Search

This paper investigated the influence of ultraviolet (UV) illumination on the corrosion behavior of 7A04 aluminum alloy in 3.5% NaCl solutions with various pH values (pH=5.0, 7.0, and 10.0) using weight loss measurement, electrochemical methods, and surface analysis techniques. The research results indicated that the corrosion products of 7A04 alloy in salt solutions with different pH values all exhibited n-type semiconductor properties and could trigger the photovoltaic effect under UV illumination. Simultaneously, UV illumination reduced the compactness of the corrosion products, inhibited the enrichment of copper compounds (Cu2O), and promoted the generation of hydroxyl radicals in the solution. Therefore, UV illumination significantly accelerated the corrosion process of 7A04 alloy, with the overall acceleration effect ranking as follows: alkaline > neutral > acidic. In addition, the corrosion mechanism of 7A04 alloy in the test solutions with and without UV illumination was also discussed in this paper.

In this research, graphene oxide was prepared by Hamers' improved method, then, with the electric arc method, silver nanoparticles enter the graphene oxide environment diluted with deionized water, and a colloid of core-shell,silver-silver oxide is prepared. After the samples were prepared, graphene oxide plates containing silver nanoparticles were fixed on them, and samples with the same concentration and volume were placed under ultraviolet radiation for 0, 30, 60, 120, and 240 minutes, respectively. Then, various spectra are prepared from the samples and their linear and non-linear behavior is studied in two experiments, Z-scan and phase spatial modulation. The results of ultraviolet-visible spectroscopy, infrared Fourier transform, and X-ray diffraction show that the resulting solution contains graphene oxide nanoplates and silver oxide nanoparticles. Investigating the nonlinear optical properties of the samples also shows that the nonlinear refractive index of the samples is of the order of , which by ultraviolet radiation to the samples, their nonlinear refractive index changes slightly, and on the other hand, the diffraction pattern with two peaks is observed in the formed structure.

In this research, Co0.5Zn0.5Al2O4 spinel oxides photocatalysts were elaborated from layered double hydroxides Co-Zn-Al/CO3 precursor by calcination at 300, 400, 500, 600, 800, and 1000 °C. XRD, FTIR, TGA/DTA, and SEM/EDX analysis were used for characterized of prepared photocatalysts. The photocatalytic efficiency of the prepared materials was tested by photodegradation of methyl orange (MO) azo dye as a model of textile contaminants under UV illumination. The effect of various operational factors such as irradiation time, initial pH, catalyst dose, methyl orange concentration and reuse were investigated. The enhancement of the photodegradation was strongly dependent on the calcination temperature. A synergic effect between the adsorption and photodegradation was observed. After 50 min of irradiation, the catalyst calcined at 400 °C showed the highest efficiency (98.2%). After regeneration (up to five cycles), the photocatalyst showed high stability.

We investigate the effect of pure darkness and UV illumination on the corrosion process of 3Ni weathering steels involved in both marine atmospheric environments. The corrosion behavior of 3Ni steel in both environments was assessed by cyclic acceleration experiments, electrochemical measurements, morphological analysis and physical phase analysis. The results show that UV illumination affects the corrosion process through the photovoltaic effect of the corrosion products, with photoelectrons and photo-vacancies participating in the redox reaction between the substrate and the atmospheric environment, thereby affecting the corrosion rate of 3Ni steel, the physical composition of the corrosion products and the denseness of the rust layer.

Austenitic stainless steels are commonly used as the base material for dry storage canisters in nuclear power plants because of their excellent corrosion resistance and mechanical properties. Dry storage canisters are often exposed to chloride-containing atmosphere near seashores that could induce localized stress corrosion cracking in these stainless steels near the welded regions. Titanium dioxide (TiO2) coatings applied on stainless steel substrates (i.e. Type 304 L stainless steels) along with ultraviolet irradiation have been proposed as a mitigation measure against corrosion in canister materials. In this study, TiO2 coatings were applied on stainless steel samples using a dip-coating method. The coated samples were then thermally treated under different annealing temperatures. Corrosion behavior and photocatalytic responses of the coated samples with and without UV illumination were evaluated by electrochemical polarization analyses and open circuit potential measurements. Surface morphologies of the samples and the crystal structures were studied by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD). It was found that the TiO2 coating not only showed markedly enhanced photocathodic protection on Type 304 L stainless steels during UV illumination but also maintain more active open circuit potentials for several hours after the cutoff of UV illumination. Results from electrochemical polarization analyses further supported the superior corrosion resistance of the coated samples under UV illumination conditions. In addition, the specifically processed TiO2 coatings once irradiated with UV could lead to a prolonged corrosion resistance of the samples even hours without UV illumination.

GaN high-electron-mobility transistors (HEMTs) have attracted widespread attention for high-power microwave applications, owing to their superior properties. However, the charge trapping effect has limitations to its performance. To study the trapping effect on the device large-signal behavior, AlGaN/GaN HEMTs and metal-insulator-semiconductor HEMTs (MIS-HEMTs) were characterized through X-parameter measurements under ultraviolet (UV) illumination. For HEMTs without passivation, the magnitude of the large-signal output wave (X21FB) and small-signal forward gain (X2111S) at fundamental frequency increased, whereas the large-signal second harmonic output wave (X22FB) decreased when the device was exposed to UV light, resulting from the photoconductive effect and suppression of buffer-related trapping. For MIS-HEMTs with SiN passivation, much higher X21FB and X2111S have been obtained compared with HEMTs. It suggests that better RF power performance can be achieved by removing the surface state. Moreover, the X-parameters of the MIS-HEMT are less dependent on UV light, since the light-induced performance enhancement is offset by excess traps in the SiN layer excited by UV light. The radio frequency (RF) power parameters and signal waveforms were further obtained based on the X-parameter model. The variation of RF current gain and distortion with light was consistent with the measurement results of X-parameters. Therefore, the trap number in the AlGaN surface, GaN buffer, and SiN layer must be minimized for a good large-signal performance of AlGaN/GaN transistors.

Controllable wettability is important for a wide range of applications, including intelligent switching, self-cleaning and oil/water separation. In this work, rapid switching and extreme wettability changes upon ultraviolet (UV) illumination were investigated. TiO2 nanoparticles were modified in solutions of trimethoxy(alkyl)silane, and the suspensions were sprayed on glass substrates. For such samples, the water contact angle (WCA) was shown to transition from a superhydrophobic (WCA ≈ 165°) to a superhydrophilic (WCA ≈ 0°) state within 10 min upon UV illumination and subsequent recovery to superhydrophobicity occurred after heat treatment. It was found that the changes in the trimethoxy(alkyl)silane upon UV illumination can explain the rapid decrease of the WCA from more than 165° to almost 0°. To further investigate the wettability transition, trimethoxy(alkyl)silane and Al2O3 nanoparticles (which are not photocatalytic) were mixed and spray-coated onto the glass substrates as the control samples. Then the unrecoverable change of trimethoxy(alkyl)silane under UV illumination can be confirmed. It was found that the presence of trimethoxy(alkyl)silane in the TiO2–trimethoxy(alkyl)silane coating served to speed up the super-wettability transition time from superhydrophobicity to superhydrophilicity, but also limited the number of wettability recycle times. With this understanding, the effect of the trimethoxy(alkyl)silane concentration on the number of recycle cycles was investigated.

Antifogging surfaces with unique properties to migrate severe fog formation have gained extensive interest, which is of particular interest for transparent substrates to obtain high visibility and transparency. To date, a large number of strategies including superhydrophilic or superhydrophobic surfaces and titanium dioxide (TiO2)-based composite coatings have been developed based on different mechanisms. Although these surfaces exhibit effective antifogging properties, the rigid nanostructures, cumbersome preparation, and the need for UV light excitation largely limit their widespread applications. Herein, we report a zwitter-wettable antifogging and frost-resisting coating through a fast UV-curable cross-linking of copolymer with benzophenone groups. A series of random copolymers consisting of hydrophilic hydroxyethyl methacrylate (HEA), hydrophobic methyl methacrylate (MMA), and benzophenone-based acrylate units are developed by thermally triggered free-radical polymerization. Upon UV light irradiation, a highly efficient antifogging/frost-resisting coating is covalently bonded on a polycarbonate plate surface, maintaining a light transmission higher than 85%, which was confirmed in both high and low temperature anti-fog tests. Moreover, the wetting behaviors reveal that the antifogging performance exhibited by the zwitter-wettable surface mainly relies on its surface water-adsorbing capability to imbibe condensed water vapor on the surface outmost layer. Notably, the antifogging/frost-resisting behaviors can be well regulated by adjusting the hydrophilic/hydrophobic units, due to the proper balance between the water-adsorption and coating stability. Owing to its simplicity, low-cost preparation and high efficiency, this UV-curable acrylate antifogging coating may find a wide range of applications in various display devices in analytical and detection instruments.

The photoelectrochemical quantification of phenolic compounds such as hydroquinone (HQ) and 4-aminophenol (4-AP) is accomplished by integrating a photoelectrochemical cell into a flow injection analysis (FIA) setup. It is a well-known fact that during the electroanalysis of phenolic compounds, the electrode surface is susceptible to poisoning. However, electrode fouling can be reduced significantly by using the FIA system with periodic washing of the electrode. Reactive oxygen species (ROS), which are generated on the surface of TiO2 under UV light, can oxidize phenolic compounds such as 4-AP. The oxidized form of 4-AP is reduced back at the electrode surface, generating a measurable signal proportional to its concentration. The factors influencing the performance of the sensor, such as flow rate, applied potential for back reduction and pH, are investigated in detail. In the concentration range 0.0125–1.0 µM, a linear correlation between the photocurrent and the concentration of 4-AP was observed with a sensitivity of 0.6 A M−1 cm−2 and a limit of detection of 18 nM. A straightforward analytical methodology for the on-site, highly sensitive and low-cost quantification of phenolic compounds is presented, based on the use of TiO2 in a photoelectrochemical flow cell.

A two-dimensional (2D) Dy2O3-Pd-PDA/rGO heterojunction nanocomposite has been synthesised and tested for hydrogen (H2) gas sensing under various functioning conditions, including different H2 concentrations (50 ppm up to 6000 ppm), relative humidity (up to 25 %RH) and working temperature (up to 200 °C). The material characterisation of Dy2O3-Pd-PDA/rGO nanocomposite performed using various techniques confirms uniform distribution of Pd NPs and 2D Dy2O3 nanostructures on multi-layered porous structure of PDA/rGO nanosheets (NSs) while forming a nanocomposite. Moreover, fundamental hydrogen sensing mechanisms, including the effect of UV illumination and relative humidity (%RH), are investigated. It is observed that the sensing performance is improved as the operating temperature increases from room temperature (RT = 30 °C) to the optimum temperature of 150 °C. The humidity effect investigation revealed a drastic enhancement in sensing parameters as the %RH increased up to 20%. The highest response was found to be 145.2% towards 5000 ppm H2 at 150 °C and 20 %RH under UV illumination (365 nm). This work offers a highly sensitive and selective hydrogen sensor based on a novel 2D nanocomposite using an environmentally friendly and energy-saving synthesis approach, enabling us to detect hydrogen molecules experimentally down to 50 ppm.

Ultraviolet (UV) radiation has been considered a deleterious agent that living organisms must avoid. However, many of the acclimation changes elicited by UV induce a wide range of positive effects in plant physiology through the elicitation of secondary antioxidant metabolites and natural defenses. Therefore, this fact has changed the original UV conception as a germicide and potentially damaging agent, leading to the concept that it is worthy of application in harvested commodities to take advantage of its beneficial responses. Four decades have already passed since postharvest UV radiation applications began to be studied. During this time, UV treatments have been successfully evaluated for different purposes, including the selection of raw materials, the control of postharvest diseases and human pathogens, the elicitation of nutraceutical compounds, the modulation of ripening and senescence, and the induction of cross-stress tolerance. Besides the microbicide use of UV radiation, the effect that has received most attention is the elicitation of bioactive compounds as a defense mechanism. UV treatments have been shown to induce the accumulation of phytochemicals, including ascorbic acid, carotenoids, glucosinolates, and, more frequently, phenolic compounds. The nature and extent of this elicitation have been reported to depend on several factors, including the product type, maturity, cultivar, UV spectral region, dose, intensity, and radiation exposure pattern. Even though in recent years we have greatly increased our understanding of UV technology, some major issues still need to be addressed. These include defining the operational conditions to maximize UV radiation efficacy, reducing treatment times, and ensuring even radiation exposure, especially under realistic processing conditions. This will make UV treatments move beyond their status as an emerging technology and boost their adoption by industry.

Nanocarbon materials have the advantages of biocompatibility, thermal stability and chemical stability and have shown excellent electrical properties in electronic devices. In this study, Al/MWCNT:GQD/ITO memristors with rewritable nonvolatile properties were prepared based on composites consisting of multiwalled carbon nanotubes (MWCNTs) and graphene quantum dots (GQDs). The switching current ratio of such a device can be tuned in two ways. Due to the ultraviolet light sensitivity of GQDs, when the dielectric material is illuminated by ultraviolet light, the charge capture ability of the GQDs decreases with an increasing duration of illumination, and the switching current ratio of the device also decreases with an increasing illumination duration (103–10). By exploiting the charge capture characteristics of GQDs, the trap capture level can be increased by increasing the content of GQDs in the dielectric layer. The switching current ratio of the device increases with increasing GQD content (10–103). The device can be programmed and erased more than 100 times; the programmable switching state can withstand 105 read pulses, and the retention time is more than 104 s. This memristor has a simple structure, low power consumption, and enormous application potential for data storage, artificial intelligence, image processing, artificial neural networks, and other applications.

UV-B illumination facilitates aggregation of alpha-lactalbumin (α-LA) by intramolecular disulfide bond cleavage followed by intermolecular thiol-disulfide exchange reactions. However, long term exposure to UV-B illumination may induce undesired oxidative modifications of amino acid residues in the protein. The purpose of this study was to examine the effect of UV-induced aggregation of apo-α-LA (a calcium-depleted form of α-LA) under aerobic and anaerobic conditions and by addition of tryptophan (Trp) as a photosensitizer. The addition of Trp to apo-α-LA illuminated under anaerobic conditions facilitated the highest level of free thiol release and disulfide-mediated aggregation as compared to without addition of Trp under both anaerobic and aerobic conditions. Addition of Trp under aerobic condition resulted in the lowest level of free thiols and disulfide-mediated aggregation and the aerobic conditions caused oxidation of the free Trp with formation of kynurenine and 5-hydroxy-Trp. Minor levels of the Trp oxidation product, 3-hydroxy-kynurenine (2% converted from Trp), was formed in apo-α-LA with added Trp under both aerobic and anaerobic conditions after UV-B treatment.

Tin sulfide (SnS) is known for its effective gas-detecting ability at low temperatures. However, the development of a portable and flexible SnS sensor is hindered by its high resistance, low response, and long recovery time. Like other chalcogenides, the electronic and gas-sensing properties of SnS strongly depend on its surface defects. Therefore, understanding the effects of its surface defects on its electronic and gas-sensing properties is a key factor in developing low-temperature SnS gas sensors. Herein, using thin SnS films annealed at different temperatures, we demonstrate that SnS exhibits n-type semiconducting behavior upon the appearance of S vacancies. Furthermore, the presence of S vacancies imparts the n-type SnS sensor with better sensing performance under UV illumination at room temperature (25 °C) than that of a p-type SnS sensor. These results are thoroughly investigated using various experimental analysis techniques and theoretical calculations using density functional theory. In addition, n-type SnS deposited on a polyimide substrate can be used to fabricate high-stability flexible sensors, which can be further developed for real applications.

A low cost, highly rectifying, nano heterojunction (p-ZnO/n-Si) diode was fabricated using solution-processed, p-type, ZnO nanoparticles and an n-type Si substrate. p-type ZnO nanoparticles were synthesized using a chemical synthesis route and characterized by XRD and a Hall effect measurement system. The device was fabricated by forming thin film of synthesized p-ZnO nanoparticles on an n-Si substrate using a dip coating technique. The device was then characterized by current–voltage (I–V) and capacitance–voltage (C–V) measurements. The effect of UV illumination on the I–V characteristics was also explored and indicated the formation of a highly rectifying, nano heterojunction with a rectification ratio of 101 at 3 V, which increased nearly 2.5 times (232 at 3 V) under UV illumination. However, the cut-in voltage decreases from 1.5 V to 0.9 V under UV illumination. The fabricated device could be used in switches, rectifiers, clipper and clamper circuits, BJTs, MOSFETs and other electronic circuitry.

In this paper, the UV illumination effect for microwave gas sensors based on the tin dioxide was verified. A UV LED with emission wavelength close to the absorption edge of the SnO2 gas-sensing layer was selected as the UV source. The developed gas sensors were tested under exposure to acetone in the 0−200 ppm range at room temperature. The sensor’s complex reflection coefficient corresponding to target gas concentration was measured with the use of a five-port reflectometer system exhibiting enhanced uncertainty distribution, which allows for the detection of low gas concentration. The UV illumination significantly emphasizes the sensors’ response in terms of both magnitude and phase for low gas concentrations, in contrast to previously reported results, in which only the reflection coefficient’s phase was affected. The highest responses were obtained for modulated UV illumination.

ZnO film was deposited by the magnetron sputtering method. The thickness of ZnO film is approximately 2 μm. The influence of UV light illumination on C2H5OH sensing properties of ZnO film was investigated. Gas sensing results revealed that the UV-illuminated ZnO film displays excellent C2H5OH characteristics in terms of high sensitivity, excellent selectivity, rapid response/recovery, and low detection limit down to 0.1 ppm. The excellent sensing performance of the sensor with UV activation could be attributed to the photocatalytic oxidation of ethanol on the surface of the ZnO film, the planar film structure with high utilizing efficiency of UV light, high electron mobility, and a good surface/volume ratio of of ZnO film with a relatively rough and porous surface.