Lesliejenkins3684

Metal-free photocatalysts with excellent visible-light absorption and highly efficient photocatalytic activity are attractive in the field of photocatalysis owing to their environmental friendliness. Black phosphorus (BP) shows a great potential in photoelectric conversion and photocatalysis due to its tunable band gap and two-dimensional structure. In this work, a stabilized metal-free photocatalyst, reduced graphene oxide (rGO)-wrapped BP heterostructure, was prepared by assembling BP and GO nanosheets in aqueous solution followed by partial reduction and lyophilization. The surface tension of the partially reduced GO during lyophilization could make rGO nanosheets tightly wrap on both surfaces of exfoliated BP nanosheets. This wrapped heterostructure with tight bonding between rGO and BP nanosheets led to a high photocatalytic activity, owing to the rapid transfer of the photogenerated electron-hole pairs at the rGO/BP heterojunction and the high stability of rGO protecting BP from oxygen attack. This work not only provided a general method to prepare the sandwiched heterojunction based on GO with good interface binding capability but also constructed a highly active, stable, metal-free photocatalyst based on BP.The defect-tolerant nature of lead halide perovskites renders outstanding luminescence by simple space-confined growth in nanopores. The fluorescence turn-on and wavelength-shift phenomena could be found in the formation of methylammonium lead tribromide (MAPbBr3) nanocrystals in hollow SiO2 nanospheres triggered by the reaction between methylamine (MA) gas and HPbBr3/PbBr2@SiO2 nanospheres. The enhanced fluorescence intensity is linear with the MA concentration in the range of 1.0-95 ppm with a limit of detection (LOD) of 70 ppb (S/N = 3). In addition, the maximum emission wavelength is consistently red-shifted from 478.7 to 510.6 nm as the MA concentration increases from 1.0 to 95 ppm, imparting the potential for colorimetric sensing. By combining the fluorescence turn-on and colorimetric sensing modes, the flexible method meets the demands for visual discrimination and point-of-care determination with portable devices.As a bridge between homogeneous and heterogeneous catalyses, single-atom catalysts (SACs), especially the noble metal atoms, have received extensive attention from both the fundamental and applied perspectives recently. High cost and difficulty in synthesis are considerable factors, however, limiting the development and practical applications of SACs. Thus, seeking for non-noble SACs for substituting the noble ones is not only of vital importance but also a long-standing challenge. Herein, a surface modification strategy by introducing an oppositely charged dopant and inducing the charge transfer between the SAC and the substrate was proposed to improve the stability and catalytic performance of the non-noble Cu SAC. Using first-principles density functional theory (DFT) calculations, it was demonstrated that the introduction of C in the MoS2 monolayer (CMoS2, experimentally available) can assist in stabilizing Cu and make it more positively charged, which will facilitate the adsorption of the reactants and further enhance the activity for CO oxidation. Strikingly, our results show that CO oxidation over Cu-CMoS2 is more favorable than over the Pt atom deposited on the pristine MoS2 (Pt-MoS2), exhibiting its potential in noble metal substitution and low-temperature CO oxidation. Additionally, Cu-CMoS2 was observed to have a response to visible light, which manifests that it may be a promising photocatalyst. this website The strategy proposed here provides an efficient route to regulate the electronic structures of SACs through charge transfer, which further promotes the reactivity of the non-noble metal SACs. We hope that this strategy can contribute to design more SACs with low cost and high efficiency, which will be beneficial for their practical applications.Topology and defects are of fundamental importance for ordered structures on all length scales. Despite extensive research on block copolymer self-assembly in solution, knowledge about topological defects and their effect on nanostructure formation has remained limited. Here, we report on the self-assembly of block copolymer discs and polymersomes with a cylinder line pattern on the surface that develops specific combinations of topological defects to satisfy the Euler characteristics for closed spheres as described by Gauss-Bonnet theorem. The dimension of the line pattern allows the direct visualization of defect emergence, evolution, and annihilation. On discs, cylinders either form end-caps that coincide with λ+1/2 disclinations or they bend around τ+1/2 disclinations in 180° turns (hairpin loops). On polymersomes, two λ+1/2 defects connect into three-dimensional (3D) Archimedean spirals, while two τ+1/2 defects form 3D Fermat spirals. Electron tomography reveals two complementary line patterns on the inside and outside of the polymersome membrane, where λ+1/2 and τ+1/2 disclinations always eclipse on opposing sides ("defect communication"). Attractive defects are able to annihilate with each other into +1 disclinations and stabilize anisotropic polymersomes with sharp tips through screening of high-energy curvature. This study fosters our understanding of the behavior of topological defects in self-assembled polymer materials and aids in the design of polymersomes with preprogrammed shapes governed by synthetic block length and topological rules.Oxazolidinones are a novel class of antibacterials with excellent activity against resistant Gram-positive bacteria including strains causing multidrug-resistant tuberculosis (TB). Despite their excellent efficacy, optimal dosing strategies to limit their toxicities are still under development. Here, we developed a novel synthetic strategy for fluorine-18-radiolabeled oxazolidinones. As proof-of-concept, we performed whole-body 18F-linezolid positron emission tomography (PET) in a mouse model of pulmonary TB for noninvasive in situ measurements of time-activity curves in multiple compartments with subsequent confirmation by ex vivo tissue gamma counting. After intravenous injection, 18F-linezolid rapidly distributed to all organs with excellent penetration into Mycobacterium tuberculosis-infected lungs. Drug biodistribution studies with PET can provide unbiased, in situ drug measurements, which could boost efforts to optimize antibiotic dosing strategies.