO₂ materials (MK-TiO₂, MS-TiO₂, and MU-TiO₂) were synthesized for the dye-sensitized solar cell (DSSC) by using different silica templates such as KIT-6, SBA-15, and MSU-H. To prepare a photoelectrode in DSSC, cis-bis(isothiocyanato)bis(2,2′-bipyridyl-4,4′-dicarboxylato)-ruthenium(II)bis-tetrabutylammonium dye (N719) was adsorbed onto the synthesized nanoporous TiO₂ materials. The samples were characterized by XRD, TEM, FE-SEM, AFM, and N₂ adsorption analyses. The photovoltaic performance of DSSC was evaluated from the overall conversion efficiency, fill factor, open-circuit voltage, and short-circuit current from the I-V curves measured. It was found that the photoelectric performance is highly dependent on the adsorption properties of N719 dye molecules on the nanoporous TiO₂ replicas (MK-TiO₂, MS-TiO₂, and MU-TiO₂) synthesized from different silica templates.     

Material properties controlling photocurrent on TiO2 aggregates with plane orientation for dye-sensitized solar cells

Effective design of a dye-sensitized solar cell (DSSC) requires a clear understanding of the reaction mechanisms of the constituent cell materials. The relationship between structural and photo-electrochemical properties of the photo-anodic materials is of the first priority for such investigations. Highly oriented aggregates of anatase phase TiO₂ nanoparticles were deposited on Indium Tin oxide (ITO) glass substrates; over which N719 dyes were adsorbed through electrophoretic deposition under a strong magnetic field. The properties were evaluated by electrochemical measurements, UV–VIS spectroscopy, and electrical resistance measurements. The results showed that the absorbed photon number in the TiO₂ aggregates with adsorbed dye and their resistivity showed different dependences on the orientation of the crystal plane in the TiO₂ particle. The dependence of the photocurrent on the plane orientation of aggregates of dye-sensitized TiO₂ nanoparticles has been determined from a combination of the electrical conductivity of TiO₂ aggregate and the amount of dye adsorbed on the surface of TiO₂.     

Preparation of nitrogen-doped titanium dioxide with visible-light photocatalytic activity using a facile hydrothermal method

Nitrogen-doped TiO₂ (N-TiO₂) nanoparticles have been successfully prepared via a direct and simple hydrothermal reaction of a commercial Degussa P25 with triethanol amine as solvent and nitrogen source. As-prepared N-TiO₂ was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet-visible light (UV-vis) absorption spectra, electron probe microanalysis (EPMA) and X-ray photoelectron spectroscopy (XPS) techniques. The results confirm that hydrothermal reaction is an effective way to incorporate nitrogen into the TiO₂ lattice, especially nitrogen substitute for titanium. The nitrogen concentration in TiO₂ can be as high as 21% (molar ratio), which is described as Ti_1−yO_2−xN_x+y (in this paper, x=0.36, y=0.27, i.e., Ti_0.73O_1.64N_0.63). The chemical statuses of N have been assigned to N-Ti-O and O-N-O in the TiO₂ lattice as identified by XPS. Photocatalytic degradation of methyl orange has been carried out in both UV-vis (simulated solar light) and the visible region (λ>400 nm). N-TiO₂ exhibits higher activity than the Degussa P25 TiO₂ photocatalyst, particularly under visible-light irradiation. This study has developed a promising and practical pathway to new nitrogen-doped photocatalysts.     

Application of TiO2 nano-particles on the electrode of dye-sensitized solar cells

In this study, nano-TiO₂ thin film electrode and solar cell have been investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), ultraviolet-visible absorption spectra, contact angle, X-ray photoelectron spectroscopy (XPS), and current-voltage characteristics analyses. X-ray diffraction patterns show that the best sintering temperature of a nano-TiO₂ film is 600 °C, at which TiO₂ anatase phase forms best and the particle size of 8-10 nm can be obtained. The SEM images of a nano-TiO₂ thin film show that the surface of the film is smooth and porous, and the thickness of the nano-TiO₂ film is 4 μm. The measurements of contact angle between nano-TiO₂ film and deionized water (DI water) reveal that the nano-TiO₂ film is super-hydrophilic when solarized under ultraviolet. The electrode of dye-sensitized solar cell is used as a free-base porphyrin with carboxyl group, 5,10,15,20-tetrakis (4-carboxyphenyl) porphyrin (TCPP) as the sensitizer to adsorb onto the TiO₂ thin film. From the results of ultraviolet-visible absorption spectra and XPS analyses of the electrode, the effects of nano-TiO₂ particles’ addition to the electrode of dye-sensitized solar cell can improve the absorption of visible light (400-700 nm) and increase electrons transferred from TCPP to the conduction band of TiO₂, resulting in the enhancement of efficiency for dye-sensitized solar cells.     

Preparation and characterization of ZnS/CdS bi-layer for CdTe solar cell application

In this work, bilayer ZnS/CdS film was prepared as an improved window layer of CdTe solar cell. TEM was used to observe the cross section of the bilayer structure. The total thickness of ZnS/CdS film was about 60 nm, which could allow more photons to pass through it and contribute to the photocurrent. Optical properties of the bilayers were investigated using UV–vis spectroscopy. Compared with poor transmission of standard CdS film in the short wavelength range of 350–550 nm, the transmission of ZnS/CdS was improved and reached above 50%. The ZnS/CdS was annealed with CdCl₂. X-ray photoelectron spectroscopy (XPS) was used to investigate its chemical properties. A possible diffusion between CdS and ZnS was observed after annealing. The efficiency of standard CdS/CdTe solar cell was 9.53%. The device based on ZnS/CdS window layer had a poor 6% efficiency. With annealing treatment on ZnS/CdS layer, the performance was improved and reached 10.3%. In addition, the homogeneity of solar cell performance was improved using ZnS/CdS window layer. A thin ZnS layer was quite effective to reduce the possible shunt paths and short parts of window layer and consequently contributed to fabrication of a homogeneous CdTe solar cell.     

Preparation and improvement in photovoltaic performance of dye-sensitized solar cells using carbon dioxide

We report preparation and improvement in photovoltaic performance of N719-based dye-sensitized solar cells (DSSCs) using pressurized carbon dioxide (CO₂) as a co-solvent for the absorption process on the TiO₂ photoelectrode surface. Effective absorption of the N719 molecules on the TiO₂ surface was achieved using CO₂ processing, and the absorption time was shortened drastically from 24 h (in the dip process) to less than 3 h. The cells prepared under pressurized CO₂ for the absorption showed greater photovoltaic performance, especially higher short-circuit current density and conversion efficiency, compared with that from typical dip method. It was revealed that the suitable CO₂ pressure for the absorption was 5 MPa and the efficiency was achieved to be more than 7.5 %. Prevention of back electron transfer reactions from TiO₂ to oxidized dyes or iodides was caused currently, because the homogeneous coverage of N719 molecules on the TiO₂ surface was obtained by the use of pressurized CO₂.     

Evolution of structural and optical properties of rutile TiO2 thin films synthesized at room temperature by chemical bath deposition method

Nanocrystalline thin films of TiO₂ were prepared on glass substrates from an aqueous solution of TiCl₃ and NH₄OH at room temperature using the simple and cost-effective chemical bath deposition (CBD) method. The influence of deposition time on structural, morphological and optical properties was systematically investigated. TiO₂ transition from a mixed anatase–rutile phase to a pure rutile phase was revealed by low-angle XRD and Raman spectroscopy. Rutile phase formation was confirmed by FTIR spectroscopy. Scanning electron micrographs revealed that the multigrain structure of as-deposited TiO₂ thin films was completely converted into semi-spherical nanoparticles. Optical studies showed that rutile thin films had a high absorption coefficient and a direct bandgap. The optical bandgap decreased slightly (3.29–3.07 eV) with increasing deposition time. The ease of deposition of rutile thin films at low temperature is useful for the fabrication of extremely thin absorber (ETA) solar cells, dye-sensitized solar cells, and gas sensors.     

Sol-gel derived S,I-codoped mesoporous TiO2 photocatalyst with high visible-light photocatalytic activity

A mesoporous S,I-codoped TiO₂ photocatalyst with high visible light photocatalytic activity was synthesized through the hydrolysis and condensation of titanium isopropoxide with thiourea and iodic acid as the precursors. The as-prepared catalysts were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), UV-vis diffuse reflectance (DRS), X-ray photoelectron spectroscopy (XPS), Fourier translation infrared spectroscopy (FT-IR), and N₂ adsorption. The results showed that the cations of S⁶⁺ and I⁵⁺ could substitute for some of the lattice titanium (Ti⁴⁺). The S,I-codoping forms the new bands above the valence band and narrows the band-gap of the TiO₂, then shifts the absorption edge from UV light region to visible light range. The activity of the catalyst was examined by photodegradation of methylene blue in an aqueous solution under visible light irradiation. The activity of the S,I-codoped catalyst is far superior to that of single S or I-doped TiO₂ counterpart. The high visible light photocatalytic activity could be attributed to the strong absorption of light, well-crystalline anatase phase, and mesoporous microstructure.     

Crystallization study of sol-gel un-doped and Pd-doped TiO2 materials

Sol-gel nanostructured titania materials have been reported to have applications in areas ranging from optics via solar energy to gas sensors. In order to enhance the photocatalytic activity, there are many studies regarding the doping of titanium dioxide (TiO₂) material with either non-metals (S, C, N, P) or metals (Ag, Pt, Nd, Fe). The present work has studied some un-doped and Pd-doped sol-gel TiO₂ materials (films and gels), with various surface morphologies and structures, obtained by simultaneous gelation of both precursors Ti(OEt)₄ and Pd(acac)₂. Their structural evaluation and crystallization behavior with thermal treatment were followed by DTA/TG analysis, infrared (IR) spectroscopy, Fourier transform infrared (FTIR), spectroellipsometry (SE), X-ray diffraction (XRD) and atomic force microscope (AFM). The influence of Pd on TiO₂ crystallization for both supported and un-supported materials was studied (lattice parameters, crystallite sizes, internal microstrains). The changes in the optical properties of the TiO₂-based vitreous materials were correlated with the changes of the structure. The hydrophilic properties of the films were also connected with their structure, composition and surface morphology.     

Effect of Dy substitution on structural,magnetic and optical properties of BiFeO3 ceramics

Bi_1−xDy_xFeO₃ (x=0.0, 0.03, 0.05, 0.07, 0.10 and 0.12) ceramics were synthesized by solid state reaction method. Effects of Dy substitution on structural distortion, magnetic and optical properties of BiFeO₃ were examined by X-ray diffraction, Raman and UV–Visible spectroscopy. The samples were found to crystallize in rhombohedral structure of BiFeO₃ with R3c space group. The reduction in lattice parameters and unit cell volume indicate the distortion in FeO₆ octahedra of the rhombohedral structure without any signature of phase transformation up to x=0.12. The predictable weak ferromagnetic hysteresis loops can be observed in the Dy doped samples with maximum remnant magnetization of 0.2103 emu/g for x=0.12. The weak ferromagnetism is ascribed to the suppressed spiral spin structure and magnetically active characteristic of Dy³⁺ ions together with ferromagnetic coupling between Dy³⁺ and Fe³⁺ ions. With optical band gap in visible region, Dy doped BiFeO₃ ceramics are potential material for optoelectronic device and solar cell applications.     

Photocatalytic photodegradation of xanthate over C, N, S-tridoped TiO2 nanotubes under visible light irradiation

C, N, S-tridoped TiO₂ nanotubes were synthesized via hydrothermal synthesis and post-treatment, and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectra (XPS), the Brunauer-Emmett-Teller method (BET), and UV-vis diffuse reflectance spectroscopy (DRS). The UV-diffuse reflectance spectra of all the C, N, S-tridoped TiO₂ nanotubes greatly extended the absorption edge to the visible light region, and the absorbance in the visible region increased with increasing molar ratio of thiourea to Ti (R), which could be attributed to C, N, S-tridoping in the form of cation C-doping, interstitial N-doping, cation S-doping, and adsorbed ions’ states. The photocatalytic activity of C, N, S-tridoped TiO₂ nanotubes was evaluated by photocatalytic photodegradation of potassium ethyl xanthate (KEX) under visible light irradiation. It was found that the photocatalytic activity of the prepared samples increased with increasing molar ratio of thiourea to Ti (R). At R=6, the photocatalytic activity of the tridoped sample TNTS-6 reached a maximum value. With further increase in R, photocatalytic activity of the sample decreased, which could be attributed to the high visible light activity resulting from the balance between visible light absorption and recombination of electron/hole pairs.     

Hydrothermal synthesis of well-dispersed ultrafine N-doped TiO2 nanoparticles with enhanced photocatalytic activity under visible light

Ultrafine nitrogen-doped TiO₂ nanoparticles with narrow particle size distribution, good dispersion, and high surface area were synthesized in the presence of urea and PEG-4000 via a hydrothermal procedure. TEM observation, N₂ adsorption, XRD, UV-vis spectroscopy, the Raman spectroscopy and XPS analysis were conducted to characterize the synthesized TiO₂ particles. The synthesized TiO₂ particles were a mixture of 49.5% anatase and 50.5% rutile with a size of around 5 nm. The photocatalytic activities were tested in the degradation of an aqueous solution of a reactive Brilliant Blue KN-R under both UV and visible light. The synthesized TiO₂ particles showed much higher photocatalytic activity than a commercial P25 TiO₂ powder under both UV and visible light irradiations. The high performance is associated to N doping, the reduced particle size, good dispersion, high surface area, and a quantum size effect.     

Transparent nano composite PVA–TiO2 and PMMA–TiO2 thin films: Optical and dielectric properties

Transparent nano composite PVA–TiO₂ and PMMA–TiO₂ thin films were prepared by an easy and cost effective dip coating method. Al/PVA–TiO₂/Al and Al/PMMA–TiO₂/Al sandwich structures were prepared to study the dielectric behavior. The presence of metal–oxide (Ti–O) bond in the prepared films was confirmed by Fourier transform infrared spectroscopy. X-ray diffraction pattern indicated that the prepared films were predominantly amorphous in nature. Scanning electron micrographs showed cluster of TiO₂ nanoparticles distributed over the film surface and also there were no cracks and pin holes on the surface. The transmittance of the films was above 80% in the visible region and the optical band gap was estimated to be about 3.77 eV and 3.78 eV respectively for PVA–TiO₂ and PMMA–TiO₂ films by using Tauc's plot. The determined refractive index (n) values were between 1.6 and 2.3. High value of dielectric constant (?′ = 24.6 and ?′ = 26.8) was obtained for the prepared composite films. The conduction in the composite films was found to be due to electrons. The observed amorphous structure, good optical properties and dielectric behavior of the prepared nano composite thin films indicated that these films could be used in opto-electronic devices and in thin film transistors.