Co-emission of UV, violet and green photoluminescence of ZnO/TiO2 thin film

ZnO/TiO₂ thin films were fabricated on quartz glass substrates by E-beam evaporation. The structural and optical properties were investigated by X-ray diffraction (XRD), Raman spectra, optical transmittance and photoluminescence. XRD analysis indicates that the TiO₂ buffer layer can increase the preferential orientation along the (002) plane of the ZnO film. PL measurements suggest that co-emission of strong UV peak at 378 nm, violet peak at 423 nm and weak green luminescence at 544 nm is observed in the ZnO/TiO₂ thin film. The violet luminescence emission at 423 nm is attributed to the interface trap in the ZnO film grain boundaries.     

Optical properties of TiO2 thin films deposited on polycarbonate by ion beam assisted evaporation

TiO₂ thin films were deposited on polycarbonate (PC) substrate by ion beam assisted evaporation. The grain size increased with the ion anode voltage and film thickness. The TiO₂ thin films had an amorphous structure. Moiré deflectometry was used to measure the nonlinear refractive indices of TiO₂ thin films on PC substrates. The nonlinear refractive index was measured to be of the order of 10^− 8 cm² W^− 1 and a change in refractive index was of the order of 10^− 5. Dense TiO₂ films exhibited high linear refractive indices, red-shift of the optical absorbance, and absorbance in the near-IR region.     

Optical properties of TiO2 thin films after Ag ion implantation

Metal plasma ion implantation has being successfully developed for improving the electronic and optical properties of semiconductor materials. Prior to deposition, a TiO₂ colloidal suspension was synthesized by microwave-induced thermal hydrolysis of the titanium tetrachloride aqueous solution. The TiO₂ thin film was optimized to obtain a high-purity crystalline anatase phase by calcinations at 550 °C. The TiO₂ coating was uniform without aggregation, which provided good photo conversion efficiency. Ag ion implantation into the as-calcined TiO₂ thin films was conducted with 1 × 10¹⁵ ~ 1 × 10¹⁶ ions/cm² at 40 keV. The peak position and intensity of the photoluminescence and UV-Vis absorption spectra are quite sensitive to Ag doping. The optical characterization showed a shift in optical absorption wavelength towards infrared ray side, which was correlated with the structure variation of the Ag⁺ implanted TiO₂. Due to the strong capability of forming compounds between the energetic silver ions and TiO₂, the photoluminescence emission and UV-Vis absorption efficiencies were improved.     

Low-temperature hydrothermal synthesis of flower-like ZnO microstructure and nanorod array on nanoporous TiO2 film

A novel ZnO architecture, with flower-like microstructure on the top layer and nanorod arrays on the bottom layer, was hydrothermally synthesized on the Fluorine-doped SnO₂ (FTO) conducting glass pre-coated with nanoporous TiO₂ film. The as-prepared architecture was characterized with Field-emission scanning electron microscopy (FE-SEM) and X-ray diffractometer (XRD). Dye-sensitized solar cell studies showed that the power conversion efficiency (η) was 1.26% for this novel ZnO architecture-covered TiO₂ electrode.     

Preparation of anatase TiO2 thin films by vacuum arc plasma evaporation

Anatase titanium dioxide (TiO₂) thin films with high photocatalytic activity have been prepared with deposition rates as high as 16 nm/min by a newly developed vacuum arc plasma evaporation (VAPE) method using sintered TiO₂ pellets as the source material. Highly transparent TiO₂ thin films prepared at substrate temperatures from room temperature to 400 °C exhibited photocatalytic activity, regardless whether oxygen (O₂) gas was introduced during the VAPE deposition. The highest photocatalytic activity and photo-induced hydrophilicity were obtained in anatase TiO₂ thin films prepared at 300 °C, which correlated to the best crystallinity of the films, as evidenced from X-ray diffraction. In addition, a transparent and conductive anatase TiO₂ thin film with a resistivity of 2.6 × 10^− 1 Ω cm was prepared at a substrate temperature of 400 °C without the introduction of O₂ gas.     

Anomalous phase formation during annealing of La2O3 thin films deposited by ion beam assisted electron beam evaporation

The fifty seven nm thick La₂O₃ thin films were deposited on Si (100) substrates. After deposition, the amorphones thin films, were amorphous, were annealed at 750 and 900 °C for 1 h. It was found that their amorphous structure had been crystallized to hexagonal and cubic structures, respectively. The phase formation of the La₂O₃ thin films was anomalous at higher annealing temperatures. The theory of heterogeneous nucleation was used to interpret the anomalous phase formation of La₂O₃ films. To investigate the effects of the phase structure on these properties, Refractive indexes and dielectric constants of different structures of La₂O₃ films were measured.     

Cr-doped TiO2 thin films deposited by RF-sputtering

Cr-doped TiO₂ thin films with different band gaps were prepared. Higher Cr doping was beneficial to the formation of the rutile-TiO₂ phase over the anatase-TiO₂ phase. A 4.8% Cr-doped thin film indicated a band gap of 2.95 eV, which was lower than the band gap of the rutile-TiO₂. Cr doping was accompanied by the formation of not only the rutile-TiO₂ phase but also the Cr₂O₃ phase, lead to the degradation of the hydrophilicity. The TiO₂ thin films with the mixed phase were not desirable to improve the hydrophilicity.     

Photo-fixation of SO2 in nanocrystalline TiO2 films prepared by reactive DC magnetron sputtering

We report on photo-fixation of SO₂ onto nanostructured TiO₂ thin films prepared by reactive DC magnetron sputtering. The films were exposed to 50 ppm SO₂ gas mixed in synthetic air and illuminated with UV light at 298 and 473 K. The evolution of the adsorbed SO_x species was monitored by in situ Fourier transform infrared specular reflection spectroscopy. Significant photo-fixation occurred only in the presence of UV illumination. The SO₂ uptake was dramatically enhanced at elevated temperatures and then produced strongly bonded surface-coordinated SO_x complexes. The total SO_x uptake is consistent with Langmuir adsorption kinetics. The sulfur doping at saturation was estimated from X-ray photoelectron spectroscopy to be ~ 2.2 at.% at 473 K. These films were pale yellowish and had an optical absorption coefficient being ~ 3 times higher than in undoped film. The S-doped films exhibit interesting oleophobic properties, exemplified by the poor adherence of stearic acid. Our results suggest a new method for sulfur doping of TiO₂ to achieve combined anti-grease and photocatalytic properties.     

Structural and photocatalytic properties of TiO2/SiOx/TiOx multi-layer prepared by electron-beam evaporation method

TiO₂/SiO_x/TiO_x multi-layers on quartz glass were prepared by electron-beam evaporation method and their structural and photocatalytic properties were investigated. The photocatalytic activity of the TiO₂/SiO_x/TiO_x multi-layer was evaluated by the photodecomposition of methylene blue in aqueous solution. As the thickness of the SiO_x inter-layer increased, the surface roughness of the TiO₂/SiO_x/TiO_x multi-layer increased but the anatase crystallite size decreased. The TiO₂/SiO_x(80 nm)/TiO_x multi-layer exhibited excellent photocatalytic activity resulting from higher surface roughness and more trap levels in the SiO_x(80 nm) inter-layer.     

Photocatalytic properties of Cr-doped TiO2 films prepared by oxygen cluster ion beam assisted deposition

We prepared Cr-doped titanium dioxide (TiO₂) films by oxygen (O₂) cluster ion beam assisted deposition method, and investigated photocatalytic properties of the films as well as crystallographic property, optical property and surface morphology. The films prepared at a substrate temperature below 200 °C were found to be amorphous from the X-ray diffraction measurement. For the substrate temperatures such as 300 °C and 400 °C, the films exhibited rutile and/or anatase structures. The film surface measured by the atomic force microscope (AFM) was smooth at an atomic level. Furthermore, the optical band gap decreased with increase of Cr-composition, and it was approximately 3.3 eV for the non-doped films, 3.2 eV for the 1% Cr-doped films and 3.1 eV for the 10% Cr-doped films, respectively. With regard to the photocatalytic properties of the Cr-doped TiO₂ films, we measured the change of contact angle as well as the photocatalytic degradation of methylene blue by the UV light irradiation. Compared with the non-doped films, the 1% Cr-doped films prepared at a substrate temperature of 400 °C showed high degradation efficiency. In addition, the contact angle of the 1% Cr-doped films with an initial value of 60° decreased to 10° by the UV light irradiation for 20 min, and the films exhibited the predominant properties of photocatalytic hydrophilicity even for the UV light irradiation with longer wavelengths.     

Superhydrophilic anatase TiO2 film with the micro- and nanometer-scale hierarchical surface structure

Nanosized anatase TiO₂ film on the ITO glass has been fabricated via spin coat process, with sodium dodecylbenzenesulfonate modified TiO₂ nanoparticles, which is synthesized by a sol-hydrothermal method, and also characterized mainly by means of field emission scanning electron microscopy (FESEM). The results show that the as-prepared anatase TiO₂ film exhibits superhydrophilic characteristic although it is not exposed to ultraviolet irradiation. The high roughness resulting from hierarchical surface structure is responsible for its superhydrophilicity. This work would provide a new route to fabricate newly nanostructured semiconductor films.     

Study of optical and structural properties of Cu2ZnSnS4 thin films

Cu₂ZnSnS₄ is a promising semiconductor to be used as absorber in thin film solar cells. In this work, we investigated optical and structural properties of Cu₂ZnSnS₄ thin films grown by sulphurization of metallic precursors deposited on soda lime glass substrates. The crystalline phases were studied by X-ray diffraction measurements showing the presence of only the Cu₂ZnSnS₄ phase. The studied films were copper poor and zinc rich as shown by inductively coupled plasma mass spectroscopy. Scanning electron microscopy revealed a good crystallinity and compactness. An absorption coefficient varying between 3 and 4 × 10⁴cm^− 1 was measured in the energy range between 1.75 and 3.5 eV. The band gap energy was estimated in 1.51 eV. Photoluminescence spectroscopy showed an asymmetric broad band emission. The dependence of this emission on the excitation power and temperature was investigated and compared to the predictions of the donor-acceptor-type transitions and radiative recombinations in the model of potential fluctuations. Experimental evidence was found to ascribe the observed emission to radiative transitions involving tail states created by potential fluctuations.     

Structural, thermal and optical characterization of TiO2:ZrO2 thin films prepared by sol-gel method

We have studied the structural and optical properties of thin films of TiO₂, doped with 5% ZrO₂ and deposited on glass substrate (by the sol-gel method). The dip-coated thin films have been examined at different annealing temperatures (350 to 450 °C) and for various layer thicknesses (63-286 nm). Refractive index and porosity were calculated from the measured transmittance spectrum. The values of the index of refraction are in the range of 1.62-2.29 and the porosity is in the range of 0.21-0.70. The coefficient of transmission varies from 50 to 90%. In the case of the powder of TiO₂, doped with 5% ZrO₂, and aged for 3 months in ambient temperature, we have noticed the formation of the anatase phase (tetragonal structure with 14.8 nm grains). However, the undoped TiO₂ exhibits an amorphous phase. After heat treatments of thin films, titanium oxide starts to crystallize at the annealing temperature 350 °C. The obtained structures are anatase and brookite. The calculated grain size, depending on the annealing temperature and the layer thickness, is in the range (8.58-20.56 nm).     

Comparison of photostability, optical and structural properties of TiO2/conjugated polymer hybrid composites prepared via different methods

In this work, we have synthesized high quality TiO₂ nanocrystallites by sol-gel method (TiO₂ white (w)) and compared its properties with the ones synthesized by the simple hydrolysis method in aqueous solution (TiO₂ transparent (t)). The TiO₂/MEH-PPV nanocomposites are formed mainly by two ways: (i) Prepared in the form of the colloidal solution by adding the known concentration of the TiO₂ in MEH-PPV and then sonicate it well; (ii) In the thin film form by depositing the above solution over a glass substrate by spin coating. The properties of the resulting dispersions could be tailored by varying the composition and concentration of TiO₂ nanoparticles in CP's. The TiO₂ nanoparticles prepared by both methods show anatase character of TiO₂ as elucidated by X-ray diffraction (XRD) studies. Transmission electron microscopic (TEM) studies reveal that the transparent colloidal suspension of TiO₂ exhibits agglomeration of TiO₂ nanoparticles (size ~ 150-300 nm) and this trend is maintained in the MEH-PPV matrix for TiO₂/MEH-PPV composites as well. However, the composite obtained by mixing MEH-PPV with sol-gel prepared TiO₂(w) shows uniform nanoscale dispersion of TiO₂ (size ~ 20 nm) in MEH-PPV matrix. The UV-VIS absorption, photoluminescence (PL) and lifetime studies confirm the presence of dynamic quenching effect indicating efficient photoinduced charge transfer in TiO₂/MEH-PPV hybrid composites particularly with white TiO₂. It is conjectured that the devices containing TiO₂/MEH-PPV composites for TiO₂ prepared by the sol-gel method should lead to significant improvement in the photovoltaic performance of TiO₂/MEH-PPV hybrid solar cells.     

Nanocrystalline anatase TiO2 prepared via a facile low temperature route

Nanocrystalline anatase TiO₂ was prepared by a facile sol-gel route at a temperature of 65 °C under mild conditions. Tetrabutyl titanate was used as a titanium precursor, glacial acetic acid was used as an inhibitor, and anhydrous ethanol was used as a solvent. XRD, TEM, FT-IR and XPS spectra were applied to characterize the crystal phase, microstructure, and other physicochemical properties of the nanoanatase TiO₂. The results showed that as prepared ellipse-shaped anatase TiO₂ with an average diameter of 7 nm, which is rich in surface hydroxyl groups, was found to exhibit high dispersibility.     

Optical and electrical properties of TiOx thin films deposited by electron beam evaporation

The TiO_x thin films were prepared by electron beam evaporation using TiO as the starting material. The effect of the annealing temperature on the optical and electrical properties was investigated. The spectra of X-ray photoelectron spectroscopy reveal that Ti in the films mainly exist in the forms of Ti²⁺ and Ti³⁺ below 400 °C 24 h annealing. The charge transfer between different titanium ion contribute greatly to the color, absorption, and electrical resistance of the films.     

TiO2-SnO2 system for gas sensing—Photodegradation of organic contaminants

Catalytic photodegradation of organic contaminants by means of UV light has been demonstrated for gas sensors based on composites of TiO₂-SnO₂. Thin film resistive-type gas sensors of TiO₂-SnO₂ have been deposited at 350 °C by RF sputtering from a Ti-SnO₂ target with varying surface ratio of SnO₂/Ti. Photodegradation experiments of bromothymol blue by UV light have been performed by means of the optical spectrophotometry over the wavelength range extending from 300 nm to 600 nm. The influence of the UV illumination on the sensor response to 100-20,000 ppm of H₂ has been investigated in situ on motor oil contaminated sensors. It has been found that sequential exposures to UV light lead to a partial recovery of the sensor signal to hydrogen.     

Nanostructured TiO2 — morphological and structural changes

Chemical modification of titanium to form TiO₂ is being extensively pursued. We compare the influence of acid pickling and post processing on the crystallinity and morphology of TiO₂ grown by H₂O₂ oxidation. Subsequent oxidation using two concentrations of H₂O₂ (15% and 30% by mass) indicates a variation in the fine surface morphology, apparent at low magnifications. No discernable difference in the quality of TiO₂ that was produced when evaluated by SEM, Raman or XRD (glancing angle and θ:2θ) could be detected between the samples oxidised in different H₂O₂ concentrations. The photoactivity of TiO₂ produced from ultra thin Ti films was confirmed by the photocatalytic reduction of Ag⁺ cations to Ag⁰.     

Effect of TiO2-SiO2 sol-gel coating on the cpTi-porcelain bond strength

The effects of TiO₂-SiO₂ sol-gel coating with different firing temperatures (300 °C, 500 °C, and 750 °C) on the cpTi-porcelain bond strength were investigated in the present study. Prior to applying the low-fusing dental titanium porcelain, the phase, surface morphology, surface roughness and static water contact angle of the intermediate layer were evaluated. The cpTi-porcelain bond strength was measured using the three-point flexure test according to ISO 9693 standard. Statistical analyses were made using one-way ANOVA and Dunnett-t test. Significantly higher bond strength of TiO₂-SiO₂/750 °C (specimens coated with TiO₂-SiO₂ sol-gel coating and fired at 750 °C for 1 h) when compared to the control group was observed (p < 0.05). No rutile phase was found in all the tested specimens coated with TiO₂-SiO₂ sol-gel coating. The surface morphology of the intermediate layer was apparently different with different firing temperatures. It was found that the static water contact angle of TiO₂-SiO₂/750 °C significantly decreased (p < 0.05). However, no markedly different R_a of TiO₂-SiO₂/500 °C and TiO₂-SiO₂/750 °C in comparison to that of the control group was observed (p > 0.05). The results show that the TiO₂-SiO₂ sol-gel coating fired at 750 °C for 1 h can notably improve the cpTi-porcelain bond strength and may be suitable for clinical use.     

Photocatalytic performance of very thin TiO2/SnO2 stacked-film prepared by magnetron sputtering

TiO₂/SnO₂ stacked-layers are synthesized by reactive sputter deposition on the glass substrate. Very thin TiO₂/SnO₂ bilayer-photocatalysts exhibited a very high photocatalytic activity for a degradation of gaseous acetaldehyde. Both the control of an electronic structure of TiO₂ overlayer in the near-surface region and the interfacial separation of photogenerated electrons/holes in the TiO₂/SnO₂ stacked-layer are keys to improve the photocatalytic performance.