Degradation of Tetracycline on SiO2-TiO2-C Aerogel Photocatalysts under Visible Light

SiO₂-TiO₂-C aerogel photocatalysts with different carbon loadings were synthesized by using sol-gel chemistry. The anatase crystal and nonmetal carbon dopant were introduced during the sol preparation and formed by hydrothermal treatment, which can simultaneously enhance the adsorption ability and visible light photo-activity. A high surface area (759 g cm⁻³) SiO₂-TiO₂-C aerogel composite can remove up to 80% tetracycline hydrochloride within 180 min under visible light. The characterization of the gel structures shows that the homogeneous dispersion of O, Si, Ti and C in the skeleton, indicating that hydrothermal synthesis could provide a very feasible way for the preparation of composite materials. n(C):n(Ti) molar ratio of 3.5 gives the best catalytic performance of the hybrid aerogel, and the cyclic test still confirms over 60% degradation activity after seven use cycles. All catalysis reaction followed the pseudo-first-order rate reaction with high correlation coefficient. The electrons and holes in the compound could be effectively restrained with doping proper amount of C, and ESR results indicate that the oxidation process was dominated by the hydroxyl radical (•OH) and superoxide radical (•O₂⁻) generated in the system.     

Hydrolytic Modification of SiO2 Microspheres with Na2SiO3 and the Performance of Supported Nano-TiO2 Composite Photocatalyst

Modified microspheres (SiO₂-M) were obtained by the hydrolytic modification of silicon dioxide (SiO₂) microspheres with Na₂SiO₃, and then, SiO₂-M was used as a carrier to prepare a composite photocatalyst (SiO₂-M/TiO₂) using the sol-gel method; i.e., nano-TiO₂ was loaded on the surface of SiO₂-M. The structure, morphology, and photocatalytic properties of SiO₂-M/TiO₂ were investigated. Besides, the mechanism of the effect of SiO₂-M was also explored. The results show that the hydrolytic modification of Na₂SiO₃ coated the surface of SiO₂ microspheres with an amorphous SiO₂ shell layer and increased the quantity of hydroxyl groups. The photocatalytic performance of the composite photocatalyst was slightly better than that of pure nano-TiO₂ and significantly better than that of the composite photocatalyst supported by unmodified SiO₂. Thus, increasing the loading capacity of nano-TiO₂, improving the dispersion of TiO_2, and increasing the active surface sites are essential factors for improving the functional efficiency of nano-TiO₂. This work provides a new concept for the design of composite photocatalysts by optimizing the performance of the carrier.     

Application of Turkevich Method for Gold Nanoparticles Synthesis to Fabrication of SiO2@Au and TiO2@Au Core-Shell Nanostructures

The Turkevich synthesis method of Au nanoparticles (AuNPs) was adopted for direct fabrication of SiO₂@Au and TiO₂@Au core-shell nanostructures. In this method, chloroauric acid was reduced with trisodium citrate in the presence of amine-functionalized silica or titania submicroparticles. Core-shells obtained in this way were compared to structures fabricated by mixing of Turkevich AuNPs with amine-functionalized silica or titania submicroparticles. It was found that by modification of reaction conditions of the first method, such as temperature and concentration of reagents, control over gold coverage on silicon dioxide particles has been achieved. Described method under certain conditions allows fabrication of semicontinuous gold films on the surface of silicon dioxide particles. To the best of our knowledge, this is the first report describing use of Turkevich method to direct fabrication of TiO₂@Au core-shell nanostructures.     

Preparation of Colored Microcapsule Phase Change Materials with Colored SiO2 Shell for Thermal Energy Storage and Their Application in Latex Paint Coating

This article reports the design and manufacture of colored microcapsules with specific functions and their application in architectural interior wall coating. Utilizing reactive dyes grafted SiO₂ shell to encapsulate paraffin through interfacial polymerization and chemical grafting methods, this experiment successfully synthesized paraffin@SiO₂ colored microcapsules. The observations of surface morphology demonstrated that the colored microcapsules had a regular spherical morphology and a well-defined core-shell structure. The analysis of XRD and FT-IR confirmed the presence of amorphous SiO₂ shell and the grafting reactive dyes, and the paraffin possessed high crystallinity. Compared with pristine paraffin, the thermal conductivity of paraffin@SiO₂ colored microcapsules was significantly enhanced. The results of DSC revealed that the paraffin@SiO₂ colored microcapsules performed high encapsulation efficiency and desirable latent heat storage capability. Besides, the examinations of UV-vis and TGA showed that the paraffin@SiO₂ colored microcapsules exhibited good thermal reliability, thermal stability, and UV protection property. The analysis of infrared imaging indicated that the prepared latex paint exhibited remarkable temperature-regulated property. Compared with normal interior wall coatings, the temperature was reduced by about 2.5 °C. With such incomparable features, the paraffin@SiO₂ colored microcapsules not only appeared well in their solar thermal energy storage and temperature-regulated property, but also make the colored latex paint coating have superb colored fixing capabilities.     

Design an Epoxy Coating with TiO2/GO/PANI Nanocomposites for Enhancing Corrosion Resistance of Q235 Carbon Steel

In this work, a ternary TiO₂/Graphene oxide/Polyaniline (TiO₂/GO/PANI) nanocomposite was synthesized by in situ oxidation and use as a filler on epoxy resin (TiO₂/GO/PANI/EP), a bifunctional in situ protective coating has been developed and reinforced the Q235 carbon steel protection against corrosion. The structure and optical properties of the obtained composites are characterized by XRD, FTIR, and UV–vis. Compared to bare TiO₂ and bare Q235, the TiO₂/GO/PANI/EP coating exhibited prominent photoelectrochemical properties, such as the photocurrent density increased 0.06 A/cm² and the corrosion potential shifted from −651 mV to −851 mV, respectively. The results show that the TiO₂/GO/PANI nanocomposite has an extended light absorption range and the effective separation of electron-hole pairs improves the photoelectrochemical performance, and also provides cathodic protection to Q235 steel under dark conditions. The TiO₂/GO/PANI/EP coating can isolate the Q235 steel from the external corrosive environment, and may generally be regarded a useful protective barrier coating to metallic materials. When the TiO₂/GO/PANI composite is dispersed in the EP, the compactness of the coating is improved and the protective barrier effect is enhanced.     

Preparation of SiO2-Protecting Metallic Fe Nanoparticle/SiO2 Composite Spheres for Biomedical Application

Functionalized Fe nanoparticles (NPs) have played an important role in biomedical applications. In this study, metallic Fe NPs were deposited on SiO₂ spheres to form a Fe/SiO₂ composite. To protect the Fe from oxidation, a thin SiO₂ layer was coated on the Fe/SiO₂ spheres thereafter. The size and morphology of the SiO₂@Fe/SiO₂ composite spheres were examined by transmission electron microscopy (TEM). The iron form and its content and magnetic properties were examined by X-ray diffraction (XRD), inductively-coupled plasma mass spectrometry (ICP-MS) and a superconducting quantum interference device (SQUID). The biocompatibility of the SiO₂@Fe/SiO₂ composite spheres was examined by Cell Counting Kit-8 (CCK-8) and lactate dehydrogenase (LDH) tests. The intracellular distribution of the SiO₂@Fe/SiO₂ composite spheres was observed using TEM. XRD analysis revealed the formation of metallic iron on the surface of the SiO₂ spheres. According to the ICP-MS and SQUID results, using 0.375 M FeCl₃·6H₂O for Fe NPs synthesis resulted in the highest iron content and magnetization of the SiO₂@Fe/SiO₂ spheres. Using a dye loading experiment, a slow release of a fluorescence dye from SiO₂@Fe/SiO₂ composite spheres was confirmed. The SiO₂@Fe/SiO₂ composite spheres co-cultured with L929 cells exhibit biocompatibility at concentrations <16.25 µg/mL. The TEM images show that the SiO₂@Fe/SiO₂ composite spheres were uptaken into the cytoplasm and retained in the endosome. The above results demonstrate that the SiO₂@Fe/SiO₂ composite spheres could be used as a multi-functional agent, such as a magnetic resonance imaging (MRI) contrast agent or drug carriers in biomedical applications.     

Tribological and Thermo-Mechanical Properties of TiO2 Nanodot-Decorated Ti3C2/Epoxy Nanocomposites

The micromorphology of fillers plays an important role in tribological and mechanical properties of polymer matrices. In this work, a TiO₂-decorated Ti₂C₃ (TiO₂/Ti₃C₂) composite particle with unique micro-nano morphology was engineered to improve the tribological and thermo-mechanical properties of epoxy resin. The TiO₂/Ti₃C₂ were synthesized by hydrothermal growth of TiO₂ nanodots onto the surface of accordion-like Ti₃C₂ microparticles, and three different decoration degrees (low, medium, high density) of TiO₂/Ti₃C₂ were prepared by regulating the concentration of TiO₂ precursor solution. Tribological test results indicated that the incorporation of TiO₂/Ti₃C₂ can effectively improve the wear rate of epoxy resin. Among them, the medium density TiO₂/Ti₃C₂/epoxy nanocomposites gained a minimum wear rate. This may be ascribed by the moderate TiO₂ nanodot protuberances on the Ti₃C₂ surface induced a strong mechanical interlock effect between medium-density TiO₂/Ti₃C₂ and the epoxy matrix, which can bear a higher normal shear stress during sliding friction. The morphologies of worn surfaces and wear debris revealed that the wear form was gradually transformed from fatigue wear in neat epoxy to abrasive wear in TiO₂/Ti₃C₂/epoxy nanocomposites. Moreover, the results of thermo-mechanical property indicated that incorporation of TiO₂/Ti₃C₂ also effectively improved the storage modulus and glass transition temperature of epoxy resin.     

Remarkable Reduction in IG with an Explicit Investigation of the Leakage Conduction Mechanisms in a Dual Surface-Modified Al2O3/SiO2 Stack Layer AlGaN/GaN MOS-HEMT

We demonstrated the performance of an Al₂O₃/SiO₂ stack layer AlGaN/GaN metal–oxide semiconductor (MOS) high-electron-mobility transistor (HEMT) combined with a dual surface treatment that used tetramethylammonium hydroxide (TMAH) and hydrochloric acid (HCl) with post-gate annealing (PGA) modulation at 400 °C for 10 min. A remarkable reduction in the reverse gate leakage current (I_G) up to 1.5×10−12 A/mm (@ V_G = −12 V) was observed in the stack layer MOS-HEMT due to the combined treatment. The performance of the dual surface-treated MOS–HEMT was significantly improved, particularly in terms of hysteresis, gate leakage, and subthreshold characteristics, with optimized gate annealing treatment. In addition, an organized gate leakage conduction mechanism in the AlGaN/GaN MOS–HEMT with the Al₂O₃/SiO₂ stack gate dielectric layer was investigated before and after gate annealing treatment and compared with the conventional Schottky gate. The conduction mechanism in the reverse gate bias was Poole–Frankel emission for the Schottky-gate HEMT and the MOS–HEMT before annealing. The dominant conduction mechanism was ohmic/Poole-Frankel at low/medium forward bias. Meanwhile, gate leakage was governed by the hopping conduction mechanism in the MOS–HEMT without gate annealing modulation at a higher forward bias. After post-gate annealing (PGA) treatment, however, the leakage conduction mechanism was dominated by trap-assisted tunneling at the low to medium forward bias region and by Fowler–Nordheim tunneling at the higher forward bias region. Moreover, a decent product of maximum oscillation frequency and gate length (f_max × L_G) was found to reach 27.16 GHz∙µm for the stack layer MOS–HEMT with PGA modulation. The dual surface-treated Al₂O₃/SiO₂ stack layer MOS–HEMT with PGA modulation exhibited decent performance with an I_DMAX of 720 mA/mm, a peak extrinsic transconductance (G_MMAX) of 120 mS/mm, a threshold voltage (V_TH) of −4.8 V, a higher I_ON/I_OFF ratio of approximately 1.2×109, a subthreshold swing of 82 mV/dec, and a cutoff frequency(f_t)/maximum frequency of (f_max) of 7.5/13.58 GHz.     

First-Principles Calculation of the Bonding Strength of the Al2O3-Fe Interface Enhanced by Amorphous Na2SiO3

In this paper, the interfacial adhesion work (W_ad), tensile strength, and electronic states of the Fe-amorphous Na₂SiO₃-Al₂O₃ and Fe-Al₂O₃ interfaces are well-investigated, utilizing the first-principles calculations. The results indicate that the Fe-amorphous Na₂SiO₃-Al₂O₃ interface is more stable and wettable than the interface of Fe-Al₂O₃. Specifically, the interfacial adhesion work of the Fe-amorphous Na₂SiO₃ interface is 434.89 J/m², which is about forty times that of the Fe-Al₂O₃ interface, implying that the addition of amorphous Na₂SiO₃ promotes the dispersion of Al₂O₃ particle-reinforced. As anticipated, the tensile stress of the Fe-amorphous Na₂SiO₃-Al₂O₃ interface is about 46.58 GPa over the entire critical strain range, which is significantly greater than the Fe-Al₂O₃ interface control group. It could be inferred that the wear resistance of Al₂O₃ particle-reinforced is improved by adding amorphous Na₂SiO₃. To explain the electronic origin of this excellent performance, the charge density and density of states are investigated and the results indicate that the O atom in amorphous Na₂SiO₃ has a bonding action with Fe and Al; the amorphous Na₂SiO₃ acts as a sustained release. This study provides new ideas for particle-reinforced composites.     

Thermal Annealing Effect on Optical Properties of Binary TiO2-SiO2 Sol-Gel Coatings

TiO₂-SiO₂ binary coatings were deposited by a sol-gel dip-coating method using tetrabutyl titanate and tetraethyl orthosilicate as precursors. The structure and chemical composition of the coatings annealed at different temperatures were analyzed by Raman spectroscopy and Fourier Transform Infrared (FTIR) spectroscopy. The refractive indices of the coatings were calculated from the measured transmittance and reflectance spectra. An increase in refractive index with the high temperature thermal annealing process was observed. The Raman and FTIR results indicate that the refractive index variation is due to changes in the removal of the organic component, phase separation and the crystal structure of the binary coatings.     

Printability and Setting Time of CSA Cement with Na2SiO3 and Gypsum for Binder Jetting 3D Printing

The purpose of this study is to optimize the composition of CSA (calcium sulfoaluminate) cement with sodium silicate (Na₂SiO₃) and gypsum for binder jetting 3D printing. The preliminary test was carried out with an applicator to decide the proper thickness of one layer before using the 3D printer. A liquid binder was then selected to maintain the shape of the particles. Based on the results, the optimal mixture of dry materials and a liquid activator was derived through various parametric studies. For dry materials, the optimum composition of CSA cement, gypsum, and sand was suggested, and the liquid activator made with sodium silicate solution and VMA (viscosity modified agent) were selected. The setting time with gypsum and sodium silicate was controlled within 30 s. In case of the delayed setting time and the rapid setting mixture, the jetting line was printed thicker or thinner and the accuracy of the printout was degraded. In order to adjust the viscosity of the liquid activator, 10% of the VMA was used in 35% of sodium silicate solution and the viscosity of 200–400 cP was suitable to be sprayed from the nozzle. With this optimal mixture, a prototype of atypical decorative wall was printed, and the compressive strength was measured at about 7 MPa.     

Fabrication of CIS Absorber Layers with Different Thicknesses Using A Non-Vacuum Spray Coating Method

In this study, a new thin-film deposition process, spray coating method (SPM), was investigated to deposit the high-densified CuInSe₂ absorber layers. The spray coating method developed in this study was a non-vacuum process, based on dispersed nano-scale CuInSe₂ precursor and could offer a simple, inexpensive, and alternative formation technology for CuInSe₂ absorber layers. After spraying on Mo/glass substrates, the CuInSe₂ thin films were annealed at 550 °C by changing the annealing time from 5 min to 30 min in a selenization furnace, using N₂ as atmosphere. When the CuInSe₂ thin films were annealed, without extra Se or H₂Se gas used as the compensation source during the annealing process. The aim of this project was to investigate the influence of annealing time on the densification and crystallization of the CuInSe₂ absorber layers to optimize the quality for cost effective solar cell production. The thickness of the CuInSe₂ absorber layers could be controlled as the volume of used dispersed CuInSe₂-isopropyl alcohol solution was controlled. In this work, X-ray diffraction patterns, field emission scanning electron microscopy, and Hall parameter measurements were performed in order to verify the quality of the CuInSe₂ absorber layers obtained by the Spray Coating Method.     

Fabrication of TiO2 – KH550 – PEG Super-Hydrophilic Coating on Glass Surface without UV/Plasma Treatment for Self-Cleaning and Anti-Fogging Applications

In this study, we have developed a self-cleaning transparent coating on a glass substrate by dip coating a TiO₂ – KH550 – PEG mixed solution with super-hydrophilicity and good antifogging properties. The fabrication of the thin-film-coated glass is a one-step solution blending method that is performed by depositing only one layer of modified TiO₂ nanoparticles at room temperature. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to determine the structure and morphology of the nanoparticles and the thin-film-coated glass. The surface functional groups were investigated using Fourier-transform infrared spectroscopy (FT-IR), and the optical properties of the glass coating were measured using a UV/Vis spectrometer. The results revealed that the KH-500-modified TiO₂ film coating was in an anatase crystalline form. The hydrophilicity of the coated and uncoated glass substrates was observed by measuring their water contact angle (WCA) using a contact angle instrument. The maximum transparency of the coated glass measured in the visible region (380–780 nm) was approximately 70%, and it possessed excellent super-hydrophilic properties (WCA ~0°) at an annealing temperature of 350 °C without further need of UV or plasma treatment. These results demonstrate the super-hydrophilic coated glass surface has potential for use in self-cleaning and anti-fogging applications.     

Quasi-Solid-State SiO2 Electrolyte Prepared from Raw Fly Ash for Enhanced Solar Energy Conversion

Quasi-solid-state electrolytes in dye-sensitized solar cells (DSSCs) prevent solvent leakage or evaporation and stability issues that conventional electrolytes cannot; however, there are no known reports that use such an electrolyte based on fly ash SiO₂ (FA_SiO₂) from raw fly ash (RFA) for solar energy conversion applications. Hence, in this study, quasi-solid-state electrolytes based on FA_SiO₂ are prepared from RFA and poly(ethylene glycol) (PEG) for solar energy conversion. The structural, morphological, chemical, and electrochemical properties of the DSSCs using this electrolyte are characterized by X-ray diffraction (XRD), high-resolution field-emission scanning electron microscopy (HR-FESEM), X-ray fluorescence (XRF), diffuse reflectance spectroscopy, electrochemical impedance spectroscopy (EIS), and incident photon-to-electron conversion efficiency (IPCE) measurements. The DSSCs based on the quasi-solid-state electrolyte (SiO₂) show a cell efficiency of 5.5%, which is higher than those of nanogel electrolytes (5.0%). The enhancement of the cell efficiency is primarily due to the increase in the open circuit voltage and fill factor caused by the reduced electron recombination and improved electron transfer properties. The findings confirm that the RFA-based quasi-solid-state (SiO₂) electrolyte is an alternative to conventional liquid-state electrolytes, making this approach among the most promising strategies for use in low-cost solar energy conversion devices.     

Influence of TiO2 Nanoparticles on the Resistance of Cementitious Composite Materials to the Action of Fungal Species

The development of mold films on the cement surfaces of buildings is a health and safety problem for the population, aesthetic but also in terms of their durability. The use of specific performance of cementitious composites containing TiO₂ nanoparticles, photoactivated by UV radiation, can be a viable solution to mitigate to eliminate these problems. The experimental studies presented aim to analyze the capacity to inhibit the development of mold type Aspergillus and Penicillium on the surface of composite materials with nano-TiO₂ content and the identification of the optimal range of nanomaterial addition. The identification and analysis of the inhibition halo (zone with a biological load of maximum 1–10 colonies of microorganisms) confirmed the biocidal capacity of the cementitious composites, but also indicated the possibility that an excess of TiO₂ nanoparticles in the mixture could induce a development of cell resistance, which would be unfavorable both in terms of behavior and in terms of cost.     

Chemical and Structural Changes by Gold Addition Using Recharge Method in NiW/Al2O3-CeO2-TiO2 Nanomaterials

NiWAu trimetallic nanoparticles (NPs) on the surface of support Al₂O₃-CeO₂-TiO₂ were synthesized by a three-step synthetic method in which Au NPs were incorporated into presynthesized NiW/Al₂O₃-CeO₂-TiO₂. The recharge method, also known as the redox method, was used to add 2.5 wt% gold. The Al₂O₃-CeO₂-TiO₂ support was made by a sol–gel method with two different compositions, and then two metals were simultaneously loaded (5 wt% nickel and 2.5 wt% tungsten) by two different methods, incipient wet impregnation and ultrasound impregnation method. In this paper, we study the effect of Au addition using the recharge method on NiW nanomaterials supported on mixed oxides on the physicochemical properties of synthesized nanomaterials. The prepared nanomaterials were characterized by scanning electron microscopy, BET specific surface area, X-ray diffraction, diffuse reflectance spectroscopy in the UV–visible range and temperature-programmed desorption of hydrogen. The experimental results showed that after loading of gold, the dispersion was higher (46% and 50%) with the trimetallic nanomaterials synthesized by incipient wet impregnation plus recharge method than with impregnation plus ultrasound recharge method, indicating a greater number of active trimetallic (NiWAu) sites in these materials. Small-sized Au from NiWAu/ACTU1 trimetallic nanostructures was enlarged for NiWAu/ACT1. The strong metal NPs–support interaction shown for the formation of NiAl₂O₄, Ni-W-O and Ni-Au-O species simultaneously present in the surface of trimetallic nanomaterial probably plays an important role in the degree of dispersion of the gold active phase.     

Study on Crystallization Process of Li2O–Al2O3–SiO2 Glass-Ceramics Based on In Situ Analysis

In this paper, we used differential scanning calorimetry (DSC), high-temperature X-ray diffraction (HT-XRD), and confocal scanning laser microscopy (CSLM) to investigate the Li₂O–Al₂O_3–SiO₂ glass crystallization process. At 943 K, lithium disilicate (Li₂Si₂O₅) phase crystals began to precipitate in the Li₂O–Al₂O₃–SiO₂ glass with a crystal size of 50–70 nm. At the temperature of 1009 K, petalite (LiAlSi₄O₁₀) crystals began to precipitate in the vitreous phase, forming composite spherical crystals of LiAlSi₄O₁₀ and Li₂Si₂O₅ with size in the range of 90–130 nm. Furthermore, the Kissinger method and KAS method of the JMAK model were used to calculate the crystallization activation energy and the Avrami index “n”. It was found that the precipitation mechanism of the two kinds of crystals is whole crystallization; accordingly, the selection of crystallization heat treatment system was guided to determine the nucleation and crystallization temperature.     

Effect of Spraying Power on Oxidation Resistance of MoSi2-ZrB2 Coating for Nb-Si Based Alloy Prepared by Atmospheric Plasma

The MoSi₂-ZrB₂ coatings were prepared on Nb-Si based alloy by atmospheric plasma spraying with the spraying power 40, 43 and 45 kW. The effect of spraying power on the microstructure and oxidation resistance of MoSi₂-ZrB₂ coating at 1250 °C were studied. The results showed that the main constituent phases of coatings were MoSi₂ at all spraying power. The coating became more compact as the spraying power increased. The coating prepared at 45 kW was dense and uniform, which exhibited the best oxidation resistance due to the formation of a dense and uniform glass layer consisting of SiO₂ and ZrSiO₄.     

Fabrication and Evaluation of Nano-TiO2 Superhydrophobic Coating on Asphalt Pavement

In order to address water damage of asphalt pavement, reduce the occurrence of water-related potholes, deformation, and other diseases, and improve the performance and service life of the pavement, a nano-TiO₂ superhydrophobic coating (PSC) on asphalt pavement was prepared from waterborne polyurethane and nano-TiO₂ modified by stearic acid. FT-IR measured stearic acid successfully modified low surface energy substance on the surface of nano-TiO₂. The SEM image shows that the PSC has a rough surface structure. The contact angle and rolling angle of the PSC in the contact angle test are 153.5° and 4.7°, respectively. PSC has a super-hydrophobic ability, which can improve the water stability of the asphalt mixture. Although the texture depth and pendulum value have been reduced by 2.5% and 4.4%, respectively, they all comply with the standard requirements. After the abrasion resistance test, the PSC coating still has a certain hydrophobic ability. These results surface PSC coating can effectively reduce water damage on asphalt pavement, and has considerable application value.     

Optical Constants of Crystallized TiO2 Coatings Prepared by Sol-Gel Process

Titanium oxide coatings have been deposited by the sol-gel dip-coating method. Crystallization of titanium oxide coatings was then achieved through thermal annealing at temperatures above 400 °C. The structural properties and surface morphology of the crystallized coatings were studied by micro-Raman spectroscopy and atomic force microscopy, respectively. Characterization technique, based on least-square fitting to the measured reflectance and transmittance spectra, is used to determine the refractive indices of the crystallized TiO₂ coatings. The stability of the synthesized sol was also investigated by dynamic light scattering particle size analyzer. The influence of the thermal annealing on the optical properties was then discussed. The increase in refractive index with high temperature thermal annealing process was observed, obtaining refractive index values from 1.98 to 2.57 at He-Ne laser wavelength of 633 nm. The Raman spectroscopy and atomic force microscopy studies indicate that the index variation is due to the changes in crystalline phase, density, and morphology during thermal annealing.