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Neurogenomic observations to the conduct and oral continuing development of the actual zebra finch.
The conversion of CO2 driven by solar energy into carbon-containing fuel has huge potential applications. However, most photocatalysts can only promote the two-electron reduction process to generate CO, and it is difficult to produce eight-electron CH4, which is more valuable and can store more solar energy. Herein, we prepared porous silver cyanamide nanocrystals with tunable morphologies via a facile synthesis strategy. Compared with ball/rectangular plate (RAP) and ball/leaf-like plate (SAP), the ball/porous leaf-like plate (LAP) can provide more internal reaction microenvironment, which is not only conducive to the transport of photoinduced charge carriers, but also can expand the active sites for photocatalytic CO2 reduction. Moreover, the suitable band gap of LAP sample can capture more visible light to provide more photoinduced electron-hole pairs to participate in the reduction reaction. Consequently, the LAP sample can convert CO2 to CH4 with remarkable activity and high selectivity (nearly 100%) without cocatalyst and photosensitizer under visible light irradiation. This work provides a promising way to design new photocatalysts for various applications in solar energy conversion.The scaffold materials with good mechanical and structural properties, controlled drug release performance, biocompatibility and biodegradability are important tenet in tissue engineering. click here In this work, the functional core-shell nanofibers with poly(ε-caprolactone) (PCL) as shell and silk fibroin heavy chain (H-fibroin) as core were constructed by emulsion electrospinning. The transmission electron microscopy confirmed that the nanofiber with core-shell structure were successfully prepared. The constructed nanofiber materials were characterized by the several characterization methods. The results showed that ethanol treatment could induce the formation of β-sheet of H-fibroin in composite nanofibers, thus improving the mechanical properties of PCL/H-fibroin nanofiber scaffold. In addition, we evaluated the potential of PCL/H-fibroin nanofiber membrane as a biological scaffold. It was found that PCL/H-fibroin nanofiber scaffold was more conducive to cell adhesion and proliferation with the increment of H-fibroin. Finally, in vitro drug release presented that PCL/H-fibroin core-shell nanofibers could effectively reduce the prophase burst of drug molecules and show the sustained drug release. The PCL/H-fibroin nanofiber scaffolds constructed in this work have good mechanical properties, biocompatibility, and display good potential in biomedical applications, such as drug carriers, tissue engineering and wound dressings, etc.The oxide-based hybrid photocatalysts, especially TiO2-based, have attracted tremendous attentions because of their prominent photocatalytic performance. Currently, theoretical understandings on the relationship between the interface of TiO2-based heterostructures and their photocatalytic activity are still lacking. Here we systematically investigated the effects of interface structure on electronic properties of the g-C3N4/TiO2 heterostructure using density functional theory (DFT) calculation. The interaction between monolayer g-C3N4 and TiO2 surface [with Anatase (101)/(001) facet] was explored, where a van der Waals heterojunction is formed. The presence of oxygen vacancy, nitrogen doping and hydrogen passivation on TiO2 surface is found to dramatically alter the electronic properties of g-C3N4/TiO2 heterostructure. Furthermore, the enhanced separation of electron - hole pairs and inhibited carrier recombination in the g-C3N4/TiO2 interface was analyzed based on the Bader charge analysis and charge density difference. The theoretical analysis revealed that oxygen vacancy and hydrogen passivation on TiO2 A001 surface induces the more significant charge separation, which may be the origin of enhanced photocatalytic efficiency of the g-C3N4/TiO2 heterostructures.Self-assembly of colloidal nanoparticles (NPs) into well-defined superstructures has been recognized as one of the most promising ways to fabricate rationally-designed functional materials for a variety of applications. Introducing hierarchical mesoporosity into NP superstructures will facilitate mass transport while simultaneously enhancing the accessibility of constituent NPs, which is of critical importance for widening their applications in catalysis and energy-related fields. Herein, we develop a colloidal co-assembly strategy to construct mesostructured, carbon-coated Co0.5Fe2.5O4 NP superstructures (M-C@CFOSs), which show great promise as highly efficient electrocatalysts for the oxygen evolution reaction (OER). Specifically, organically-stabilized SiO2 NPs are employed as both building blocks and sacrificial template, which co-assemble with Co0.5Fe2.5O4 NPs to afford binary NP superstructures through a solvent drying process. M-C@CFOSs are obtainable after in situ ligand carbonization followed by the selective removal of SiO2 NPs. The hierarchical mesoporous structure of M-C@CFOSs, combined with the conformal graphitic carbon coating derived from the native organic ligands, significantly improves their electrocatalytic performance as OER electrocatalysts when compared with nonporous Co0.5Fe2.5O4 NP superstructures. This work establishes a new and facile approach for designing NP superstructures with hierarchical mesoporosity, which may find wide applications in energy storage and conversion.Pentlandite is reported to exhibit good catalytic activity in hydrogen evolution reaction (HER). Many studies have paid attention to metal catalysis of pentlandite. However, the nonmetal catalysis is not considered for HER. Here, we unravel one probable catalytic mechanism of pentlandite toward HER using density functional theory. In our study models, (001) and (100) surfaces are created because there are three types of S-bridged M-M groups on them. Our study reveals that (Fe-Ni)-S center has a moderate value of Gibbs free energy while the corresponding value for (Fe-Fe)-S or (Ni-Ni)-S center is largely positive or negative. In (Fe-Ni)-S group, Fe and Ni can regulate the antibonding state of S, and then balance adsorption and desorption of proton. In addition, an intrinsic electronic potential difference exists between Fe and Ni in (Fe-Ni)-S group, which may boost the charge transfer. Particularly, (Fe-Ni)-S groups are perpendicular to the surface, and four of them make up one closed loop in the surface. It is suggested that the behaviors of such configuration composed of reaction centers resemble edge sites along the layers of MoS2 toward HER.
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