Browse
Submit Data
Databases
API
Help

Dataset Information

24 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Visible-Light-Driven Ag-Modified TiO₂ Thin Films Anchored on Bamboo Material with Antifungal Memory Activity against Aspergillus niger.

ABSTRACT: A round-the-clock photocatalyst with energy-storage ability has piqued the interest of researchers for removing microbial contaminants from indoor environments. This work presents a moderate round-the-clock method for inhibiting the growth of fungus spores on bamboo materials using Ag-modified TiO₂ thin films. Photoactivated antifungal coating with catalytic memory activity was assembled on a hydrophilic bamboo by first anchoring anatase TiO₂ thin films (TB) via hydrogen bonding and then decorating them with Ag nanoparticles (ATB) via electrostatic interactions. Antifungal test results show that the Ag/TiO₂ composite films grown on the bamboo surface produced a synergistic antifungal mechanism under both light and dark conditions. Interestingly, post-illumination catalytic memory was observed for ATB, as demonstrated by the inhibition of Aspergillus niger (A. niger) spores, in the dark after visible light was removed, which could be attributed to the transfer of photoexcited electrons from TiO₂ to Ag, their trapping on Ag under visible-light illumination, and their release in the dark after visible light was removed. The mechanism study revealed that the immobilized Ag nanoparticles served the role of "killing two birds with one stone": increasing visible-light absorption through surface plasmon resonance, preventing photogenerated electron-hole recombination by trapping electrons, and contributing to the generation of ●O₂^-and ●OH. This discovery creates a pathway for the continuous removal of indoor air pollutants such as volatile organic compounds, bacteria, and fungus in the day and night time.

SUBMITTER: Li J

PROVIDER: S-EPMC8397055 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Switched photocurrent direction in Au/TiO2 bilayer thin films.

Project description:Switched photocurrent direction in photoelectrodes is a very interesting phenomenon and has demonstrated their potentials in important applications including photodiodes, phototransistors, light-driven sensors and biosensors. However, the design and mechanism understanding of such photoelectrodes remain challenging to date. Here we report a new phenomenon of sequence-driven the photocurrent direction on a simple bilayer structure of 5 nm thick Au and 10 nm TiO2 under visible-light irradiation. It is found that when Au layer are deposited as the outer layer on TiO2 coated fluorine doped tin oxide (FTO) substrate (designated as FTO/TiO2/Au), anodic photocurrent is obtained due to the band bending formed at the electrode-electrolyte interface. Interestingly, simply swapping the deposition sequence of Au and TiO2 leads to cathodic photocurrent on FTO/Au/TiO2 electrode. Characterization and calculations on the photoelectrode reveals that the photogenerated electrons can be easily trapped in the energy well formed between the band bending and the Schottky contact, which allows electronic tunnelling through the 1.6 nm thick space charge layer, resulting in a unique anodic to cathodic photocurrent conversion. The understanding of this new phenomenon can be important for designing new generation optoelectronic converting devices in a low-cost and facile manner.

| S-EPMC4450582 | biostudies-literature

Optically Active TiO2:Er Thin Films Deposited by Magnetron Sputtering.

Project description:Titanium dioxide photoanodes for hydrogen generation suffer from a profound mismatch between the optical absorption of TiO2 and the solar spectrum. To solve the problem of low solar-to-chemical efficiency, optically active materials are proposed. In this work, TiO2 thin films containing erbium were deposited by radio frequency RF magnetron sputtering under ultrahigh vacuum conditions UHV. Morphology, structural, optical and electronic properties were studied. TiO2:Er thin films are homogenous, with uniform distribution of Er ions and high transparency over the visible VIS range of the light spectrum. However, a profound 0.4 eV blue shift of the fundamental absorption edge with respect to undoped TiO2 was observed, which can be attributed either to the size effect due to amorphization of TiO2 host or to the onset of precipitation of Er2Ti2O7 nanocrystals. Near-infrared NIR to VIS up-conversion is demonstrated upon excitation at 980 nm, while strong green photoluminescence at 525 and 550 nm occurs upon photon absorption at 488 nm.

| S-EPMC8348420 | biostudies-literature

A spectrally selective visible microbolometer based on planar subwavelength thin films.

Project description:In this work, we experimentally demonstrate a new type of compact, low-cost, visible microbolometer based on metal-insulator-metal (MIM) planar subwavelength thin films, which exploits resonant absorption for spectral selectivity without additional filters and has the advantages of compact design, simple structure, cost-efficiency, and large format fabrication. The experimental results show that a proof-of-principle microbolometer exhibits spectrally selective properties in the visible frequency range. At a resonant absorption wavelength of 638 nm, a responsivity of about 10 mV W-1 is achieved at room temperature at a bias current of 0.2 mA, which is about one order of magnitude higher than that of the control device (a bare Au bolometer). Our proposed approach provides a viable solution for the development of compact and inexpensive detectors.

| S-EPMC10044596 | biostudies-literature

Effect of Ag Concentration Dispersed in HfOx Thin Films on Threshold Switching.

Project description:A sneak path current-a current passing through a neighboring memory cell-is an inherent and inevitable problem in a crossbar array consisting of memristor memory cells. This serious problem can be alleviated by serially connecting the selector device to each memristor cell. Among the various types of selector device concepts, the diffusive selector has garnered considerable attention because of its excellent performance. This selector features volatile threshold switching (TS) using the dynamics of active metals such as Ag or Cu, which act as an electrode or dopant in the solid electrolyte. In this study, a diffusive selector based on Ag-doped HfOx is fabricated using a co-sputtering system. As the Ag concentration in the HfOx layer varies, different electrical properties and thereby TS characteristics are observed. The necessity of the electroforming (EF) process for the TS characteristic is determined by the proper Ag concentration in the HfOx layer. This difference in the EF process can significantly affect the parameters of the TS characteristics. Therefore, an optimized doping condition is required for a diffusive selector to attain excellent selector device behavior and avoid an EF process that can eventually degrade device performance.

| S-EPMC6990205 | biostudies-literature

Near infrared photothermoelectric effect in transparent AZO/ITO/Ag/ITO thin films.

Project description:A new concept of oxide-metal-oxide structures that combine photothermoelectric effect with high reflectance (~ 80%) at wavelengths in the infrared (> 1100 nm) and high transmittance in the visible range is reported here. This was observed in optimized ITO/Ag/ITO structure, 20 nm of Silver (Ag) and 40 nm of Indium Tin Oxide (ITO), deposited on Aluminum doped Zinc Oxide (AZO) thin film. These layers show high energy saving efficiency by keeping the temperature constant inside a glazed compartment under solar radiation, but additionally they also show a photothermoelectric effect. Under uniform heating of the sample a thermoelectric effect is observed (S = 40 mV/K), but when irradiated, a potential proportional to the intensity of the radiation is also observed. Therefore, in addition to thermal control in windows, these low emission coatings can be applied as transparent photothermoelectric devices.

| S-EPMC8692428 | biostudies-literature

High quality transparent conductive Ag-based barium stannate multilayer flexible thin films.

Project description:Transparent conductive multilayer thin films of silver (Ag)-embedded barium stannate (BaSnO3) structures have been deposited onto flexible polycarbonate substrates by magnetron sputtering at room temperature to develop an indium free transparent flexible electrode. The effect of thicknesses of Ag mid-layer and barium stannate layers on optical and electrical properties were investigated, and the mechanisms of conduction and transmittance were discussed. The highest value of figure of merit is 25.5 × 10-3 Ω-1 for the BaSnO3/Ag/BaSnO3 multilayer flexible thin films with 9 nm thick silver mid-layer and 50 nm thick barium stannate layers, while the average optical transmittance in the visible range from 380 to 780 nm is above 87%, the resistivity is 9.66 × 10-5 Ω · cm, and the sheet resistance is 9.89 Ω/sq. The change rate of resistivity is under 10% after repeated bending of the multilayer flexible thin films. These results indicate that Ag-based barium stannate multilayer flexible thin films can be used as transparent flexible electrodes in various flexible optoelectronic devices.

| S-EPMC5427918 | biostudies-literature

Adsorption of Polarized Molecules for Interfacial Band Engineering of Doped TiO2 Thin Films.

Project description:Owing to their chemical and mechanical stability, metal-oxides have emerged as potential alternatives for conventional pure-metal and organic molecule-based solid-state electronic devices. Traditionally, band engineering of these metal-oxides has been performed to improve the efficiency of solar cells and transistors. However, recent advancements in the field of oxide-based electronic devices demand reversible band structure engineering for applications in next-generation adaptive electronics and memory devices. Therefore, this work aims to reversibly engineer the surface band structure of doped metal-oxides using stable organic ligands with weak dipoles. Para-substituted benzoic acid (BZA) ligands with positive and negative dipole moments were adsorbed in situ on the surface of TiO2:Ni2+ thin film to modify the interfacial dipole moment, and the valence band structure was probed using surface-sensitive ultraviolet photoelectron spectroscopy (UPS). UPS, paired with density functional theory (DFT) simulations, demonstrate the ability to selectively tune interfacial electronic/chemical landscapes with ligand-dependent dipole moment. The unique ability to reversibly tune the band bending at the organic-inorganic interface of doped metal-oxide semiconductors using molecular dipoles is expected to play a key role in the development of metal-oxide-based adaptive electronics that outperform the conventional polymer-based and Si-based devices.

| S-EPMC7304897 | biostudies-literature

Antibacterial property of Ag nanoparticle-impregnated N-doped titania films under visible light.

Project description:Photocatalysts produce free radicals upon receiving light energy; thus, they possess antibacterial properties. Silver (Ag) is an antibacterial material that disrupts bacterial physiology. Our previous study reported that the high antibacterial property of silver nanoparticles on the surfaces of visible light-responsive nitrogen-doped TiO2 photocatalysts [TiO2(N)] could be further enhanced by visible light illumination. However, the major limitation of this Ag-TiO2 composite material is its durability; the antibacterial property decreased markedly after repeated use. To overcome this limitation, we developed TiO2(N)/Ag/TiO2(N) sandwich films in which the silver is embedded between two TiO2(N) layers. Various characteristics, including silver and nitrogen amounts, were examined in the composite materials. Various analyses, including electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and ultraviolet-visible absorption spectrum and methylene blue degradation rate analyses, were performed. The antibacterial properties of the composite materials were investigated. Here we revealed that the antibacterial durability of these thin films is substantially improved in both the dark and visible light, by which bacteria, such as Escherichia coli, Streptococcus pyogenes, Staphylococcus aureus, and Acinetobacter baumannii, could be efficiently eliminated. This study demonstrated a feasible approach to improve the visible-light responsiveness and durability of antibacterial materials that contain silver nanoparticles impregnated in TiO2(N) films.

| S-EPMC4496671 | biostudies-literature

In Situ Formation of Ag Nanoparticles in Mesoporous TiO<sub>2</sub> Films Decorated on Bamboo via Self-Sacrificing Reduction to Synthesize Nanocomposites with Efficient Antifungal Activity.

Project description:We developed a novel green approach for the in situ fabrication of Ag NPs in mesoporous TiO2 films via the bamboo self-sacrificing reduction of Ag(NH3)2+ ions, which can inhibit fungal growth on the bamboo surface. Mesoporous anatase TiO2 (MT) films were first synthesized on bamboo via a hydrothermal method. Then, Ag NPs with a 5.3 nm mean diameter were incorporated into the pore channels of optimal MT/bamboo (MTB) samples at room temperature without the addition of reducing agents, such that the Ag NPs were almost entirely embedded into the MT films. Our analysis indicated that the solubilized lignin from bamboo, which is rich in oxygen-containing functional groups, serves as a green reductant for reducing the Ag(NH3)2+ ions to Ag NPs. Antifungal experiments with Trichoderma viride under dark conditions highlighted that the antifungal activity of the Ag/MT/bamboo samples were greater than those of naked bamboo, MTB, and Ag/bamboo, suggesting that these hybrid nanomaterials produce a synergistic antifungal effect that is unrelated to photoactivity. The inhibition of Penicillium citrinum effectively followed a similar trend. This newly developed bamboo protection method may provide a sustainable, eco-friendly, and efficient method for enhancing the antifungal characteristics of traditional bamboo, having the potential to prolong the service life of bamboo materials, particularly under dark conditions.

| S-EPMC6862692 | biostudies-literature

Enhanced Visible-Light Photocatalytic Activity of Ag QDs Anchored on CeO2 Nanosheets with a Carbon Coating.

Project description:Ag quantum dots (QDs) anchored on CeO2 nanosheets with a carbon coating (Ag/CeO2@C) (composites) were prepared via an in situ reduction approach for the photocatalytic degradation of Cr(VI) and tetracycline hydrochloride (TCH) in the visible-light region. The photocatalytic activity of Ag/CeO2@C was greatly affected by carbon content, Ag-doping content, Cr(VI) concentration, pH value, and inorganic ions. Enhanced photocatalytic activity was obtained by Ag/CeO2@C (compared to CeO2 and CeO2@C), of which 3-Ag/CeO2@C-2 with an Ag-doping content of 5.41% presented the best removal efficiency and the most superior stability after five cycles. ·O2- and ·OH radicals were crucial for the photocatalytic capacity of 3-Ag/CeO2@C-2. The combined effect of the surface plasma resonance (SPR) of Ag QDs, an electron trapper of carbon shells, and the redox activity of the Ce(III)/Ce(IV) coupling induced efficient charge transfer and separation, suppressing the recombination of electron-hole pairs.

| S-EPMC6915373 | biostudies-literature