摘要：Homogeneous redox mediation is efficient in alleviating the shuttling effect and slow redox kinetics of lithium polysulfides in lithium-sulfur ***,their perfect performance is not fulfilled owning to the fact that the multi-step transformation of lithium polysulfides requests the multifunctional active positions for the tandem *** on the redox comediation principles,a promoter of mixing organodiselenide and organoditelluride(mixed-Se/Te)was raised to induce tandem catalysis and boost the effective electrochemical conversion of lithium *** specifically,diphenyl diselenide facilitated the liquid-liquid and solid-liquid transformation between lithium polysulfides and sulfur,while diphenyl ditelluride improved the solid-liquid transformation concerning lithium sulfide ***,even under high sulfur loading of 6.5 mg cm^(−2) and low electrolyte/sulfur ratio of 5.88μL mg^(−1),the 10 mM low concentration mixed-Se/Te promoter offered a high discharge capacity of 6.6 mAh cm^(−2) and high rate performance of 4.1 mAh cm^(−2) at 0.5 ***,the assembled 1.5 Ah-level lithium-sulfur pouch cells provide an energy density of 332 Wh kg^(−1) at 0.05 C and good cycling *** research demonstrates the applicability of propelling continuous sulfur conversion reactions with detached active positions and is anticipated to stimulate deep molecular design of kinetic promoter to targeted energy-associated redox reactions.

摘要：Inorganic-organic composite electrolyte is proved an effective way to enhance the overall performance of the ***,simply combining powder fillers with polymers is not sufficient for the application of composite *** this work,we designed an ultrathin organic-inorganic composite solid electrolyte with high mechanical strength and ionic conductivity,in which the inorganic Li1.5Al0.5Ge1.5(PO_(4))3(LAGP)solid electrolyte is prefiberized into a three-dimensional nanofiber network to serve as a self-supporting skeleton for the polyethylene oxide(PEO)*** continuous skeleton structure not only significantly improves the mechanical strength of the PEO-based electrolyte,but also forms a continuous lithium-ion conduction path,promoting the rapid migration of lithium *** fiber-reinforced composite electrolyte has an ionic conductivity of 8.27×10^(−4) S cm^(-1) at 60°C and a tensile strength of up to 4.29 ***,it exhibits a reduced overpotential and stable long-term cycling performance over 1700 h when used in Li/Li symmetric *** LiFePO_(4)(LFP)|Li cell assembled with the fiber-reinforced composite electrolyte also delivers a specific capacity of about 142 mAh g^(−1) over 300 cycles at 0.5 C and maintains good cycling *** work provides a novel idea for designing the next generation of safe and reliable organic-inorganic composite solid-state electrolyte membranes.

摘要：The development of low-cost,highly active platinum(Pt)-based electrocatalysts for oxygen reduction reaction(ORR)is crucial for widespread applications of fuel *** effective approach lies in alloying Pt with non-noble transition metals to modulate the physicochemical state of the Pt ***,fundamental challenges remain in understanding the structure-performance relationship due to the complexity of composition,crystal type,and surface structure during the alloying *** this study,we synthesized a series of PtCo bimetallic solid solutions with varying ratios using a liquid-phase synthesis *** exploiting the characteristics of solid solutions,the resulting PtCo bimetallic alloy maintains the face-centered cubic crystal structure of pure platinum,minimizing the complexities introduced during alloying and facilitating mechanism ***,under controlled alloy composition and crystal structure,we investigated the dependence of the electrocatalytic activity for the oxygen reduction reaction on the surface strain of the platinum *** S-PtCo-SNPs cathode designed accordingly endows both proton exchange membrane fuel cell(PEMFC)(2.08 W cm^(−2) at 4 A cm^(−2))and Zn-air battery(ZAB)(143.1 mW cm^(−2) at 214.5 mA cm^(−2))with outstanding performance.

摘要：The A–D–A′–D–A-type non-fused ring electron acceptors(NFREAs),consisting of electron-donating unit(D)as the bridge to link electron-accepting units(A and A′),have emerged as promising electron acceptors for organic solar cells(OSCs)and organic photodetectors(OPDs).As the units are linked by the carbon–carbon single bonds,these electron acceptors generally possess feasible synthesis and tunable optoelectronic ***,the recent progress of A–D–A′–D–A-type NFREAs is reviewed,including molecular design,device performance,structure–property relationships,and their applications in OSCs and ***,we discuss the challenges and propose the perspectives for the further development of A–D–A′–D–A-type NFREAs.

摘要：Solid oxide cells(SOCs)are emerging devices for efficient energy storage and ***,during SOC operation,gaseous chromium(Cr)species released from Fe-Cr alloy interconnect can lead to Cr deposition and poisoning of air electrodes,causing substantial degradation in electrochemical performance and compromising the longterm stability of *** mini-review examines the mechanism of Cr deposition and poisoning in air electrodes under both fuel-cell and electrolysis ***,emphasis is placed on the recent advancements in strategies to mitigate Cr poisoning,offering insights into the rational design and development of active and Cr-tolerant air electrodes for SOCs.

摘要：Multi-walled carbon nanotubes(MWCNTs)modified with silane coupling agent A-1120(MWCNTs-A1120)were *** with the raw MWCNTs,acidified MWCNTs(MWCNTs-COOH),and MWCNTs grafted with EDA(MWCNTs-NH2),MWCNTs-A1120 have the best dispersion in fluoroelastomer at the same doping ***,fluoroelastomer/MWCNTs-A1120 composite has the best mechanical properties with tensile strength of 13.92 MPa and elongation at break of 111.78%.Then,the effects of doping amount of MWCNTs-A1120 on the electrical properties of the composites were *** dielectric constant of the composite increases with the increase of MWCNTs-A1120,and the dielectric loss does not change much at the low doping amount such as 0.5 wt%.When the doping amount of MWCNTs-A1120 is 5 wt%,the dielectric constant and the dielectric loss value are greatly increased,and the volume resistivity is greatly decreased,which proves that the conductive network is formed in the composite,so the filling amount of 5 wt%is the percolation *** tensile deformation of the sample also affects the electrical properties of the *** the tensile deformation increases,the dielectric constant and dielectric loss of the composite *** the composite with 5 wt%MWCNTs-A1120,excessive tensile deformation will destroy the conductive network structure of the composite,so the composite will change from conductive material to dielectric ***,such composite is a good candidate for flexible conductive material or flexible dielectric material used in harsh environments such as high temperatures and various aggressive solvents.

摘要：The influences of the ratio of the radius of atom A（rA） to radius of atom B（rB）, electronegativity and electron number were discussed on the Laves phase formation and the characteristics of Zr-based AB2 type hydrogen storage alloy. An enthalpy model of Zr-based AB2 alloy was obtained from known data and twelve Zr-based alloys were designed to test the model. The results show that the predicted values are in good agreement with the experimental values. The model can be used for predicting enthalpy values of Zr-based hydrogen storage alloys and settles a foundation for experiments.

摘要：Alkali-water electrolyzers and hydroxide exchange membrane fuel cells are emerging as promising technologies to realize hydrogen *** cost-effective electrode materials with high activities towards corresponding hydrogen evolution(HER)and oxidation(HOR)reactions plays a crucial role in commercial hydrogen production and ***,we fabricated a V-doped Ni_(3)N/Ni heterostructure(V-Ni_(3)N/Ni)through a controlled nitridation treatment on a V-incorporated nickel hydroxide *** resultant catalyst exhibits comparable catalytic activity and durability to commercial Pt/C in terms of both HER(a low overpotential of 44 mV at the current density of 10 mA·cm^(-2))and HOR(a high current density of 1.54 mA·cm^(-2)at 0.1 V versus reversible hydrogen electrode)under alkaline *** superior activity of V-Ni_(3)N/Ni grown on different substrates further implies its intrinsic *** functional theory(DFT)calculations reveal that the coupled metallic Ni and doped V can promote the water adsorption,accelerate the Volmer step of alkaline HER,as well as optimize the adsorption and desorption of hydrogen intermediate(H^(*))to reach a balancedΔGH*value.

摘要：The multiple quantum transitions within d-band correlation oxides such as rare-earth nickelates(RENiO_(3))triggered by critical temperatures and/or hydrogenation opened up a new paradigm for correlated electronics applications,*** electric field sensor,bio-sensor,and neuron synapse logical ***,these applications are obstructed by the present ineffectiveness in the thin film growth of the metastable RENiO_(3)with flexibly adjustable rare-earth compositions and electronic ***,we demonstrate a metal-organic decompositions(MOD)approach that can effectively grow metastable RENiO_(3)covering a large variety of the rare-earth composition without introducing any vacuum *** the previous chemical growths for RENiO_(3)relying on strict interfacial coherency that limit the film thickness,the MOD growth using reactive isooctanoate percussors is tolerant to lattice defects and therefore achieves comparable film thickness to vacuum *** indicated by positron annihilation spectroscopy,the RENiO_(3)grown by MOD exhibit large amount of lattice defects that improves their hydrogen incorporation amount and electron transfers,as demonstrated by the resonant nuclear reaction analysis and near edge X-ray absorption fine structure *** effectively enlarges the magnitude in the resistance regulations in particular for RENiO_(3)with lighter RE,shedding a light on the extrinsic regulation of the hydrogen induced quantum transitions for correlated oxides semiconductors kinetically via defect engineering.

摘要：In order to further improve the potential application of nickel-cobalt oxide(NiCoO) in supercapacitors,we use controlled calcination of diffe rent Ni-Co-MOF([NiCo(HBTC)(4,4’-bipy)]) composites to obtain five kinds of nickel doped NiCoO(N-NiCoO) with different Ni/Co molar *** N-NiCoO materials with unique hexagonal nanoplates structure,high specific surface area and high porosity indicate high and stable electrochemical *** particular,N-NiCoO-2 with a Ni/Co molar ratio of 2:1 exhibits the highest 945.79 F/g specific capacitance at 1 A/g and a high cycle stability of only 6.7% attenuation after 5000 *** from the certain percentage of NiCoO with higher conductivity,nitrogen doping provides more reactive sites and the specific porous hexagonal nanoplates structure of the product itself accelerate electron transfer and promote electrolyte diffusion can more effectively enhance the electrochemical ***,N-NiCoO synthesized via a simple method exhibit exciting potential and can be used as an electrode material for supercapacitors with good performance.