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Visible light-induced photocatalytic and antibacterial adhesion properties of superhydrophilic TiO₂ nanoparticles.

ABSTRACT: Bacterial infections triggered by patient or healthcare worker contact with surfaces are a major cause of medically acquired infections. By controlling the kinetics of tetrabutyl titanate hydrolysis and condensation during the sol-gel process, it is possible to regulate the content of Ti³⁺ and oxygen vacancies (OVs) in TiO₂, and adjust the associated visible light-induced photocatalytic performance and anti-bacterial adhesion properties. The results have shown that the Ti³⁺ content in TiO₂ was 9.87% at the calcination temperature of the reaction system was 300 °C and pH was 1.0, corresponding to optimal photocatalytic and hydrophilic properties. The formation of a hydrated layer on the superhydrophilic surface provided resistance to bacterial adhesion, preventing cross-contamination on high-touch surfaces. The excellent photocatalytic self-cleaning performance and anti-bacterial adhesion properties can be attributed to synergistic effects associated with the high specific surface area of TiO₂ nanoparticles, the mesoporous structure, and the presence of Ti³⁺ and OVs. The formation of superhydrophilic self-cleaning surfaces under visible light can serve as the basis for the development of a new class of anti-bacterial adhesion materials.

SUBMITTER: Zhou M

PROVIDER: S-EPMC10995203 | biostudies-literature | 2024 Apr

REPOSITORIES: biostudies-literature

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Visible light-induced photocatalytic and antibacterial adhesion properties of superhydrophilic TiO2 nanoparticles.

Zhou Mingzhu M Zhang Xingran X Quan Yuanxia Y Tian Yu Y Chen Jie J Li Li L

Scientific reports 20240404 1

Bacterial infections triggered by patient or healthcare worker contact with surfaces are a major cause of medically acquired infections. By controlling the kinetics of tetrabutyl titanate hydrolysis and condensation during the sol-gel process, it is possible to regulate the content of Ti3+ and oxygen vacancies (OVs) in TiO2, and adjust the associated visible light-induced photocatalytic performance and anti-bacterial adhesion properties. The results have shown that the Ti<s ...[more]

PMID: 38575777

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Project description:Flexible fiber membranes for pollutant removal have received increasing attention due to their high adsorption performance and easy recycling characteristics. However, due to the lack of environmentally friendly regeneration, some adsorption membranes have low regeneration efficiency, especially in terms of chemical adsorption, so they lack reusability. This study prepares a series of conducting polymer [PAn (polyaniline) or PPy (polypyrrole) or PTh (polythiophene)] graphene quantum dots (GQDs, the size of GQDs is about 20 nm)/TiO2 ternary fiber membranes via a facile electrospinning method with chemical deposition. Remarkably, this creates an anatase TiO2 and π-conjugated system. The combination is beneficial to the photocatalytic degradation of organic pollutants, showing synergistic promotion in both the degradation rate and the degree of decomposition. The UV-vis test shows that the combination of GQDs broadens the optical response threshold of TiO2, from near ultraviolet region excitation to visible region excitation. At the same time, the conductive polymer load further reduces the energy required for photogenerated electron transfer, which theoretically improves the degradation effect. Photocatalytic degradation tests showed that the PTh/GQDs/TiO2 fiber membrane exhibited significant high photocatalytic activity of visible-light in the methylene blue (MB) and TC degradation. The degradation rate level is 92.90% and 80.58%, respectively and the MB removal is more than 4 times that of bare TiO2 membrane. After photocatalytic regeneration four times, the regeneration efficiency can be maintained above 95%. Notably, various experimental results show that the interface charge transfer mechanism between GQDs/TiO2 and PTh follows the Z-scheme heterojunction, which maximizes the retention of strong reducing electrons and oxidation holes. In the degradation, the active species of ·O2 - and ·OH, make different contributions in the photocatalysts, which oxidize and break down the pollutant molecules into small molecules and then to harmless substances. According to the electronegativity difference of the material itself, PTh acts as electron acceptor in the degradation system, and TiO2 fiber membrane doped with GQDs acts as electron donor. The present research, not only offers feasibility of the PTh/GQDs/TiO2 flexible fiber membrane as an environment-friendly catalyst, but also motivates researchers to develop flexible fiber materials for future photocatalytic technology.

Project description:Graphitic carbon nitride (g-C₃N₄) and titanium dioxide (TiO₂) were chosen as a model system to investigate photocatalytic abilities of heterojunction system under UV and visible light conditions. The use of g-C₃N₄ has been shown to be effective in the reduction in recombination through the interaction between the two interfaces of TiO₂ and g-C₃N₄. A simple method of preparing g-C₃N₄ through the pyrolysis of melamine was employed, which was then added to undoped TiO₂ material to form the g-C₃N₄-TiO₂ system. These materials were then fully characterized by X-ray diffraction (XRD), Brunauer Emmett Teller (BET), and various spectroscopic techniques including Raman, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), diffuse absorbance, and photoluminescence analysis. Photocatalysis studies were conducted using the model dye, rhodamine 6G utilizing visible and UV light irradiation. Raman spectroscopy confirmed that a composite of the materials was formed as opposed to a mixture of the two. Using XPS analysis, a shift in the nitrogen peak to that indicative of substitutional nitrogen was detected for all doped samples. This is then mirrored in the diffuse absorbance results, which show a clear decrease in band gap values for these samples, showing the effective band gap alteration achieved through this preparation process. When g-C₃N₄-TiO₂ samples were analyzed under visible light irradiation, no significant improvement was observed compared that of pure TiO₂. However, under UV light irradiation conditions, the photocatalytic ability of the doped samples exhibited an increased reactivity when compared to the undoped TiO₂ (0.130 min-1), with 4% g-C₃N₄-TiO₂ (0.187 min-1), showing a 43.9% increase in reactivity. Further doping to 8% g-C₃N₄-TiO₂ lead to a decrease in reactivity against rhodamine 6G. BET analysis determined that the surface area of the 4% and 8% g-C₃N₄-TiO₂ samples were very similar, with values of 29.4 and 28.5 m²/g, respectively, suggesting that the actual surface area is not a contributing factor. This could be due to an overloading of the system with covering of the active sites resulting in a lower reaction rate. XPS analysis showed that surface hydroxyl radicals and oxygen vacancies are not being formed throughout this preparation. Therefore, it can be suggested that the increased photocatalytic reaction rates are due to successful interfacial interactions with the g-C₃N₄-doped TiO₂ systems.

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Visible light-induced photocatalytic and antibacterial adhesion properties of superhydrophilic TiO₂ nanoparticles.

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Visible light-induced photocatalytic and antibacterial adhesion properties of superhydrophilic TiO<sub>2</sub> nanoparticles.

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