Titanium Dioxide Thin Films Research Articles

Low-temperature stabilization of rutile in W-doped Titania thin films deposited by magnetron Co-Sputtering

Tungsten doped Titania thin films were sputtered on a silicon substrate by magnetron co-sputtering. The influence of tungsten on Vickers hardness and crystallographic changes was studied in films subjected to stepped annealing treatments. Rutile is the dominant phase with crystallite size ∼ 10 nm after 500 °C annealing. The films, doped with 1.79 % W, exhibit the highest hardness (20.88 GPa), a rutile-anatase mixture (80:20) and a preferential shift in crystallographic orientation from (101) to (110). The homogeneous distribution of tungsten in TiO2 stabilizes rutile at 500 °C, providing an innovative and simple strategy for its synthesis, thus expanding the options for substrate materials.

Demonstration of the Optical Isotropy of TiO2 Thin Films Prepared by the Sol-Gel Method.

Titanium dioxide (TiO2) thin films prepared by the sol-gel technique have been shown to be optically isotropic and, unlike the films obtained by competitive methods, do not exhibit measurable birefringence. A series of submicrometer-thin titanium dioxide films were prepared using the sol-gel technique and then thermally annealed at different temperatures. The samples were analyzed by spectroscopic ellipsometry using the Mueller matrix formalism, X-ray diffractometry and scanning electron microscopy. The conversion of amorphous titanium dioxide to polycrystalline anatase occurred at 400 °C or higher. Crystallites of a few percent of the film thickness were observed. Nevertheless, the crystallization process did not trigger the appearance of birefringence. These observations demonstrate that high-quality planar optical waveguides can be successfully fabricated on flexible substrates, in particular those composed of efficient polymers that can withstand the aforementioned temperatures.

Amorphous titanium oxide (aTiO2) thin films biofunctionalized with CAP-p15 induce mineralized-like differentiation of human oral mucosal stem cells (hOMSCs)

Insufficient osseointegration of titanium-based implants is a factor conditioning their long-term success. Therefore, different surface modifications, such as multifunctional oxide coatings, calcium phosphates, and the addition of molecules such as peptides, have been developed to improve the bioactivity of titanium-based biomaterials. In this work, we investigate the behavior of human oral mucosal stem cells (hOMSCs) cultured on amorphous titanium oxide (aTiO2), surfaces designed to simulate titanium (Ti) surfaces, biofunctionalized with a novel sequence derived from cementum attachment protein (CAP-p15), exploring its impact on guiding hOMSCs towards an osteogenic phenotype. We carried out cell attachment and viability assays. Next, hOMSCs differentiation was assessed by red alizarin stain, ALP activity, and western blot analysis by evaluating the expression of RUNX2, BSP, BMP2, and OCN at the protein level. Our results showed that functionalized surfaces with CAP-p15 (1 µg ml−1) displayed a synergistic effect increasing cell proliferation and cell attachment, ALP activity, and expression of osteogenic-related markers. These data demonstrate that CAP-p15 and its interaction with aTiO2 surfaces promote osteoblastic differentiation and enhanced mineralization of hOMSCs when compared to pristine samples. Therefore, CAP-p15 shows the potential to be used as a therapeutical molecule capable of inducing mineralized tissue regeneration onto titanium-based implants.

Simultaneous determination of the phase boundary thermal resistance and thermal conductivity in phase-separated TiO2 thin films

Phase boundaries, most often between crystalline and amorphous phases of a material, are ubiquitous lattice imperfections in thin films, particularly deposited by low temperature processes such as atomic layer deposition (ALD). Thermal resistances from these boundaries may impede phonon transport and reduce thermal conductivity. However, to date, there have been no reports on the direct measurement of the phase boundary thermal resistance, due in part to challenges associated with fabricating an atomically flat yet geometrically planar interface between different phases within a film. Here, we present a systematic study to simultaneously determine the phase boundary thermal resistance and thermal conductivity in a series of phase-separated titanium oxide (TiO2) thin films prepared via plasma-enhanced ALD (PEALD). A precise implementation of per-cycle plasma treatment enables extremely localized crystallization—i.e., plasma-assisted atomic layer annealing (ALA)—and the fabrication of crystalline/amorphous layered structures with their respective thicknesses systematically varied. Frequency-domain thermoreflectance measures the effective thermal conductivity of each film and its top and bottom interfaces, confirmed independently using time-domain thermoreflectance. We simultaneously solve a system of linear equations generated by applying a series resistor model to each film, yielding the phase boundary thermal resistance of 5.1 m2 K GW–1 between crystalline and amorphous TiO2, as well as the thermal conductivities of 5.1 and 2.1 W m–1 K–1 for crystalline and amorphous TiO2, respectively. The results suggest that the crystalline/amorphous phase boundary acts like a layer of crystalline (amorphous) TiO2 with equivalent thickness ∼26 (∼11) nm.

Properties of Ti films produced on atomically smooth GaAs substrates by magnetron sputtering

In this study, the morphology and crystallographic properties of thin titanium (Ti) films grown on atomically smooth gallium arsenide (GaAs) substrates are examined. The films were grown by direct current magnetron sputtering in an argon (Ar) flow. The surface is found to be atomically smooth with steps up to 0.1 nm in height and a morphology close to that of the Ti film substrate with nominal thicknesses of 5 and 10 nm. Increasing the film thickness to 60 nm leads to a noticeable surface reconstruction, associated with the formation of clusters up to 16 nm in height. As per X-ray diffraction studies, all films show a crystal structure of the α-Ti phase. In this case, an increase in the crystallite size from 7 to 20 nm and an increase in the film nominal thickness from 5 to 60 nm are also typical. Based on atomic force microscopy analysis, a change is observed in surface morphology. When the film thickness increases from 10 to 60 nm, clusters are formed on the Ti film surface, measuring 1 µm in diameter and 16 nm in height.

Study the Influence of Tin Oxide SnO2 Doping on the Optical and Structural Properties of Titanium Oxide TiO2

Titanium dioxide thin films, along with varying tin oxide ratios, were applied onto quartz substrates through pulsed laser deposition. The samples included pure TiO2 and doped versions ranging from 5% to 25%. The deposition parameters were kept constant at an energy level of 1000 mJ and a frequency of 6 Hz. Analysis via atomic force microscopy revealed that higher doping percentages correlated with increased surface roughness and grain diameter, indicating larger particle growth. Additionally, the absorption coefficient rose with higher doping ratios, peaking at 25% SnO2. This increase in absorption coefficient accompanied a decrease in the optical energy gap due to thicker film deposition, leading to higher absorbance and lower transmittance.

Assessing the Aging Effect on Ti/Au Bilayers for Transition-Edge Sensor (TES) Detectors.

Transition-edge sensor (TES) microcalorimeters are advanced cryogenic detectors that use a superconducting film for particle or photon detection. We are establishing a new production line for TES detectors to serve as cryogenic anticoincidence (i.e., veto) devices. These detectors are made with a superconducting bilayer of titanium (Ti) and gold (Au) thin films deposited via electron beam evaporation in a high vacuum condition on a monocrystalline silicon substrate. In this work, we report on the development of such sensors, aiming to achieve stable sensing performance despite the effects of aging. For this purpose, patterned and non-patterned Ti/Au bilayer samples with varying geometries and thicknesses were fabricated using microfabrication technology. To characterize the detectors, we present and discuss initial results from repeated resistance-temperature (R-T) measurements over time, conducted on different samples, thereby augmenting existing literature data. Additionally, we present a discussion of the sensor's degradation over time due to aging effects and test a potential remedy based on an easy annealing procedure. In our opinion, this work establishes the groundwork for our new TES detector production line.

Strong coupling in an asymmetric two-dimensional guided mode resonance metasurface structure and enhancement for optical third-harmonic generation

A two-dimensional guided mode resonance structure supports a transverse magnetic (TM) resonant mode in the direction of incident polarization and a transverse electric (TE) resonant mode in the direction perpendicular to the polarization. In this work, the coupling between the transverse magnetic and the transverse electric resonant modes in an asymmetric two-dimensional dielectric metasurface structure is investigated. The asymmetric structure consists of a two-dimensional square nanohole array etched in a titanium dioxide thin film on a transparent silica substrate. With finite difference time domain simulations, anti-crossing of the resonant spectra of the TM and TE modes is observed by adjusting the asymmetry of the structure. The anti-crossing indicates that the interaction between TM and TE resonant modes results in a strong coupling state. A coupled harmonic oscillator model is used to explain the strong coupling effect. The results of the coupled harmonic oscillator modeling agree well with the results of numerical simulations. Furthermore, it is shown that the strong coupling can significantly enhance the third harmonic generation intensity compared with the uncoupled TM and TE resonant modes.

Cobalt Ion-Modified Titanium Oxide Nanorods: A Promising Approach for High-Performance Electrochromic Application

The development of novel cathodic materials with tailored nanostructures is crucial for the advancement of electrochromic devices. In this study, we synthesized cobalt-doped titanium dioxide (Ti-Co) thin films using a facile hydrothermal method to investigate the effects of cobalt doping on their structural, morphological, and electrochromic properties. Comprehensive characterization techniques, including X-ray diffraction and Raman analysis, confirmed the highly crystalline nature of the Ti-Co thin films, with specific Raman bands indicating distinct modifications due to cobalt incorporation. The TiO2 nanorods, optimally doped with cobalt (TC-3), demonstrated enhanced charge transport and mobility, significantly improving the electrochromic performance. Among the various compositions studied, the TC-3 sample exhibited superior lithium-ion accommodation, achieving an optical modulation of 73.6% and a high coloration efficiency of 81.50 cm2/C. It also demonstrated excellent electrochromic stability, maintaining performance for up to 5000 s of coloring/bleaching cycles. These results confirm the beneficial impact of cobalt doping on the structural and functional properties of the host material. Furthermore, the practical effectiveness of the TC-3 thin film was validated through the fabrication of an electrochromic device, which showed efficient coloration and bleaching capabilities. This comprehensive research enhances the understanding and functionality of Ti-Co nanorod architectures, highlighting their promising potential for advanced electrochromic applications.

Characterization of the structure, morphology, and optical properties of titanium dioxide thin film deposited by spray pyrolysis technique for self-cleaning glass

Abstract The research in material science has actively pursued the creation of self-cleaning materials, especially for windows. Titanium dioxide (TiO2) is considered a promising substance for developing hydrophilic self-cleaning surfaces due to its photocatalytic activity. In this research, TiO2 nanoparticles were synthesized using TiCl3 as the precursor and co-precipitation as the experimental method in order to obtain anatase phase. The nanoparticles, then, was deposited by spray pyrolysis technique with different spraying time; 1, 2, 3, and 4 minutes and different types of TiO2 nanoparticles—synthesis and commercial—as the primary variations. TiO2 thin film was formed using ethyl cellulose as binder and isopropyl alcohol as solvent. The synthesized TiO2 nanoparticles and deposited thin film were, then, characterized using XRD, Maud software, UV-Visible Spectrophotometer, optical microscope, and SEM. The higher band gap energy value of TiO2 thin films was obtained with the average of 3.746 eV and 3.744 eV for TI(S) and TI(C), respectively, as a result of ethyl cellulose composition on the thin film. The thin film was categorized as hydrophilic.

Laser printing of certain pixels of graphene nanoribbons

A possibility of laser printing of graphene nanoribbon pixels while preserving the integrity of the structure and shape on the silicon substrate in accordance with the irradiated laser spot is demonstrated. To provide the transfer, a target consisting of a transparent sapphire plate and an absorbing thin titanium film (500 nm thick) coated with a film consisting of graphene nanoribbons is irradiated with a KrF excimer laser (λ=248 nm, τ=20 ns). Optimal conditions for laser irradiation are determined and a technique is developed for transferring a carbon nanomaterial from a growth nickel surface to a titanium film aimed at creating stronger bonds between the nanoribbons. Raman spectroscopy confirms the preservation of structural features of the synthesized atomically precise 7-atoms-wide graphene nanoribbons with an armchair edge during laser transfer.

Enhancement of electrochromic efficiency of TiO2 nanorods

In this study, the rutile TiO2 nanorods thin films were deposited via hydrothermal method on fluorine-doped tin oxide (FTO) substrate. To form a porous morphology layer, a thin film of amorphous titanium oxide (TiOx) was deposited on the TiO2 nanorods through sputtering at high pressure. The samples were annelid at 450ᵒC to transform the amorphous surface to anatase phase. Structural, optical, morphology and electrochemical properties of the samples were examined via X-ray diffraction (XRD), Raman scattering, UV–Vis NIR and photoluminescence (PL) spectroscopies, field-emission scanning electron microscopy (FE-SEM) and Potentiostat device respectively. The samples exhibited a large optical bandgap of 3.35–3.40 eV and high transparency of over 77 % at a wavelength of 555 nm. Raman analysis confirmed the formation of anatase phase on the rutile nanorods under thermal treatment. PL analysis indicated that the oxygen vacancies reached their maximum after sputtering, while the intensity of PL emission significantly increased after annealing. Investigation of the electrochromic properties revealed an increase in coloration efficiency from 2.6 C−1cm2 for bare nanorods to 10.0 C−1cm2 for nanorods after sputtering deposition, which decreased to 5.4 C−1cm2 after thermal treatment.

Structural and optical properties of highly Ag-doped TiO2 thin films prepared by flash thermal evaporation

The present study investigates the structural and optical properties of silver (Ag)-doped titanium dioxide (TiO2) thin films prepared via flash thermal evaporation using TiO2 and Ag powders mixture at various mass ratios. The crystallinity and surface morphology of the films were studied by varying the percentage of Ag content. Structural properties were characterized using X-ray diffraction (XRD), Raman spectroscopy, and scanning electron microscopy (SEM), while optical properties were assessed through optical transmission spectra analysis. Results indicate that Ag doping enhances crystallinity, as evidenced by XRD and Raman spectroscopy, and induces surface plasmon resonance (SPR) absorption attributed to Ag nanoparticles. SEM micrographs reveal agglomerated silver particles on the film surface, confirming Ag diffusion during annealing. Surface analysis through Secondary Ion Mass Spectrometry (SIMS) measurements illustrated the diffusion of Ag within the TiO2 samples and its subsequent accumulation at the surface. We have suggested that the crystallization observed in the evaporated TiO2-Ag thin films may primarily result from the thermal diffusion of Ag metal rather than the annealing process alone. Optical transmission spectra demonstrate a shift in the absorption edge towards the visible region with increasing Ag concentration, indicating enhanced light absorption properties.

Optical response and temperature shielding coatings using tri-layer structure composed of titania/silica/titania

The fabrication of metamaterials with inspiration from nature paved the door for the creation of revolutionary passive and active devices. Butterfly wings are one of them, and their multilayered structure motivated nanotechnologists, physicists, and other optoelectronic and photonic engineers to develop photonic crystals, dielectric reflectors, and Bragg reflectors for use in visible light communication, solar cells, and other photonic and optoelectronic applications. We report the sol–gel spin coating of a dielectric reflector on the glass substrate, an optical passive component consisting of titania and silica thin films for infrared radiation reflection. Individual thin films of titania and silica on glass substrates were studied using an x-ray diffractometer, which indicated anatase of titania and the amorphous nature of silica at a Bragg angle of 25° with a sharp and wide peak, respectively. The multilayer structure of titania/silica/titania was further investigated using Fourier transform infrared spectroscopy, which revealed the presence of Ti–O–Ti and Si–O–Si vibrational bonds at wavenumbers 546 and 973 cm−1, respectively, as well as the presence of Ti–O–Si vibrational bond at 1100 cm−1. The thickness of the multilayer titania/silica/titania was measured using a cross-sectional field emission scanning electron microscope (FESEM) and found to be 160/240/160 nm, respectively. Finally, reflection investigation on the multilayer structure using ultraviolet–visible–near-infrared spectroscopy validated the reflection of the infrared spectrum area by around 70% and showed to be beneficial for temperature shielding applications on glass furnishings.

Structural and optical characteristics of Cr-doped TiO2 thin films synthesized by sol-gel method

In this paper, undoped and 7 %, and 20 % chromium doped titanium dioxide thin films were synthesized on silicon and quartz substrates by utilizing the sol-gel spin coating process. The films were then annealed at 450 °C. The synthesis process and the effects of doping on the structural, optical, and vibrational properties were studied. XRD analysis showed that the undoped thin film had an anatase phase with a crystalline size of about 15.4 nm. However, as the concentration of chromium increased, the crystalline size decreased, and we obtained a mixed phase of rutile and anatase for doped films. The FTIR spectra revealed that undoped films had Ti–O bonding at 435 cm−1 and bond with stretching at 619 cm−1 wavenumbers, which decreased to 379 cm−1 and 377 cm−1 wavenumbers for 7 % and 20 % Cr doping, respectively. The optical measurements showed that the films were homogeneous and had high transmission, reaching 95 % in the visible range for the undoped thin film and 80 % for higher doping levels of chromium. These films have a remarkable level of transparency, and because of that they are highly regarded in the field of thin-film solar cells. Their optical properties make them an excellent choice for use as optical windows in these types of solar cells. As the amount of chromium in the film increases, the optical bandgap decreases from 3.23 eV to 2.26 eV. This suggests that chromium has a significant impact on the optical properties of these films, which might be helpful to researchers and professionals working in the fields of solar energy, optoelectronic devices, photocatalytic systems, gas sensors, and solar cell passivation.

Highly-selective optical filter for NADH fluorescence detection in multiphoton microscopy

Colorectal cancer (CRC) is a pressing global health concern, emphasizing the need for early detection tools. In this study an optical filter for precise detection of nicotinamide adenine dinucleotide (NADH) fluorescence via two-photon excitation fluorescence (TPEF) was developed. Fabricated with silicon dioxide and titanium dioxide thin films in a Fabry-Perot structure, the filter achieved a peak transmittance of about 95% at 483 nm, with a 12 nm full-width at half maximum. TPEF measurements using a tailored setup and NADH liquid phantoms underscored the filter's significance in selectively capturing NADH fluorescence while mitigating interference from other fluorophores. This work marks a substantial stride towards integrating multiphoton microscopy into conventional colonoscopy, enabling non-invasive, objective optical biopsy for colorectal tissue analysis. Further refinements of the experimental setup are imperative to advance tissue differentiation and enhance CRC diagnosis.

Effects of thermal treatment on the electrical behavior of titanium dioxide thin-films

AbstractElectrochemical biosensors made of titanium dioxide have generated significant interest due to their high sensitivity and selectivity for the detection of a variety of diseases. This study focuses on the impact of thermal treatment in an oxygen environment on the electrical properties of titanium dioxide thin films deposited on silicon substrates using pulsed laser deposition; the films were subjected to temperatures of $$\varvec{100\,\,^{\circ }C}$$ 100 ∘ C , $$\varvec{400\,\,^{\circ }C}$$ 400 ∘ C , and $$\varvec{600\,\,^{\circ }C}$$ 600 ∘ C . The primary objective was to explore how thermal processing influences the electrical characteristics of the thin films, with the goal of enhancing their capacitance and thereby improving the performance of sensors developed by functionalizing these films; X-ray photoelectron spectroscopy revealed the presence of Ti$$^{4+}$$ 4 + , Ti$$^{3+}$$ 3 + and TiO$$_x$$ x species in the untreated thin film and in the heat-treated films, with an increase in TiO$$_x$$ x species observed after oxygen heat treatment. Atomic force microscopy demonstrated a decrease in the surface homogeneity of the films at elevated treatment temperatures, which corresponded to a reduction in capacitive behavior; this was further corroborated by Nyquist plots derived from electrochemical capacitance spectroscopy (ECS). The study found that the electrochemical capacitance at lower frequencies decreased significantly from $$\varvec{1.02\,\, \mu Fcm^{-2}}$$ 1.02 μ F c m - 2 to $$\varvec{0.25\,\, \mu Fcm^{-2}}$$ 0.25 μ F c m - 2 when the treatment temperature was increased to $$\varvec{600\,\,^{\circ }C}$$ 600 ∘ C

Electrochemical Studies of The Corrosion Resistance of Bismuth Titanate Thin Films Deposited by RF Sputtering

Thin films of bismuth titanate were grown on stainless steel (316L) and titanium alloy (Ti6Al4V) substrates using the magnetron sputtering technique. The surface morphology of these films was observed with a scanning electron micrograph (SEM). The electrochemical studies used to evaluate the corrosion resistance of the substrate-coating set were the potentiodynamic polarization (Tafel) tests and electrochemical impedance spectroscopy (EIS), both done in a solution of NaCl (3%) as an electrolyte. The SEM showed that the morphology of the coatings grown on a titanium alloy Ti6Al4V substrate was generally homogeneous with a smooth surface but with unmelted material in some regions, while the morphology of the thin films grown on stainless steel 316L was mainly granular, with the presence of a few holes or craters. The potentiodynamic polarization curves showed that the corrosion resistance of the coated samples was better than that of the bare substrate because the corrosion current obtained from the coated samples was lower by two orders of magnitude than that exhibited by the uncoated substrates, and in addition, the corrosion potential of the coated samples was greater than that of the bare substrate. The EIS test showed the presence of a passive thin film of titanium oxide on the titanium alloy substrate.

A study on the fabrication procedure for a high-D/Ti-ratio-deuterated-titanium film on the disk-type neutron generator target

This study aims to present thin film deposition and deuterium adsorption procedure to fabricate disk-type targets with high D/Ti values for a neutron generator and increase their lifespan. The neutron target consists of a titanium thin film with hydrogen loading, and a copper substrate for heat removal. We optimized the incident deuterium ion beam energy and thin film thickness using Geant4 simulations. Additionally, we calculated the expected neutron yield under the optimized conditions. The hydrogen adsorption conditions were optimized by comparing the H/Ti results as per hydrogen adsorption temperature and loading time using titanium foils of different thickness values. Hydrogen (or deuterium) adsorption ratio is strongly influenced by the surface condition and the deposition conditions of the thin film. A titanium film was deposited in various conditions of plasma DC power and substrate temperature. The quality of the thin film was evaluated through surface roughness evaluation and thin film sheet resistance for each deposition conditions. Subsequently, the hydrogen adsorption results were compared according to the quality of the thin titanium films, and the thin titanium film deposition conditions with the highest hydrogen adsorption ratio were confirmed. The selected conditions were applied to conduct deuterium adsorption. In conclusion, this study underscores the critical relationship between thin film quality and hydrogen (or deuterium) adsorption ratio, reinforcing the importance of optimizing thin film deposition parameters for the design of neutron generator disk-type targets with high quality of film and extended lifespan.

Characterization of Flower Based Organic Dyes and Titanium Dioxide Thin Film for Dye Sensitized Solar Cell

In the present study, we described the organic dye extraction process from local flowers employing different methods and solvents (a mixture of acetic acid and ethanol, another is only acetic acid); especially we completed our research by exploring dye from red gerbera flower as it showed higher absorbance. Both dry and fresh petals of the flower were used for extracting dyes. The results revealed that the mixture-based dye extraction from dry red gerbera yielded a higher absorbance value of 4.579 a.u., whereas the acetic acid-based extraction from the same source exhibited a lower absorbance value of 2.778 a.u. The choice of solvent for dye extraction was found to significantly influence the absorption spectrum. Additionally, the Beer-Lambert law was employed to analyze the relationship between the absorbance and the concentration of the extracted dyes. For the electrode, a TiO2 film was created using the spin coating technique. From the XRD graph, we found the band gap energy of TiO2 which is 2.81eV (annealed at 450°C), the type of nanoparticle of the thin film. Also found a Crystallite size of 32.95nm and a specific Surface Area (SSA) of 43.048 m2.g−1, Microstrain (ε) of 5e-3 and Dislocation Density (δ) of 9.2e-4cm−2.