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Keywords = ZnO nanofilms

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16 pages, 3467 KiB  
Article
Incorporation of Nano-Zinc Oxide as a Strategy to Improve the Barrier Properties of Biopolymer–Suberinic Acid Residues Films: A Preliminary Study
by Aleksandra Jeżo, Faksawat Poohphajai, Rene Herrera Diaz and Grzegorz Kowaluk
Materials 2024, 17(15), 3868; https://doi.org/10.3390/ma17153868 - 5 Aug 2024
Viewed by 1169
Abstract
Finishing coatings in the wood-based composites industry not only influence the final appearance of the product but also serve to protect against fungi and molds and reduce the release of harmful substances, particularly formaldehyde and volatile organic compounds (VOCs). Carbon-rich materials, such as [...] Read more.
Finishing coatings in the wood-based composites industry not only influence the final appearance of the product but also serve to protect against fungi and molds and reduce the release of harmful substances, particularly formaldehyde and volatile organic compounds (VOCs). Carbon-rich materials, such as those derived from birch bark extraction, specifically suberin acids, can fulfill this role. Previous research has demonstrated that adding suberin acid residues (SAR) at 20% and 50% by weight significantly enhances the gas barrier properties of surface-finishing materials based on poly(lactide) (PLA) and polycaprolactone (PCL), particularly in terms of total VOC (TVOC) and formaldehyde emissions. This study aims to explore whether these properties can be further improved through the incorporation of nano-zinc oxide (nano-ZnO). Previous research has shown that these nanoparticles possess strong resistance to biological factors and can positively affect the characteristics of nanofilms applied as surface protection. The study employed PLA and PCL finishing layers blended with SAR powder at 10% w/w and included 2% and 4% nano-zinc oxide nanoparticles. The resulting blends were milled to create a powder, which was subsequently pressed into 1 mm-thick films. These films were then applied to raw particleboard surfaces. TVOC and formaldehyde emission tests were conducted. Additionally, the fungal resistance of the coated surfaces was assessed. The results showed that PLA/SAR and PCL/SAR composites with the addition of nano-zinc oxide nanoparticles exhibited significantly improved barrier properties, offering a promising avenue for developing biodegradable, formaldehyde-free coatings with enhanced features in the furniture industry. Furthermore, by utilizing SAR as a post-extraction residue, this project aligns perfectly with the concept of upcycling. Full article
(This article belongs to the Special Issue Preparation and Characterization of Functional Composite Materials)
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<p>Antibacterial mechanism of ZnO NPs (own elaboration based on [<a href="#B46-materials-17-03868" class="html-bibr">46</a>]).</p>
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<p>The results of the relative hardness of the examined coatings (red—PLA and PLA blends; blue—PCL and PCL blends).</p>
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<p>The average mold grade of the examined coatings exposed to <span class="html-italic">A. niger</span> and <span class="html-italic">C. cladosporioides</span>.</p>
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<p>PCL tested with <span class="html-italic">Cladosporium cladosporiodies</span> (scale bar: 3 mm).</p>
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<p>PCL tested with <span class="html-italic">Aspergillus niger</span> (scale bar: 3 mm).</p>
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<p>PLA tested with <span class="html-italic">Cladosporium cladosporiodies</span> (scale bar: 3 mm).</p>
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<p>PLA tested with <span class="html-italic">Aspergillus niger</span> (scale bar: 3 mm).</p>
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<p>The relative hardness of the samples after one and after repeated processing.</p>
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17 pages, 5233 KiB  
Article
Synthesis of Ag/ZnO/BiOCl Composite Material and Its Photodegradation Performance on Ciprofloxacin
by Danye Zuo, Yuhong Yin, Liming Jiang, Zhi Xia, Chong Tan, Junsheng Li, Jinlong Zuo and Yuyang Wang
Coatings 2024, 14(2), 192; https://doi.org/10.3390/coatings14020192 - 1 Feb 2024
Cited by 2 | Viewed by 1277
Abstract
This study focuses on synthesizing a composite material of Ag/ZnO/BiOCl using Ag, ZnO, and BiOCl as raw materials. The material was prepared by loading Ag and BiOCl onto ZnO nanofilms, aiming to enhance the photocatalytic degradation of ciprofloxacin (CIP). Optimization of the photocatalytic [...] Read more.
This study focuses on synthesizing a composite material of Ag/ZnO/BiOCl using Ag, ZnO, and BiOCl as raw materials. The material was prepared by loading Ag and BiOCl onto ZnO nanofilms, aiming to enhance the photocatalytic degradation of ciprofloxacin (CIP). Optimization of the photocatalytic degradation process through single-factor experiments revealed that under conditions of an initial CIP pH of 9, an Ag/ZnO/BiOCl dosage of 1 g/L, and an initial CIP concentration of 5 mg/L the conversion efficiency of CIP reached 98.79% after 150 min of exposure to a 250 W xenon lamp simulating sunlight. Furthermore, the composite material maintained a conversion efficiency of 86.17% for CIP even after five cycles of reuse, demonstrating its excellent stability. The optical properties, elemental composition, valence state, crystallinity, and morphology of the samples were analyzed using techniques such as X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), photoluminescence (PL), UV–visible diffuse reflectance spectroscopy (UV-vis DRS), Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The results indicate that the introduction of Ag expanded the light response range of ZnO, while the addition of BiOCl improved the separation efficiency of electron–hole pairs in the composite nanomaterial. The photocatalytic mechanism was further elucidated through radical scavenging experiments, confirming that ·OH and h+ are the main active species in the degradation process. Full article
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<p>XRD patterns of Ag/ZnO/BiOCl, Ag/ZnO, and BiOCl composites.</p>
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<p>FTIR spectra of ZnO, Ag/ZnO, and Ag/ZnO/BiOCl.</p>
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<p>SEM image of (<b>a</b>): ZnO; (<b>b</b>): Ag/ZnO; (<b>c</b>): Ag/ZnO/BiOCl; (<b>d</b>): EDS spectrum and element distribution diagram of Ag/ZnO/BiOCl.</p>
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<p>(<b>a</b>) XPS full spectrum of ZnO, Ag/ZnO, and Ag/ZnO/BiOCl; (<b>b</b>) Bi 4f; (<b>c</b>) Cl 2p; (<b>d</b>) Zn 2p; (<b>e</b>) Ag 3d; (<b>f</b>) O 1s high resolution XPS spectrogram.</p>
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<p>(<b>a</b>) UV-vis DRS spectra of ZnO, Ag/ZnO, BiOCl, and Ag/ZnO/BiOCl; (<b>b</b>) optical band gap diagram of ZnO, Ag/ZnO, and BiOCl Ag/ZnO/BiOCl.</p>
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<p>PL spectra of ZnO, Ag/ZnO, and Ag/ZnO/BiOCl.</p>
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<p>Photocatalytic Activity Test of ZnO, Ag/ZnO, Ag/ZnO/BiOCl, and P25.</p>
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<p>(<b>a</b>) Degradation diagram of CIP by catalysts under different pH conditions; (<b>b</b>) the effect of initial pH value of solution on conversion efficiency.</p>
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<p>(<b>a</b>) Degradation diagram of CIP by catalysts under different catalyst dosage conditions; (<b>b</b>) effect of dosage on conversion efficiency.</p>
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<p>(<b>a</b>) Degradation maps of CIP by catalysts under different initial concentrations of CIP; (<b>b</b>) effect of initial concentration of CIP on photocatalytic conversion efficiency.</p>
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<p>Recycling stability of Ag/ZnO/BiOCl for photocatalytic degradation of CIP.</p>
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<p>Degradation map of CIP by different free radical capturing agents.</p>
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<p>Photocatalytic mechanism diagram.</p>
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19 pages, 11461 KiB  
Article
Novel Photocatalyst Ag/ZnO/BC Nanofilms Degradation of Low Concentration Ammonia Nitrogen Wastewater
by Junsheng Li, Sihang Li, Liming Jiang, Jialun Xu, Jiahui Li, Zhi Xia, Chong Tan, Jinlong Zuo and Yuyang Wang
Coatings 2023, 13(12), 2043; https://doi.org/10.3390/coatings13122043 - 5 Dec 2023
Cited by 1 | Viewed by 1247
Abstract
In this study, an innovative Ag/ZnO/BC nanofilms composite material was synthesized by loading zinc oxide and silver on biochar nanofilms using a combination of hydrothermal and calcination methods using zinc oxide, silver and biochar as raw materials. Subsequent characterization analysis confirmed the successful [...] Read more.
In this study, an innovative Ag/ZnO/BC nanofilms composite material was synthesized by loading zinc oxide and silver on biochar nanofilms using a combination of hydrothermal and calcination methods using zinc oxide, silver and biochar as raw materials. Subsequent characterization analysis confirmed the successful synthesis of Ag/ZnO/BC nanofilms photocatalysts, and the Ag/ZnO nanocomposite particles were effectively loaded on the biochar nanofilms (BC). The composite exhibited robust photocatalytic removal under visible light irradiation under simulated wastewater conditions with an ammonia nitrogen concentration of 50 mg/L. The photocatalytic removal of ammonia and nitrogen pollutants in the composite was achieved by the use of Ag/ZnO nanoparticles. Specifically, the degradation of ammonia nitrogen pollutant reached a peak efficiency of 83.28%. Notably, the photocatalyst maintained over 80% degradation efficiency after four cycles, highlighting its sustained photocatalytic activity and stability. In conclusion, this study elucidated a feasible method to fabricate metal oxide–biochar thin-film composites with excellent adsorption and photocatalytic properties, thus providing a promising pathway for the remediation of organic wastewater, especially wastewater containing ammonia and nitrogen pollutants. Full article
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<p>1—UVlamp; 2—Quartz glass; 3—The rotor; 4—Magnetic stirrer.</p>
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<p>XRD spectrum of ZnO, Ag/ZnO and Ag/ZnO/BC nanofilm composites.</p>
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<p>(<b>a</b>) shows the SEM of ZnO; Figure (<b>b</b>,<b>c</b>) shows the SEM of Ag/ZnO; Figure (<b>d</b>) shows the SEM of BC; Figure (<b>e</b>,<b>f</b>) shows the SEM of Ag/ZnO/BC nanofilms composite.</p>
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<p>EDS energy spectrum and elemental distribution of Ag/ZnO/BC nanofilm composites.</p>
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<p>EDS energy spectrum and elemental distribution of Ag/ZnO/BC nanofilm composites.</p>
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<p>Raman spectra of ZnO, Ag/ZnO and Ag/ZnO/BC nanofilms.</p>
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<p>(<b>a</b>) XPS full spectra of ZnO, Ag/ZnO and Ag/ZnO/BC nanofilm composites; (<b>b</b>) high resolution XPS spectra of Zn 2p; (<b>c</b>) O 1s; (<b>d</b>) C1s; (<b>e</b>) Ag 3d.</p>
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<p>Infrared spectra of ZnO, Ag/ZnO and Ag/ZnO composites.</p>
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<p>(<b>a</b>) UV-Vis DRS spectra of BC, ZnO, Ag/ZnO and Ag/ZnO/BC nanofilm composites; (<b>b</b>) optical band gap maps of ZnO, Ag/ZnO and Ag/ZnO/BC nanofilm composites.</p>
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<p>PL spectra of ZnO, Ag/ZnO and Ag/ZnO/BC nanofilms.</p>
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<p>Nitrogen adsorption–desorption isotherms for ZnO, Ag/ZnO and Ag/ZnO/BC nanofilms.</p>
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<p>Degradation of 50 mg/L ammonia nitrogen simulated wastewater by Ag/ZnO and Ag/ZnO/BC nanofilms at different compound ratios.</p>
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<p>Photocatalytic activity test of Ag/ZnO/BC nanofilms.</p>
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<p>Results of linear fitting of kinetics for the degradation of 50 mg/L ammonia nitrogen simulated wastewater for each sample.</p>
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<p>Effect of number of catalyst uses on photocatalytic performance.</p>
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<p>Free radical degradation masking rate.</p>
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<p>Photocatalytic mechanism diagram.</p>
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16 pages, 5118 KiB  
Article
Fabrication of a Highly NO2-Sensitive Gas Sensor Based on a Defective ZnO Nanofilm and Using Electron Beam Lithography
by Zhifu Feng, Damiano Giubertoni, Alessandro Cian, Matteo Valt, Matteo Ardit, Andrea Pedrielli, Lia Vanzetti, Barbara Fabbri, Vincenzo Guidi and Andrea Gaiardo
Micromachines 2023, 14(10), 1908; https://doi.org/10.3390/mi14101908 - 6 Oct 2023
Cited by 1 | Viewed by 1156
Abstract
Hazardous substances produced by anthropic activities threaten human health and the green environment. Gas sensors, especially those based on metal oxides, are widely used to monitor toxic gases with low cost and efficient performance. In this study, electron beam lithography with two-step exposure [...] Read more.
Hazardous substances produced by anthropic activities threaten human health and the green environment. Gas sensors, especially those based on metal oxides, are widely used to monitor toxic gases with low cost and efficient performance. In this study, electron beam lithography with two-step exposure was used to minimize the geometries of the gas sensor hotplate to a submicron size in order to reduce the power consumption, reaching 100 °C with 0.09 W. The sensing capabilities of the ZnO nanofilm against NO2 were optimized by introducing an enrichment of oxygen vacancies through N2 calcination at 650 °C. The presence of oxygen vacancies was proven using EDX and XPS. It was found that oxygen vacancies did not significantly change the crystallographic structure of ZnO, but they significantly improved the electrical conductivity and sensing behaviors of ZnO film toward 5 ppm of dry air. Full article
(This article belongs to the Special Issue Micro and Nano Technology in Gas Sensing)
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<p>ZnO gas sensor layout patterning steps: (<b>a</b>) first step, fabrication of SMHP pads; (<b>b</b>) second step, fabrication of heater circuit; (<b>c</b>) exposure of active area for sensing material ZnO deposition.</p>
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<p>Hotplate fabrication process: (<b>a</b>) preparation of wafer with top insulating stack structure; (<b>b</b>) spin-coating photoresist on the wafer; (<b>c</b>) first step, EBL exposure on the electrode part; (<b>d</b>) second step, EBL exposure on the heater circuit; (<b>e</b>) metal Pt/Ti sputtering deposition; (<b>f</b>) lift-off process.</p>
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<p>ZnO sensing material deposition: (<b>a</b>) photoresist spin-coating; (<b>b</b>) ZnO deposition area; (<b>c</b>) ZnO nanofilm sputtering; (<b>d</b>) lift-off; (<b>e</b>) calcination.</p>
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<p>Images of ZnO gas sensor: (<b>a</b>) images of ZnO gas sensor structure; (<b>b</b>) SEM image of ZnO1 film on SMHP; (<b>c</b>) SEM image of ZnO2 film on SMHP.</p>
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<p>Images of ZnO gas sensor: (<b>a</b>) images of ZnO gas sensor structure; (<b>b</b>) SEM image of ZnO1 film on SMHP; (<b>c</b>) SEM image of ZnO2 film on SMHP.</p>
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<p>(<b>a</b>) AFM images and (<b>b</b>) the roughness values of ZnO1 and ZnO2.</p>
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<p>(<b>a</b>) XRD patterns of ZnO1 and ZnO2; (<b>b</b>) XRD pattern comparison of substrate cristobalite α phase and ZnO.</p>
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<p>XPS spectra: (<b>a</b>) full scan of samples; (<b>b</b>) Zn 2p spectrum; (<b>c</b>) O 1s splitting peaks of ZnO1 and ZnO2.</p>
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<p>The voltage-dependent performance of the (<b>a</b>) current and resistance of hotplate, (<b>b</b>) working temperature and power consumption of hotplate, (<b>c</b>) resistance change in ZnO1 and ZnO2.</p>
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<p>(<b>a</b>) ZnO sensing curves toward 5 ppm NO<sub>2</sub> gas at different conditions; (<b>b</b>) ZnO sensing trend toward 5 ppm NO<sub>2</sub> under different humidities; (<b>c</b>) ZnO2 sensing response/recovery time toward 5 ppm NO<sub>2</sub> under different humidities; (<b>d</b>) ZnO2 sensing response toward NO<sub>2</sub> with different concentrations in dry air.</p>
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<p>Sensing response repeatability of ZnO2 sensor vs. 5 ppm of NO<sub>2</sub> over one week of measurements.</p>
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<p>Schematic representation of the conduction mechanisms through ZnO nanoparticles on O<sub>2</sub> (<b>a</b>) and NO<sub>2</sub> gases (<b>b</b>).</p>
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22 pages, 5862 KiB  
Article
Perovskite Nano-Powder and Nano-Film Catalysts in Mineralization of Aqueous Organic Contaminants through Solar Simulated Radiation
by Tamara Zorba, Heba Nassar, Muath H. S. Helal, Jeheon Song, Tae Woo Kim, Shehdeh Jodeh and Hikmat S. Hilal
Processes 2023, 11(8), 2378; https://doi.org/10.3390/pr11082378 - 7 Aug 2023
Cited by 1 | Viewed by 1107
Abstract
Water contamination with various contaminants, including organic species, is a global concern. Reclamation through safe, economic and technically feasible methods is imperative. Two perovskites, zinc titanate (ZnTiO3) and manganese titanate (MnTiO3), mixed with TiO2 phases, were prepared as [...] Read more.
Water contamination with various contaminants, including organic species, is a global concern. Reclamation through safe, economic and technically feasible methods is imperative. Two perovskites, zinc titanate (ZnTiO3) and manganese titanate (MnTiO3), mixed with TiO2 phases, were prepared as nano-powders and nano-films. The materials were characterized and used as catalysts in photodegradation of aqueous methylene blue, a hazardous model contaminant, using solar simulated radiation. The effects of various reaction conditions on the photodegradation were examined. The kinetics indicated the suitability of using the process at various contaminant concentrations and catalyst loadings. Both powder and film catalysts completely removed the contaminant in less than 6 h. Powder and film forms of the MnTiO3 mixture were more efficient than their ZnTiO3 counterparts. In both perovskite mixtures, the films exhibited higher catalytic efficiency than the powders. The film materials exhibited high catalytic efficiency in both the continuous flow and batch processes. Water contaminated with various methylene blue concentrations can be treated by the film catalysts that can be recovered and reused with no technical difficulties. The results open new horizons for larger-scale water purification processes. Full article
(This article belongs to the Special Issue Synthesis and Applications of Novel Functional Materials)
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<p>Photoluminescence emission spectra for (<b>a</b>) ZnTiO<sub>3</sub> and (<b>b</b>) MnTiO<sub>3</sub> suspensions.</p>
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<p>Solid state electronic absorption spectra measured for perovskites. (<b>a</b>) ZnTiO<sub>3</sub>, (<b>b</b>) MnTiO<sub>3</sub>. The spectra were measured as suspensions in water against a water baseline.</p>
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<p>SEM micrographs measured for perovskites in their various forms. Powder forms of (<b>a</b>) ZnTiO<sub>3</sub> and (<b>b</b>) MnTiO<sub>3</sub>. Film forms of (<b>c</b>) ZnTiO<sub>3</sub> and (<b>d</b>) MnTiO<sub>3</sub>. Cross-sectional films of (<b>e</b>) ZnTiO<sub>3</sub> and (<b>f</b>) MnTiO<sub>3</sub>.</p>
Full article ">Figure 3 Cont.
<p>SEM micrographs measured for perovskites in their various forms. Powder forms of (<b>a</b>) ZnTiO<sub>3</sub> and (<b>b</b>) MnTiO<sub>3</sub>. Film forms of (<b>c</b>) ZnTiO<sub>3</sub> and (<b>d</b>) MnTiO<sub>3</sub>. Cross-sectional films of (<b>e</b>) ZnTiO<sub>3</sub> and (<b>f</b>) MnTiO<sub>3</sub>.</p>
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<p>Measured XRD patterns for perovskite powders (<b>a</b>) ZnTiO<sub>3</sub> and (<b>b</b>) MnTiO<sub>3</sub>. * for perovskite reflections.</p>
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<p>XPS spectra measured for the ZnTiO<sub>3</sub> and MnTiO<sub>3</sub> films.</p>
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<p>Reaction profiles showing continued disappearance of methylene blue over time. The reactions were conducted using various forms of perovskites at room temperature and pH 8.5.</p>
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<p>Effect of pH (<span style="color:#4472C4">●</span> 3.5, <span style="color:#ED7D31">♦</span> 7, <span style="color:#C00000">■</span> 8.5, and <span style="color:#70AD47">▲</span>11) on the methylene blue photodegradation reaction using various perovskite forms. (<b>a</b>) ZnTiO<sub>3</sub> powder (0.1 g), (<b>b</b>) MnTiO<sub>3</sub> powder (0.1 g), (<b>c</b>) ZnTiO<sub>3</sub> film (2.3 × 10<sup>−3</sup> g) and (<b>d</b>) MnTiO<sub>3</sub> film (1.8 × 10<sup>−3</sup> g). All reactions were conducted at room temperature.</p>
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<p>Effect of pH (<span style="color:#4472C4">●</span> 3.5, <span style="color:#ED7D31">♦</span> 7, <span style="color:#C00000">■</span> 8.5, and <span style="color:#70AD47">▲</span>11) on the methylene blue photodegradation reaction using various perovskite forms. (<b>a</b>) ZnTiO<sub>3</sub> powder (0.1 g), (<b>b</b>) MnTiO<sub>3</sub> powder (0.1 g), (<b>c</b>) ZnTiO<sub>3</sub> film (2.3 × 10<sup>−3</sup> g) and (<b>d</b>) MnTiO<sub>3</sub> film (1.8 × 10<sup>−3</sup> g). All reactions were conducted at room temperature.</p>
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<p>Schematic showing changes in methylene blue structures associated with solution pH. Reproduced with permission from Elsevier [<a href="#B50-processes-11-02378" class="html-bibr">50</a>].</p>
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<p>Reaction profiles with time for methylene blue degradation using various initial contaminant concentrations for various catalysts. (<b>a</b>) ZnTiO<sub>3</sub> powder, (<b>b</b>) MnTiO<sub>3</sub> powder, (<b>c</b>) ZnTiO<sub>3</sub> film and (<b>d</b>) MnTiO<sub>3</sub> film. All reactions were conducted at room temperature and pH 7.</p>
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<p>Effect of powder catalyst loading on methylene blue photodegradation reactions. (<b>a</b>) ZnTiO<sub>3</sub> and (<b>b</b>) MnTiO<sub>3</sub>. Reactions performed at room temperature and pH 7. (<span style="color:#70AD47">♦</span> 0.05 gm, <span style="color:#4472C4">▲</span> 0.1 gm, <span style="color:#ED7D31">●</span> and <span style="color:#C00000">●</span> 0.15 gm and <span style="color:#A6A6A6">■</span> 0.2 gm).</p>
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<p>Effect of perovskite catalyst form on methylene blue photodegradation (<b>a</b>) for powder forms (0.1 g each catalyst) and (<b>b</b>) for film forms ZnTiO<sub>3</sub> (2.4 × 10<sup>−3</sup> g and MnTiO<sub>3</sub> (1.8 × 10<sup>−3</sup> g). Reactions were performed at room temperature and pH 7. <span style="color:#4472C4">■</span> ZnTiO<sub>3</sub> and <span style="color:#C00000">●</span> MnTiO<sub>3</sub>.</p>
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<p>Comparison between continuous flow <span style="color:#C00000">●</span> and batch <span style="color:#4472C4">▲</span> experiments for methylene blue photodegradation using the film perovskites (<b>a</b>) ZnTiO<sub>3</sub> and (<b>b</b>) MnTiO<sub>3</sub>.</p>
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14 pages, 3351 KiB  
Article
Tunable Resistive Switching Behaviors and Mechanism of the W/ZnO/ITO Memory Cell
by Zhiqiang Yu, Jinhao Jia, Xinru Qu, Qingcheng Wang, Wenbo Kang, Baosheng Liu, Qingquan Xiao, Tinghong Gao and Quan Xie
Molecules 2023, 28(14), 5313; https://doi.org/10.3390/molecules28145313 - 10 Jul 2023
Cited by 4 | Viewed by 1396
Abstract
A facile sol–gel spin coating method has been proposed for the synthesis of spin-coated ZnO nanofilms on ITO substrates. The as-prepared ZnO-nanofilm-based W/ZnO/ITO memory cell showed forming-free and tunable nonvolatile multilevel resistive switching behaviors with a high resistance ratio of about two orders [...] Read more.
A facile sol–gel spin coating method has been proposed for the synthesis of spin-coated ZnO nanofilms on ITO substrates. The as-prepared ZnO-nanofilm-based W/ZnO/ITO memory cell showed forming-free and tunable nonvolatile multilevel resistive switching behaviors with a high resistance ratio of about two orders of magnitude, which can be maintained for over 103 s and without evident deterioration. The tunable nonvolatile multilevel resistive switching phenomena were achieved by modulating the different set voltages of the W/ZnO/ITO memory cell. In addition, the tunable nonvolatile resistive switching behaviors of the ZnO-nanofilm-based W/ZnO/ITO memory cell can be interpreted by the partial formation and rupture of conductive nanofilaments modified by the oxygen vacancies. This work demonstrates that the ZnO-nanofilm-based W/ZnO/ITO memory cell may be a potential candidate for future high-density, nonvolatile, memory applications. Full article
(This article belongs to the Collection Green Energy and Environmental Materials)
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<p>(<b>a</b>) XRD pattern of the ZnO nanofilms. FESEM images of the ZnO nanofilms: (<b>b</b>) the cross-sectional FESEM image, (<b>c</b>) the high magnification, top-view FESEM image. (<b>d</b>) The size distribution histogram of ZnO nanograins.</p>
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<p>(<b>a</b>) Survey XPS spectra of the as-prepared ZnO nanofilms. (<b>b</b>) Zn 2<span class="html-italic">p</span> and (<b>c</b>) O 1<span class="html-italic">s</span> high-resolution XPS spectra of the as-prepared ZnO nanofilms.</p>
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<p>(<b>a</b>) UV–visible absorption spectra and (<b>b</b>) the Tauc plots of the ZnO nanofilms.</p>
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<p>(<b>a</b>) The semi-logarithmic <span class="html-italic">I</span>-<span class="html-italic">V</span> curves of the W/ZnO/ITO memory cell for 100 successive cycles; inset is the schematic configuration of the device. (<b>b</b>) The double-logarithmic <span class="html-italic">I</span>-<span class="html-italic">V</span> curve of the device. (<b>c</b>) Endurance performance of the device. (<b>d</b>) Retention test of the device.</p>
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<p>(<b>a</b>) The semi-logarithmic <span class="html-italic">I</span>-<span class="html-italic">V</span> curves and (<b>b</b>) retention capabilities of the W/ZnO/ITO memory cell under different set voltages.</p>
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<p>Schematic of the resistive switching mechanism of the W/ZnO/ITO memory cell.</p>
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21 pages, 12105 KiB  
Article
Distinct Optical and Structural (Nanoyarn and Nanomat-like Structure) Characteristics of Zinc Oxide Nanofilm Derived by Using Salvia officinalis Leaves Extract Made without and with PEO Polymer
by Adnan H. Alrajhi, Naser M. Ahmed, Mohd Mahadi Halim, Abeer S. Altowyan, Mohamad Nurul Azmi and Munirah A. Almessiere
Materials 2023, 16(13), 4510; https://doi.org/10.3390/ma16134510 - 21 Jun 2023
Cited by 4 | Viewed by 1268
Abstract
This paper reports the optical properties of zinc oxide nanofilm fabricated by using organic natural products from Salvia officinalis leaves (SOL) extract and discusses the effect of the nanocrystal (NC) structure (nanoyarn and nanomat-like structure) on nanofilm optical properties. The surface-active layer of [...] Read more.
This paper reports the optical properties of zinc oxide nanofilm fabricated by using organic natural products from Salvia officinalis leaves (SOL) extract and discusses the effect of the nanocrystal (NC) structure (nanoyarn and nanomat-like structure) on nanofilm optical properties. The surface-active layer of the nanofilm of ZnO nanoparticles (ZnO NPs) was passivated with natural organic SOL leaves hydrothermally, then accumulated on zinc oxide nanorods (ZnO NRs). The nanofilms were fabricated (with and without PEO) on glass substrate (at 85 °C for 16 h) via chemical solution deposition (CSD). The samples were characterized by UV-vis, PL, FESEM, XRD, and TEM measurements. TEM micrographs confirmed the nucleation of ZnO NPs around 4 nm and the size distribution at 1.2 nm of ZnO QDs as an influence of the quantum confinement effect (QCE). The nanofilms fabricated with SOL surfactant (which works as a capping agent for ZnO NPs) represent distinct optoelectronic properties when compared to bulk ZnO. FESEM images of the nanofilms revealed nanoyarn and nanomat-like structures resembling morphologies. The XRD patterns of the samples exhibited the existence of ZnO nanocrystallites (ZnO NCs) with (100), (002), and (101) growth planes. The nanofilms fabricated represented a distinct optical property through absorption and broad emission, as the optical energy band gap reduced as the nanofilms annealed (at 120 ). Based on the obtained results, it was established that phytochemicals extracted from organic natural SOL leaves have a distinct influence on zoic oxide nanofilm fabrication, which may be useful for visible light spectrum trapping. The nanofilms can be used in photovoltaic solar cell applications. Full article
(This article belongs to the Special Issue The Composite Materials of Today and Tomorrow)
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<p>Steps of ZnO NRs preparation.</p>
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<p>FESEM image micrographs of the (<b>a</b>) ZnO seeds layer, and (<b>b</b>) ZnO NRs.</p>
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<p>Mechanism of active layer formation, (ZnO NPs onto ZnO NRs stacking in the nanofilm).</p>
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<p>Absorption spectra of ZnO NRs. Insets contain the corresponding optical band gap energy (<math display="inline"><semantics> <mrow> <msub> <mi>E</mi> <mi>g</mi> </msub> </mrow> </semantics></math>).</p>
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<p>PL emission spectra of the proposed ZnO NRs. Insets contain the corresponding CIE diagram exhibiting color purity.</p>
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<p>(<b>a</b>) Various stages of nanofilm fabrication, (<b>b</b>) illustration of ZnO NPs thin film; FESEM image micrograph of (<b>c</b>) ZnO NPs thin film (500 μm), (<b>d</b>) nanoyarn and nanomat-like structures (30 μm), (<b>d′</b>) optical absorbance of the film containing ZnO NPs (5 μm), and (<b>d″</b>) emission spectra of nanofilm with ZnO NPs (10 μm).</p>
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<p>Absorption spectra of ZnO NPs coated with SOL capping agent: (<b>a</b>) with PEO, (<b>b</b>) without PEO. Insets contain the corresponding optical band gap energy (<math display="inline"><semantics> <mrow> <msub> <mi>E</mi> <mi>g</mi> </msub> </mrow> </semantics></math>).</p>
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<p>PL emission spectra of the proposed ZnO NPs synthesized with <span class="html-italic">Salvia officinalis</span> phytochemicals: (<b>a</b>) with PEO, (<b>b</b>) without PEO. Insets contain the circular CIE diagram exhibiting color purity.</p>
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<p>(<b>a</b>–<b>c</b>) TEM image of ZnO NPs/SOL-PEO: sizes of several particles, particle size distribution, and ZnO NPs capped with SOL + PEO shells, respectively. (<b>d</b>–<b>f</b>) TEM image of ZnO NPs/SOL: sizes of several particles, particle size distribution, and ZnO NPs capped with SOL shell, respectively.</p>
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<p>Phenolic components from SOL extract: (<b>a</b>) flavonoids [<a href="#B59-materials-16-04510" class="html-bibr">59</a>], (<b>b</b>) phenolic acids [<a href="#B59-materials-16-04510" class="html-bibr">59</a>].</p>
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<p>FESEM image of (<b>a</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>b</b>) ZnO NPs/SOL nanofilm. EDX spectra of (<b>c</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>d</b>) ZnO NPs/SOL nanofilm.</p>
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<p>Cross-section view of (<b>a</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>b</b>) ZnO NPs/SOL nanofilm. EDX spectra of (<b>c</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>d</b>) ZnO NPs/SOL nanofilm.</p>
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<p>XRD profiles of nanofilms (<b>a</b>) ZnO NPs/SOL-PEO, (<b>b</b>) ZnO NPs/SOL, (<b>c</b>) ZnO NPs/SOL-PEO annealed at <math display="inline"><semantics> <mrow> <mn>120</mn> <mo> </mo> <mo>℃</mo> </mrow> </semantics></math> for 2 h, and (<b>d</b>) ZnO NPs/SOL annealed at <math display="inline"><semantics> <mrow> <mn>120</mn> <mo> </mo> <mo>℃</mo> </mrow> </semantics></math> for 2 h.</p>
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<p>Absorption spectra of the nanofilms: (<b>a</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>b</b>) ZnO NPs/SOL nanofilm. Insets contain the corresponding optical band gap energy (<math display="inline"><semantics> <mrow> <msub> <mi>E</mi> <mi>g</mi> </msub> </mrow> </semantics></math>).</p>
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<p>PL emission spectra of the nanofilms: (<b>a</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>b</b>) ZnO NPs/SOL nanofilm. Insets contain the corresponding CIE diagram exhibiting color purity.</p>
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<p>Absorption spectra of the annealed (at <math display="inline"><semantics> <mrow> <mn>120</mn> <mo> </mo> <mo>℃</mo> </mrow> </semantics></math> for 2 h) nanofilms: (<b>a</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>b</b>) ZnO NPs/SOL nanofilm. Insets contain the corresponding optical band gap energy (<math display="inline"><semantics> <mrow> <msub> <mi>E</mi> <mi>g</mi> </msub> </mrow> </semantics></math>).</p>
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<p>PL emission spectra of the annealed (at <math display="inline"><semantics> <mrow> <mn>120</mn> <mo> </mo> <mo>℃</mo> </mrow> </semantics></math> for 2 h) nanofilms: (<b>a</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>b</b>) ZnO NPs/SOL nanofilm. Insets contain the corresponding CIE diagram exhibiting color purity.</p>
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<p>PL emission spectra of the annealed (at <math display="inline"><semantics> <mrow> <mn>120</mn> <mo> </mo> <mo>℃</mo> </mrow> </semantics></math> for 2 h) nanofilms: (<b>a</b>) ZnO NPs/SOL-PEO nanofilm, and (<b>b</b>) ZnO NPs/SOL nanofilm. Insets contain the corresponding CIE diagram exhibiting color purity.</p>
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<p>(<b>a</b>) Absorption spectra of various fabricated ZnO NP nanofilms. (<b>b</b>) Optical band gap energy (<math display="inline"><semantics> <mrow> <msub> <mi>E</mi> <mi>g</mi> </msub> </mrow> </semantics></math>) variant with (αhν)2 of ZnO NP nanofilms.</p>
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16 pages, 10919 KiB  
Article
Atomic Layer Deposition of Chlorine Containing Titanium–Zinc Oxide Nanofilms Using the Supercycle Approach
by Denis Nazarov, Lada Kozlova, Aida Rudakova, Elena Zemtsova, Natalia Yudintceva, Elizaveta Ovcharenko, Alexandra Koroleva, Igor Kasatkin, Ludmila Kraeva, Elizaveta Rogacheva and Maxim Maximov
Coatings 2023, 13(5), 960; https://doi.org/10.3390/coatings13050960 - 20 May 2023
Cited by 5 | Viewed by 2271
Abstract
Atomic layer deposition (ALD) is a useful tool for producing ultrathin films and coatings of complex composition with high thickness control for a wide range of applications. In this study, the growth of zinc–titanium oxide nanofilms was investigated. Diethyl zinc, titanium tetrachloride, and [...] Read more.
Atomic layer deposition (ALD) is a useful tool for producing ultrathin films and coatings of complex composition with high thickness control for a wide range of applications. In this study, the growth of zinc–titanium oxide nanofilms was investigated. Diethyl zinc, titanium tetrachloride, and water were used as precursors. The supercycle approach was used, and wide ZnO/TiO2 (ZTO) ALD cycles were prepared: 5/1, 3/1, 2/1, 1/1, 1/2, 1/3, 1/5, 1/10, 1/20. Spectral ellipsometry, X-ray reflectometry, X-ray diffraction, scanning electron microscopy, SEM-EDX, and contact angle measurements were used to characterize the thickness, morphology, and composition of the films. The results show that the thicknesses of the coatings differ considerably from those calculated using the rule of mixtures. At high ZnO/TiO2 ratios, the thickness is much lower than expected and with increasing titanium oxide content the thickness increases significantly. The surface of the ZTO samples contains a significant amount of chlorine in the form of zinc chloride and an excessive amount of titanium. The evaluation of the antibacterial properties showed significant activity of the ZTO–1/1 sample against antibiotic-resistant strains and no negative effect on the morphology and adhesion of human mesenchymal stem cells. These results suggest that by tuning the surface composition of ALD-derived ZTO samples, it may be possible to obtain a multi-functional material for use in medical applications. Full article
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<p>The difference between the theoretical (calculated) and real thickness of coatings depending on the composition of supercycles.</p>
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<p>XRD patterns of the as-prepared (<b>a</b>) and annealed at 350 °C (<b>b</b>) samples.</p>
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<p>Plan-view SEM images of ZnO, TiO<sub>2</sub>, and ZTO samples at magnification of 300,000. (<b>a</b>) ZnO, (<b>b</b>) ZTO–5/1 (<b>c</b>) ZTO–3/1, (<b>d</b>) ZTO–1/1 (<b>e</b>) ZTO–1/3 (<b>f</b>) ZTO–1/5 (<b>g</b>) ZTO–1/10 (<b>h</b>) ZTO–1/20 (<b>i</b>) TiO<sub>2</sub>.</p>
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<p>Plan-view SEM images and results of local EDX analysis of ZnO, TiO<sub>2</sub>, and ZTO samples at magnification 30,000. (<b>a</b>) ZnO, (<b>b</b>) ZTO–5/1 (<b>c</b>) ZTO–3/1, (<b>d</b>) ZTO–1/1 (<b>e</b>) ZTO–1/3 (<b>f</b>) ZTO–1/5 (<b>g</b>) ZTO–1/10 (<b>h</b>) ZTO–1/20 (<b>i</b>) TiO<sub>2</sub>. The circles indicate the areas of the surface composition study by the EDX containing particles, and the rectangles are the areas without particles.</p>
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<p>Results of quantitative analysis of surface composition measured by XPS.</p>
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<p>XPS spectra of all studied coatings (<b>a</b>) C1s, (<b>b</b>) O1s, (<b>c</b>) Cl2p, (<b>d</b>) Ti2p, and (<b>e</b>) Zn2p.</p>
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<p>Results of water contact angle measurements. Data are presented as mean ± C.I. from at least 12 independent series of experiments (<span class="html-italic">p</span> &lt; 0.05) in different areas of the samples.</p>
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<p>Immunofluorescent images of FetMSC cells cultivated on the cover glasses coated by ALD. FetMSc actin cytoskeleton (red), nuclei (blue). (<b>a</b>) control sample without coatings, (<b>b</b>) TiO<sub>2</sub>, (<b>c</b>) ZTO–1/20, (<b>d</b>) ZTO–1/1, and (<b>e</b>) ZnO.</p>
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<p>Comparison of the experimental and the theoretical composition of the surface calculated according to the rule of mixture.</p>
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11 pages, 2814 KiB  
Article
Preparation of Ti-Doped ZnO/Bi2O3 Nanofilm Heterojunction and Analysis of Microstructure and Photoelectric Properties
by Zhenying Chen, Xiuqing Cao, Yuyang Huang, Shuang Zhang, Wenjian Pan and Wen Deng
Crystals 2023, 13(2), 264; https://doi.org/10.3390/cryst13020264 - 2 Feb 2023
Cited by 4 | Viewed by 1525
Abstract
Ti-doped ZnO (TZO) and Bi2O3 thin films were designed and deposited by magnetron sputtering successively on ITO glass substrate to form a Ti-doped ZnO/Bi2O3 (TZO/Bi2O3) heterojunction. Microstructure and photoelectric properties of TZO, Bi [...] Read more.
Ti-doped ZnO (TZO) and Bi2O3 thin films were designed and deposited by magnetron sputtering successively on ITO glass substrate to form a Ti-doped ZnO/Bi2O3 (TZO/Bi2O3) heterojunction. Microstructure and photoelectric properties of TZO, Bi2O3, and TZO/Bi2O3 films were tested and characterized. The results showed that TZO film with a hexagonal wurtzite structure was preferentially grown along the crystal plane (002), had a good crystallization state, and was an N-type semiconductor film with high transmittance (90%) and low resistivity (4.68 × 10−3 Ω·cm). However, the Bi2O3 film sputtered in an oxygen-containing atmosphere and was a polycrystalline film that was preferentially grown along the crystal plane (111). It had a lower crystallization quality than TZO film and was a P-type semiconductor film with low transmittance (68%) and high resistance (1.71 × 102 Ω·cm). The I–V curve of TZO/Bi2O3 composite films showed that it had an obvious heterojunction rectification effect, which indicates that the PN heterojunction successfully formed in TZO/Bi2O3 films. Full article
(This article belongs to the Section Inorganic Crystalline Materials)
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<p>Schematics of TZO/Bi<sub>2</sub>O<sub>3</sub> film.</p>
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<p>SEM micrographs of TZO and Bi<sub>2</sub>O<sub>3</sub> films.</p>
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<p>A cross-sectional SEM image of TZO/Bi<sub>2</sub>O<sub>3</sub> thin film heterojunction.</p>
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<p>XRD analysis for each layer of TZO/Bi<sub>2</sub>O<sub>3</sub> heterojunction film.</p>
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<p>Optical transmittance spectra of each layer of TZO/Bi<sub>2</sub>O<sub>3</sub> heterojunction film.</p>
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<p>Plots of (<span class="html-italic">α</span>hυ)<sup>2</sup> versus photon energy (hυ) of (<b>a</b>) TZO and (<b>b</b>) Bi<sub>2</sub>O<sub>3</sub> films.</p>
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<p>I–V measurement curve of adjacent layer of TZO/Bi<sub>2</sub>O<sub>3</sub> heterojunction film.</p>
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15 pages, 3491 KiB  
Article
Synthesis and Characterization of Chitosan-Containing ZnS/ZrO2/Graphene Oxide Nanocomposites and Their Application in Wound Dressing
by Yousef A. A. Alghuwainem, Mohamed Gouda, Mai M. Khalaf, Abraham Elmushyakhi, Manal F. Abou Taleb and Hany M. Abd El-Lateef
Polymers 2022, 14(23), 5195; https://doi.org/10.3390/polym14235195 - 29 Nov 2022
Cited by 8 | Viewed by 1948
Abstract
The development of scaffold-based nanofilms for the acceleration of wound healing and for maintaining the high level of the healthcare system is still a challenge. The use of naturally sourced polymers as binders to deliver nanoparticles to sites of injury has been highly [...] Read more.
The development of scaffold-based nanofilms for the acceleration of wound healing and for maintaining the high level of the healthcare system is still a challenge. The use of naturally sourced polymers as binders to deliver nanoparticles to sites of injury has been highly suggested. To this end, chitosan (CS) was embedded with different nanoparticles and examined for its potential usage in wound dressing. In detail, chitosan (CS)-containing zinc sulfide (ZnS)/zirconium dioxide (ZrO2)/graphene oxide (GO) nanocomposite films were successfully fabricated with the aim of achieving promising biological behavior in the wound healing process. Morphological examination by SEM showed the formation of porous films with a good scattering of ZnS and ZrO2 nanograins, especially amongst ZnS/ZrO2/GO@CS film. In addition, ZnS/ZrO2/GO@CS displayed the lowest contact angle of 67.1 ± 0.9°. Optically, the absorption edge records 2.35 eV for pure chitosan, while it declines to 1.8:1.9 scope with the addition of ZnS, ZrO2, and GO. Normal lung cell (WI-38) proliferation inspection demonstrated that the usage of 2.4 µg/mL ZnS/ZrO2/GO@CS led to a cell viability % of 142.79%, while the usage of 5000 µg/ mL led to a viability of 113.82%. However, the fibroblast malignant cell line exposed to 2.4 µg/mL ZnS/ZrO2/GO@CS showed a viability % of 92.81%, while this percentage showed a steep decline with the usage of 5000 µg/ mL and 2500 µg/mL, reaching 23.28% and 27.81%, respectively. Further biological assessment should be executed with a three-dimensional film scaffold by choosing surrounding media characteristics (normal/malignant) that enhance the selectivity potential. The fabricated scaffolds show promising selective performance, biologically. Full article
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<p>Structural investigation using XRD (<b>A</b>) and FTIR (<b>B</b>) spectra of CS-based NC films.</p>
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<p>EDX of ZnS/ZrO<sub>2</sub>/GO@CS film.</p>
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<p>SEM micrographs of CS-based nanofilms.</p>
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<p>Wettability of CS-based nanofilms.</p>
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<p>Thermal behavior of ZnS/ZrO<sub>2</sub>/GO@CS film.</p>
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<p>Optical behavior of CS-based polymeric films.</p>
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<p>Cell viability of ZnS/ZrO<sub>2</sub>/GO@CS film (<b>A</b>) using normal lung cells; (<b>B</b>) anticancer activity against fibroblast cancerous cells.</p>
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<p>Optical microscope images clarifying the different concentrations of ZnS/ZrO<sub>2</sub>/GO@CS. (<b>a</b>–<b>c</b>) Cell viability of the normal lung cells (AI-38) after the incubation period, while the cells were exposed to a concentration of (<b>a</b>) 4000 µg/mL, (<b>b</b>) 2000 µg/mL, or (<b>c</b>) 500 µg/mL. (<b>d</b>–<b>f</b>) Cell viability of the cancer lung cells (A549) after the incubation period, while the cells were exposed to a concentration of (<b>d</b>) 4000 µg/mL, (<b>e</b>) 2000 µg/mL, or (<b>f</b>) 500 µg/mL. (The magnification is maintained at 100×).</p>
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14 pages, 29106 KiB  
Article
Graphene Reinforced Anticorrosion Transparent Conductive Composite Film Based on Ultra-Thin Ag Nanofilm
by Xiaowei Fan, Zenghua Zhao, Xiaoping Liang, Xuguo Huai, Chan Wang, Juncheng Liu and Chunyang Duan
Materials 2022, 15(14), 4802; https://doi.org/10.3390/ma15144802 - 9 Jul 2022
Cited by 2 | Viewed by 1776
Abstract
Transparent conductive films are widely used in electronic products and industrial fields. Ultra-thin Ag conductive nanofilm (ACF) was prepared on a soda lime silica glass (ordinary architectural glass) substrate with industrial magnetron sputtering equipment with AZO (Al2O3 doped ZnO) as [...] Read more.
Transparent conductive films are widely used in electronic products and industrial fields. Ultra-thin Ag conductive nanofilm (ACF) was prepared on a soda lime silica glass (ordinary architectural glass) substrate with industrial magnetron sputtering equipment with AZO (Al2O3 doped ZnO) as the crystal bed and wetting layer. In order to improve the corrosion resistance and conductivity of the ACF, graphene nanosheets were modified on the surface of the ACF by electrospraying for the first time. The results show that this graphene modification could be carried out continuously on a meter scale. With the modification of the graphene layer, the corrosion rate of graphene-decorated ACF (G/ACF) can be reduced by 74.56%, and after 72 h of salt spray test, the conductivity of ACF samples without modification of graphene can be reduced by 34.1%, while the conductivity of G/ACF samples with modification of graphene can be reduced by only 6.5%. This work proves the potential of graphene modified ACF to prepare robust large-area transparent conductive film. Full article
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<p>(<b>a</b>) Scheme of ultra-thin Ag conductive film (ACF) preparation procedure. (<b>b</b>) SEM image of ACF. (<b>c</b>) Optical photo of large-scale ACF samples deposited on the glass surface. (<b>d</b>) Sheet resistance and transmission of ACF with different thicknesses.</p>
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<p>(<b>a</b>) Scheme of ultra-thin Ag conductive film (ACF) preparation procedure. (<b>b</b>) SEM image of ACF. (<b>c</b>) Optical photo of large-scale ACF samples deposited on the glass surface. (<b>d</b>) Sheet resistance and transmission of ACF with different thicknesses.</p>
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<p>XPS spectra of the sample: (<b>a</b>) the full spectrum and (<b>b</b>) Ag 3d5/2 peak fitting spectrum.</p>
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<p>(<b>a</b>) Scheme of electrospraying for G/ACF film preparation procedure. (<b>b</b>) SEM image of graphene nanosheets. (<b>c</b>) TEM image of graphene nanosheets. (<b>d</b>) Raman spectra of graphene nanosheets. (<b>e</b>) Tyndall effect of graphene nanosheets suspension. (<b>f</b>) Image of the Raman mapping area. (<b>g</b>,<b>h</b>) Raman mapping results of G/ACF film.</p>
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<p>(<b>a</b>–<b>d</b>) Reflection and transmission spectra of ACF and G/ACF samples. (<b>e</b>) Sheet resistance of ACF and G/ACF samples.</p>
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<p>(<b>a</b>) Scheme of corrosion electrochemical test diagram of ACF and G/ACF samples. (<b>b</b>,<b>c</b>) Tafel plots of ACF and G/ACF samples. (<b>d</b>) Corrosion rates of ACF and G/ACF samples.</p>
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<p>(<b>a</b>,<b>b</b>) SEM images of ACF (<b>a</b>) and G/ACF (<b>b</b>) samples after salt spray test. (<b>c</b>,<b>d</b>) Contact angles of the surface of ACF (<b>a</b>) and G/ACF (<b>b</b>) samples. (<b>e</b>,<b>f</b>) Surface resistance (<b>e</b>) and transmission (<b>f</b>) of ACF samples and G/ACF samples after 72 h salt spray test.</p>
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13 pages, 3627 KiB  
Article
Preparation of Au@ZnO Nanofilms by Combining Magnetron Sputtering and Post-Annealing for Selective Detection of Isopropanol
by Guodong Wang, Pengju Wu, Lanlan Guo, Wei Wang, Wenqiang Liu, Yuanyuan Wang, Tingyu Chen, Haohan Wang, Yonghao Xu and Yingli Yang
Chemosensors 2022, 10(6), 211; https://doi.org/10.3390/chemosensors10060211 - 3 Jun 2022
Cited by 12 | Viewed by 2161
Abstract
We demonstrate the highly sensitive and fast response/recovery gas sensors for detecting isopropanol (IPA), in which the Au-nanoparticles-modified ZnO (Au@ZnO) nanofilms act as the active layers. The data confirm that both the response and the response/recovery speed for the detection of IPA are [...] Read more.
We demonstrate the highly sensitive and fast response/recovery gas sensors for detecting isopropanol (IPA), in which the Au-nanoparticles-modified ZnO (Au@ZnO) nanofilms act as the active layers. The data confirm that both the response and the response/recovery speed for the detection of IPA are significantly improved by adding Au nanoparticles on the surface of ZnO nanofilms. The gas sensor with an Optimum Au@ZnO nanofilm exhibits the highest responses of 160 and 7 to the 100 and 1 ppm IPA at 300 °C, which indicates high sensitivity and a very low detecting limit. The sensor also exhibits a very short response/recovery time of 4/15 s on the optimized Au@ZnO nanofilm, which is much shorter than that of the sensor with a pure ZnO nanofilm. The mechanisms of the performance improvement in the sensors are discussed in detail. Both the electronic sensitization and the chemical sensitization of the ZnO nanofilms are improved by the modified Au nanoparticles, which not only regulate the thickness of the depletion layer but also increase the amount of adsorbed oxygen species on the surfaces. This work proposes a strategy to develop a highly sensitive gas sensor for real-time monitoring of IPA. Full article
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<p>Schematic illustration for the preparation process of Au@ZnO nanofilms.</p>
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<p>XRD patterns of as-obtained samples (<b>a</b>) and high-resolution SEM images of S1 (<b>b</b>); S2 (<b>c</b>); S3 (<b>d</b>); S4 (<b>e</b>); size distribution of Au nanoparticles (<b>f</b>).</p>
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<p>The XPS spectra of pure ZnO and Au@ZnO nanofilms; (<b>a</b>) survey; (<b>b</b>) Zn 2p; (<b>c</b>) Au 4f and Zn 3p; (<b>d</b>) O 1s.</p>
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<p>The initial resistance of as-obtained samples at various temperatures (<b>a</b>); the response of as-obtained samples toward 100 ppm IPA with operating temperatures (<b>b</b>); variation of initial resistance of all as-obtained samples at 300 °C with Au sputtering time (<b>c</b>); variation of response of all as-obtained samples toward 100 ppm IPA at 300 °C with Au sputtering time (<b>d</b>).</p>
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<p>The dynamic response curves of as-obtained samples with time to 100 ppm IPA. (<b>a</b>) S1; (<b>b</b>) S2; (<b>c</b>) S3; (<b>d</b>) S4.</p>
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<p>Selectivity of the four samples measured at 300 °C (<b>a</b>); long-term stability of S3 toward 100 ppm IPA at 300 °C (<b>b</b>).</p>
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<p>Transient response/recovery curves of pure ZnO nanofilm ranging from 30 to 200 ppm (<b>a</b>) and of Au@ZnO nanofilms ranging from 1 to 200 ppm (<b>b</b>); linearly fitting curve of response for the as-obtained samples (<b>c</b>); six periods of transient response/recovery curves of the Au@ZnO nanofilms to 100 ppm IPA at 300 °C (<b>d</b>).</p>
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<p>Schematic diagram of the sensing mechanism for pure ZnO nanofilm (<b>a</b>,<b>b</b>) and Au@ ZnO nanofilms (<b>c</b>,<b>d</b>).</p>
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11 pages, 7663 KiB  
Article
Plasmon Enhanced Second Harmonic Generation from ZnO Nanofilms on Vertical Au Nanorod Arrays
by Qiang Ma, Chengda Pan, Yingxian Xue, Zhiyun Fang, Shiyu Zhang, Botao Wu and E Wu
Nanomaterials 2021, 11(10), 2597; https://doi.org/10.3390/nano11102597 - 2 Oct 2021
Cited by 3 | Viewed by 2321
Abstract
Vertically aligned gold nanorod arrays have attracted much attention for their fascinating optical properties. Different from longitudinal surface plasmon wavelength (LSPW) and edge-to-edge spacing of gold nanorods, the role of gold nanorod diameter in plasmonic enhancement ability of vertical gold nanorod arrays has [...] Read more.
Vertically aligned gold nanorod arrays have attracted much attention for their fascinating optical properties. Different from longitudinal surface plasmon wavelength (LSPW) and edge-to-edge spacing of gold nanorods, the role of gold nanorod diameter in plasmonic enhancement ability of vertical gold nanorod arrays has rarely been explored. In this work, we selected gold nanorods with similar LSPW but two different diameters (22 and 41 nm), the optical properties of which are dominated by absorption and scattering cross sections, respectively. The vertically aligned arrays of these gold nanorods formed by evaporation self-assembly are coupled with nonlinear ZnO nanocrystal films spin-coated on their surfaces. It was found that the gold nanorod array with a larger diameter can enhance the second harmonic generation (SHG) of ZnO nanofilm by a factor of 27.0, while it is about 7.3 for the smaller gold nanorod array. Theoretical simulations indicate that such stronger enhancement of the larger vertical gold nanorod array compared with the smaller one is due to its stronger scattering ability and greater extent of near-field enhancement at SHG fundamental wavelength. Our work shows that the diameter of gold nanorods is also an important factor to be considered in realizing strong plasmon enhancement of vertically aligned gold nanorod arrays. Full article
(This article belongs to the Special Issue State-of-the-Art Nanophotonic and Optical Nanomaterials in China)
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<p>Experimental setup for the SHG measurement of ZnO nanofilms.</p>
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<p>(<b>a</b>) Absorption spectra of Au nanorods with the diameters of 22 and 41 nm in water; (<b>b</b>) SEM image of Au nanorods with a 22 nm diameter; (<b>c</b>) SEM image of Au nanorods with a 41 nm diameter; (<b>d</b>) simulated absorption, scattering and extinction spectra for Au nanorods with a 22 nm diameter; (<b>e</b>) simulated absorption, scattering and extinction spectra for Au nanorods with a 41 nm diameter. The insets in (<b>d</b>,<b>e</b>) are dark-field scattering images of individual Au nanorods deposited on glass substrates.</p>
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<p>(<b>a</b>–<b>c</b>) SEM images of Au nanorods with a diameter of 22 nm at low, medium and high magnification; (<b>d</b>–<b>f</b>) SEM images of Au nanorods with a diameter of 41 nm at low, medium and high magnification.</p>
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<p>(<b>a</b>) XRD pattern of ZnO nanocrystals; (<b>b</b>) TEM image of ZnO nanocrystals; (<b>c</b>) SEM surface image of ZnO nanofilm; (<b>d</b>) cross section SEM image of ZnO nanofilm.</p>
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<p>(<b>a</b>) Representative SHG spectrum of ZnO nanofilm; (<b>b</b>) SHG enhancement factor of ZnO nanofilms on the vertical Au nanorod arrays with the diameters of 22 and 41 nm.</p>
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<p>(<b>a</b>) SHG spectra at different excitation powers and (<b>b</b>) SHG intensity vs. excitation power in a logarithmic scale for the vertical Au nanorod array with a diameters of 22 nm; (<b>c</b>) SHG spectra at different excitation powers and (<b>d</b>) SHG intensity vs. excitation power in a logarithmic scale for the vertical Au nanorod array with a diameters of 41 nm.</p>
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<p>Simulated near-field |<span class="html-italic">E</span>/<span class="html-italic">E</span><sub>0</sub>|<sup>2</sup> distributions of vertical Au nanorod arrays with the diameters of 22 and 41 nm at the logarithmic scale: (<b>a</b>) harmonic wavelength (400 nm); (<b>b</b>) fundamental wavelength (800 nm).</p>
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13 pages, 3982 KiB  
Article
A High-Efficiency TiO2/ZnO Nano-Film with Surface Oxygen Vacancies for Dye Degradation
by Huizhong Ma, Baofei Hao, Wentao Song, Jinpeng Guo, Mingyuan Li and Lan Zhang
Materials 2021, 14(12), 3299; https://doi.org/10.3390/ma14123299 - 15 Jun 2021
Cited by 12 | Viewed by 2379
Abstract
Photocatalytic degradation of organic pollutants in water is a highly efficient and green approach. However, the low quantum efficiency is an intractable obstacle to lower the photocatalytic efficiency of photocatalysts. Herein, the TiO2/ZnO heterojunction thin films combined with surface oxygen vacancies [...] Read more.
Photocatalytic degradation of organic pollutants in water is a highly efficient and green approach. However, the low quantum efficiency is an intractable obstacle to lower the photocatalytic efficiency of photocatalysts. Herein, the TiO2/ZnO heterojunction thin films combined with surface oxygen vacancies (OVs) were prepared through magnetron sputtering, which was designed to drive rapid bulk and surface separation of charge carriers. The morphology and structural and compositional properties of films were investigated via different techniques such as SEM, XRD, Raman, AFM, and XPS. It has been found that by controlling the O2/Ar ratio, the surface morphology, thickness, chemical composition, and crystal structure can be regulated, ultimately enhancing the photocatalytic performance of the TiO2/ZnO heterostructures. In addition, the heterojunction thin film showed improved photocatalytic properties compared with the other nano-films when the outer TiO2 layer was prepared at an O2/Ar ratio of 10:35. It degraded 88.0% of Rhodamine B (RhB) in 90 min and 90.8% of RhB in 120 min. This was attributed to the heterojunction interface and surface OVs, which accelerated the separation of electron–hole (e–h) pairs. Full article
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<p>SEM side-view images of ZnO/TiO<sub>2</sub> films: (<b>a</b>) ZT1; (<b>b</b>) ZT2; (<b>c</b>) ZT3; (<b>d</b>) ZT4; (<b>e</b>) ZT5.</p>
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<p>SEM top-view images of ZnO/TiO<sub>2</sub> films: (<b>a</b>) ZT1; (<b>b</b>) ZT2; (<b>c</b>) ZT3; (<b>d</b>) ZT4; (<b>e</b>) ZT5.</p>
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<p>(<b>a</b>) XRD patterns of ZT1, ZT2, ZT3, ZT4, and ZT5; (<b>b</b>) Zoomed-in details of ZT2, ZT3 and ZT4.</p>
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<p>Raman spectrum of ZT3 and ZT4.</p>
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<p>AFM side-view images of ZnO/TiO<sub>2</sub> films: (<b>a</b>) ZT1; (<b>b</b>) ZT2; (<b>c</b>) ZT3; (<b>d</b>) ZT4; (<b>e</b>) ZT5.</p>
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<p>(<b>a</b>) Survey spectra; (<b>b</b>) Ti 2p; (<b>c</b>) O1s; and (<b>d</b>) Zn 3d XPS spectra of as-prepared samples.</p>
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<p>The transmittance (<b>a</b>) and the bandgap values (<b>b</b>) of the ZT1, ZT2, ZT3, ZT4, and ZT5.</p>
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<p>Transient photocurrent responses of the as-prepared simples.</p>
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<p>(<b>a</b>) The photocatalytic degeneration of RhB over ZT1, ZT2, ZT3, ZT4, and ZT5; (<b>b</b>) the photocatalytic degeneration of RhB with various scavengers over ZT3; (<b>c</b>) the stability of the ZT3; and (<b>d</b>) the SEM image of ZT3 after the photocatalytic test.</p>
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<p>The reaction rate constants of ZT1, ZT2, ZT3, ZT4, and ZT5. The reaction rate constants of ZT1, ZT2, ZT3, ZT4, and ZT5.</p>
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<p>ZnO/TiO<sub>2</sub> film degradation RhB solution mechanism.</p>
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11 pages, 4709 KiB  
Article
Influence of InGaZnO Films with Different Ratios on Refractive Index Sensing Characteristics of LPFG
by Huanhuan Yan, Li Wang, Shufeng Li, Huisong Zhang, Jin Wang and Peng Cheng
Coatings 2020, 10(10), 978; https://doi.org/10.3390/coatings10100978 - 14 Oct 2020
Cited by 2 | Viewed by 1880
Abstract
Sensitive materials are widely used in the field of optical fiber sensing because of their unique advantages such as rich types, controllable composition ratio and diverse structure distribution. In this paper, the surface of long-period fiber gratings with InGaZnO [(In2O3 [...] Read more.
Sensitive materials are widely used in the field of optical fiber sensing because of their unique advantages such as rich types, controllable composition ratio and diverse structure distribution. In this paper, the surface of long-period fiber gratings with InGaZnO [(In2O3):(Ga2O3):(ZnO)] nano films with different compositions were coated by pulse laser deposition (PLD) technology. The best sensing ratio and the high sensitivity sensing of the refractive index of long-period fiber grating (LPFG) were achieved through the analysis of the influence of different ratios of InGaZnO nano films on the refractive index sensing characteristics of grating. High sensitivities of 337 nm/RIU (refractive index unit) and 145 dB/RIU of the LPFG are achieved when the best doping ratio of InGaZnO is 7:1:2. Full article
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<p>Effective refractive index of the first 10 cladding modes varies with the environmental refractive index, (<b>a</b>) R<sub>InGaZnO</sub> = 1.6, (<b>b</b>) R<sub>InGaZnO</sub> = 1.65, (<b>c</b>) R<sub>InGaZnO</sub> = 1.68, (<b>d</b>) R<sub>InGaZnO</sub> = 1.7.</p>
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<p>Relationship between coupling coefficient and film refractive index of long-period fiber grating (LPFG).</p>
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<p>(<b>a</b>) Grating cleaning and coating process (<b>b</b>) Vacuum cavity structure (<b>c</b>) Four layer membrane structure of LPFG.</p>
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<p>Transmission spectrum of nano film with different ratios.</p>
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<p>Relationship between refractive index of thin film.</p>
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<p>Atomic force microscopy (AFM) image of InGaZnO film at different content ratio, PA (In2O3):(Ga<sub>2</sub>O<sub>3</sub>):(ZnO) content is (<b>a</b>) 6:1:3, (<b>b</b>) 7:1:2, (<b>c</b>) 7.5:1:1.5.</p>
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<p>Change of square root mean roughness of InGaZnO film with the doping ratio of In<sub>2</sub>O<sub>3</sub>.</p>
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<p>(<b>a</b>) X-ray diffraction (XRD) patterns of IGZO films, (<b>b</b>) energy-dispersive X-ray (EDX) image of IGZO film, (<b>c</b>) X-ray photoelectron spectroscopy (XPS) patterns of InGaZnO film.</p>
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<p>Scanning electron microscope (SEM) image of InGaZnO.</p>
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<p>Transmission spectra of LPFG in different NaCl solutions, (<b>a</b>) uncoated LPFG, (<b>b</b>) LPFG coated with (In<sub>2</sub>O<sub>3</sub>):(Ga<sub>2</sub>O<sub>3</sub>):(ZnO) 6:1:3, (<b>c</b>) LPFG coated with (In<sub>2</sub>O<sub>3</sub>):(Ga<sub>2</sub>O<sub>3</sub>):(ZnO) 7:1:2, (<b>d</b>) LPFG coated with In<sub>2</sub>O<sub>3</sub>):(Ga<sub>2</sub>O<sub>3</sub>):(ZnO) 7.5:1:1.5.</p>
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<p>(<b>a</b>) Resonance wavelength of LPFG shifts with the mass of dissolved NaCl. (<b>b</b>) Resonance intensity of LPFG moves with the mass of dissolved NaCl.</p>
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