Strandcombs6780

This work highlights the desirable design and potential application of plasmonic photocatalysts for solar-driven coproduction of H2 fuel and high-value chemicals.Exploring high-efficiency metal-free electrocatalysts towards N2 reduction reaction (NRR) is of great interest for the development of electrocatalytic N2 fixation technology. Herein, we combined boron nitride quantum dots (BNQDs) and graphitic carbon nitride (C3N4) to design a metal-free BNQDs/C3N4 heterostructure as an effective and durable NRR catalyst. The electronically coupled BNQDs/C3N4 presented an NH3 yield as high as 72.3 μg h-1 mg-1 (-0.3 V) and a Faradaic efficiency of 19.5% (-0.2 V), far superior to isolated BNQDs and C3N4, and outperforming nearly all previously reported metal-free catalysts. Theoretical computations unveiled that the N2 activation could be drastically enhanced at the BNQDs-C3N4 interface where interfacial BNQDs and C3N4 cooperatively adsorb N2 and stabilize *N2H intermediate, leading to the significantly promoted NRR process with an ultra-low overpotential of 0.23 V.Strain-sensitive and conductive hydrogels have attracted extensive research interest due to their potential applications in various fields, such as healthcare monitoring, human-machine interfaces and soft robots. However, low electrical signal transmission and poor tensile properties still limit the application of flexible sensing hydrogels in large amplitude and high frequency motion. In this study, a novel ionic liquid segmental polyelectrolyte hydrogel consisting of acrylic acid (AAc), 1-vinyl-3-butylimidazolium bromide (VBIMBr) and aluminum ion (Al3+) was prepared by molecular design and polymer synthesis. GSK-4362676 order The cationic groups and amphiphilicity of ionic liquid chain segments effectively improve the tensile behavior of the polyelectrolyte hydrogel, with a maximum tensile strength of 0.16 MPa and a maximum breaking strain of 604%. The introduction of ionic liquid segments increased the current carrying concentration of polyelectrolyte hydrogel, and the conductivity reached the initial 4.8 times (12.5 S/m), which is a necessary condition for detecting various amplitude and high frequency limb movements. The flexible electronic sensor prepared by this polyelectrolyte hydrogel efficiently detects the movement of different parts of the human body stably and sensitively, even in extreme environment (-20 °C). These outstanding advantages demonstrate the great potential of this hydrogel in healthcare monitoring and wearable flexible strain sensors.Layered metal sulfides are considered as promising candidates for potassium ion batteries (KIBs) owing to the unique interlayer passages for ion diffusion. However, the insufficient electronic conductivity, inevitable volume expansion, and sulfur loss hinder the promotion of K-ion storage performance. Herein, few-layered Ti3C2Tx nanosheets were selected as the multi-functional substrate for cooperating few-layered SnS2 nanosheets, constructing SnS2/Ti3C2Tx hetero-structural nanosheets (HNs) with the thickness as thin as about 5 nm. In this configuration, the formed Ti-S bonds provide robust interaction between SnS2 and Ti3C2Tx nanosheets, which hinders the agglomeration of SnS2 and the restack of Ti3C2Tx, endowing the hybrid material with robust nanostructure. Thus, the shortcomings of the SnS2 anode are muchly relieved. In this way, the as-prepared SnS2/Ti3C2Tx HNs electrode delivers reversible capacities of 462.1 mAh g-1 at 0.1 A g-1 and 166.1 mAh g-1 at 2.0 A g-1, respectively, and a capacity of 85.5 mAh g-1 is remained even after 460 cycles at 2.0 A g-1. These results are superior to those of the counterpart electrode, confirming aggressive promotion of K-ion storage performance of SnS2 anode brought by the cooperation of Ti3C2Tx, and presenting a reliable strategy to improve the electrochemical performance of sulfide anodes.Sulfonated polydivinylbenzene bamboo-like nanotube (SPDVB) with effective olefins oxidation activity is prepared by combining cationic polymerization and sulfonation. By merely adjusting sulfonation time, SPDVB with different sulfonic acid group (-SO3H) contents is achieved. SPDVB is used as both a solid emulsifier and catalyst to fabricate Pickering emulsion interface catalytic system for oxidizing olefins with 30% H2O2 acting as oxidant/water phase and olefins acting as reactants/oil phase. It is shown that Pickering emulsion interface catalytic system stabilized by SPDVB exhibits enhanced olefins oxidation efficiency than the conventional ones. At the optimum catalyst and reaction condition, the conversion of olefins by Pickering emulsion interface catalytic system stabilized by SPDVB for cyclohexene, 1-methylcyclohexene, cyclooctene, 2,3-dimethyl-2-butene oxidation is higher than 90.00% and the corresponding 1,2-diol selectivity exceeds 93.00% except the selectivity to 1-methyl-1,2-cyclohexanediol. The catalytic system also exhibits excellent cycling performance (>95.00% olefins conversion and >89.00% 1,2-diol selectivity for cyclohexene/2,3-dimethyl-2-butene oxidation after four cycles). A possible mechanism for oxidation of olefins to 1,2-diol by SPDVB stabilized Pickering emulsion is proposed the high catalytic interface area between sulfonic acid group and H2O2 in water phase enhances the sulfonic acid group of SPDVB to convert into peroxysulfonic acid (catalytic activity centre) firstly; then the formed peroxysulfonic acid attacks the double bond of olefins to form epoxide intermediates, which will be hydrolyzed to 1,2-diol.New tin-based metal-phosphine complexes of [Sn(OH)4(PPh3)2] and [Sn(OH)2(PPh3)2] have been successfully synthesized and used as supercapacitor electrodes for the first time, exhibiting a high specific capacitance, a good rate capability, and an excellent cycling stability. The specific capacitances (highest specific capacitance for tin-based materials) of 1204F g-1 and 764F g-1 for two samples at a current density of 1 A g-1 in 6 M KOH can respectively be achieved, and their capacitance retention remained at 95.1% and 89.2% even after 15,000 cycles at a current density of 10 A g-1. Furthermore, a flexible quasi-solid-state asymmetric supercapacitor composed of Sn(OH)2(PPh3)2 and activated carbon was assembled and exhibited a specific capacitance of 290.6 mF cm-2 at a current density of 1 mA cm-2. More importantly, this device also displayed excellent cyclic stability of ∼100% for 1800 cycles during the galvanostatic charge/discharge process at 5 mF cm-2.As a pseudocapacitive electrode material, nickel-cobalt bimetallic phosphide has attracted wide attention with its advantage in capacitance and chemical activity. While, like Ni-Co oxides or sulfides, the application of nickel-cobalt bimetallic phosphide is generally hampered by its confined conductivity, low chemical stability and unsatisfactory cycle durability. Herein, this work demonstrates a NiCoP@CNT@PPy (NCP@CNT@PPy) composite that is obtained by polymerizing pyrrole monomer on the surface of NiCoP@CNT complex. According to density functional theory (DFT), it is theoretically demonstrated that the bimetallic Ni-Co phosphide (NiCoP) can exhibit more electrons near the Fermi level than single Ni or Co phosphide. Under the combined effects of carboxylic carbon nanotubes (c-CNTs) and polypyrrole (PPy), the NCP@CNT@PPy electrode exhibits excellent electrochemical performance. In addition, a flexible asymmetric supercapacitor (ASC) is prepared, which demonstrated high energy density and admirable heat-resistance and flexibility performance, showing huge potential in the application of heat-resistant storage energy systems and portable wearable devices.Core-shell architecture enables to impart unique customized properties to microparticles, through the proper selection of composition and aggregation state of the inner and outer materials. Here, the synthesis of microparticles with a chiral dielectric core and a metallic shell of gold nanoparticles is demonstrated. The chiral core is obtained by UV induced polymerization of the self-organized droplets of a cholesteric reactive mesogen in a chloroauric acid aqueous solution. Gold nanoparticles precipitation contemporarily occurs upon UV irradiation, covering the microparticles surface. Electron microscopy and optical spectroscopy investigations give evidence that the degree of coverage of the core by gold nanoparticles, with size less than 100 nm, depends on the chloroauric acid concentration, while their aggregation is influenced by the polymeric surface morphology. The optical properties of the chiral microparticles are modified by the gold shell. Specifically, gold coating of dye doped chiral microparticles, working as Bragg onion resonators, clearly improves the stability of omnidirectional microlasers. The proposed strategy, due to the flexibility of the chiral material and of the method, opens a route toward fabrication of microdevices with wide control over light manipulation, in term of intensity, polarization, generation.Transition metal sulfides have been intensively investigated as an effective catalyst for overall water splitting application due to their inexorable bifunctional oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) activity. However, the chalcogenides are oxidised during the OER process and hence limit the stability of the electrocatalyst. The synthesized materials should have a higher oxidation state corresponding to the active species in order to improve the stability. In this study, we have employed a one-step chemical bath deposition (CBD) route to synthesis bimetallic copper nickel sulfide (CuNiS) electrocatalyst. We have accomplished a superior OER electrocatalytic activity with a lower overpotential of 337 mV at 10 mA/cm2 current density and a small Tafel slope of 43 mV/dec. Also, we have achieved an excellent HER activity with a very low overpotential of 99 mV at 10 mA/cm2 and a Tafel slope of 63 mV/dec. The constructed electrolyzer attained a lower cell voltage of only 1.55 V to reach the current density of 10 mA/cm2. The stability test carried at a high current density of 200 mA/cm2 for 50 h showed less than 5% increase in Ni3+ active species at the surface ensure the stable performance nature. Thus, this work provides a promising methodology for the synthesis of bimetallic sulfides for enhanced electrocatalytic water splitting with exceptional reliability.

Potassium usnate (KU), a water-soluble form of usnic acid, shows anticancer activity. However, the underlying mechanisms have not been fully elucidated.

We aimed to identify the pathways involved in anticancer effects of KU in human gastric cancer (GC) and colorectal cancer (CRC) cells using RNA-sequencing (RNA-seq) based transcriptome analysis.

We analyzed the cytotoxic effects of KU to identify the common molecular events in GC and CRC cells upon KU exposure using unbiased approaches.

Cell viability assays and western blot experiments were used to examine apoptotic changes, cell cycle arrest, and endoplasmic reticulum (ER) stress-induced cellular responses in KU-treated cells. Total RNA from KU-treated human GC and CRC cells was prepared for RNA-seq analysis. Gene ontology term and gene set enrichment analyses were used to identify the key mediators of the cytotoxic effects of KU. The expression of ER stress-induced apoptotic markers was evaluated using quantitative reverse-transcription PCR and western blot analysis.