Enhanced photoelectrochemical properties of TiO2 nanorod arrays decorated with CdS nanoparticles

TiO₂ nanorod arrays (TiO₂ NRAs) sensitized with CdS nanoparticles were fabricated via successive ion layer adsorption and reaction (SILAR), and TiO₂ NRAs were obtained by oxidizing Ti NRAs obtained through oblique angle deposition. The TiO₂ NRAs decorated with CdS nanoparticles exhibited excellent photoelectrochemical and photocatalytic properties under visible light, and the one decorated with 20 SILAR cycles CdS nanoparticles shows the best performance. This can be attributed to the enhanced separation of electrons and holes by forming heterojunctions of CdS nanoparticles and TiO₂ NRAs. This provides a promising way to fabricate the material for solar energy conversion and wastewater degradation.     

TiO2 inverse opal based CdS/CdSe quantum dot co-sensitized solar cells

CdS and CdSe quantum dots were introduced as co-sensitizers into TiO₂ inverse opal quantum dot sensitized solar cells. Herein, the three-dimensionally ordered porous TiO₂ inverse opal film leads to a better infiltration of both sensitizers and hole transporting material, and the smaller surface area of TiO₂ inverse opal film is effectively offset by the incorporating of co-sensitization. It was found that the presence of CdS/CdSe co-sensitizers provides enhanced light absorption, and leads to a lower recombination rate of the electrons due to the stepwise structure of band edge in TiO₂/CdS/CdSe, which resulted in the observed enhanced photocurrent and energy conversion efficiency of the solar cells. A cell efficiency of 1.01 % has been attained.     

Chemically deposited TiO2/CdS bilayer system for photoelectrochemical properties

In the present investigation, TiO₂, CdS and TiO₂/CdS bilayer system have been deposited on the fluorine doped tin oxide (FTO) coated glass substrate by chemical methods. Nanograined TiO₂ was deposited on FTO coated glass substrates by successive ionic layers adsorption and reaction (SILAR) method. Chemical bath deposition (CBD) method was employed to deposit CdS thin film on pre-deposited TiO₂ film. A further study has been made for structural, surface morphological, optical and photoelectrochemical (PEC) properties of FTO/TiO₂, FTO/CdS and FTO/TiO₂/CdS bilayers system. PEC behaviour of FTO/TiO₂/CdS bilayers was studied and compared with FTO/CdS single system. FTO/TiO₂/CdS bilayers system showed improved performance of PEC properties over individual FTO/CdS thin films.     

Double-sided transparent electrodes of TiO2 nanotube arrays for highly efficient CdS quantum dot-sensitized photoelectrodes

A novel double-sided CdS quantum dots-sensitized TiO₂ nanotube (TNT)/ITO photoelectrode is fabricated to improve the energy conversion efficiencies of quantum dots-sensitized solar cells (QDSCs). Our experimental results show that the double-sided CdS quantum dots-sensitized TNT/ITO photoelectrodes show enhanced light absorption. As a consequence, the photoelectrochemical response of the CdS/TNT/ITO photoelectrode is much improved compared with single-sided CdS sensitized TNT arrays on Ti substrate (i.e., CdS/TNT/Ti photoelectrode). An optimum conversion efficiency of 7.5 % is achieved by the double-sided CdS(15)/TNT/ITO photoelectrode, which is an enhancement of about 120 % when compared with the single-sided CdS/TNT/Ti photoelectrode. Our results demonstrate that the energy conversion efficiencies of QDSCs can be improved by designing a new photoelectrode structure.     

Chemical synthesis of CdS onto TiO2 nanorods for quantum dot sensitized solar cells

A quantum dot sensitized solar cell (QDSSC) is fabricated using hydrothermally grown TiO₂ nanorods and successive ionic layer adsorption and reaction (SILAR) deposited CdS. Surface morphology of the TiO₂ films coated with different SILAR cycles of CdS is examined by Scanning Electron Microscopy which revealed aggregated CdS QDs coverage grow on increasing onto the TiO₂ nanorods with respect to cycle number. Under AM 1.5G illumination, we found the TiO₂/CdS QDSSC photoelectrode shows a power conversion efficiency of 1.75%, in an aqueous polysulfide electrolyte with short-circuit photocurrent density of 4.04 mA/cm² which is higher than that of a bare TiO₂ nanorods array.     

CdS quantum dot sensitized nanocrystalline Gd-doped TiO2 thin films for photoelectrochemical solar cells

CdS quantum dot sensitized Gd-doped TiO₂ nanocrystalline thin films have been prepared by chemical method. X-ray diffraction analysis reveals that TiO₂ and Gd-doped TiO₂ nanocrystalline thin films are of anatase phase. The absorption spectra revealed that the absorption edge of CdS quantum dot sensitized Gd-doped TiO₂ thin films shifted towards longer wavelength side (red shift) when compared to that of CdS quantum dot sensitized TiO₂ films. CdS quantum dots with a size of 5 nm have been deposited onto Gd-doped TiO₂ film surface by successive ionic layer adsorption and reaction method and the assembly of CdS quantum dot with Gd-doped TiO₂ has been used as photo-electrode in quantum dot sensitized solar cells. CdS quantum dot sensitized Gd-doped TiO₂ based solar cell exhibited a power conversion efficiency of 1.18 %, which is higher than that of CdS quantum dot sensitized TiO₂ (0.91 %).     

Photoelectrochemical performance of CdS nanorods grafted vertically aligned TiO2 nanorods

In this study, TiO₂ nanorods/CdS nanorods composite samples were successfully synthesized by grafting CdS nanorods on vertically aligned TiO₂ nanorods. A two-step hydrothermal method was used to prepare the samples. Some properties of the samples, such as morphological, structural, and optical properties were characterized by energy-dispersive X-ray detection, field emission scanning electron microscopy, X-ray diffraction, Raman spectroscopy, and ultraviolet-visible spectroscopy. Moreover, photoelectrochemical properties were studied via current-voltage and photocurrent spectrum measurements. The results showed that CdS nanorods grafted on top of TiO₂ nanorods like a lawn. The amount grafted as well as the diameter and crystallinity of CdS nanorods increased first and then decreased as the grafting time increased, due to Ostwald ripening. Under the back-side illumination, the composite film with 2 h grafting time exhibited the highest photocurrent density which was almost twice of that of the pure TiO₂ nanorods.     

Enhanced photovoltaic performance of solar cell based on front-side illuminated CdSe/CdS double-sensitized TiO2 nanotube arrays electrode

Free-standing TiO₂ nanotube (NT) arrays have been prepared by a two-step anodization method. These translucent TiO₂ NT arrays can be transferred to the fluorine-doped tin oxide glass substrates to form front-side illuminated TiO₂ NT electrodes. The TiO₂ NT electrodes were double-sensitized by CdSe/CdS quantum dots (QDs) through successive ionic layer adsorption and reaction (SILAR) process. The absorption range of the TiO₂ NT electrode was extended from ~380 to 700 nm after sensitization with CdSe/CdS QDs. The SILAR cycles were investigated to find out the best combination of CdS and CdSe QDs for photovoltaic performance. The power conversion efficiency of 2.42 % was achieved by the CdSe(10)/CdS(8)/TiO₂ NT solar cell. A further improved efficiency of 2.57 % was obtained with two cycles of ZnS overlayer on the CdSe(10)/CdS(8)/TiO₂ NT electrode, which is 45.19 % higher than that of back-side illuminated solar cell. Furthermore, the ZnS(2)/CdSe(10)/CdS(8)/TiO₂ NT solar cell possesses a higher stability than CdSe(10)/CdS(8)/TiO₂ NT solar cell during the same period. The better photovoltaic performance of the ZnS(2)/CdSe(10)/CdS(8)/TiO₂ NT solar cell has demonstrated the promising value to design quantum dots-sensitized solar cells with double-sensitized front-side illuminated TiO₂ NT arrays strategy.     

Synthesis of TiO2 nanotubes coupled with CdS nanoparticles and production of hydrogen by photocatalytic water decomposition

The CdS/TiO₂NTs composite was prepared by a simple two-step chemical solution routes to directly transfer trititanate nanotubes to TiO₂NTs and simultaneously coupled with CdS nanoparticles. The results of XRD, TEM, Diffuse reflectance UV-Visible absorption spectra revealed that the CdS nanoparticles were homogeneously embedded on the surface of TiO₂NTs and the absorption spectrum of TiO₂NTs was extended to visible region. The activity of hydrogen production by photocatalytic water decomposition for the CdS/TiO₂NTs composite was examined under visible light irradiation (λ > 400 nm) and the quantity of H₂ evolution was ca. 1708 μL/g for 6 h.     

TiO2 nanowires sensitized with CdS quantum dots and the surface photovoltage properties

TiO₂ nanowires prepared by thermal annealing of anodized Ti foil were sensitized with CdS quantum dots (QDs) via chemical bath deposition (CBD). Microstructural characterizations by SEM, TEM and XRD show that the CdS nanocrystals with the cubic structure have intimate contact to the TiO₂ nanowires. The amount of CdS QDs can be controlled by varying the CBD cycles. The experiment results demonstrate that the surface photovoltage (SPV) response intensity was significantly enhanced and the surface photovoltage response region was also expanded obviously for the TiO₂ NWs sensitized by CdS QDs.     

Sonochemical preparation of TiO2 nanoparticles

TiO₂ nanoparticles with mean diameter of about 20 nm, average crystallite size of 15 nm and BET specific surface area of 78.88 m²/g, were prepared through a simple sonochemical method and initial treatment in 10 M NaOH aqueous solution. XRD results exhibited that the obtained nanoparticles composed of pure rutile phase. During the initial treatment with NaOH aqueous solution, the Ti–O–Ti bonds in the TiO₆ octahedra structure of the raw material were broken, and new octahedras formed after ultrasonic irradiation. It is supposed that edge sharing was favored during ultrasonic treatment, leading to formation of the rutile nanoparticles.     

Microstructure Evolution and Isothermal Compaction in TiO2-Al-C Combustion Reaction

Combustion reaction in the TiO₂-Al-C system was investigated by the combustion wave freezing technique with a wedge-shaped copper-made quenching block. The combustion reaction was a combined process in which the aluminothermic reduction of TiO₂ (3TiO₂ + 4Al 2Al₂O₃ + 3Ti) and TiC formation reaction (Ti + C TiC) occur in series. First, the aluminothermic reduction was activated by wet spreading of molten Al into interspaces between TiO₂ particles to produce rounded Al₂O₃ grains embedded in the Ti-rich liquid phase. In the later combustion stage, the Ti-rich phase reacted with the reactant C to produce TiC grains in the Ti-rich liquid phase. The three-dimensionally interconnected Al₂O₃ structure typically shown in this system mainly originated from interconnection between the rounded Al₂O₃ grains due to the high combustion temperature from the high exothermic TiC formation reaction. With decreasing the combustion temperature and controlling the C and TiC content, the interconnected Al₂O₃ structure changed to isolated. The isolated Al₂O₃ structure showed superior isothermal compaction behavior to the interconnected. Finally, it is suggested that the microstructure of combustion reaction should be one of the important factors in the SHS compaction process.     

Synthesis and characterization of CdS doped TiO2 nanocrystalline powder: A spectroscopic study

This report aimed to study the effect of CdS doping in TiO₂ on the phase transformation of TiO₂ from anatase to rutile using X-ray diffraction (XRD) and Raman spectroscopy. CdS-doped TiO₂ nanocomposites have been prepared and characterized using Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM). We have observed that contrary to bare TiO₂, phase transformation of TiO₂ from anatase to rutile is hindered when doped with CdS at high temperature. Raman spectroscopy is found to be more sensitive for detection of the surface of TiO₂ as compared to XRD.     

Enhanced photocatalytic activity of TiO2 nanofibers and their flexible composite films: Decomposition of organic dyes and efficient H2 generation from ethanol-water mixtures

TiO₂ nanofibers decorated with Pt and Pd nanoparticles have been synthesized and studied in various photocatalytic processes. Excellent photocatalytic behavior in the decomposition of organic dyes in water, degradation of organic stains on the surface of flexible freestanding cellulose/catalyst composite films and in generation of hydrogen from ethanol using both suspended and immobilized catalysts are demonstrated. The performance of the nanofiber-based TiO₂ materials is competitive with??and in some cases outperforms??their conventional nanoparticle-based counterparts. In all cases, Pd-decorated TiO₂ nanoparticles and nanofibers proved to be more efficient than their Pt-based counterparts, which could be explained on the basis of the formation of nano-sized Schottky interfaces at the contacts between TiO₂ and metal nanoparticles. The feasibility of forming cellulose/catalyst composites provides a novel way of utilizing photocatalyst materials in large-area coatings and freestanding films.      

Titanium local environment and electrical conductivity of TiO2-doped stabilized tetragonal zirconia

Solid state reactions in the ZrO₂-Y₂O₃-TiO₂system have been studied and the solid solubility limit of TiO₂ in yttria stabilized tetragonal zirconia Y-TZP has been stablished. Structural characterization was carried out by XRD studies, and the changes in local structures with increasing TiO₂ in yttria stabilized tetragonal zirconia was analyzed for the first time by EXAFS and XANES measurements. The XANES results indicate a displacement of Ti ions from the center of symmetry with increasing titania content leading to assume a non randomly substitution of Ti on Zr sites in the tetragonal zirconia lattice. From the Ti-O and Ti-Ti measured distances, it has been assumed that the found electrical conductivity decrease with increasing titania content was due to both a trapping of the oxygen ion vacancies at Ti ions (Ti_Zr Vö) and the formation of more complex associations like (Ti_Zr Vö Ti_Zr Vö), which giving rise to a reduction in the global concentration of moving oxygen vacancies.     

Fabrication of quantum dot-sensitized solar cells with multilayer TiO2/PbS(X)/CdS/CdSe/ZnS/SiO2 photoanode and optimization of the PbS nanocrystalline layer

In this work, two multilayer photoanode structures of TiO₂/PbS(X)/CdS/ZnS/SiO₂ and TiO₂/PbS(X)/CdS/CdSe/ZnS/SiO₂ were fabricated and applied in quantum dot-sensitized solar cells (QDSCs). Then, the effect of PbS QDs layer on the photovoltaic performance of corresponding cells was investigated. The sensitization was carried out by PbS and CdS QDs layers deposited on TiO₂ scaffold through successive ionic layer adsorption and reaction (SILAR) method. The CdSe QDs film was also formed by a fast, modified chemical bath deposition (CBD) approach. Two passivating ZnS and SiO₂ layers were finally deposited by SILAR and CBD methods, respectively. It was shown that the reference cell with TiO₂/CdS/ZnS/SiO₂ photoanode demonstrated a power conversion efficiency (PCE) of 3.0%. This efficiency was increased to 4.0% for the QDSC with TiO₂/PbS(2)/CdS/ZnS/SiO₂ photoelectrode. This was due to the co-absorption of incident light by low-bandgap PbS nanocrystalline film and also the CdS QDs layer and well transport of the charge carriers. For the CdSe included QDSCs, the PbS-free reference cell represented a PCE of 4.1%. This efficiency was improved to 5.1% for the optimized cell with TiO₂/PbS(2)/CdS/CdSe/ZnS/SiO₂ photoelectrode. The maximized efficiency was enhanced about 25% and 70% compared to the PbS-free reference cells with and without the CdSe QDs layer.

     

In Situ Irradiated X‐Ray Photoelectron Spectroscopy Investigation on a Direct Z‐Scheme TiO2/CdS Composite Film Photocatalyst

Inspired by nature, artificial photosynthesis through the construction of direct Z‐scheme photocatalysts is extensively studied for sustainable solar fuel production due to the effectiveness in enhancing photoconversion efficiency. However, there is still a lack of thorough understanding and direct evidence for the direct Z‐scheme charge transfer in these photocatalysts. Herein, a recyclable direct Z‐scheme composite film composed of titanium dioxide and cadmium sulfide (TiO₂/CdS) is prepared for high‐efficiency photocatalytic carbon dioxide (CO₂) reduction. In situ irradiated X‐ray photoelectron spectroscopy (ISI‐XPS) confirms the direct Z‐scheme charge‐carrier migration pathway in the photocatalytic system. Furthermore, density functional theory simulation identifies the intrinsic cause for the formation of the direct Z‐scheme heterojunction between the TiO₂ and the CdS. Thanks to the significantly enhanced redox abilities of the charge carriers in the direct Z‐scheme system, the photocatalytic CO₂ reduction performance of the optimized TiO₂/CdS is 3.5, 5.4, and 6.3 times higher than that of CdS, TiO₂, and commercial TiO₂ (P25), respectively, in terms of methane production. This work is a valuable guideline in preparation of highly efficient recyclable nanocomposite for photoconversion applications.     

Nanostructured mesoporous Au/TiO2 for photocatalytic degradation of a textile dye: the effect of size similarity of the deposited Au with that of TiO2 pores

Mesoporous Au/TiO₂ nanocomposites with different Au particle size (7.3–11.8 nm) were synthesized via deposition–precipitation method. The synthesized nanocomposites have been characterized by XRD, TEM, XPS, DLS, ICP-OES, N₂ sorpometry, and UV–Vis spectroscopy. Au/TiO₂ showed higher quantum yield and greater photocatalytic efficiency compared to pure TiO₂ under both ultraviolet and sunlight illumination. The increase of the photocatalytic efficiency of TiO₂ upon deposition with gold nanoparticles, Au NPs, is due to the interface electron transfer from Au nanoparticles to TiO₂ under visible light illumination and from TiO₂ to Au nanoparticles under UV illumination. For the first time, the effect of Au particle sizes when it is very similar to the interparticles pores of TiO₂ has been investigated. The highest reaction rate (5.7 × 10^?2 min^?1) and degradation efficiency of Safranin-O (SO) dye (97 %) were observed when the deposited gold nanoparticles are the smallest among the studied samples (sAu/TiO₂). In spite of blocking a high percentage of the TiO₂ pores, the sAu/TiO₂ sample demonstrated a complete degradation of SO dye in 50 min which is more efficient than any other reported catalysts in the literature.     

A novel method for fabrication of CdS quantum dot-sensitized solar cells

In this report, a novel and facile in situ gas–solid reaction method has been developed for the deposition of CdS quantum-dots (QDs) on a mesoscopic TiO₂ film. In the approach, cadmium nitrate solution was first coated on mesoporous TiO₂ films, and subsequently transformed into CdS QDs (with size about 2–3 nm) by reaction with hydrogen sulfide (H₂S) gas generated in a closed container at room temperature. Different from the conventional solution techniques, this method offers new opportunities for rapid and facile deposition of CdS QD-coated TiO₂ films without the introduction of the by-products. With the CdS QDs-decorated TiO₂ active electrodes, the liquid and solid solar cells were fabricated with power conversion efficiencies (PCEs) of 1.90 and 0.80%, respectively.     

Photoelectrochemical properties of TiO<Subscript>2</Subscript>/CdS heterostructures

The photoelectrochemical properties of TiO₂, CdS, and TiO₂/CdS anodes have been studied. The results demonstrate that, under illumination, CdS anodes are subject to photocorrosion, and Cd²⁺ ions pass into solution. Corrosion-resistant films of TiO₂ prevent CdS photocorrosion, and the CdS/TiO₂ system exhibits good photosensitivity in the visible range.