scholarly journals Wetting and Photocatalytic Properties of TiO2Nanotube Arrays Prepared via Anodic Oxidation of E-Beam Evaporated Ti Thin Films

2015 ◽  
Vol 2015 ◽  
pp. 1-6
Author(s):  
Soon Wook Kim ◽  
Hong Ki Kim ◽  
Jong Won Yun ◽  
Eui Jung Kim ◽  
Sung Hong Hahn

TiO2nanotube arrays (TNAs) are fabricated on quartz substrate by anodizing E-beam evaporated Ti films. E-beam evaporated Ti films are directly anodized at various anodizing voltages ranging from 20 to 45 V and their morphological, wetting, and photocatalytic properties are examined. The photocatalytic activity of the prepared TNAs is evaluated by the photodecomposition of methylene blue under UV illumination. The TNAs prepared at an anodizing voltage of 30 V have a high roughness of 30.1 nm and a low water contact angle of 7.5°, resulting in a high photocatalytic performance. The surface roughness of the TNAs is found to correlate inversely with the water contact angle. High roughness (i.e., high surface area), which leads to high hydrophilicity, is desirable for effective photocatalytic activity.

2018 ◽  
Vol 2 (4) ◽  
pp. 74 ◽  
Author(s):  
Abinash Tripathy ◽  
Patryk Wąsik ◽  
Syama Sreedharan ◽  
Dipankar Nandi ◽  
Oier Bikondoa ◽  
...  

Functional ZnO nanostructured surfaces are important in a wide range of applications. Here we report the simple fabrication of ZnO surface structures at near room temperature with morphology resembling that of sea urchins, with densely packed, μm-long, tapered nanoneedles radiating from the urchin center. The ZnO urchin structures were successfully formed on several different substrates with high surface density and coverage, including silicon (Si), glass, polydimethylsiloxane (PDMS), and copper (Cu) sheets, as well as Si seeded with ZnO nanocrystals. Time-resolved SEM revealed growth kinetics of the ZnO nanostructures on Si, capturing the emergence of “infant” urchins at the early growth stage and subsequent progressive increases in the urchin nanoneedle length and density, whilst the spiky nanoneedle morphology was retained throughout the growth. ε-Zn(OH)2 orthorhombic crystals were also observed alongside the urchins. The crystal structures of the nanostructures at different growth times were confirmed by synchrotron X-ray diffraction measurements. On seeded Si substrates, a two-stage growth mechanism was identified, with a primary growth step of vertically aligned ZnO nanoneedle arrays preceding the secondary growth of the urchins atop the nanoneedle array. The antibacterial, anti-reflective, and wetting functionality of the ZnO urchins—with spiky nanoneedles and at high surface density—on Si substrates was demonstrated. First, bacteria colonization was found to be suppressed on the surface after 24 h incubation in gram-negative Escherichia coli (E. coli) culture, in contrast to control substrates (bare Si and Si sputtered with a 20 nm ZnO thin film). Secondly, the ZnO urchin surface, exhibiting superhydrophilic property with a water contact angle ~ 0°, could be rendered superhydrophobic with a simple silanization step, characterized by an apparent water contact angle θ of 159° ± 1.4° and contact angle hysteresis ∆θ < 7°. The dynamic superhydrophobicity of the surface was demonstrated by the bouncing-off of a falling 10 μL water droplet, with a contact time of 15.3 milliseconds (ms), captured using a high-speed camera. Thirdly, it was shown that the presence of dense spiky ZnO nanoneedles and urchins on the seeded Si substrate exhibited a reflectance R < 1% over the wavelength range λ = 200–800 nm. The ZnO urchins with a unique morphology fabricated via a simple route at room temperature, and readily implementable on different substrates, may be further exploited for multifunctional surfaces and product formulations.


Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1366
Author(s):  
Jinyuan Zhang ◽  
Hui Zhang ◽  
Wenjun Li ◽  
Limeng Yang ◽  
Hailiang Wu ◽  
...  

In this study, the photocatalytic properties of novel keratin char-TiO2 composite films, made through the calcination of wool keratin coatings containing TiO2 precursors at 400 °C, were investigated for the photodegradation of organic contaminants under visible light irradiation. Its structural characteristics and photocatalytic performance were systematically examined. It was shown that a self-cleaning hydrophobic keratin char-TiO2 composite film containing meso- and micro-pores was formed after the keratin—TiO2 precursors coating was calcined. In comparison with calcinated TiO2 films, the keratin char-TiO2 composite films doped with the elements of C, N, and S from keratins resulted in decreased crystallinity and a larger water contact angle. The bandgap of the char-TiO2 composite films increased slightly from 3.26 to 3.32 eV, and its separation of photogenerated charge carriers was inhibited to a certain degree. However, it exhibited higher photodegradation efficiency to methyl blue (MB) effluents than the pure calcinated TiO2 films. This was mainly because of its special porous structure, large water contact angle, and high adsorption energy towards organic pollutants, confirmed by the density functional theory calculations. The main active species were 1O2 radicals in the MB photodegradation process.


2021 ◽  
Author(s):  
Ranran Zhang ◽  
Jiaying Jin ◽  
Lumeng Jia ◽  
Bo Shi ◽  
Rufen Chen

Abstract The Ti3C2 and g-C3N4NS were obtained first, and the CdS/Ti3C2/g-C3N4NS Z-scheme composites were prepared via a facile hydrothermal synthesis and their photocatalytic properties were investigated. The g-C3N4NS with a high surface area displayed higher adsorption and degradation capacity. Compared with Ti3C2/g-C3N4NS and CdS, the optimal ternary composites exhibited significantly enhanced visible light (vis) photocatalytic activity. The Fabrication of CdS/Ti3C2/g-C3N4NS Z-scheme heterostructure not only enhanced vis absorption, but also improved the separation ability of the photoinduced e−-h+ pairs and the redox ability of the catalyst, thereby leading to the improvement of visible-light-driven photocatalytic activity. This finding provides new insights into the construction of high efficiency Z-scheme heterostructure photocatalyst.


2020 ◽  
Author(s):  
Muayad Al-shaeli ◽  
Stefan J. D. Smith ◽  
Shanxue Jiang ◽  
Huanting Wang ◽  
Kaisong Zhang ◽  
...  

<p>In this study, novel <a>mixed matrix polyethersulfone (PES) membranes</a> were synthesized by using two different kinds of metal organic frameworks (MOFs), namely UiO-66 and UiO-66-NH<sub>2</sub>. The composite membranes were characterised by SEM, EDX, FTIR, PXRD, water contact angle, porosity, pore size, etc. Membrane performance was investigated by water permeation flux, flux recovery ratio, fouling resistance and anti-fouling performance. The stability test was also conducted for the prepared mixed matrix membranes. A higher reduction in the water contact angle was observed after adding both MOFs to the PES and sulfonated PES membranes compared to pristine PES membranes. An enhancement in membrane performance was observed by embedding the MOF into PES membrane matrix, which may be attributed to the super-hydrophilic porous structure of UiO-66-NH<sub>2</sub> nanoparticles and hydrophilic structure of UiO-66 nanoparticles that could accelerate the exchange rate between solvent and non-solvent during the phase inversion process. By adding the MOFs into PES matrix, the flux recovery ratio was increased greatly (more than 99% for most mixed matrix membranes). The mixed matrix membranes showed higher resistance to protein adsorption compared to pristine PES membranes. After immersing the membranes in water for 3 months, 6 months and 12 months, both MOFs were stable and retained their structure. This study indicates that UiO-66 and UiO-66-NH<sub>2</sub> are great candidates for designing long-term stable mixed matrix membranes with higher anti-fouling performance.</p>


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Andrzej Sikora ◽  
Dariusz Czylkowski ◽  
Bartosz Hrycak ◽  
Magdalena Moczała-Dusanowska ◽  
Marcin Łapiński ◽  
...  

AbstractThis paper presents the results of experimental investigations of the plasma surface modification of a poly(methyl methacrylate) (PMMA) polymer and PMMA composites with a [6,6]-phenyl-C61-butyric acid methyl ester fullerene derivative (PC61BM). An atmospheric pressure microwave (2.45 GHz) argon plasma sheet was used. The experimental parameters were: an argon (Ar) flow rate (up to 20 NL/min), microwave power (up to 530 W), number of plasma scans (up to 3) and, the kind of treated material. In order to assess the plasma effect, the possible changes in the wettability, roughness, chemical composition, and mechanical properties of the plasma-treated samples’ surfaces were evaluated by water contact angle goniometry (WCA), atomic force microscopy (AFM), attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS). The best result concerning the water contact angle reduction was from 83° to 29.7° for the PMMA material. The ageing studies of the PMMA plasma-modified surface showed long term (100 h) improved wettability. As a result of plasma treating, changes in the samples surface roughness parameters were observed, however their dependence on the number of plasma scans is irregular. The ATR-FTIR spectra of the PMMA plasma-treated surfaces showed only slight changes in comparison with the spectra of an untreated sample. The more significant differences were demonstrated by XPS measurements indicating the surface chemical composition changes after plasma treatment and revealing the oxygen to carbon ratio increase from 0.1 to 0.4.


Author(s):  
Wei Lee Lim ◽  
Shiplu Roy Chowdhury ◽  
Min Hwei Ng ◽  
Jia Xian Law

Tissue-engineered substitutes have shown great promise as a potential replacement for current tissue grafts to treat tendon/ligament injury. Herein, we have fabricated aligned polycaprolactone (PCL) and gelatin (GT) nanofibers and further evaluated their physicochemical properties and biocompatibility. PCL and GT were mixed at a ratio of 100:0, 70:30, 50:50, 30:70, 0:100, and electrospun to generate aligned nanofibers. The PCL/GT nanofibers were assessed to determine the diameter, alignment, water contact angle, degradation, and surface chemical analysis. The effects on cells were evaluated through Wharton’s jelly-derived mesenchymal stem cell (WJ-MSC) viability, alignment and tenogenic differentiation. The PCL/GT nanofibers were aligned and had a mean fiber diameter within 200–800 nm. Increasing the GT concentration reduced the water contact angle of the nanofibers. GT nanofibers alone degraded fastest, observed only within 2 days. Chemical composition analysis confirmed the presence of PCL and GT in the nanofibers. The WJ-MSCs were aligned and remained viable after 7 days with the PCL/GT nanofibers. Additionally, the PCL/GT nanofibers supported tenogenic differentiation of WJ-MSCs. The fabricated PCL/GT nanofibers have a diameter that closely resembles the native tissue’s collagen fibrils and have good biocompatibility. Thus, our study demonstrated the suitability of PCL/GT nanofibers for tendon/ligament tissue engineering applications.


Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 215
Author(s):  
Ewa Wierzbicka ◽  
Karolina Syrek ◽  
Klaudia Mączka ◽  
Grzegorz D. Sulka

High surface area, self-organized nanoporous ZrO2 arrays with perfect adhesion to the Zr substrate were synthesized by anodization in an aqueous electrolyte containing (NH4)2SO4 and NH4F. The obtained semiconductor materials were tested as photocatalysts for decolorization of the methyl red (MR) as a model azo dye pollutant. It was demonstrated that as-synthesized anodic ZrO2 anodic layers are already crystalline and, therefore, do not require further thermal treatment to provide a high photocatalytic performance. However, photocatalytic efficiency could be improved by annealing at a relatively low-temperature of 350 °C. Higher annealing temperatures caused a gradual drop of photocatalytic activity. The photocatalytic behavior was correlated with the crystal phase transformation in anodic ZrO2. It was found that higher photocatalytic activity was observed for the tetragonal phase over the monoclinic phase (predominant at elevated temperatures). It results from the optimal and complex electronic structure of annealed ZrO2 with three different energy states having absorption edges at 2.0, 4.01 and 5.28 eV.


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