Search Results (353)

Complex oxides with the general formula Gd₂(Ti_1−xZr_x)₂O₇ are promising candidates for radioactive waste immobilization due to their capacity to withstand radiation by dissipating part of the free energy driving defect creation and phase transitions. In this study, samples with varying zirconium content (xZr = 0.00, 0.15, 0.25, 0.375, 0.56, 0.75, 0.85, 1.00) were synthesized via the sol–gel method and thermally treated at 500 °C to obtain nanosized powders mimicking the defective structure of irradiated materials. Synchrotron-based techniques were employed to investigate their structural properties: High-Resolution X-ray Powder Diffraction (HR-XRPD) was used to assess long-range structure, while Pair Distribution Function (PDF) analysis and Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy provided insights into the local structure. HR-XRPD data revealed that samples with low Zr content (xZr ≤ 0.25) are amorphous. Increasing Zr concentration led to the emergence of a crystalline phase identified as defective fluorite (xZr = 0.375, 0.56). Samples with the highest Zr content (xZr ≥ 0.75) were fully crystalline and exhibited only the fluorite phase. The experimental G(r) functions of the fully crystalline samples in the low r range are suitably fitted by the Weberite structure, mapping the relaxations induced by structural disorder in defective fluorite. These structural insights informed the subsequent EXAFS analysis at the Zr-K and Gd-L₃ edges, confirming the splitting of the cation–cation distances associated with different metal species. Moreover, EXAFS provided a local structural description of the amorphous phases, identifying a consistent Gd-O distance across all compositions. Full article

The sustainable valorization of electrolytic manganese residue (EMR) and fly ash (FA) presents critical environmental challenges. This study systematically investigates the performance optimization of EMR-FA ceramic composites through the coordinated regulation of raw material ratios, sintering temperatures, and additive effects. While the composite with 85 g FA exhibits the highest mechanical strength, lowest porosity, and minimal water absorption, the formulation consisting of 45 wt% EMR, 40 wt% FA, and 15 wt% kaolin is identified as a balanced composition that achieves an effective compromise between mechanical performance and solid waste utilization efficiency. Sintering temperature studies revealed temperature-dependent property enhancement, with controlled sintering at 1150 °C preventing the over-firing phenomena observed at 1200 °C while promoting phase evolution. XRD-SEM analyses confirmed accelerated anorthite formation and the morphological transformations of FA spherical particles under thermal activation. Additive engineering demonstrated that 8 wt% CaO addition enhanced structural densification through hydrogrossular crystallization, whereas Na₂SiO₃ induced sodium-rich calcium silicate phases that suppressed anorthite development. Contrastingly, ZrO₂ facilitated zircon nucleation, while TiO₂ enabled progressive performance enhancement through amorphous phase modification. This work establishes fundamental phase–structure–property relationships and provides actionable engineering parameters for sustainable ceramic production from industrial solid wastes. Full article

The superhydrophobic coatings for outdoor use need to be exposed to sunlight for a long time; therefore, their UV-aging resistances are crucial in practical applications. In this study, the primary product of titanium dioxide (P-TiO₂) was used as the raw material. Nano-silica (SiO₂) was coated onto the surface of P-TiO₂ by the acid precipitation method to prepare P-TiO₂-SiO₂ composite particles. Then, they were modified and sprayed simply to obtain a superhydrophobic P-TiO₂-SiO₂/HDTMS coating. The results indicated that amorphous nano-SiO₂ was coated on the P-TiO₂ surface, forming a micro–nano binary structure, which was the essential structure to form superhydrophobic coatings. Additionally, the UV-aging property of P-TiO₂ was significantly enhanced after being coated with SiO₂. After continuous UV irradiation for 30 days, the color difference (ΔE*) and yellowing index (Δb*) values of the coating prepared with P-TiO₂-SiO₂ increased from 0 to 0.75 and 0.23, respectively. In contrast, the ΔE* and Δb* of the coating prepared with P-TiO₂ increased from 0 to 1.68 and 0.74, respectively. It was clear that the yellowing degree of the P-TiO₂-SiO₂ coating was lower than that of P-TiO₂, and its UV-aging resistance was significantly improved. After modification with HDTMS, the P-TiO₂-SiO₂ coating formed a superhydrophobic P-TiO₂-SiO₂/HDTMS coating. The water contact angle (WCA) and water slide angle (WSA) on the surface of the coating were 154.9° and 1.3°, respectively. Furthermore, the coating demonstrated excellent UV-aging resistance. After continuous UV irradiation for 45 days, the WCA on the coating surface remained above 150°. Under the same conditions, the WCAs of the P-TiO₂/HDTMS coating decreased from more than 150° to 15.3°. This indicated that the retention of surface hydrophobicity of the P-TiO₂-SiO₂/HDTMS coating was longer than that of P-TiO₂/HDTMS, and the P-TiO₂-SiO₂/HDTMS coating’s UV-aging resistance was greater. The superhydrophobic P-TiO₂-SiO₂/HDTMS self-cleaning coating reported in this study exhibited outstanding UV-aging resistance, and it had the potential for long-term outdoor use. Full article

To investigate the application potential of amorphous transition metal chalcogenides in catalysis, this study successfully synthesized amorphous molybdenum telluride (MoTe_x) materials and systematically explored their structural characteristics, compositional modulation, and catalytic performance. Experimental results indicate that the synthesized amorphous system consists of particles of approximately 200–300 nm in size. This distinct microstructure facilitates the exposure of abundant active sites and enhances physical adsorption capacity. The amorphous MoTe₂/MoTe₃ catalysts achieve an approximately 30%/40% degradation of methylene blue (MB) within 90 min, demonstrating significantly enhanced photocatalytic efficiency compared to that of crystalline MoTe₂ (≈20% degradation under identical conditions). Furthermore, when integrated with titanium dioxide (TiO₂), the composite exhibits exceptional co-catalytic performance, achieving a 90% degradation of MB within 90 min under visible-light irradiation, representing a catalytic efficiency improvement exceeding 160% compared to the results for pristine TiO₂. Furthermore, through comparative analysis of the catalytic behavior and microstructural variations between amorphous MoTe₃ (a-MoTe₃) and MoTe₂ (a-MoTe₂), we observed that the catalytic activity of molybdenum tellurides exhibits a weak correlation with the tellurium content, with co-catalytic efficacy jointly governed by the density of the active sites and the physical adsorption properties. This research provides new methods and insights for the study and improvement of catalytic performance in chalcogenide materials. Full article

A SiO₂-Al₂O₃-B₂O₃-CaO-MgO-Na₂O glass-based protective lubricant coating was developed for Ti-6Al-4V alloy forging, featuring a fully non-toxic formulation. The coating consisted of a composite glass matrix formed by blending two phases with distinct softening temperatures, extending its operational window to 700–950 °C. The composite glass showed initial softening at 700 °C and complete melting at 800 °C, with contact angle measurements confirming superior wettability (θ < 90°) across the forging range (800~950 °C). With an increase in temperature, the surface tension of the composite glass melt decreased, and subsequently, the wettability of the composite glass melt was significantly improved. XRD revealed that the uncoated Ti-6Al-4V formed a 22 μm thick rutile TiO₂ scale with a porous structure and interfacial cracks, while the coated sample retained an amorphous glass layer with no TiO₂. Cross-sectional SEM showed a crack-free, poreless interface with strong metallurgical bonding, in contrast to the uncoated sample’s spalled oxide layer. EDS showed minimal oxygen diffusion of the glass coating into the substrate. Ring upsetting tests showed that the coating reduced friction from 0.5–0.7 to 0.3 (50–57% decrease). Collectively, the glass protective lubricant coating showed good performance in terms of protection and lubrication. Full article

In response to escalating global energy demands and environmental challenges, electrochromic (EC) smart windows have emerged as a transformative technology for adaptive solar modulation. Herein, we report the rational design and fabrication of a bilayer WO₃/TiO₂ heterostructure via a synergistic two-step strategy involving the electrochemical deposition of amorphous WO₃ and the controlled hydrothermal crystallization of TiO₂. Structural and morphological analyses confirm the formation of phase-pure heterostructures with a tunable TiO₂ crystallinity governed by reaction time. The optimized WTi-5 configuration exhibits a hierarchically organized nanostructure that couples the fast ion intercalation dynamics of amorphous WO₃ with the interfacial stability and electrochemical modulation capability of crystalline TiO₂. Electrochromic characterization reveals pronounced redox activity, a high charge reversibility (98.48%), and superior coloration efficiency (128.93 cm²/C). Optical analysis confirms an exceptional transmittance modulation (ΔT = 82.16% at 600 nm) and rapid switching kinetics (coloration/bleaching times of 15.4 s and 6.2 s, respectively). A large-area EC device constructed with the WTi-5 electrode delivers durable performance, with only a 3.13% degradation over extended cycling. This study establishes interface-engineered WO₃/TiO₂ bilayers as a scalable platform for next-generation smart windows, highlighting the pivotal role of a heterostructure design in uniting a high contrast, speed, and longevity within a single EC architecture. Full article

TiO₂ is an abundant material on Earth, essential for the sustainable and cost-effective development of various technologies, with anatase being the most effective polymorph for photocatalytic and photovoltaic applications. Bulk crystalline anatase TiO₂ exhibits a band gap energy E_gA = 3.2 eV, for tetragonal lattice parameters a_A = 0.3785 nm and c_A = 0.9514 nm, but these characteristics vary for amorphous or polycrystalline thin films. Reactive magnetron sputtering has proven suitable for the preparation of TiO₂ coatings on glass fiber substrates, with structural and optical characteristics that change during growth. Below a minimum thickness (t < 0.2 μm), the films have an amorphous nature or extremely small crystallite sizes not observable by X-ray diffraction. Afterwards, compressed quasi-randomly orientated crystallites are detected (volume strain ΔV = −0.02 and stress σ_V = −3.5 GPa for t = 0.2 μm) that evolve into relaxed and preferentially (004) orientated crystallites, reaching the standard anatase values at t ~ 1.4 μm with σ_V = 0.0 GPa. The band gap energy increases with lattice distortion according to the relation ∆E_g (eV) = −6∆V, and a further increase is observed for the thinnest coatings (∆E_g = 0.24 eV for t = 0.05 μm). Full article

We report the photocatalytic (PC) response of titanium oxide (TiO_x) films grown by reactive DC magnetron sputtering under oblique-angle-deposition (OAD) and subjected to post-deposition flash-lamp-annealing (FLA). Under ballistic growth conditions, OAD yields TiO_x films with either compact or inclined columnar structure as the deposition incidence angle (α) with respect to the substrate normal varies from zero to grazing. On the one hand, films produced for α ≤ 45° display a compact and opaque structure comprising the formation of nanocrystalline cubic titanium monoxide (c-TiO) phase. On the other hand, films grown at larger α (≥60°) display tilted columns with amorphous structure, yielding highly porous films and an increased transparency for α > 75°. For TiO_x films grown at large α, FLA induces phase transformation to nanocrystalline anatase from the amorphous state. In contrast to as-grown samples, FLA samples display PC activity as assessed by bleaching of methyl orange dye. The best PC performance is attained for an intermediate situation (α = 60–75°) between compact and columnar structures. The obtained photoactivity is discussed in terms of the different microstructures obtained by OAD and posterior phase formation upon FLA. Full article

This study developed a hydrothermal-crystallization coupling strategy for selective titanium extraction from low-grade titanium-bearing blast furnace slag. Systematic parametric optimization revealed that an optimum titanium extraction efficiency of 92.3% was achieved under mild hydrothermal conditions. Phase evolution analysis demonstrated that the leaching residues comprised commercially valuable calcium oxalate hydrate and amorphous silica aggregates, while titanium primarily existed as stable Ti(OH)₂(C₂O₄)₂²⁻ complexes in the leachate. Subsequently, 99.4% of titanium in the leachate was precipitated through the hydrothermal decomposition method, and mixed-phase titanium oxides with a grade of 90.5% were obtained through alkaline washing. Comparative analysis highlights three notable advantages over conventional metallurgical processes: (1) selective extraction specificity for low-concentration titanium minerals, (2) process intensification through integrated hydrothermal-crystallization operations, and (3) environmental benignancy via reagent recyclability. Full article

Nickel-decorated carbocatalysts were synthesized by the evaporation-induced self-assembly (EISA) method. The influence of the metal content and pyrolysis temperature upon the photoactivity was assessed through rhodamine B degradation under UV irradiation. The characterization revealed a mesoporous framework with a granular morphology composed of amorphous carbon, where the pyrolysis temperature influenced the metal dispersion on the carbon surface. The primary metallic phases consisted of elemental nickel crystallites and nickel carbide phases. The kinetic parameters for adsorption and dye photodegradation under UV irradiation were determined and compared to TiO₂-P25. Correlations were found between the adsorption parameters, photocatalytic activity, and nickel content, the pyrolysis method (one-step vs. two-step pyrolysis), and the pyrolysis temperature. The sample with a 1:1:0.25 tannin/Pluronic^®F-127/Ni weight ratio pyrolyzed at 700 °C exhibited the highest photoactivity, achieving rhodamine B degradation rates up to 68 and 2.5 times greater than photolysis and TiO₂-P25. In terms of the normalized weight of the catalysts, it can be concluded that the present Ni-based catalysts are up to two orders of magnitude more photoactive than TiO₂-P25 under UV irradiation, opening a door for indoor UV-driven photoreactors. These findings demonstrate that the EISA method is an effective, low-cost, and ecofriendly approach for synthesizing Ni-decorated carbocatalysts. Full article

This report discusses the impact of nanoparticles on glass-forming systems composed of a liquid crystalline (LC) mixture E7 and paraelectric BaTiO₃ particles ($d\approx 50 \mathrm{n}\mathrm{m}$, globular), tested via broadband dielectric spectroscopy. In the isotropic phase, critical changes in the dielectric constant are shown. They are related to the weakly discontinuous nature of the isotropic–nematic transition. In the nematic phase, two primary relaxation times/processes and DC electric conductivity are considered, down to the glass temperature $T_g$. The prevalence of portrayals via the ‘double exponential’ MYEGA equation and the critical & activated Drozd-Rzoska relation for dynamic properties are shown. For the primary loss curve, critical-like changes of its maximum (peak) are evidenced: ${\epsilon }_{peak}^{″}\propto 1/\left(T-T_g^{*}\right)$ for $T_g<T<\left(T_g+25 \mathrm{K}\right)$, where $T_g^{*}<T_g$ denotes the extrapolated singular temperature. Dielectric constant monitoring revealed the permanent arrangement of rod-like LC molecules by nanoparticles’ endogenic impact in the nematic phase. The heuristic model regarding this unique behavior is presented. It considers a hypothetical link between the glass transition and a hidden near-critical discontinuous phase transition, uniquely avoiding a symmetry change. The uniaxiality of LC molecules enables the detection of critical-like features when approaching the glass transition, hypothetically associated with a specific ‘amorphous’ phase transition. Full article

Electrochromic materials have a wide range of energy-effective applications, such as in mirrors, smart windows, automobile sunroofs, and display devices. The electrochromic behavior of mixed metal oxides is focused on in this review. Extra heat absorbed by buildings is one of the major problems in our modern era, so electrochromic films have been used as components of smart windows to reduce heat absorption through glass windows. Transition metal (W, V, Ti, Mo, and Ni) oxides are considered popular electrochromic materials for this purpose. Smart windows consist of electrochromic material layers (such as metal oxide layers) and solid electrolytes sandwiched between transparent conductive layers. Few publications have studied the use of mixtures of different metal oxides as electrochromic materials. This study focuses on the results of investigations of such multicomponent materials, such as the effects on the electrochromic properties of mixed metal oxides and how they contrast with pure metal oxides. Reviewing these papers, we found WO₃- and MoO₃-based mixtures to be the most promising, especially the magnetron-sputtered, amorphous WO₃(40%)–MoO₃(60%) composition, which had 200–300 cm²/C coloration efficiency. The mixed oxide materials reported in this review have room for development (and even commercialization) in the oxide-based electrochromic device market. Full article

This review analyzes TiO₂-based coatings formed by the plasma electrolytic oxidation (PEO) process of titanium for the photocatalytic degradation of methyl orange (MO) under simulated solar irradiation conditions. PEO is recognized as a useful technique for creating oxide coatings on various metals, particularly titanium, to assist in the degradation of organic pollutants. TiO₂-based photocatalysts in the form of coatings are more practical than TiO₂-based photocatalysts in the form of powder because the photocatalyst does not need to be recycled and reused after wastewater degradation treatment, which is an expensive and time-consuming process. In addition, the main advantage of PEO in the synthesis of TiO₂-based photocatalysts is its short processing time (a few minutes), as it excludes the annealing step needed to convert the amorphous TiO₂ into a crystalline phase, a prerequisite for a possible photocatalytic application. Pure TiO₂ coatings formed by PEO have a low photocatalytic efficiency in the degradation of MO, which is due to the rapid recombination of the photo-generated electron/hole pairs. In this review, recent advances in the sensitization of TiO₂ with narrow band gap semiconductors (WO₃, SnO₂, CdS, Sb₂O₃, Bi₂O₃, and Al₂TiO₅), doping with rare earth ions (example Eu³⁺) and transition metals (Mn, Ni, Co, Fe) are summarized as an effective strategy to reduce the recombination of photo-generated electron/hole pairs and to improve the photocatalytic efficiency of TiO₂ coatings. Full article

The heterogeneous integration of ferroelectric thin films on silicon- or silicon nitride-based platforms for photonic integrated circuits plays a crucial role in the development of nanophotonic thin film modulators. For this purpose, an ultrathin seed film was recently introduced as an integration method for ferroelectric thin films such as BaTiO₃ and Pb(Zr,Ti)O₃. One issue with this self-orienting seed film is that for non-planarized circuits, it fails to act as a template film for the thin films. To circumvent this problem, we propose a method of planarization without the need for wafer-scale chemical mechanical polishing by using hydrogen silsesquioxane as a precursor to forming amorphous silica, in order to create an oxide cladding similar to the thermal oxide often present on silicon-based platforms. Additionally, this oxide cladding is compatible with the high annealing temperatures usually required for the deposition of these novel ferroelectric thin films (600–800 °C). The thickness of this silica film can be controlled through a dry etch process, giving rise to a versatile platform for integrating nanophotonic thin film modulators on a wider variety of substrates. Using this method, we successfully demonstrate a hybrid BaTiO₃-Si ring modulator with a high Pockels coefficient of $r_{wg}=155.57\pm 10.91$ pm V⁻¹ and a half-wave voltage-length product of $V_{\pi }L=2.638\pm 0.084$ V cm, confirming the integration of ferroelectric thin films on an initially non-planar substrate. Full article

This research highlights the different behaviors of titanium (Ti) wires under the action of 500 W and 800 W microwave power levels. Following the interaction between microwaves and a titanium wire placed in the node of the (TM₀₁₁—transverse magnetic mode) waveguide in air at atmospheric pressure, plasma was generated. Using optical emission spectroscopy technique it was observed that during plasma generation at 500 W and 800 W microwaves powers, metallic ions, and gas ions were created, and the plasmas fulfilled the local thermodynamic equilibrium (LTE) conditions. The XRD analysis showed that on the surface of the Ti wire exposed to 500 W microwave power a mixture of titanium dioxide (TiO₂) and titanium oxide (TiO) grew, while the Ti wire exposed to 800 W microwave power was completely vaporized and a mixture of TiO₂ and TiO nanoparticles was synthesized. The SEM analysis showed that the dimensions of the titanium oxide (TiO_x) nanoparticles generated by both microwave discharges ranged from 5 nm to 200 nm. The results of EDS analysis showed that the power of microwaves plays an important role in quantitative conversion from Ti wire into a TiO_x mixture. The TEM analysis indicates that most of the nanoparticles are either amorphous or nanocrystalline. Using this simple and inexpensive technique one can grow a TiO_x layer on the surface of titanium electrodes or can synthetize nanocrystalline TiO_x particles. Full article