Search Results (122)

Composite electrodeposited coatings hold significant potential for marine and aerospace applications due to their synergistic corrosion resistance and wear durability, yet nanoparticle agglomeration and interfacial incompatibility persistently undermine their performance. Conventional dispersion techniques—mechanical agitation, surfactants, or high-energy methods—fail to resolve these issues, often introducing residual stresses, organic impurities, or thermal damage to substrates. This study addresses these challenges through a novel thermal-assisted alkaline etching (TAE) protocol that synergistically removes surface oxides and enhances colloidal stability in β-SiC nanoparticles. By combining NaOH-based etching with low-temperature calcination (250 °C), the method achieves oxide-free SiC surfaces with elevated hydrophilicity and a ζ-potential of −25 mV, enabling submicron clustering (300 nm) without surfactants. Electrodeposited Co/SiC coatings incorporating TAE-SiC exhibited current-modulated reinforcement, achieving optimal SiC incorporation (5.9 at% Si) at 8 A/dm² through electrophoretic–hydraulic synergy, along with uniform cross-sectional distribution validated by SEM. Tribological assessments revealed shorter wear tracks in TAE-SiC-enhanced coatings compared to their untreated counterparts, suggesting enhanced interfacial coherence despite a comparable mass loss. Demonstrating scalability through cost-effective aqueous-phase chemistry, this methodology provides a generalized framework applicable to other ceramic-reinforced systems (e.g., Al₂O₃ and TiC), offering transformative potential for next-generation protective coatings in harsh operational environments. Full article

Herein, we report on the synthesis of Ni and Zn clusters on the surface of TiO₂ as well as their bimetallic NiZn analogs. The materials were prepared by incipient wet impregnation of colloidal TiO₂ followed by microwave (MW) irradiation to graft the clusters to TiO₂ surface. The materials were further immobilized onto glass slides and exhibited high surface area, high mechanical stability, and porosity with accessible pores. The main species responsible for visible light degradation of microcystin LR via the interface charge transfer (IFCT) of excited e⁻ to surface metal clusters were found to be O₂^•− and h⁺. The optimal nominal grafting concentration was 0.5 wt.% for Ni and 1.0 wt.% for Zn, while for the bimetal modification (NiZn), the optimal nominal concentration was 0.5 wt.%. Compared to monometallic, bimetallic grafting showed a lower kinetic constant, albeit still improved compared to bare TiO₂. Bimetal-modified titania showed a lower photocurrent compared to single metal-grafted TiO₂ and poorer interfacial charge transport, namely, more recombination sites—possibly at the interface between the Ni and Zn domains. This work highlights the efficiency of using MW irradiation for grafting sub-nano-sized metallic species to TiO₂ in a homogeneous way. However, further strategies using MW irradiation for the structural design of bimetallic cocatalysts can be implemented in the future. Full article

Cortisol is a key biomarker for stress detection, and its levels can be monitored using point-of-care devices with sensors such as nanoparticles and interdigitated array electrodes (IDEs). This study developed an IDE platform using barium titanate (BaTiO₃) particles synthesized via colloidal precipitation with titanium tetraisopropoxide, barium chloride, and Pluronic^® P123. The calcination temperatures varied between 160 °C and 340 °C, with optimal results observed at 160 °C. Scanning electron microscopy revealed particles with an average size of 26 nm, and Fourier transform infrared spectroscopy confirmed the molecular composition after the removal of P123. X-ray diffraction analysis revealed anatase and brookite phases. Brunauer-Emmett-Teller analysis indicated changes in pore morphology, with samples treated at 160 °C exhibiting a type IV(a) mesoporous structure, a surface area of 163 m²/g, and an average pore diameter of 5.24 nm. Higher temperatures led to transitions to type IV(b) at 260 °C and type V at 340 °C, with reduced pore size. Electrochemical impedance spectroscopy was employed to evaluate the performance of the IDE sensor integrated with BaTiO₃ nanoparticles and albumin across cortisol concentrations ranging from 5.0 to 20 ng/mL. Impedance measurements revealed a significant decrease in impedance (Z′) with increasing cortisol concentrations, indicating increased conductivity. Specifically, Nyquist plots for a saliva sample containing 5 ng/mL cortisol—within the typical physiological range—exhibited a marked increase in charge-transfer resistance (Rct), confirming the sensor’s ability to detect low hormone levels in biological fluids. These findings underscore the potential of BaTiO₃-based IDE platforms at 160 °C for stress biomarker monitoring. Full article

Colloidal copper-based chalcogenide quantum dots (QDs), particularly lead-free CuInSe₂ systems, have emerged as promising photosensitizers for optoelectronic de-vices due to their high extinction coefficients and solution processability. In this work, we demonstrate a TiO₂ photodetector enhanced through interfacial engineering with the size of 9.88 ± 2.49 nm CuInSe₂ QD_s, synthesized via controlled thermal injection. The optimized device architecture combines a 160 nm TiO₂ active layer with 60 μm horizontal channel electrodes, achieving high performance metrics. The QD-sensitized device demonstrates an impressive switching ratio of approximately 10⁵ in the 405 nm wavelength, a significant 34-times increase in responsivity at a 2 V bias, and a detection rate of 4.17 × 10⁸ Jones. Due to the limitations imposed by the TiO₂ bandgap, the TiO₂ photodetector exhibits a negligible increase in photocurrent at 565 nm. The engineered type-II heterostructure enables responsivity enhancement across an extended spectral range through sensitization while maintaining equivalent performance characteristics at both 405 nm and 565 nm wavelengths. Furthermore, the sensitized architecture demonstrates superior response kinetics, enhanced specific detectivity, and exceptional operational stability, establishing a universal design framework for broadband photodetection systems. Full article

Layered sodium trititanate (Na₂Ti₃O₇) is a promising anode material for sodium-ion batteries due to its suitable charge/discharge plateaus, cost-effectiveness, and eco-friendliness. However, its slow Na⁺ diffusion kinetics, poor electron conductivity, and instability during cycling pose significant challenges for practical applications. To address these issues, we developed a template-free method to synthesize Na₂Ti₃O₇-C hollow microspheres. The synthesis began with polymerization-induced colloid aggregation to form a TiO₂–urea–formaldehyde (TiO₂-UF) precursor, which was then subjected to heat treatment to induce inward crystallization, creating hollow cavities within the microspheres. The hollow structure, combined with a conductive carbon matrix, significantly enhanced the cycling performance and rate capability of the material. When used as an anode, the Na₂Ti₃O₇-C hollow microspheres exhibited a high reversible capacity of 188 mAh g⁻¹ at 0.2C and retained 169 mAh g⁻¹ after 500 cycles. Additionally, the material demonstrated excellent rate performance with capacities of 157, 133, 105, 77, 62, and 45 mAh g⁻¹ at current densities of 0.5, 1, 2, 5, 10, and 20C, respectively. This innovative approach provides a new strategy for developing high-performance sodium-ion battery anodes and has the potential to significantly advance the field of energy storage. Full article

Anatase-phase rod-shaped TiO₂ nanocrystals are prepared by the solvothermal method, the surface is metalated, and doped nanocrystals are achieved by thermal diffusion of surface metal ions. Incorporation of dopant ions into TiO₂ lattice enhances the visible light absorption of the material and in some cases can increase the rate of photocatalysis. Even though there are overflowing studies on the preparation of doped TiO₂ materials, there are no methods that enable the precise control of dopant concentration in TiO₂ nanocrystals. We have developed a method to load the surface of oleic acid stabilized anatase-phase rod-shaped TiO₂ nanocrystals (approx. 3 ± 1 nm diameter and 40 ± 10 nm long) with transition metal ions followed by ion diffusion to prepare metal-doped nanocrystals with exact control of the dopant concentration. Specifically, in this work, Cr³⁺ adsorbs TiO₂ nanorods to yield a green colloid, followed by ion diffusion at elevated temperature. After removal of any remaining surface Cr³⁺, tan-colored chromium-doped TiO₂ nanorods can be obtained. Electron microscopy and powder X-ray diffraction indicate no change in nanocrystal size and morphology throughout the process. The TiO₂ nanorods play an important role in photocatalysis owing to their excellent chemical and physical properties. Titanium dioxide is a low-cost, non-toxic, highly stable, chemically robust material. Doped TiO₂ materials have found application in photocatalysis (oxidative degradation of organic molecules, hydrogen evolution), photovoltaics, solar cells, lithium-ion batteries, supercapacitors, and sensors. TiO₂ photocatalysis is also the basis for clean energy technologies, such as dye-sensitized solar cells and photoelectrochemical cells. In photocatalysis applications, nanocrystalline TiO₂ presents advantages of a high surface area, ability to control the surface facet, and minimized bulk recombination. Full article

In this report, the nonlinear optical (NLO) properties of titanium dioxide nanoparticles (TiO₂ NPs) have been explored experimentally using femtosecond laser light along with the Z-scan approach. The synthesis of TiO₂ NPs was carried out in distilled water through nanosecond second harmonic Nd:YAG laser ablation. Characterization of the TiO₂ NPs colloids was conducted using UV-visible absorption spectroscopy, transmission electron microscopy (TEM), inductively coupled plasma (ICP), and energy-dispersive X-ray spectroscopy (EDX). The TEM analysis indicated that the size distribution and average particle size of the TiO₂ NPs varied from 8.3 nm to 19.1 nm, depending on the laser ablation duration. The third-order NLO properties of the synthesized TiO₂ NPs were examined at different excitation laser wavelengths and incident powers through both open- and closed-aperture Z-scan techniques, utilizing a laser pulse duration of 100 fs and a high repetition rate of 80 MHz. The nonlinear absorption (NLA) coefficient and nonlinear refractive (NLR) index of the TiO₂ NPs colloidal solutions were found to be influenced by the incident power, excitation wavelength, average size, and concentration of TiO₂ NPs. Maximum values of 4.93 × 10⁻⁹ cm/W for the NLA coefficient and 15.39 × 10⁻¹⁵ cm²/W for the NLR index were observed at an excitation wavelength of 800 nm, an incident power of 0.6 W, and an ablation time of 15 min. The optical limiting (OL) effects of the TiO₂ NPs solution at different ablation times were investigated and revealed to be concentration and average size dependent. An increase in concentration results in a more limiting effect. Full article

Fly ash (FA) is the main solid waste emitted from coal-fired power plants. Due to its high yield, low utilization rate, and occupation of a large amount of land, it exerts enormous pressure on the Earth’s environment. With the deepening of the concept of sustainable development, exploring the reuse of industrial waste such as FA has become a key strategy. If FA can be combined with commonly used jewelry in people’s lives, it will be of great significance to promote the high-net-worth utilization of FA. Therefore, this study synthesized a fly-ash-based composite material with color-changing function and combined it with necklaces as the main material. In the first stage, after blending fly ash and slag, an alkaline activator with a total mass of 10% was added. When the proportion of fly ash was 60%, the compressive strength of the prepared fly-ash-based composite material reached 10.1 MPa. This was attributed to the reaction between sodium silicate in the alkaline activator and free CaO, MgO, and other substances in the fly ash to form hydrated silicate colloids, which solidify the fly ash and transform it into a complex three-dimensional network skeleton. In the second stage, a UV resistant coating with thermochromic function was obtained by blending acrylic resin, TiO₂, and a thermosensitive color-changing agent. It was applied to the surface of fly-ash-based composite materials, and the results showed that as the content of the color-changing agent increased, the number of pores on the surface of the coating gradually decreased. When the content of color-changing agent was 10%, the prepared 10%FAB not only had good surface color but also had good thermal stability, UV absorption ability, superhydrophobicity, and mechanical properties. Therefore, 10%FAB was selected as the basic material for jewelry design. In the third stage, the traditional Chinese technique of “gold inlaid with jade” was utilized to develop jewelry applications for the FA composites. As such, 10%FAB was processed into necklaces, which not only had modern design aesthetics but also had good color-changing effects above 30 °C. And after a long period of UV aging experiments, the necklace did not show any wrinkles, bubbles, or other phenomena. Due to the excitation of TiO₂ hole–electron pairs, the necklace’s UV absorption ability was further improved. This study demonstrates the potential application of industrial waste in decorative products, expands the high-end utilization of fly ash as a low-cost material, and provides new ideas for building a low-carbon lifestyle. Full article

Ammonia (NH₃) gas is prevalent in industrial production as a health hazardous gas. Consequently, it is essential to develop a straightforward, reliable, and stable NH₃ sensor capable of operating at room temperature. This paper presents an innovative approach to modifying SnO₂ colloidal quantum dots (CQDs) on the surface of Ti₃C₂T_x MXene to form a heterojunction, which introduces a significant number of adsorption sites and enhances the response of the sensor. Zero-dimensional (0D) SnO₂ quantum dots and two-dimensional (2D) Ti₃C₂T_x MXene were prepared by solvothermal and in situ etching methods, respectively. The impact of the mass ratio between two materials on the performance was assessed. The sensor based on 12 wt% Ti₃C₂T_x MXene/SnO₂ composites demonstrates excellent performance in terms of sensitivity and response/recovery speed. Upon exposure to 50 ppm NH₃, the frequency shift in the sensor is −1140 Hz, which is 5.6 times larger than that of pure Ti₃C₂T_x MXene and 2.8 times higher than that of SnO₂ CQDs. The response/recovery time of the sensor for 10 ppm NH₃ was 36/54 s, respectively. The sensor exhibited a theoretical detection limit of 73 ppb and good repeatability. Furthermore, a stable sensing performance can be maintained after 30 days. The enhanced sensor performance can be attributed to the abundant active sites provided by the accumulation/depletion layer in the Ti₃C₂T_x/SnO₂ heterojunction, which facilitates the adsorption of oxygen molecules. This work promotes the gas sensing application of MXenes and provides a way to improve gas sensing performance. Full article

Polyvinyl alcohol (PVA)/TiO₂/colloidal photonic crystal (CPC) films with photocatalytic properties are presented, where TiO₂ nanoparticles were introduced into the PVA gel network. Such PVA/TiO₂/CPC films possess three-dimensional periodic structures that are supported with a PVA/TiO₂ composite gel. The unique structural color of CPCs can indicate the process of material preparation, adsorption, and desorption. The shift of diffraction peaks of CPCs can be more accurately determined using fiber-optic spectroscopy. The effect of the PVA/TiO₂/CPC catalyst films showed better properties as the degradation of methylene blue (MB) by the PVA/TiO₂/CPC film catalyst in 4 h was 77~90%, while the degradation of MB by the PVA/TiO₂ film was 33% in 4 h, indicating that the photonic crystal structure was 2.3~2.7 times more effective than that of the bulk structure. Full article

Metal oxides possessing a large surface area, pore volume and desirable pore size provide more varieties and active industrial potentials. Nevertheless, it is very challenging to produce crystal metal oxides while keeping satisfactory porosity features, especially for ternary compositions. High temperature is usually needed to produce crystal metal oxides, which readily leads to the collapse of the pore structure. Herein, by employing a ‘soft’ dispersant agent and a hard silica template, ZrO₂, TiO₂ and Zr-Ti solid solutions having a tetragonal crystal structure are produced and the silica-leached materials are characterized from macroscopic to atomistic scales. The micron-sized particulate powders are composed of nanoscale ‘building blocks’, with crystallite sizes between ~8 and 21 nm. These polycrystalline ceramic powders exhibit a high specific surface area (up to ~200 m²·g⁻¹) and pore volume (up to 0.5 cm³·g⁻¹), with a pore size range of ~5–20 nm. Importantly, the Zr/Ti–O–Si–OH chemical bonds exist on the particle surface, with about two-thirds of the surface covered by silica. The hydroxyl groups can further post-graft organic ligands or directly associate with species. Synthesized mesoporous metal oxides are highly homogenous and could potentially be used in various applications because of their tetragonal structure and porosity features. Full article

In this study, the optimal microwave-assisted sol-gel synthesis parameters for achieving TiO₂ nanoparticles with the highest specific surface area and photocatalytic activity were determined. Titanium isopropoxide was used as a precursor to prepare the sol (colloidal solution) of TiO₂. Isopropanol was used as a solvent; acetylacetone was used as a complexation moderator; and nitric acid was used as a catalyst. Four samples of titanium dioxide were synthesized from the prepared colloidal solution in a microwave reactor at a temperature of 150 °C for 30 min and at a temperature of 200 °C for 10, 20, and 30 min. The phase composition of the TiO₂ samples was determined by X-ray diffraction analysis (XRD) and Fourier-transform infrared spectroscopy (FTIR). Nitrogen adsorption/desorption isotherms were used to determine the specific surface area and pore size distributions using the Brunauer–Emmett–Teller (BET) method. The band-gap energy values of the TiO₂ samples were determined by diffuse reflectance spectroscopy (DRS). The distribution of Ti and O in the TiO₂ samples was determined by SEM-EDS analysis. The effects of adsorption and photocatalytic activity of the prepared TiO₂ samples were evaluated by the degradation of ciprofloxacin (CIP) as an emerging organic pollutant (EOP) under UV-A light (365 nm). The results of the photocatalytic activity of the synthesized TiO₂ nanoparticles were compared to the benchmark Degussa P25 TiO₂. Kinetic parameters of adsorption and photocatalysis were determined and analyzed. It was found that crystalline TiO₂ nanoparticles with the highest specific surface area, the lowest energy band gap, and the highest photocatalytic degradation were the samples synthesized at 200 °C for 10 min. The results indicate that CIP degradation by all TiO₂ samples prepared at 200 °C show a synergistic effect of adsorption and photocatalytic degradation in the removal process. Full article

Old Corrugated Container (OCC) pulping wastewater has a complex organic composition and high levels of biotoxicity. The presence of dissolved and colloidal substances (DCSs) is a major limiting factor for pulp and paper companies to achieve closed-water recycling. In order to solve this problem, the coupled ozone-catalyzed oxidation and biodegradation (OCB) method was used to treat OCC pulping wastewater in this study. A polyurethane sponge was used as the basic skeleton, loaded with nano TiO₂ and microorganisms, respectively, and then put into a reactor. After an 8-min ozone-catalyzed oxidation reaction, a 10-h biological reaction was carried out. The process was effective in removing organic pollutants such as COD and BOD₅ from OCC paper whitewater. The removal rates of COD and BOD₅ were 81.5% and 85.1%, respectively. By using the polyurethane sponge to construct a microenvironment suitable for microbial growth and metabolism, this study successfully applied and optimized engineered bacteria—white rut fungi (WRF)—in the system to achieve practical degradation of OCC pulping wastewater. Meanwhile, the biocompatibility of different microbial communities on the polyurethane sponge was analyzed by examining the degradation performance of OCC pulping wastewater. The structure of microbial communities loaded on the polyurethane sponge was analyzed to understand the degradation mechanism and microbial reaction behavior. White-rot fungi (Phanerochaete) contributed more to the degradation of OCC wastewater, and new strains adapted to OCC wastewater degradation were generated. Full article

The synergetic effects of electromagnetic and chemical enhancements via the combination of semiconductor nanomaterials with noble metal nanoparticles is crucial to the performance of surface-enhanced Raman scattering (SERS). Here, WO₃/TiO₂ photonic crystal films in the form of three-dimensional inverse opals were fabricated via the co-assembly of polymer colloidal templates with water-soluble precursors in order to simultaneously grow both constituent metal oxides with tailored electronic properties and photonic band gaps. The surface modification of compositionally tuned WO₃/TiO₂ inverse opals by Ag nanoparticles is demonstrated to be an efficient method to boost SERS efficiency in the detection of 4−mercaptobenzoic acid via the synergy of plasmonic effects with charge transfer and slow-light trapping. Full article

Ag nanoparticles (AgNPs) were biosynthesized using sage (Salvia officinalis L.) extract. The obtained nanoparticles were supported on SBA-15 mesoporous silica (S), before and after immobilization of 10% TiO₂ (Degussa-P25, STp; commercial rutile, STr; and silica synthesized from Ti butoxide, STb). The formation of AgNPs was confirmed by X-ray diffraction. The plasmon resonance effect, evidenced by UV-Vis spectra, was preserved after immobilization only for the sample supported on STb. The immobilization and dispersion properties of AgNPs on supports were evidenced by TEM microscopy, energy-dispersive X-rays, dynamic light scattering, photoluminescence and FT-IR spectroscopy. The antioxidant activity of the supported samples significantly exceeded that of the sage extract or AgNPs. Antimicrobial tests were carried out, in conditions of darkness and white light, on Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli and Candida albicans. Higher antimicrobial activity was evident for SAg and STbAg samples. White light increased antibacterial activity in the case of Escherichia coli (E. coli) and Pseudomonas aeruginosa (P. aeruginosa). In the first case, antibacterial activity increased for both supported and unsupported AgNPs, while in the second one, the activity increased only for SAg and STbAg samples. The proposed antibacterial mechanism shows the effect of AgNPs and Ag⁺ ions on bacteria in dark and light conditions. Full article