Editorial of Special Issue "Materials for Energy Applications 2.0".

Energy is a key factor in determining the growth of human society [...].

Metabolomics profiling of valproic acid-induced symptoms resembling autism spectrum disorders using 1H NMR spectral analysis in rat model.

Prenatal exposure to valproic acid (VPA) has been implicated in the manifestation of autism spectrum disorder (ASD)-like behavioral and functional changes both in human and rodents including mice and rats. The objective of this study was to determine metabolomics profiling and biomarkers related to VPA-induced symptoms resembling ASD using proton nuclear magnetic resonance (1H-NMR) spectral data. VPA was administered to pregnant rats at gestation day 12.5 and effects measured subsequently in male 4-week-old offspring pups. The sociability of VPA-treated animals was significantly diminished and exhibited ASD-like behavior as evidenced by reduction of social adaptation disorder and lack of social interactions. To find biomarkers related to ASD, the following were collected prefrontal brain cortices, urine bladder and blood samples directly from heart puncture. In all samples, principal component analysis (PCA) and partial least-squares discriminant analysis (PLS-DA) displayed significant clustering pattern differences between control and treated groups. Valine, taurine, myo-inositol, 3-hydroxybutyrate and 1,3-dihydroxyacetone were significantly decreased in brain cortices in treated rats. Serum metabolites of glucose, creatine phosphate, lactate, glutamine and threonine were significantly increased in VPA-administered animals. Urinary metabolites of pimelate, 3-hydroxyisovalerate and valerate were significantly reduced in VPA-treated rat, whereas galactose and galactonate levels were elevated. Various metabolites were associated with mitochondrial dysfunction metabolism and central nervous system disorders. Data demonstrated that VPA-induced alterations in endogenous metabolites of serum, urine, and brain cortex which might prove useful as biomarkers for symptoms resembling ASD as a model of this disorder.

A Flower-like In2O3 Catalyst Derived via Metal-Organic Frameworks for Photocatalytic Applications.

The most pressing concerns in environmental remediation are the design and development of catalysts with benign, low-cost, and efficient photocatalytic activity. The present study effectively generated a flower-like indium oxide (In2O3-MF) catalyst employing a convenient MOF-based solvothermal self-assembly technique. The In2O3-MF photocatalyst exhibits a flower-like structure, according to morphology and structural analysis. The enhanced photocatalytic activity of the In2O3-MF catalyst for 4-nitrophenol (4-NP) and methylene blue (MB) is likely due to its unique 3D structure, which includes a large surface area (486.95 m2 g-1), a wide spectrum response, and the prevention of electron-hole recombination compared to In2O3-MR (indium oxide-micro rod) and In2O3-MD (indium oxide-micro disc). In the presence of NaBH4 and visible light, the catalytic performances of the In2O3-MF, In2O3-MR, and In2O3-MD catalysts for the reduction of 4-NP and MB degradation were investigated. Using In2O3-MF as a catalyst, we were able to achieve a 99.32 percent reduction of 4-NP in 20 min and 99.2 percent degradation of MB in 3 min. Interestingly, the conversion rates of catalytic 4-NP and MB were still larger than 95 and 96 percent after five consecutive cycles of catalytic tests, suggesting that the In2O3-MF catalyst has outstanding catalytic performance and a high reutilization rate.

Carbon-Coated ZnS-FeS2 Heterostructure as an Anode Material for Lithium-Ion Battery Applications.

The construction of carbon-coated heterostructures of bimetallic sulfide is an effective technique to improve the electrochemical activity of anode materials in lithium-ion batteries. In this work, the carbon-coated heterostructured ZnS-FeS2 is prepared by a two-step hydrothermal method. The crystallinity and nature of carbon-coating are confirmed by the investigation of XRD and Raman spectroscopy techniques. The nanoparticle morphology of ZnS and plate-like morphology of FeS2 is established by TEM images. The chemical composition of heterostructure ZnS-FeS2@C is discovered by an XPS study. The CV results have disclosed the charge storage mechanism, which depends on the capacitive and diffusion process. The BET surface area (37.95 m2g-1) and lower Rct value (137 Ω) of ZnS-FeS2@C are beneficial to attain higher lithium-ion storage performance. It delivered a discharge capacity of 821 mAh g-1 in the 500th continuous cycle @ A g-1, with a coulombic efficiency of around 100%, which is higher than the ZnS-FeS2 heterostructure (512 mAh g-1). The proposed strategy can improve the electrochemical performance and stability of lithium-ion batteries, and can be helpful in finding highly effective anode materials for energy storage devices.

Hydrogen Production through Catalytic Water Splitting Using Liquid-Phase Plasma over Bismuth Ferrite Catalyst.

This study examined the H2 production characteristics from a decomposition reaction using liquid-phase plasma with a bismuth ferrite catalyst. The catalyst was prepared using a sol-gel reaction method. The physicochemical and optical properties of bismuth ferrite were analyzed. H2 production was carried out from a distilled water and aqueous methanol solution by direct irradiation via liquid-phase plasma. The catalyst absorbed visible-light over 610 nm. The measured bandgap of the bismuth ferrite was approximately 2.0 eV. The liquid-phase plasma emitted UV and visible-light simultaneously according to optical emission spectrometry. Bismuth ferrite induced a higher H2 production rate than the TiO2 photocatalyst because it responds to both UV and visible light generated from the liquid-phase plasma.

A radiation shielding sensitivity analysis based on metal hydrides multilayers.

In order to shield neutron and gamma rays efficiently, a multilayer model is designed with metal hydrides and heavy metals and is analysed based on Monte Carlo simulations. In terms of shielding performance, the hydrogen in metal hydrides acts as a moderator to slow down the neutron energy and heavy metals are good for absorbing gamma rays. A simulation and calculational analysis are carried out with various parameters such as spectrum change, shield thickness, and number of multilayers. In addition, the rate of DPA (displacement per atom) is analysed to estimate both the lifetime and radiation resistance with the MCNP code. From lots of simulations, ZrH2 and W couples are the best candidate especially for shielding gamma rays, while TiH2 with W is good for neutron shielding. The concept of multilayer metal hydride such as TiH2 and ZrH2 coupled with W could be one of best combinations to shield both neutron and gamma-rays in many nuclear facilities such as nuclear reactor, fusion reactor and other applications.

Facet-Dependent in Situ Growth of Nanoparticles in Epitaxial Thin Films: The Role of Interfacial Energy.

Nucleation of nanoparticles using the exsolution phenomenon is a promising pathway to design durable and active materials for catalysis and renewable energy. Here, we focus on the impact of surface orientation of the host lattice on the nucleation dynamics to resolve questions with regards to "preferential nucleation sites". For this, we carried out a systematic model study on three differently oriented perovskite thin films. Remarkably, in contrast to the previous bulk powder-based study suggesting that the (110)-surface is a preferred plane for exsolution, we identify that other planes such as (001)- and (111)-facets also reveal vigorous exsolution. Moreover, particle size and surface coverage vary significantly depending on the surface orientation. Exsolution of (111)-oriented film produces the largest number of particles, the smallest particle size, the deepest embedment, and the smallest and most uniform interparticle distance among the oriented films. Based on classic nucleation theory, we elucidate that the differences in interfacial energies as a function of substrate orientation play a crucial role in controlling the distinct morphology and nucleation behavior of exsolved nanoparticles. Our finding suggests new design principles for tunable solid-state catalyst or nanoscale metal decoration.

Decyl Glucoside Synthesized by Direct Glucosidation of D-Glucose Over Zeolite Catalysts and Its Estrogenicity as Non-Endocrine Disruptive Surfactant.

The estrogenicity of decyl glucoside was asserted as a non-endocrine disruptive surfactant with its preparation method using zeolite catalysts. Its estrogenicity was estimated using E-assay method. The decyl glucoside was synthesized by direct glucosidation from D-glucose with 1-decanol. The conversion and yield were improved with increasing of amount of acid sites of the zeolite catalysts. The decyl glucopyranoside is more hydrophilic than nonylphenol and has a high wettability. The decyl glucopyranosides exhibited extremely lower proliferation of estrogenic cell compared with nonylphenol.

Enhanced Electrochemical Performance of Carbon Nanotube with Nitrogen and Iron Using Liquid Phase Plasma Process for Supercapacitor Applications.

Nitrogen-doped carbon nanotubes (NCNTs) and iron oxide particles precipitated on nitrogen-doped carbon nanotubes (IONCNTs) were fabricated by a liquid phase plasma (LPP) process for applications to anode materials in supercapacitors. The nitrogen element and amorphous iron oxide nanoparticles were evenly disseminated on the pristine multiwall carbon nanotubes (MWCNTs). The electrochemical performance of the NCNTs and IONCNTs were investigated and compared with those of pristine MWCNTs. The IONCNTs exhibited superior electrochemical performance to pristine MWCNTs and NCNTs. The specific capacitance of the as-fabricated composites increased as the content of nitrogen and iron oxide particles increased. In addition, the charge transfer resistance of the composites was reduced with introducing nitrogen and iron oxide.

Preparation and Characterization of Cobalt/Graphene Composites Using Liquid Phase Plasma System.

Liquid phase plasma (LPP) method was applied, for the first time, to the impregnation of cabalt nanoparticles onto graphene. Nanoparticles were dispersed uniformly on the surface of the two-dimensional graphene sheet. The electron miocroscopy observation showed approximately 2-7 nm sized spherical nanoparticles deposited on the surface of graphene sheets. The XPS and EDX analyses revealed that both metal Co and CoO were present in the Co/graphene composites synthesized by the LPP method.

Electrochemical properties of chemically processed SiO x as coating material in lithium-ion batteries with Si anode.

A SiO x coating material for Si anode in lithium-ion battery was processed by using SiCl4 and ethylene glycol. The produced SiO x particles after heat treatment at 725°C for 1 h were porous and irregularly shaped with amorphous structure. Pitch carbon added to SiO x was found to strongly affect solid electrolyte interphase stabilization and cyclic stability. When mixed with an optimal amount of 30 wt% pitch carbon, the SiO x showed a high charge/discharge cyclic stability of about 97% for the 2nd to the 50th cycle. The initial specific capacity of the SiO x was measured to be 1401 mAh/g. On the basis of the evaluation of the SiO x coating material, the process utilized in this study is considered an efficient method to produce SiO x with high performance in an economical way.

Synthesis of manganese nanoparticles in the liquid phase plasma.

The liquid phase plasma reduction method was applied to prepare the polycrystalline manganese nanoparticles from the solution of manganese chloride tetrahydrate. A bipolar pulsed power supply was used to generate discharge in the aqueous solutions. While large size of dendrite-shaped manganese nanoparticles were mostly observed in the initial stage and particle size decreased with discharge time. The particles were dispersed with less and less small particles by the addition of CTAB and anisotropic shapes nanoparticles were mostly observed at long time plasma-treated. Many spots could be seen in the ED pattern for polycrystalline particles.

Preparation of carbon blacks by liquid phase plasma (LPP) process.

In this study, carbon black nanoparticles were synthesized by Liquid Phase Plasma (LPP) technique; plasma generated in the organic solvent of benzene at 4.9 kV with the pulse frequency of 15 kHz and width of 5 micros transformed the carbon atoms in the solvent into carbon blacks by oxidation and reduction reactions. Graphite phase was found to be introduced into the carbon blacks without any additional processes due to the characteristics of LPP process, resulting in a higher G/D ratio of 0.92, compared to 0.83 of commercial Ketjen carbon blacks. For the performance improvement, heat treatment was employed and its parameters such as temperature and duration time were optimized in relation to the crystallinity and specific surface area of the carbon blacks. Carbon blacks heat treated at 450 degrees C in the air for 20 min were measured to have the discharge capacity of 1750 mAh/g and irreversible charging and discharging capacity ratio of 52.6%.

Bipolar pulsed electrical discharge for decomposition of methylene blue in aqueous TiO2 nanoparticle dispersions.

The objective of this paper is to investigate the decomposition process of organic pollutants by liquid phase plasma. A bipolar pulsed power supply was used to generate discharges in the aqueous TiO2 nanoparticle dispersions. The applied voltage, pulse width, and frequency were 250 V, 5 micros, and 30 kHz, respectively. Properties of generated plasma were investigated by electrical and optical emission spectroscopy methods. The comparison of properties of the discharge operated with and without oxygen gas bubbling is shown. The results of electrical-discharge degradation of methylene blue showed that the decomposition rate increased with the TiO2 particle dosages. Addition of oxygen gas bubbles also increased the degradation rate of methylene blue.

The synthesis of nickel nanoparticles by liquid phase plasma processing.

In this work, the liquid phase plasma reduction method was applied to prepare the spherical nickel nanoparticles from the solution of nickel chloride. A bipolar pulsed power supply was used to generate discharges in the aqueous solutions. Nickel nanoparticle peaks produced by surface plasmon absorption were observed around 381 nm with electrical discharge. Spherical nickel nanoparticles were mostly observed in this study, pentagonal nanoparticles were also observed occasionally. The TEM image showed that the average particle size varied from 10 to 200 nm in diameter as discharge time was increased. Many spots could be seen in the ED pattern for polycrystalline particles.

Enhanced water splitting by Fe2O3-TiO2-FTO photoanode with modified energy band structure.

The effect of TiO2 layer applied to the conventional Fe2O3/FTO photoanode to improve the photoelectrochemical performance was assessed from the viewpoint of the microstructure and energy band structure. Regardless of the location of the TiO2 layer in the photoanodes, that is, Fe2O3/TiO2/FTO or TiO2/Fe2O3/FTO, high performance was obtained when α-Fe2O3 and H-TiNT/anatase-TiO2 phases existed in the constituent Fe2O3 and TiO2 layers after optimized heat treatments. The presence of the Fe2O3 nanoparticles with high uniformity in the each layer of the Fe2O3/TiO2/FTO photoanode achieved by a simple dipping process seemed to positively affect the performance improvement by modifying the energy band structure to a more favorable one for efficient electrons transfer. Our current study suggests that the application of the TiO2 interlayer, together with α -Fe2O3 nanoparticles present in the each constituent layers, could significantly contribute to the performance improvement of the conventional Fe2O3 photoanode.

Room-temperature ammonia gas sensing via Au nanoparticle-decorated TiO2 nanosheets.

A high-performance gas sensor operating at room temperature is always favourable since it simplifies the device fabrication and lowers the operating power by eliminating a heater. Herein, we fabricated the ammonia (NH3) gas sensor by using Au nanoparticle-decorated TiO2 nanosheets, which were synthesized via two distinct processes: (1) preparation of monolayer TiO2 nanosheets through flux growth and a subsequent chemical exfoliation and (2) decoration of Au nanoparticles on the TiO2 nanosheets via hydrothermal method. Based on the morphological, compositional, crystallographic, and surface characteristics of this low-dimensional nano-heterostructured material, its temperature- and concentration-dependent NH3 gas-sensing properties were investigated. A high response of ~ 2.8 was obtained at room temperature under 20 ppm NH3 gas concentration by decorating Au nanoparticles onto the surface of TiO2 nanosheets, which generated oxygen defects and induced spillover effect as well.

Removal of oxytetracycline from water by liquid-phase plasma process with an iron precipitated TiO2 photocatalyst.

This study developed a new water treatment method using liquid-phase plasma (LPP) process that can decompose oxytetracycline (OTC) remaining in the aquatic environment. Relatedly, the OTC causes damage to the human body and cannot be removed by traditional water treatment methods. The study also prepared Fe/TiO2 photocatalyst responding to visible light using the LPP process. In particular, the OTC decomposition efficiency of the LPP process improved by more than 10% with the use of the Fe/TiO2 photocatalyst as compared to that of the one with the use of bare TiO2 photocatalyst. Further, the optimal LPP process parameters and Fe/TiO2 photocatalyst amount in the LPP process for OTC decomposition were established in the study. Finally, the degradation pathway of the OTC in the LPP process was found based on the five intermediates of the LPP reaction that were detected by the liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) analysis. In particular, the decomposition pathway was estimated to be involving the mineralization of the OTC through demethylation, deamination, dehydration, and ring cleavage.

Preparation of hydrogen titanate nanotube/FTO glass thin film obtained by the layer-by-layer-self assembling method for water splitting.

Hydrogen titanate nanotube (H-TiNT) particles were coated porously on a fluorine-doped tin oxide glass using the layer-by-layer self assembling method and then heat-treated at temperatures below 600 degrees C for 10 min in air. The microstructure, crystallinity, and optical absorbance of the heat-treated H-TiNT thin film were investigated using scanning electron microscopy, X-ray diffraction, Raman spectroscopy, and UV-vis spectroscopy, respectively. Also, I-V characteristics of the fibrous H-TiNT particles in the thin film using linear cycle voltammetry under ultraviolet-A irradiation were analyzed to have a maximum current value at applied voltages with the increase in heating temperature for economic water splitting.

Crystalline characterization and photodecomposition properties of rod-shaped Na2Ti6O13 powder prepared by molten salt process.

To prepare one-dimensional nanostructured Na2Ti6O13 powder, the starting materials of TiO2, NaCl and Na2CO3 were mixed and then heat-treated at 1000 degrees C for 2 hrs in air under molten state of NaCl. Changes in shape and phase, photo absorbance and photocatalytic ability of TiO2 particle were observed controlling added amount of Na2CO3 under constant weight ratio of TiO2 to NaCl using SEM, X-ray diffractometer, Raman spectroscopy, and UV-Vis spectroscopy. The TiO2 particle was changed into rod-shape Na2Ti6O13 with the addition of Na2CO3, showing increase in optical energy band-gap of the powder as well as gradual decrease of the photo-decomposition ability.