Search Results (55)

Photoelectrochemical (PEC) energy conversion is a promising approach for solar-to-chemical fuel production, but its practical performance is limited by insufficient visible-light utilization and charge-carrier recombination. Here, poly(3,4-ethylenedioxythiophene) (PEDOT)-centered TiO₂ hybrid electrodes were prepared by electropolymerizing PEDOT on FTO substrates, followed by electrochemical doping/dedoping treatment and coating with commercial TiO₂ as a model oxide semiconductor. SEM, EDS, and LIBS analyses confirmed the successful deposition of TiO₂ onto PEDOT-based films. Four-probe measurements showed that electrochemical doping reduced the apparent resistance of PEDOT-based electrodes, while UV–vis spectroscopy revealed enhanced long-wavelength absorption for doped PEDOT-containing films. PEC measurements using TiO₂, PEDOT, and TiO₂–PEDOT electrodes showed that PEDOT-containing electrodes exhibited much stronger photoresponses than commercial TiO₂ alone under both HER- and OER-relevant conditions. The TiO₂–PEDOT electrode showed stable photocurrent responses under chopped illumination and retained photoresponse under illumination transmitted through a 410 nm UV-cut filter, supporting the primary role of PEDOT in visible-light utilization. Long-term chronoamperometry further showed that TiO₂–PEDOT retained approximately 99.0% of its cathodic current under HER-relevant conditions and 91.9% of its anodic current under OER-relevant conditions after 5200 s of continuous illumination. The improved response of TiO₂–PEDOT compared with PEDOT alone suggests that TiO₂/PEDOT physical contact may assist interfacial charge separation and transport. These findings demonstrate that PEDOT-centered metal oxide/conducting polymer hybrids provide a useful model platform for visible-light-responsive PEC energy-conversion applications. Full article

This study investigates the hydrothermal modification of commercial titanium dioxide (TiO₂) in the presence of a natural licorice root extract (Glycyrrhiza glabra L.), serving as a stabilizing and growth-modulating agent. The experimental framework combines hydrothermal treatment in a Teflon-lined autoclave with subsequent thermal calcination to elucidate the structural, morphological, and chemical evolution of the material. The plant-based extract significantly influences particle assembly during synthesis, fostering the formation of an initial organic–inorganic hybrid system that results in enhanced morphological homogeneity compared to pristine TiO₂. Thermal analyses (TGA and DSC) demonstrated the progressive decomposition of the organic components with increasing temperature, yielding a thermally stable, predominantly inorganic material at 600 °C. Scanning Electron Microscopy (SEM) observations confirmed a more uniform particle distribution in the modified samples. X-ray diffraction (XRD) patterns corroborated that the primary crystalline phase of TiO₂ remains intact across all conditions, with structural variations limited to peak definition and long-range organization. Furthermore, FTIR spectroscopy supported the preservation of characteristic TiO₂ vibrational features while indicating a gradual depletion of weakly bound surface species following thermal treatment. In conclusion, these findings demonstrate that natural extracts can effectively function as growth-modulating agents, steering material organization without altering its intrinsic chemical properties. This approach aligns with the principles of Green Chemistry and the circular economy, highlighting the potential of renewable plant-based resources as functional additives for the sustainable processing of inorganic materials. Rather than seeking to outperform commercial benchmarks, this work establishes a viable and low-environmental-impact strategy for morphological and structural modulation. Full article

Despite the growing adoption of Ti6Al4V-ELI made by Laser Powder Bed Fusion (LPBF) in tribologically demanding applications, the influence of hybrid nanoparticle additives on its lubrication behavior under starved contact conditions remains insufficiently explored. The tribological performance of Ti6Al4V was investigated under starved boundary-to-mixed lubrication conditions using engine oil modified with Ag-doped TiO₂ nanoparticles. Double-scan LPBF-fabricated discs were tested in a ball-on-disc configuration against AISI 52100 bearing steel using a TRB³ tribometer. Nanolubricants were prepared by dispersing TiO₂ and Ag–TiO₂ nanopowders with different Ag⁺/Ti⁴⁺ ratios (0.5%, 1.5%, and 2.5%) in SAE 10W-40 engine oil at a constant nanoparticle concentration of 0.05 wt%. Comprehensive physicochemical characterization of the nanopowders and nanolubricants was performed through structural, chemical, optical, morphological, rheological, and stability analyses. Tribological experiments were conducted following a full-factorial design combining three normal loads (5–15 N), three sliding speeds (0.10–0.20 m·s⁻¹), and four lubricant formulations. The steady-state coefficient of friction ranged between 0.281 and 0.359, while the specific wear rate varied from 2.81 × 10⁻⁴ to 4.83 × 10⁻⁴ mm³·N⁻¹·m⁻¹. The contact temperature rise remained relatively moderate, within the interval of 1.9–9.4 °C. Among the investigated formulations, the lubricant containing 1.5% Ag–TiO₂ exhibited the lowest friction coefficient, whereas the formulation with the highest Ag content showed improved stability of tribological performance across the investigated operating domain. These results indicate that Ag-modified TiO₂ nanoparticles are consistent with the formation of protective tribofilms and contribute to the stabilization of friction, wear, and thermal behavior under starved lubrication conditions. ANOVA confirmed that sliding speed and the load–lubricant interaction are the dominant factors governing friction and wear, while normal load controls the thermal response. These findings support the use of Ag–TiO₂ nanolubricants as a viable strategy for stabilizing interfacial behavior in LPBF-fabricated titanium components operating under starved lubrication conditions. Full article

Titanium dioxide (TiO₂) has evolved from a conventional photocatalyst into a sophisticated nano-platform that bridges environmental sustainability and biomedicine. This paper proposes a unified interfacial redox design framework that links the electronic-structure engineering of the TiO₂ with the spatial control of its reactive oxygen species (ROS). In the environmental sector, we highlight advances in photocatalytic detoxification, such as the cleavage of organophosphates via Ag-modified TiO₂, driven by doping and metal–support interactions. In the biomedical domain, TiO₂ is framed as an active bio-interface capable of coordinative protein binding. We specifically examine the “moonlighting” protein dihydrolipoamide dehydrogenase (DLDH) as a model for stable, oriented biofunctionalization. By integrating RGD-targeting motifs, these hybrid systems enable integrin-directed, localized photodynamic effects. We further address critical toxicological considerations, emphasizing that TiO₂ behavior is context-dependent and governed by particle size, crystallinity, and surface state. By synthesizing insights from catalysis and redox biology, this manuscript outlines principles for the rational design of safer, application-specific TiO₂ technologies. This convergence supports a transition from non-selective oxidation toward predictable, spatially confined redox outcomes in both complex environmental matrices and physiological systems. This review outlines key mechanistic insights and proposes design principles for controlled and context-dependent TiO₂ activity. Full article

EPDM is widely used as the polymer matrix for solid rocket motor (SRM) internal thermal protection because of its low density, chemical inertness, and ability to form carbonaceous residue. Practical performance is frequently limited by weak char integrity and barrier properties, char oxidation, mechanical stripping in gas-dynamic flow, and by the poor comparability of published results due to non-uniform test conditions and reporting. This review systematizes studies on 0D nanofillers in EPDM ablatives and harmonizes the key metrics, including linear and mass ablation rates (LAR, MAR), back-face temperature (T_back), and solid residue yield. The major 0D additives-nSiO₂, nTiO₂, nZnO, and carbon black (CB) are compared, and their dominant mechanisms are summarized: degradation-layer structuring, reduced gas permeability, thermo-oxidative stabilization, and effects on vulcanization. Several studies report larger improvements for hybrid systems, where CB enhances char cohesion and retention, while oxide nanoparticles improve barrier performance and resistance to oxidation. Finally, an application-oriented selection matrix is proposed that accounts for thermal protection efficiency, processability, agglomeration limits, and density penalties to support EPDM coating design and improve comparability. Full article

Advanced oxidation processes using porphyrin-based heterogeneous catalysts hold promise for removing hazardous pollutants from wastewater. Their high visible-light absorption coefficients enable absorption of light from the solar spectrum. Moreover, their conjugated aromatic skeletons and intrinsic electronic properties facilitate the delocalization of photogenerated electrons during photodegradation. Delaying the recombination of photogenerated electron–hole pairs by introducing specific materials increases efficiency, as separated charges have more time to participate in redox reactions, boosting photocatalytic activities. However, applying these photocatalysts for wastewater treatment is challenging owing to facile agglomeration, deactivation, and recovery of the photocatalyst for reuse, which can significantly increase the overall cost. Therefore, new photocatalytic systems comprising porphyrin molecules must be developed. For this purpose, porphyrins can be conjugated to nanomaterials to create hybrid materials with photocatalytic efficiencies superior to those of free-standing starting porphyrins. Various transition metal oxides (TiO₂, ZnO, and Fe₃O₄) nanoparticles, main-group-element oxides (Al₂O₃ and SiO₂) nanoparticles, metal plasmons (silver nanoparticles), carbon-based platforms (graphene, graphene oxide, and g-C₃N₄), and polymer matrices have been used as nanostructured solid supports for the successful fabrication of porphyrin-conjugated hybrid materials. The conjugation of porphyrin molecules to solid supports improves the photocatalytic degradation activity in terms of visible-light conversion ability, recyclability, active porous sites, substrate mobility, separation of photogenerated charge species, recovery for reuse, and chemical stability, along with preventing the generation of secondary pollution. This review discusses the ongoing development of porphyrin-conjugated hybrid nanomaterials for the heterogeneous photocatalytic degradation of organic dyes, pharmaceutical pollutants, heavy metals, pesticides, and human care in water. Several important results and advancements in the field allow for a more efficient wastewater remediation process. Full article

The adsorption of methylene blue (MB) on poly(vinylidene fluoride) (PVDF) and PVDF/titanium dioxide(TiO₂) membranes with 1.5 wt% dosage was examined through batch adsorption and dynamic cross-flow filtration experiments. The effects of pH, temperature, and initial MB concentration on adsorption performance were evaluated via batch experiments. The Thomas model was applied to analyze the membrane filtration process, while kinetic, isothermal, and thermodynamic models were integrated to elucidate the adsorption mechanisms. Results demonstrated that low temperature and high initial MB concentration significantly improved MB adsorption on both membranes. Under neutral pH conditions (pH = 7), the maximum adsorption capacities of PVDF and PVDF/TiO₂ membranes reached 1.518 ± 0.025 mg/g and 0.189 ± 0.008 mg/g, respectively. The adsorption processes on both membranes conformed to the pseudo-second-order kinetic model, with optimal fitting to the Langmuir isotherm model. Thermodynamic analysis revealed physical adsorption mechanisms, as evidenced by adsorption free energy (E) calculated via the Dubinin–Radushrevich model Notably, PVDF membrane exhibited a more pronounced mass transfer zone height (h_Z = 2.3 ± 0.1 cm) and achieved higher adsorption capacity (2.1 ± 0.09 mg/g) than PVDF/TiO₂ membranes (0.25 ± 0.01 mg/g). The TiO₂ incorporation reduced hybrid membrane adsorption capacity and significantly mitigated membrane fouling caused by adsorption, with PVDF/TiO₂ membranes showing a 32 ± 2.5% lower flux decline rate than PVDF membranes with less MB into the pores. This study provides fundamental data supporting the combined application of “adsorption–subsequent oxidation” using PVDF-based membranes in dye wastewater treatment. Full article

The primary goal of this study was to improve the rheological properties of water-based drilling mud using a combination of TiO₂-coated ZnO nanoparticles and activated carbon (AC) from banana peels. The TiO₂/ZnO nanocomposites were prepared using polyvinyl alcohol (PVA) as a binder under magnetic stirring and ultrasonic sonication to ensure uniform coating, followed by washing and controlled thermal treatment. NaOH-assisted chemical activation of banana peel produced activated carbon with better porosity and surface functionality than raw banana peel. The base water-based mud used in this study had different concentrations of both additives mixed in, and rheological parameters such as mud density, plastic viscosity (PV), yield point (YP), and gel strength were measured according to standard API methods. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used for structural and morphological characterization, which proved the successful coating and uniform dispersion of TiO₂ on ZnO nanoparticles. The use of mixed additives resulted in a significant improvement in mud properties, such as viscosity, gel strength, and yield point, proving to be more effective in suspension capacity and overall rheological stability. The use of this hybrid bio-nanocomposite mud system is a very economical and eco-friendly way of enhancing the drilling fluid performance, thus proving to be a supporting factor in conducting drilling operations that are both safe and efficient. Additionally, this study provides a sustainable hybrid TiO₂-ZnO and activated carbon additive that results in synergistic improvement of drilling-mud rheology and stability. Full article

Sorption and advanced oxidative processes (AOPs) are potential strategies for the removal of organic compounds, such as caffeine, from aqueous media. Such strategies tend to be more promising when combined with biopolymeric membranes as sorbents and photocatalyst supports. Therefore, the aim of the present study was to investigate sorption and AOP parameters in the performance of chitosan membranes and chitosan/TiO₂ composite membranes in individual and hybrid systems involving the photolysis, photocatalysis, and sorption of caffeine. Caffeine degradation by photolysis was 19.51 ± 1.14, 28.61 ± 0.05, and 30.64 ± 6.32%, whereas caffeine degradation by photocatalysis with catalytic membrane was 18.33 ± 2.20, 20.83 ± 1.49, and 31.41 ± 3.08% at pH 6, 7, and 8, respectively. In contrast, photocatalysis with the dispersed catalyst achieved degradation of 93.56 ± 2.12, 36.42 ± 2.59, and 31.41 ± 1.07% at pH 6, 7, and 8, respectively. These results indicate that ions present in the buffer solutions affect the net electrical charge on the surface of the composite biomaterial with the change in pH variation, occupying active sorption sites in the structure of the biomaterial, which was characterized by Fourier transform infrared spectrometry, thermogravimetric analysis, differential scanning thermogravimetry, and X-ray diffraction. Thus, it is verified that in a combined process of caffeine removal under UV irradiation and use of chitosan/TiO₂ composite membranes in phosphate-buffered medium, the photolysis mechanism is predominant, with little or no contribution from sorption, and that the TiO₂ catalyst promotes a significant reduction in the percentage of pollutant in the medium only when used dispersed and at low pH. Full article

Hybrid silane-based coatings were developed via the sol–gel process using two precursors, vinyltrimethoxysilane (VTMS) and tetraethoxysilane (TEOS), and subsequently deposited onto three titanium-based substrates: commercially pure titanium Grade 2, Ti6Al4V, and Ti13Nb13Zr. Comprehensive physicochemical characterization was performed, including microstructural (optical and SEM), topographical (3D roughness), spectroscopic (FTIR), and electrochemical (potentiodynamic) analyses. The coatings were continuous, transparent, smooth, and exhibited high gloss with no visible cracks or surface defects. Surface roughness (Sa ≈ 0.3 μm) was consistent across all samples and remained unaffected by both the VTMS to TEOS ratio and the substrate type. Coating thickness ranged from 8 to 15 μm, as confirmed by both digital microscopy and thickness gauge measurements. All coatings demonstrated strong adhesion to the substrates. FTIR analysis confirmed the presence of key functional groups, such as CH₂, C=C, C–H, Si–O–Si, Si–OH, Si–O–Ti, CH=CH₂, and O–Si–O, regardless of the substrate type. Electrochemical tests in Ringer’s solution showed excellent corrosion resistance, particularly for coatings with a VTMS to TEOS ratio of 1:1. Post-corrosion imaging confirmed the integrity of the coatings and their effectiveness as protective barriers in simulated physiological environments. These findings support the potential of VTMS/TEOS sol–gel coating as a surface modification strategy for biomedical titanium implants. Full article

The urgency to decarbonize fuels has contributed to a rise in biofuel production, which has culminated in a significant increase in the waste quantity of glycerol produced. Therefore, to convert glycerol waste into high-value products, electrochemical oxidation (EO) is a viable alternative for the co-generation of carboxylic acids, such as formic acid (FA) and green hydrogen (H₂), which are considered energy carriers. The aim of this study is the electroconversion of glycerol into FA by EO using a divided electrochemical cell, driven by a photovoltaic (PV) system, with a dimensionally stable anode (DSA, Ti/TiO₂-RuO₂-IrO₂) electrode as an anode and Ni-Fe stainless steel (SS) mesh as a cathode. To optimize the experimental conditions, studies were carried out evaluating the effects of applied current density (j), electrolyte concentration, electrolysis time, and electrochemical cell configuration (undivided and divided). According to the results, the optimum experimental conditions were achieved at 90 mA cm⁻², 0.1 mol L⁻¹ of Na₂SO₄ as a supporting electrolyte, and 480 min of electrolysis. In this condition, 256.21 and 211.17 mg L⁻¹ of FA were obtained for the undivided and divided cells, respectively, while the co-generation of 6.77 L of dry H₂ was achieved in the divided cell. The electroconversion process under the optimum conditions was also carried out with a real sample, where organic acids like formic and acetic acids were co-produced simultaneously with green H₂. Based on the preliminary economic analysis, the integrated-hybrid process is an economically viable and promising alternative when it is integrated with renewable energy sources such as solar energy. Full article

This study investigated a hybrid electrode based on titanium/titanium dioxide nanowires/reduced graphene oxide (Ti-TiO₂(NW)/rGO) that was developed in two stages. The Ti-TiO₂(NW)/rGO was obtained by hydrothermal treatment in a mixed solution of H₂O₂ and melamine for Ti-TiO₂ support, followed by a simple spin-coating deposition method and thermal oxidation in a controlled atmosphere of nitrogen gas (99%). The as-prepared structures of electrodes were characterized using ultraviolet-visible spectroscopy (UV-Vis), X-ray diffraction (XRD), Raman spectroscopy, and scanning electron microscopy (SEM). In addition, the electrochemical behavior was assessed by cyclic voltammetry (CV) in a 1M HNO₃-supporting electrolyte and in the presence of 4 mM K₄Fe(CN)₆ 3H₂O to determine the electroactive surface area and apparent diffusion coefficient of the hybrid electrode. The development of the Ti-TiO₂(NW)/rGO hybrid electrode provides a sensitive method for photo-electrooxidation of doxorubicin due to exploiting the synergistic and remarkable properties of the nanowires of TiO₂ and of reduced graphene oxide (rGO) layer on the electrode surface. Full article

The present review is related to the novel approach for improvement of the optical properties of wide bandgap metal oxides, in particular TiO₂, based on the formation of the inorganic–organic hybrids that display absorption in the visible spectral range due to the formation of interfacial charge transfer (ICT) complexes. We outlined the property requirements of TiO₂-based ICT complexes for efficient photo-induced catalytic reactions, emphasizing the simplicity of the synthetic procedure, the possibility of the fine-tuning of the optical properties supported by the density functional theory (DFT) calculations, and the formation of a covalent linkage between the inorganic and organic components of hybrids, i.e., the nature of the interface. In addition, this study provides a comprehensive insight into the potential applications of TiO₂-based ICT complexes in photo-driven catalytic reactions (water splitting and degradation of organic molecules), including the identification of the reactive species that participate in photocatalytic reactions by the spin-trapping electron paramagnetic resonance (EPR) technique. Considering the practically limitless number of combinations between the inorganic and organic components capable of forming oxide-based ICT complexes and with the knowledge that this research area is unexplored, we are confident it is worth studying, and we emphasized some further perspectives. Full article

In the pursuit of developing advanced nanofiltration membranes with high permeation flux for organic solvents, a TiO₂ nanofilm was synthesized via a vapor–liquid interfacial reaction on a flat-sheet α-Al₂O₃ ceramic support. This process involves the reaction of glycerol, an organic precursor with a structure featuring 1,2-diol and 1,3-diol groups, with TiCl₄ vapor to form organometallic hybrid films. Subsequent calcination in air at 250 °C transforms these hybrid films into carbon-doped titanium oxide nanofilms. The unique structure of glycerol plays a crucial role in determining the properties of the resulting nanopores, which exhibit high solvent permeance and effective solute rejection. The synthesized carbon-doped TiO₂ nanofiltration membranes demonstrated impressive performance, achieving a pure methanol permeability as high as 90.9 L·m⁻²·h ⁻¹·bar⁻¹. Moreover, these membranes exhibited a rejection rate of 93.2% for Congo Red in a methanol solution, underscoring their efficacy in separating solutes from solvents. The rigidity of the nanopores within these nanofilms, when supported on ceramic materials, confers high chemical stability even in the presence of polar solvents. This robustness makes the carbon-doped TiO₂ nanofilms suitable for applications in the purification and recovery of organic solvents. Full article

Anatase titanium dioxide (TiO₂) has emerged as a potential anode material for sodium-ion hybrid capacitors (SICs) in terms of its nontoxicity, high structure stability and cost-effectiveness. However, its inherent poor electrical conductivity and limited reversible capacity greatly hinder its practical application. Here, ultrathin TiO₂ nanoplates were synthesized utilizing a hydrothermal technique. The electrochemical kinetics and reversible capacity were significantly improved through sulfur and nitrogen co-doping combined with carbon coating (SN-TiO₂/C). Sulfur and nitrogen co-doping generated oxygen vacancies and introduced additional active sites within TiO₂, facilitating accelerated Na-ion diffusion and enhancing its reversible capacity. Furthermore, carbon coating provided stable support for electron transfer in SN-TiO₂/C during repeated cycling. This synergistic strategy of sulfur and nitrogen co-doping with carbon coating for TiO₂ led to a remarkable capacity of 335.3 mAh g⁻¹ at 0.1 A g⁻¹, exceptional rate property of 148.3 mAh g⁻¹ at 15 A g⁻¹ and a robust cycling capacity. Thus, the SN-TiO₂/C//AC SIC delivered an impressive energy density of 177.9 W h kg⁻¹. This work proposes an idea for the enhancement of reaction kinetics for energy storage materials through a synergistic strategy. Full article