As a result, the hybrid electrode achieved a high reversible capacity of 535 mAh g-1 at 0.1 A g-1 and superior cycling performance (343 mAh g-1 after 1000 cycles at 1 A g-1 with a capacity retention of 87%) in a fluorine-free carbonate electrolyte.We report a versatile method to form bacterial cellulose coatings through simple dip-coating of 3D objects in suspensions of cellulose-producing bacteria. The adhesion of cellulose-secreting bacteria on objects was promoted through surface roughness and chemistry. Immobilized bacteria secreted highly porous hydrogels with high water content directly from the surface of a variety of materials. The out-of-plane orientation of cellulose fibers present in this coating leads to high mechanical stability and energy dissipation with minimal cellulose concentration. The conformal, biocompatible, and lubricious nature of the in situ grown cellulose surfaces makes the coated 3D objects attractive for biomedical applications.A facile and efficient plasma treatment strategy has been applied for the first time to dope heteroatom nitrogen (N) into Q-graphene (QG) under ambient temperature toward a carbon-based green nanozyme. It was discovered that the resulting N doped QG (N-QG) nanozyme can present the greatly enhanced catalysis activity, which is nearly 5-fold higher than that of pristine QG, as comparably revealed by the kinetic studies. Herein, the plasma treatment-assisted N doping could improve the conductivity (hydrophilicity) and create the surface defects of QG so as to promote the electron transferring toward the enhanced catalytic activities of N-QG. Furthermore, the catalase, superoxide dismutase, and oxidase-like catalysis activities of N-QG were explored, indicating the N doping could endow the obtained nanozyme with a high specificity of peroxidase-like catalysis. The application feasibility of the developed N-QG nanozyme was demonstrated subsequently by the catalysis-based colorimetric assays for H2O2 in milk samples, with the linear range from 2.00 to 1500 μM. Importantly, such a plasma-assisted heteroatom doping route may open a door toward the large-scale applications for the rational designs of various enzyme mimics with improved catalysis performances.ConspectusOver the past decade, photoredox catalysis has blossomed as a powerful methodology because of its wide applicability in sustainable free-radical-mediated processes, in which light is used as a cleaner energy source to alter the redox properties of organic molecules and to drive unique chemical transformations. Numerous examples of highly selective C-C and C-heteroatom bond formation processes have been achieved this way in an efficient and waste-reducing way. Therein, the activation of widely available organic halides via single-electron reduction has been broadly applied for organic synthesis. However, in comparison with alkyl and aryl halides, the analogous utilization of vinyl halides is less developed, most likely as a consequence of the highly unstable vinyl radicals generated as intermediates along with their strong tendency to abstract hydrogen atoms from a suitable source (e.g., the solvent), resulting in a synthetically less useful reduction.Nevertheless, during the last years, a number of fter donation of an electron to the photocatalyst, (c) energy transfer corresponding to diradical formation upon triplet-triplet sensitization, and (d) dual transition metal and photocatalysis employing vinyl halides as precursors. While in the first three approaches the activation of vinyl halides is part of the photochemical step, the fourth one involves the interaction of a photochemically generated radical with a vinylnickel(II) halide obtained in turn by the oxidative addition of nickel(0) to the vinyl halide. Therefore, we highlight these important developments for conceptual comparison to the direct activation of vinyl halides by light, but they are not covered in depth in this Account.Atomically thin two-dimensional (2D) materials face significant energy barriers for synthesis and processing into functional metastable phases such as Janus structures. Here, the controllable implantation of hyperthermal species from pulsed laser deposition (PLD) plasmas is introduced as a top-down method to compositionally engineer 2D monolayers. The kinetic energies of Se clusters impinging on suspended monolayer WS2 crystals were controlled in the less then 10 eV/atom range with in situ plasma diagnostics to determine the thresholds for selective top layer replacement of sulfur by selenium for the formation of high quality WSSe Janus monolayers at low (300 °C) temperatures and bottom layer replacement for complete conversion to WSe2. Atomic-resolution electron microscopy and spectroscopy in tilted geometry confirm the WSSe Janus monolayer. Molecular dynamics simulations reveal that Se clusters implant to form disordered metastable alloy regions, which then recrystallize to form highly ordered structures, demonstrating low-energy implantation by PLD for the synthesis of 2D Janus layers and alloys of variable composition.Silicon nanocrystals (SiNCs) with bright bandgap photoluminescence (PL) are of current interest for a range of potential applications, from solar windows to biomedical contrast agents. Here, we use the liquid precursor cyclohexasilane (Si6H12) for the plasma synthesis of colloidal SiNCs with exemplary core emission. Through size separation executed in an oxygen-shielded environment, we achieve PL quantum yields (QYs) approaching 70% while exposing intrinsic constraints on efficient core emission from smaller SiNCs. Time-resolved PL spectra of these fractions in response to femtosecond pulsed excitation reveal a zero-phonon radiative channel that anticorrelates with QY, which we model using advanced computational methods applied to a 2 nm SiNC. Our results offer additional insight into the photophysical interplay of the nanocrystal surface, quasi-direct recombination, and efficient SiNC core PL.Although flexible and multifunctional textile-based electronics are promising for wearable devices, it is still a challenge to seamlessly integrate excellent conductivity into textiles without sacrificing their intrinsic flexibility and breathability.  https://www.selleckchem.com/products/apilimod.html  Herein, the vertically interconnected conductive networks are constructed based on a meshy template of weave cotton fabrics with interwoven warp and weft yarns. The two-dimensional early transition metal carbides/nitrides (MXenes), with unique metallic conductivity and hydrophilic surfaces, are uniformly and intimately attached to the preformed fabric via a spray-drying coating approach. Through adjusting the spray-drying cycles, the degree of conductive interconnectivity for the fabrics is precisely tuned, thereby affording highly conductive and breathable fabrics with integrated Joule heating, electromagnetic interference (EMI) shielding and strain sensing performances. Interestingly, triggered by the interwoven conductive architecture, the MXene-decorated fabrics with a low loading of 6 wt % (0.