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Developing cost-effective and efficient oxygen evolution reaction (OER) electrocatalyst is highly essential for energy-conversion technologies. A self-assembled NiFe-layered double hydroxide (LDH)@MnCO3 heterostructure prepared on Ni foam using a successive hydrothermal strategy shows notable catalytic activity toward the OER with a small overpotential of 275 mV to drive a geometrical current density of 10 mA cm-2 under alkaline conditions with remarkable stability for 15 h, outperforming IrO2/C electrocatalyst (350 mV@10 mA cm-2). The hierarchical NiFe-LDH@MnCO3 heterostructure possess more exposed active sites, enhanced conductivity and superior interfacial coupling effect makes them an ideal candidate for OER electrocatalyst. Antibiotic contaminants have received much attention due to the increasing serious environmental concerns. In this work, for the first time, we have fabricated a series of significant type-II p-n heterostructure with Z-scheme charge transfer between p-type B-doped g-C3N4 with different proportion of n-type BN through a simple in-situ growth process. PXRD, FTIR, UV-Vis, FESEM, HRTEM and EIS analysis were applied for the detailed characterization of the as-prepared composites to study the crystal phase, structural features, optical and electrical properties. The photocatalytic behaviour of BN/BCN photocatalyst was investigated by the degradation of tetracycline hydrochloride under solar light illumination. Experimental results revealed that about 88.1% of TCH was degraded by the BN/BCN composite containing 4 wt% BN in the BN/BCN matrix, in 60 min of solar light irradiation. Reduction in recombination rate of photo generated electron-hole pair's and enhanced visible light absorption ability is credited to the enhanced photocatalytic performance of BN/BCN composite. Trapping experiment for the scavenging agents has confirmed that superoxide (O2¯) and hydroxyl (OH) radicals are the main reactive species during the TCH degradation process. The high stability shown by the BN/BCN composite opens a new path for designing of significant BN based Z-scheme photocatalyst for prevention of environmental issues. Assembly of plasmonic nanoparticle clusters having hotspots in a specific space is an effective way to efficiently utilize their plasmonic properties. In the assembly, however, bulk-like aggregates of the nanoparticles are readily formed by strong van der Waals forces, inducing a decrease of the properties. The present work proposes an advanced method to avoid aggregation of the clusters by encapsulating into a confined space of hollow silica interior. Hollow spheres incorporating gold nanoparticle clusters were synthesized by a surface-protected etching process. The observation of inner nanoparticles with liquid cell transmission electron microscopy experimentally proved that the nanoparticles moved as a cluster instead of as dispersed nanoparticles within the water-filled hollow compartment. The hollow spheres incorporating the nanoparticle clusters were assembled in the vicinity of electrodes by application of an external AC electric field, resulting in the enhancement of Raman intensities of probe molecules. The nanoparticle-cluster-containing hollow spheres were redispersed when the electric field was turned off, showing that the hollow silica spheres can act as a physical barrier to avoid the cluster aggregation. The Raman intensities were reversibly changed by switching the electric field on and off to control the assembled or dispersed states of the hollow spheres. Core-shell Fe3C@NC nanostructures constructed by Fe3C core encapsulated in N-doped carbon nanotubes (FFCN-MP4000) is designed and readily prepared via a facile and economical solid-state chemical route. By controlling the proportion of C and N in the starting materials, the composition of FeNC core-shell nanotubes was optimized, then provided more possible active sites as electrocatalysts, exhibited superior oxygen reduction performance. Onset potential (Eonset) of 0.96 V versus reversible hydrogen electrode (RHE) and half-wave potential (E1/2) of 0.83 V vs RHE was obtained in 0.1 M KOH, which are comparable to those of the commercial Pt/C catalyst (Eonset = 0.98 V, E1/2 = 0.84 V vs RHE). Notably, the limited current density for FFCN-MP4000 can reach to 6.6 mA cm-2, and it efficiently catalyzes 4-electron reduction of oxygen (n = 3.98) with a hydrogen peroxide yield of below 2.2%. In addition, the methanol tolerance and durability are even superior to commercial Pt/C catalyst. This work provides a facile and economical strategy for the feasible design of oxygen reduction reaction (ORR) electrocatalyst with high activity and low cost in alternative commercial Pt/C electrocatalyst. Debate about the cross-cultural relevance of depression has been central to cross-cultural psychiatry and global mental health. Although there is now a wealth of evidence pertaining to symptoms across different cultural settings, the role of the health system in addressing these problems remains contentious. Depression is undetected among people attending health facilities. We carried out a thematic synthesis of qualitative evidence published in the scientific literature from sub-Saharan Africa to understand how depression is debated, deployed and described. No date limits were set for inclusion of articles. Our results included 23 studies carried out in communities, among people living with HIV, attendees of primary healthcare and with healthcare workers and traditional healers. Included studies were carried out between 1995 and 2018. In most cases, depression was differentiated from 'madness' and seen to have its roots in social adversity, predominantly economic and relationship problems, sometimes entangleg other resources available to people living with depression. Advances in molecular dynamics simulations have led to large increases across spatial and complexity scales, providing valuable molecular level insight into processes occurring on the subcellular level. this website An increasing repertoire of methods to assemble and analyse complex membrane simulations, alongside advances in structural biology methods for membrane proteins, have contributed to our increased understanding of the roles of specific lipid interactions for multiple membrane protein systems. Large scale simulations of crowded protein solutions have provided a model describing the biophysical basis for experimentally observed diffusion properties. In this review we discuss recent approaches that pave the way towards linking molecular level detail to the cellular level.
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