Nanomanufacturing

Titanium dioxide nanoparticles were synthesized via hydrothermal treatment of tetrabutyl titanate in sulfuric acid, with controlled reaction times (10 h and 24 h) and zinc sulfate as a modifier. XRD confirmed exclusive formation of the anatase phase, with longer reaction times promoting crystallite growth. SEM and BET analyses showed that introducing Zn during synthesis suppressed agglomeration, decreased the particle size, and modified porosity while maintaining the mesoporous nature of all samples. UV–Vis diffuse reflectance spectroscopy showed a band gap near 3.2 eV, which was unaffected by Zn content or morphology. Photoconductivity studies showed a several-orders-of-magnitude increase in conductivity under vacuum conditions, especially in samples heat-treated for 24 h, due to the generation of oxygen vacancies and ${\mathrm{Ti}}^{3+}$ states that prolong the carrier lifetime. In particular, the TS24Z8 sample exhibited a photoconductivity enhancement of five orders of magnitude relative to its dark conductivity and nearly 30 times higher than that of the commercial P25 benchmark. In contrast, in air, photoconductivity remained low because of strong surface recombination with adsorbed oxygen. These results emphasize the critical influence of hydrothermal duration and zinc incorporation on the defect structure and electronic response of ${\mathrm{TiO}}_2$, offering insights for improved photocatalytic and optoelectronic applications.

Given the environmental hazards of 2,4,6-trinitrophenol (TNP) and the limitations of existing detection methods, sodium-doped fluorescent carbon dots (Na-CDs) were successfully synthesized via a one-step hydrothermal method using citric acid and ascorbic acid as carbon sources. Compared with undoped carbon quantum dots, Na-CDs exhibited nearly identical surface functional groups but significantly enhanced fluorescence stability and markedly improved selective responsiveness toward TNP. Accordingly, a Na-CD-based fluorescent probe was developed for the highly selective detection of TNP. Results demonstrated a good linear relationship between the relative fluorescence intensity change (F₀ − F)/F₀ and TNP concentration ranging from 7 × 10⁻⁷ to 2 × 10⁻⁵ mol/L, with a detection limit of 3.5 × 10⁻⁸ mol/L. When applied to detect TNP in local river water samples, the method achieved recoveries of 95.40–104.0%, confirming its reliability for real-world environmental sample analysis. This study develops a novel, sensitive, and highly selective approach for monitoring TNP in environmental systems.

Metal-oxide heterostructures represent an effective strategy to overcome the limitations of pristine TiO₂, including its ultraviolet-only light absorption and rapid electron–hole recombination, which hinder its performance in solar-driven applications. Among various configurations, coupling TiO₂ with tungsten oxide (WO_x) forms a favorable type-II band alignment that enhances charge separation. However, a comprehensive understanding of how WO_x overlayer thickness affects the optical and photoelectrochemical (PEC) behavior of device-grade thin films remains limited. In this study, bilayer TiO₂/WO_x heterostructures were fabricated via reactive DC magnetron sputtering, with controlled variation in WO_x thickness to systematically investigate its influence on the structural, optical, and PEC properties. Adjusting the WO_x deposition time enabled precise tuning of light absorption, interfacial charge transfer, and donor density, resulting in markedly distinct PEC responses. The heterostructure obtained with 30 min of WO_x deposition demonstrated a significant enhancement in photocurrent density under AM 1.5G illumination, along with reduced charge-transfer resistance and improved capacitive behavior, indicating efficient charge separation and enhanced charge storage at the electrode–electrolyte interface. These findings underscore the potential of sputtered TiO₂/WO_x bilayers as advanced photoanodes for solar-driven hydrogen generation and light-assisted energy storage applications.