Synergistic Performance Boosts of Dopamine-Derived Carbon Shell Over Bi-metallic Sulfide: A Promising Advancement for High-Performance Lithium-Ion Battery Anodes.

A CoMoS composite is synthesized to combine the benefits of cobalt and molybdenum sulfides as an anodic material for advanced lithium-ion batteries (LIBs). The synthesis is accomplished using a simple two-step hydrothermal method and the resulting CoMoS nanocomposites are subsequently encapsulated in a carbonized polydopamine shell. The synthesis procedure exploited the self-polymerization ability of dopamine to create nitrogen-doped carbon-coated cobalt molybdenum sulfide, denoted as CoMoS@NC. Notably, the de-lithiation capacity of CoMoS and CoMoS@NC is 420 and 709 mAh g⁻1, respectively, even after 100 lithiation/de-lithiation cycles at a current density of 200 mA g⁻1. Furthermore, excellent capacity retention ability is observed for CoMoS@NC as it withstood 600 consecutive lithiation/de-lithiation cycles with 94% capacity retention. Moreover, a LIB full-cell assembly incorporating the CoMoS@NC anode and an NMC-532 cathode is subjected to comprehensive electrochemical and practical tests to evaluate the performance of the anode. In addition, the density functional theory showcases the increased lithium adsorption for CoMoS@NC, supporting the experimental findings. Hence, the use of dopamine as a nitrogen-doped carbon shell enhanced the performance of the CoMoS nanocomposites in experimental and theoretical tests, positioning the material as a strong candidate for LIB anode.

Dielectric constant enhancement of poly 4-vinylphenol (PVPh) via graphene flakes incorporation through electrospray atomization for energy storage.

We report on the fabrication of hybrid composite poly 4-vinlyphenol (PVPh)/graphene thin film via cost-effective electrospray atomization deposition technique. Thin films fabricated through manipulating deposition technique in two different ways which are blending and layer by layer (LBL). For investigation of PVPh/graphene hybrid composite dielectric behavior in comparison to PVPh; three asymmetric MIS thin film capacitors were fabricated, where dielectric thin films (i) PVPh and (ii & iii) hybrid composite thin films PVPh/graphene (blended and LBL) were sandwiched between electrodes i.e. indium tin oxide (ITO) and p-type semiconductor poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS). The dielectric properties of the thin films were characterized for frequencies 1 to 100 kHz while utilizing the MIS thin film capacitors. The capacitance obtained at 1 kHz frequency for PVPh/graphene (LBL) dielectric layer at the voltage range ±10 volts was 8.5 mF cm-2 while for blended PVPh/graphene thin film the capacitance at the voltage range ±3 volts was 0.40 µF cm-2 and for pristine PVPh as dielectric layer the capacitance at voltage range ±1 volts was 1.45 µF cm-2. Similarly, even at higher frequencies up to 100 kHz, the PVPh/graphene (LBL) showed stable behavior. Thus, the composite PVPh/graphene (LBL) thin film has a better dielectric nature compared to the composite PVPh/graphene (blended) thin film, even at higher frequencies with larger operational voltage window. This distinguishing nature of the composite PVP/graphene (LBL) is attributed to increase in dielectric constant due to graphene flakes in between PVPh. For the thin films LBL and blended PVPh/graphene, the calculated dielectric constant at 10 kHz is 6.7 and 0.023 while at 100 kHz it is 2 and 0.0167, respectively.

A simple microplasma reactor paired with indirect ultrasonication for aqueous phase synthesis of cobalt oxide nanoparticles.

Cobalt oxide nanoparticles are widely used owing to their distinct properties such as their larger surface area, enhanced reactivity, and their superior optical, electronic, and magnetic properties when compared to their bulk counterpart. The nanoparticles are preferably synthesized using a bottom-up approach in liquid as it allows the particle size to be more precisely controlled. In this study, we employed microplasma to synthesize Co3O4 nanoparticles because it eliminates harmful reducing agents and is efficient and cost-effective. Microplasma reactors are equipped with copper wire electrodes to generate plasma and are simple to configure. The product was characterized using UV-Vis spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM). The experimental parameters that were varied for the synthesis were: with or without stirring, with or without indirect ultrasonication, and with or without capping agents (urea and sucrose). The results showed that the microplasma enabled Co3O4 nanoparticles to be successfully synthesized, with particle sizes of 10.9-17.7 nm, depending on the synthesis conditions.

Synthesis of efficient light harvesting Cr, N Co-doped TiO2 nanoparticles for enhanced visible light photocatalytic degradation of xanthene dyes; eosin yellow and rose bengal.

To solve the problem of water pollution, using environment friendly and cost effective method in short time is the need of hour. In this work, chromium (Cr) and nitrogen (N) co-doped TiO2 nanoparticles were synthesized and were used for the photocatalytic degradation of dyes under visible light. The synergistic effect of metal and non-metal co-dopants added would result in appropriate reduction of band gap {from 3.2 eV of TiO2 to 2.67 eV}, decrease in recombination rate of charge carriers by trapping electrons and holes, and in better light harvesting capacity. Nanoparticles were synthesized by sol-gel method and characterized using ultraviolet-visible (UV-VIS) spectroscopy, fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), zeta potential, X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) analysis, field emission scanning electron microscopy (FE-SEM), and RAMAN spectroscopy. Eosin yellow (EY) and rose bengal (RB) were subjected to photocatalytic degradation under solar light to check the photocatalytic activity of the synthesized nanoparticles. Effects of dye concentration, the concentration of nanoparticles, time, and pH were investigated to optimize the parameters. The results obtained were remarkable for 20 ppm EY solution took 10 min using 1 gL-1 NPs at pH 3 and 10 ppm RB solution took 5 min using 0.75 gL-1 NPs at pH 5.78 (original pH) for complete degradation. Kinetics studies were also performed and both dyes followed pseudo-second-order kinetics with R2 values 0.99312 and 0.99712 for EY and RB, respectively. The study of degraded products was conducted using high-performance liquid chromatography (HPLC) hyphenated with electron spray ionization mass spectroscopy (ESI-MS) (LC-MS) and possible degradation pathways were made for both dyes. A reusability test was also performed showing the efficiency of the particles was up to 88% after 3 cycles of use. These notable results can be attributed to the efficient removal of organic pollutants using the proposed dopants in this study.

Visible-Light Driven Photodegradation of Industrial Pollutants Using Nitrogen-Tungsten Co-Doped Nanocrystalline TiO2: Spectroscopic Analysis of Degradation Reaction Path.

The purpose to conduct this research work is to study the effect of photocatalytic degradation by developing cost-effective and eco-friendly nitrogen and tungsten (metal/non-metal) co-doped titania (TiO2). The inherent characteristics of synthesized nanoparticles (NPs) were analyzed by Fourier transform infra-red spectroscopy (FT-IR), ultra-violet visible (UV-Vis) spectroscopy, Raman spectroscopy, Field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDX), dynamic light scattering (DLS), X-ray diffraction (XRD) spectrometry, and atomic force microscopy (AFM). Co-doping of metal and non-metal has intensified the photocatalysis trait of TiO2 nanoparticles in an aqueous medium. This co-doping of transition metal ions and modification of nitrogen extended the absorption into the visible region subsequently restraining the recombination of electrons/holes pair. The stronger light absorption in the visible region was required for the higher activity of photodegradation of dye under visible light illumination to confine bandgap energy which results in accelerating the rate of photodegradation. After efficient doping, the bandgap of titania reduced to 2.38 eV and caused the photodegradation of malachite green in visible light. The results of photocatalytic degradation were confirmed by using UV/Vis. spectroscopy and high-performance liquid chromatography coupled with a mass spectrophotometer (HPLC-ESI-MS) was used for the analysis of intermediates formed during photocatalytic utility of the work.

Activated carbon derived from cherry flower biowaste with a self-doped heteroatom and large specific surface area for supercapacitor and sodium-ion battery applications.

Herein, cherry flower waste-derived activated carbon (CFAC) with self-doped nitrogen is synthesized as a viable energy storage material for green and sustainable energy solutions. The activated carbon derived in this way is examined as an electric double-layer capacitance (EDLC)-type electrode material and sodium-ion battery (NIB) electrode material, and commendable performance is demonstrated for both of these energy storage applications. The specific surface area (SSA) and nitrogen content are observed to play a very delicate role in determining the charge storage ability of the CFAC, and the performance is optimized only by carefully balancing both of these properties. The optimized CFAC electrode supplied an excellent performance with a specific capacitance of 333.8 F g-1 and capacity is maintained to more than 96% even after 38,000 charge-discharge cycles as an EDLC-type supercapacitor electrode material. Likewise, the CFAC/NIB also yielded remarkable performance with an average specific capacity of 150 mAh g-1 and capacity retention of more than 84% after 200 charge-discharge cycles. Furthermore, an electrokinetic study was performed for both supercapacitor and NIB applications to identify the contribution from surface and diffusion type charge storage phenomena, consequently highlighting the role of the SSA and nitrogen content in the CFAC matrix.

Plasma-catalytic ethylene removal by a ZSM-5 washcoat honeycomb monolith impregnated with palladium.

The effective removal of dilute ethylene in a novel honeycomb plasma reactor was investigated using a honeycomb catalyst (Pd/ZSM-5/monolith) sandwiched between two-perforated electrodes operating at ambient temperature. Herein, the dependence of catalyst performance on the binder fraction, catalyst preparation method, and catalyst loading was examined. Ethylene removal was carried out by a process comprising cycles of 30-min adsorption conjugated with 15-min plasma-catalytic oxidation. Interestingly, the performance of the cyclic process was superior to continuous plasma-catalytic oxidation and thermally activated catalyst in terms of energy conservation, i.e., ~36 compared to ~105 and ~300 J/L, respectively. Hence, the novel cyclic process can be considered advanced-oxidation technology that features room-temperature oxidation, offers low energy consumption, negligible hazardous by-products emissions such as NOx and O3. Moreover, the process operated under described conditions: low-pressure drop, ambient atmosphere, a mechanically stable system, and a simple reactor configuration, suggesting the practical applicability of this plasma process.

Removal of ethyl acetate in air by using different types of corona discharges generated in a honeycomb monolith structure coated with Pd/γ-alumina.

A method based on the corona discharge produced by high voltage alternating current (AC) and direct current (DC) over a Pd/γ-Al2O3 catalyst supported on a honeycomb structure monolith was developed to eliminate ethyl acetate (EA) from the air at atmospheric pressure. The characteristics of the AC and DC corona discharge generated inside the honeycomb structure monolith were investigated by varying the humidity, gas hourly space velocity (GHSV), and temperature. The results showed that the DC corona discharge is more stable and easily operated at different operating conditions such as humidity, GHSV, and gas temperature compared to the AC discharge. At a given applied voltage, the EA conversion in the DC honeycomb catalyst discharge is, therefore, higher compared with that in the AC honeycomb catalyst discharge (e.g., 96% of EA conversion compared with approximately 68%, respectively, at 11.2 kV). These new results can open opportunities for wide applications of DC corona discharge combined with honeycomb catalysts to VOC treatment.

Enhancement of seed germination and microbial disinfection on ginseng by cold plasma treatment.

BACKGROUND: This study aimed to investigate the effect of cold plasma treatment on the improvement of seed germination and surface sterilization of ginseng seeds. METHODS: Dehisced ginseng (Panax ginseng) seeds were exposed to dielectric barrier discharge (DBD) plasma operated in argon (Ar) or an argon/oxygen mixture (Ar/O2), and the resulting germination and surface sterilization were compared with those of an untreated control group. Bacterial and fungal detection assays were performed for plasma-treated ginseng seeds after serial dilution of surface-washed suspensions. The microbial colonies (fungi and bacteria) were classified according to their phenotypical morphologies and identified by molecular analysis. Furthermore, the effect of cold plasma treatment on the in vitro antifungal activity and suppression of Cylindrocarpon destructans in 4-year-old ginseng root discs was investigated. RESULTS: Seeds treated with plasma in Ar or Ar/O2 exhibited a higher germination rate (%) compared with the untreated controls. Furthermore, the plasma treatment exhibited bactericidal and fungicidal effects on the seed surface, and the latter effect was stronger than the former. In addition, plasma treatment exhibited in vitro antifungal activity against C. destructans and reduced the disease severity (%) of root rot in 4-year-old ginseng root discs. The results demonstrate the stimulatory effect of plasma treatment on seed germination, surface sterilization, and root rot disease suppression in ginseng. CONCLUSION: The results of this study indicate that the cold plasma treatment can suppress the microbial community on the seed surface root rot in ginseng.

Efficient removal of anionic, cationic textile dyes and salt mixture using a novel CS/MIL-100 (Fe) based nanofiltration membrane.

The purification of hazardous textile dyeing wastewater has exhibited many challenges because it consists of a complex mixture, including dyestuff, additives, and salts. It is necessary to fabricate membranes with enhanced permeability, fouling resistance, stability, and superior dyes and salts removal from wastewater. Incorporating a highly water stable metal-organic framework (MOFs) into membranes would meet the requirements for the efficient purification of textile wastewater. In this study, nanofiltration (NF) membranes are fabricated by incorporating MIL-100 (Fe) into the chitosan (CS) through film casting technique. The effect of MIL-100 (Fe) loadings on chitosan characterized by FT-IR, XRD, contact angle measurement, FESEM-EDS, XPS, zeta potential, and surface roughness analysis. The membrane characterization confirmed the enhanced surface roughness, pore size, surface charge, and hydrophilicity. The CS/MIL-100 (Fe) membrane exhibited an improved pure water flux from 5 to 52 L/m2h as well as 99% rejection efficiency for cationic methylene blue (MB) and anionic methyl orange (MO). We obtained the rejection efficiency trend for the MB mixed salts in the order of MgSO4 (Mg2+ - 51.6%, SO42- - 52.5%) > Na2SO4 (Na+ - 26.3%, SO42- - 29.3%) > CaCl2 (Ca2+ - 21.4%, Cl- - 23.8%) > NaCl (Na+ - 16.8%, Cl- - 19.2%). In addition, the CS/MIL-100 (Fe) composite membrane showed excellent rejection efficiency and antifouling performances with high recycling stability. These stunning results evidenced that the CS/MIL-100 (Fe) nanofiltration membrane is a promising candidate for removing toxic pollutants in the textile dyeing wastewater.

High-Throughput NOx Removal by Two-Stage Plasma Honeycomb Monolith Catalyst.

A two-stage plasma catalyst system for high-throughput NOx removal was investigated. Herein, the plasma stage involved the large-volume plasma discharge of humidified gas and was carried out in a sandwich-type honeycomb monolith reactor consisting of a commercial honeycomb catalyst (50 mm high; 93 mm in diameter) located between two parallel perforated disks that formed the electrodes. The results demonstrated that, in the plasma stage, the reduction of NOx did not occur at room temperature; instead, NO was only oxidized to NO2 and n-heptane to oxygenated hydrocarbons. The oxidation of NO and n-heptane in the honeycomb plasma discharge state was largely affected by the humidity of the feed gas. Furthermore, the oxidation of NO to NO2 occurs preferably to that of n-heptane with a tendency of the NO oxidation to decrease with increasing feed gas humidity. The reason is that the generation of O3 decreases as the amount of water vapor in the feed gas increases. Compared to the catalyst alone, the two-stage plasma catalyst system increased NOx removal by 29% at a temperature of 200 °C and an energy density of 25 J/L.

Effective practical removal of acetaldehyde by a sandwich-type plasma-in-honeycomb reactor under surrounding ambient conditions.

The effective removal of acetaldehyde by humidified air plasma was investigated with a high throughput of contaminated gas in a sandwiched honeycomb catalyst reactor at surrounding ambient temperature. Here, acetaldehyde at the level of a few ppm was successfully oxidized by the honeycomb plasma discharge despite the harsh condition of large water content in the feed gas. The conversion rate of acetaldehyde increased significantly with the presence of catalysts coating on the surface channels. The increased conversion rate was also obtained with a high specific energy input (SEI) and total flow rate. Interestingly, the conversion changed negligibly under the acetaldehyde concentration range from 5 to 20 ppm. However, the conversion rate decreased toward increased water amount in the feed gas. Notably, about 60% of acetaldehyde in the feed was oxidized under SEI of 40 J/L at water amounts ≤ 2.5%, approximately 0.5 g/kWh for acetaldehyde removal. Also, the plasma-catalyst reaction was superior to the thermal reactive catalyst for acetaldehyde removal in airborne pollutants. In comparison with other plasma-catalyst sources for acetaldehyde removal, the energy efficiency under the condition is comparable. Moreover, the honeycomb plasma discharge features high throughput, avoiding pressure drop, and straightforward reactor configuration, suggesting potential practical applications.

Dependence of humidified air plasma discharge performance in commercial honeycomb monoliths on the configuration and key parameters of the reactor.

The effect of the reactor configuration and several key parameters such as the gas temperature, humidity, and flow rate on the corona discharge plasma in honeycomb monoliths was investigated. The AC corona discharge-based plasma reactor consisted of two parallel electrodes (perforated disk/wire-mesh) placed at both ends of the honeycomb monolith. Although the wire-mesh electrode offers increased sharpness, the perforated disk electrode, where the corona discharge started at the sharp edges of the holes, produced more discharge power because of the larger effective electrode area. Loading a small amount of metal onto the monolith was found to increase the discharge power significantly. Coating the monolith with a zeolite such as ZSM-5 (Si/Al: 23.9) led to a decrease in the discharge power because of its hydrophobic nature and large surface area. The result also revealed that the operating temperature, the humidity of the feed gas, and the gas velocity were key factors affecting the discharge performance. The discharge power was inversely proportional to the temperature. On the other hand, the use of a high-velocity feed gas with high water vapor content was found to be particularly advantageous for obtaining high discharge power.

Nonthermal plasma in practical-scale honeycomb catalysts for the removal of toluene.

Nonthermal plasma combined with a practical-scale honeycomb catalyst of 5.0 cm in height and 9.3 cm in diameter was investigated for the removal of toluene. The creation of plasma in the honeycomb catalyst greatly depended on the humidity of the feed gas and the presence of metals on the honeycomb surface. Compared to the bare ceramic honeycomb, the metal-loaded one gave higher toluene removal efficiency because the decomposition of toluene by the plasma-generated reactive species occurred not only homogeneously in the gas phase but also heterogeneously on the catalyst surface. The present plasma-catalytic reactor was able to successfully remove about 80% of dilute toluene (15 ppm in air) at a large flow rate of 60 L/min with a specific energy input of 58 J/L. The honeycomb-based plasma-catalytic reactor system is promising for practical applications since it can overcome such problems as high-pressure drop and difficulty in scale-up encountered in packed-bed reactors.

Synergistic effects of nanocarbon spheres sheathed on a binderless CoMoO4 electrode for high-performance asymmetric supercapacitor.

An essential key to enhancing the specific capacity and cyclic stability of transition metal oxide materials is the hybridization of carbon compounds by binder-free methods for supercapacitors. Carbonaceous compounds shorten the electron-ion diffusion pathways due to their high active surface area and conductivity. Herein, we focus on improving the specific energy, stability, and conductivity of the electrode by the incorporation of nanosized carbon material. The integration of nano carbons from viable eco-friendly glucose with CoMoO4 enhanced the experimental specific capacity of the electrode. The self-grown CoMoO4 on a nickel foam (CMO-NF) was confirmed as the best approach after extensive optimization process by the feasible hydrothermal (HT) method. The amount of carbon deposited and the structural morphology on the fabricated CoMoO4-glucose-derived carbon (CMO-GC) electrode was varied by adjusting the concentration of glucose by the viable HT technique. Notably, the hybrid CMO-GC-2 achieved a maximum specific capacity of 851.85 C g-1 at 1 A g-1, and it is relatively higher than that of CMO-NF (301.4 C g-1). The asymmetric supercapacitor device (CMO-GC-2//AC) demonstrated excellent energy density (36.86 W h kg-1 for 152.84 W kg-1), power density (3209.35 W kg-1 for 11.19 W h kg-1), and extensive capacity retention of 87% for up to 5000 cycles. The high performance is related to the synergetic effect of EDLC and the redox reaction, with nano-architecture and well-defined morphology of the electrode material.

Free-Standing PVDF/Reduced Graphene Oxide Film for All-Solid-State Flexible Supercapacitors towards Self-Powered Systems.

The development of polymer-based devices has attracted much attention due to their miniaturization, flexibility, lightweight and sustainable power sources with high efficiency in the field of wearable/portable electronics, and energy system. In this work, we proposed a polyvinylidene fluoride (PVDF)-based composite matrix for both energy harvesting and energy storage applications. The physicochemical characterizations, such as X-ray diffraction, laser Raman, and field-emission scanning electron microscopy (FE-SEM) analyses, were performed for the electrospun PVDF/sodium niobate and PVDF/reduced graphene oxide composite film. The electrospun PVDF/sodium niobate nanofibrous mat has been utilized for the energy harvester which shows an open circuit voltage of 40 V (peak to peak) at an applied compressive force of 40 N. The PVDF/reduced graphene oxide composite film acts as the electrode for the symmetric supercapacitor (SSC) device fabrication and investigated for their supercapacitive properties. Finally, the self-charging system has been assembled using PVDF/sodium niobate (energy harvester), and PVDF/reduced graphene oxide SSC (energy storage) and the self-charging capability is investigated. The proposed self-charging system can create a pathway for the all-polymer based composite high-performance self-charging system.

Innovative Approach of Non-Thermal Plasma Application for Improving the Growth Rate in Chickens.

As an innovative technology in biological applications-non-thermal plasma technique-has recently been applied to living cells and tissues. However, it is unclear whether non-thermal plasma treatment can directly regulate the growth and development of livestock. In this study, we exposed four-day-incubated fertilized eggs to plasma at 11.7 kV for 2 min, which was found to be the optimal condition in respect of highest growth rate in chickens. Interestingly, plasma-treated male chickens conspicuously grew faster than females. Plasma treatment regulated the reactive oxygen species homeostasis by controlling the mitochondrial respiratory complex activity and up-regulating the antioxidant defense system. At the same time, growth metabolism was improved due to the increase of growth hormone and insulin-like growth factor 1 and their receptors expression, and the rise of thyroid hormones and adenosine triphosphate levels through the regulation of demethylation levels of growth and hormone biosynthesis-related genes in the skeletal muscles and thyroid glands. To our knowledge, this study was the first to evaluate the effects of a non-thermal plasma treatment on the growth rate of chickens. This safe strategy might be beneficial to the livestock industry.

MicroRNA-7450 regulates non-thermal plasma-induced chicken Sertoli cell apoptosis via adenosine monophosphate-activated protein kinase activation.

Non-thermal plasma treatment is an emerging innovative technique with a wide range of biological applications. This study was conducted to investigate the effect of a non-thermal dielectric barrier discharge plasma technique on immature chicken Sertoli cell (SC) viability and the regulatory role of microRNA (miR)-7450. Results showed that plasma treatment increased SC apoptosis in a time- and dose-dependent manner. Plasma-induced SC apoptosis possibly resulted from the excess production of reactive oxygen species via the suppression of antioxidant defense systems and decreased cellular energy metabolism through the inhibition of adenosine triphosphate (ATP) release and respiratory enzyme activity in the mitochondria. In addition, plasma treatment downregulated miR-7450 expression and activated adenosine monophosphate-activated protein kinase α (AMPKα), which further inhibited mammalian target of rapamycin (mTOR) phosphorylation in SCs. A single-stranded synthetic miR-7450 antagomir disrupted mitochondrial membrane potential and decreased ATP level and mTOR phosphorylation by targeting the activation of AMPKα, which resulted in significant increases in SC lethality. A double-stranded synthetic miR-7450 agomir produced opposite effects on these parameters and ameliorated plasma-mediated apoptotic effects on SCs. Our findings suggest that miR-7450 is involved in the regulation of plasma-induced SC apoptosis through the activation of AMPKα and the further inhibition of mTOR signaling pathway.

Non-thermal plasma treatment improves chicken sperm motility via the regulation of demethylation levels.

The quality of avian semen is an important economic trait in poultry production. The present study examines the in vitro effects of non-thermal dielectric barrier discharge plasma on chicken sperm to determine the plasma conditions that can produce the optimum sperm quality. Exposure to 11.7 kV of plasma for 20 s is found to produce maximum sperm motility by controlling the homeostasis of reactive oxygen species and boosting the release of adenosine triphosphate and respiratory enzyme activity in the mitochondria. However, prolonged exposure or further increase in plasma potential impairs the sperm quality in a time- and dose-dependent manner. Optimal plasma treatment of sperm results in upregulated mRNA and protein expression of antioxidant defense-related and energetic metabolism-related genes by increasing their demethylation levels. However, 27.6 kV of plasma exerts significant adverse effects. Thus, our findings indicate that appropriate plasma exposure conditions improve chicken sperm motility by regulating demethylation levels of genes involved in antioxidant defense and energetic metabolism.

Tailoring the wettability of glass using a double-dielectric barrier discharge reactor.

A double dielectric barrier discharge reactor operated at a low power frequency of 400 Hz and atmospheric pressure was utilized for regulating the wettability of glass surface. The hydrophobic treatment was performed by plasma polymerization of tetramethylsilane (TMS, in argon gas). The obtained results showed that the TMS coatings formed on the glass substrates without oxygen addition were smooth, uniform films with the maximum water contact angle (WCA) of about 106°, which were similar to those obtained by low pressure, high power frequency plasmas reported in the literature. The addition of oxygen into TMS/Ar plasma gas decreased the WCA and induced the formation of SiOSi and/or SiOC linkages, which dominated the existence of Si(CH2)nSi network formed in TMS/Ar (without oxygen) plasma.