Coupling ZnIn2S4 Nanosheets with MoS2 Hollow Nanospheres as Visible-Light-Active Bifunctional Photocatalysts for Enhancing H2 Evolution and RhB Degradation.

In this study, Mo-glycerate was used as a precursor to create MoS2 hollow nanospheres (HNS), which were then used for the first time to modify ZnIn2S4 nanosheets to create MoS2 HNS/ZnIn2S4 photocatalysts. The findings demonstrate that MoS2 HNS/ZnIn2S4 heterojunctions exhibited remarkably boosted photocatalytic properties and excellent reusability for both RhB degradation and H2 evolution without the use of Pt as a co-catalyst. Among the heterojunctions, the RhB degradation and H2 evolution efficiencies of the optimized MoS2 HNS/ZnIn2S4-3 wt % composite were almost 5 and 34 times higher than those of ZnIn2S4, respectively. The excellent performance of MoS2 HNS/ZnIn2S4-3 wt % might be attributed to the expansion of the visible-light response range and the accelerated separation efficiency of photo-induced carriers, according to the findings of the optical property tests. Based on the established band gap position and characterization results, a potential mechanism for appealing photocatalytic activity over MoS2 HNS/ZnIn2S4 heterojunctions was also postulated.

Fabrication and enhanced visible-light photocatalytic H2production of B-doped N-deficient g-C3N4/CdS Hybrids with robust 2D/2D hetero-interface interaction.

2D layered photocatalysts with proper electronic structure have sparked much attention in the field of visible-light photocatalysis for H2production. Herein, by simply calcining the mixture of ultrathin g-C3N4(CNN) and NaBH4, heteroatom B and N defect were simultaneously introduced into g-C3N4. The obtained modified g-C3N4(BDCNN) was further coupled with 2D flower-like CdS nanosheet. The optimal 2D/2D BDCNN/CdS-15% heterojunction behaved ideal photocatalytic activity for H2revolution by water splitting, and the highest H2revolution rate was as high as 1013.8µmol g-1h-1, which was 6.7 times, 2 times, and 5.8 times of the corresponding values of pristine CNN, BDCNN and CdS respectively. It was evidenced that the band structure of 2D/2D BDCNN/CdS-15% was well tuned for better visible-light adsorption and higher separation efficiency of photo-induced carriers for enhancing H2revolution performance. The achievement in this study provided informative principles for exploring g-C3N4based heterojunctions with higher H2-production performance.

Enhanced H2evolution performance by carbonized SiC/g-C3N4heterojunction under visible-light illumination.

In this study, carbonized silicon carbide/graphitic carbon nitride ((SiC/C)/g-C3N4) composites were fabricated via a facile calcination method. The optimal SiC/C/g-C3N4composite shows an excellent visible-light photocatalytic activity for water splitting, with the highest hydrogen evolution amount being 200.2µmol, which is four times higher than that of pure g-C3N4when triethanolamine and platinum (1.0 wt%) are used as the sacrificial agent and cocatalyst, respectively. With an intimate interface between SiC/C and g-C3N4, the energy band structure of g-C3N4was well engineered for photocatalytic H2production. This study provides a novel method for fabricating g-C3N4-based heterojunctions for application in environmental conservation.

In situself-assembly fabrication of ultrathin sheet-like CuS modified g-C3N4heterojunction and its enhanced visible-light photocatalytic performance.

Photocatalysts with heterojunction structure have been widely used for organic degradation. In this study, CuS/g-C3N4heterojunction was formed byin situself-assembly via a simply hydrothermal method. A series of characterizations were applied to analyzing the morphology, structure, optical properties and photo-induced electron transfer of the samples. The effect of CuS mass ratio in the CuS/g-C3N4composite on methyl blue (10 mg l-1) degradation under visible-light illumination was discussed. When CuS mass ratio was 60%, CuS/g-C3N4behaved the highest photocatalytic efficiency which is 17 times higher than that of pure g-C3N4, and the optimal heterojunction exhibited promising photocatalytic stability as well. The synthesized CuS/g-C3N4with intimate contact and promising photocatalytic performance provides important implications on analogous researches on g-C3N4-based heterojunctions for photocatalytic applications.

Construction of 3D CrN@nitrogen-doped carbon nanosheet arrays by reactive magnetron sputtering for the free-standing electrode of supercapacitor.

Owing to their favorable chemical stabilities and electronic conductivities, transition metal nitrides (TMNs) have been targeted as the potential electrode materials for the supercapacitors. Herein, 3D CrN@nitrogen-doped carbon nanosheet arrays (NCs) were successfully deposited on carbon paper (CP) by reactive magnetron sputtering method. The CrN@NCs@CP electrode exhibited satisfactory electrochemical properties: initially, the electrode showed a 132.1 mF cm-2specific capacitance at 1.0 mA cm-2current density; subsequently, the electrode demonstrated a 95.9% capacitance retention after 20 000 galvanostatic charge-discharge cycles at 5.0 mA cm-2current density. The specific capacitance of the CrN@NCs@CP electrode was significantly higher than that of the CrN@CP electrode (4.1 mF cm-2at 1.0 mA cm-2). Furthermore, the symmetric supercapacitor that incorporated two CrN@NCs@CP electrodes demonstrated 5.28µWh cm-2(2.7 Wh kg-1) energy density at 0.41 mW cm-2power density. These findings exemplify the suitability of the 3D composite electrodes of TMNs for energy storage application.

TiO2-graphene composites with exposed {001} facets produced by a one-pot solvothermal approach for high performance photocatalyst.

TiO2-graphene (TOG) composites with exposed TiO2 {001} facets were prepared by a solvothermal approach without any addition of surfactants or capping agents, only using titanium isopropoxide and graphene oxide ethanol suspension as the precursors. Graphene was covered uniformly and densely with anatase TiO2 nanoparticles, exposing the {001} facets. The X-ray photoelectron spectroscopy, photoluminescence spectroscopy and photocurrent measurements show the presence of electron transfer between TiO2 and graphene. The electron transfer between TiO2 and graphene will greatly retard the recombination of photoinduced charge carriers and prolong electron lifetime, which will contribute to the enhancement of photocatalytic performance. Accordingly, the TOG composites show high photocatalytic activity of methyl orange under UV light, likely due to the effective separation of photoinduced charge, exposure of highly reactive {001} facets and great adsorptivity of dyes.

Erosion effects of atomic oxygen on polyhedral oligomeric silsesquioxane-polyimide hybrid films in low earth orbit space environment.

A novel polyimide (PI) hybrid nanocomposite containing polyhedral oligomeric silsesquioxane (POSS) had been prepared by copolymerization of trisilanolphenyl-POSS, 4,4'-oxydianiline (ODA), and pyromellitic dianhydride (PMDA). The AO resistance of these PI/POSS hybrid films was tested in the ground-based AO simulation facility. Exposed and unexposed surfaces were characterized by SEM and X-ray photoelectron spectroscopy. SEM images showed that the surface of the 20 wt% PI/POSS became much less rough than that of the pristine polyimide. Mass measurements of the samples showed that the erosion yield of the PI/POSS (20 wt.%) hybrid film was 1.2 x 10(-25) cm3/atom, and reduced to 4% of the polyimide film. The XPS data indicated that the carbon content of the near-surface region was decreased from 60.1 to 13.2 at% after AO exposure. The oxygen and silicon concentrations in the near-surface region increased to 1.96 after AO exposure. The nanometer-sized structure of POSS, with its large surface area, had led AO-irradiated samples to form a SiO2 passivation layer, which protected the underlying polymer from further AO attack. The incorporation of POSS into the polyimide could dramatically improve the AO resistance of polyimide films in low earth orbit environment.

Facile Construction of 2D/2D ZnIn2S4-Based Bifunctional Photocatalysts for H2 Production and Simultaneous Degradation of Rhodamine B and Tetracycline.

A two-dimensional/two-dimensional (2D/2D) TiO2/ZnIn2S4 photocatalyst was reasonably proposed and constructed by a two-step oil bath-hydrothermal method. TiO2 nanosheets uniformly grown on the surface of ZnIn2S4 nanosheets and a synergetic effect between the TiO2 and ZnIn2S4 could highly contribute to improving the specific surface area and hydrophilicity of ZnIn2S4 as well as accelerating the separation and transfer of photon-generated e--h+ pairs, and thus enhancing the visible-light photocatalytic degradation and H2 evolution performance of ZnIn2S4. Rhodamine B (RhB) and tetracycline (TC) were simultaneously selected as the target pollutants for degradation in the work. The optimum photocatalytic RhB and TC degradation properties of TiO2/ZnIn2S4-10 wt% were almost 3.11- and 8.61-fold higher than that of pure ZnIn2S4, separately, while the highest photocatalytic hydrogen evolution rate was also observed in the presence of TiO2/ZnIn2S4-10wt% and 4.28-fold higher than that of ZnIn2S4. Moreover, the possible photocatalytic mechanisms for enhanced visible-light photocatalytic degradation and H2 evolution were investigated and proposed in detail. Our research results open an easy pathway for developing efficient bifunctional photocatalysts.

Effect of kerosene combustion atmosphere on the mild steel oxide layer.

In arson cases, accelerants were usually used by criminals to achieve the purpose of rapid arson. Therefore, fire investigators aim to determine whether accelerants was used in the fire scene. Metallic material has to react with corrosive gas around it at high temperature and the oxidation products may store the information of reactants. Accelerants present in fire scenes impart some oxidative characteristics on metallic materials. The aim of this work is to figure out the possibility to identify the presence of accelerant in a fire according to the oxidation patterns of metallic material. This paper researched the oxidation behavior of mild steel at high temperature in a simulated flame environment. The surface morphological and cross-sectional microstructural features of the samples were characterized by X-ray diffractions, X-ray photoelectron spectroscopy and scanning electron microscopy with energy-dispersive spectroscopy analysis after oxidation. The carbon in the combustion atmosphere had a carburizing effect on the metal oxide layer. It was mostly C-C, C-O and C=O of organic matter could be used as in fire investigation. Various oxidizing atmosphere composite systems promote the formation of metal oxide layers. And bidirectional oxidation mode in the oxide layer further accelerates the oxidation rate. The (wustite) FeO phase was not found in the oxide layer because of the strong oxidation of the combustion atmosphere. These results offer complementary information in fire characteristics, which combining the characterization of surface scale with traditional chemical analysis of recovering ignitable liquid residues from fire debris are expected to offer crucial information for determining the presence of combustion accelerants at a fire scene.

In situ fabrication of a novel CdS/ZnIn2S4/g-C3N4 ternary heterojunction with enhanced visible-light photocatalytic performance.

In this study, a novel g-C3N4-based ternary heterojunction was rationally designed and constructed by the in situ growth of ZnIn2S4 nanosheets and CdS nanoparticles onto the g-C3N4 nanosheets using a facile two-step oil-bath method. Through optimizing the proportion of ZnIn2S4 and CdS component, g-C3N4 nanosheets coupled with ZnIn2S4 nanosheets and CdS nanoparticles (denoted as CdS/ZnIn2S4/g-C3N4) exhibited obviously higher photocatalytic properties for RhB removal than the single-component and dual-component systems. Among the as-obtained ternary photocatalysts, it was found that the ternary CdS/ZnIn2S4/g-C3N4-0.2 photocatalyst displayed the optimum photocatalytic property (96%) within a short time (30 min), which was almost 27.42 and 1.17 times higher than that of pure g-C3N4 and binary ZnIn2S4/g-C3N4-0.7 composite. The excellent activity of the ternary CdS/ZnIn2S4/g-C3N4 heterostructure is assigned to the synergetic effects of CdS nanoparticles, ZnIn2S4 nanosheets and g-C3N4 nanosheets, which not only broaden the visible-light absorption range, but also improve the charge mobility and separation rate, thus boosting the visible-light-driven photocatalytic property of g-C3N4.