摘要：WS2 nanomaterials have attracted great attention in the field of electromagnetic wave absorption due to their high specific surface area,layered structure,and peculiar electronic ***,further improvements on their limited electromagnetic absorbing(EMA)capacity and bandwidth are urgently required for their practical application as EMA *** this work,WS2/NiO hybrids with heterostructures are prepared by a hydrothermal method and developed into EMA *** maximum reflection loss of the hybrids with 20%NiO loading could reach-53.31 dB at a thickness of 4.30 mm;the bandwidth with a reflection loss value of less than-10 dB is determined to be13.46 GHz(4.54–18 GHz)when the thickness of the absorbent is between 3.5 and 5.5 *** is found that the enhanced EMA performance of WS2/NiO hybrids is caused by the addition of magnetic NiO,which could result in the interfaces between WS2 and NiO being responsible for the synergetic magnetic loss and dielectric loss in the *** work provides a new approach for the design of excellent EMA materials for practical applications.

摘要：It is a great challenge to finely tune the morphology of iron oxides for energy storage. In this work, we introduced a facile hydrothermal method to obtain single crystalline hematite （α-Fe2O3） nano-coffee beans （NCBs） with the assistance of acetic acid. Interestingly, α-Fe2O3 nanos- tructures with this special morphology were formed under the effect of Ostwald ripening and oriented etching of H^＋ ions along [001] direction, which could be proved by the scanning electron microscope/transmission electron microscope and X-ray diffraction. After calcination at high temperature, the as-prepared α-Fe2O3 NCBs were used as potential anode ma- terials, showing a very high reversible capacity of 810 mA h g^-1 （0.2 C）, excellent cycling stability, and high-rate performance for lithium storage. Hence, in virtue of the good performances, the structural design of nanomaterials would be promoted in the fabrication of electrode materials for lithiumion batteries.

摘要：Vectored non-covalent interactions—mainly hydrogen bonding and aromatic interactions—extensively contribute to(bio)-organic self-assembling processes and significantly impact the physicochemical properties of the associated ***,vectored non-covalent interaction-driven assembly occursmainly along one-dimensional(1D)or three-dimensional(3D)directions,and a two-dimensional(2D)orientation,especially that of multilayered,graphene-like assembly,has been reported *** this present research,by introducing amino,hydroxyl,and phenyl moieties to the triazine skeleton,supramolecular layered assembly is achieved by vectored non-covalent *** planar hydrogen bonding network results in high stability,with a thermal sustainability of up to about 330°C and a Young’s modulus of up to about 40 *** introducing wrinkles by biased hydrogen bonding or aromatic interactions to disturb the planar organization,the stability ***,the intertwined aromatic interactions prompt a red edge excitation shift effect inside the assemblies,inducing broad-spectrum fluorescence covering nearly the entire visible light region(400–650 nm).We show that bionic,superhydrophobic,pillar-like arrays with contact angles of up to about 170°can be engineered by aromatic interactions using a physical vapor deposition approach,which cannot be realized through hydrogen *** findings show the feasibility of 2D assembly with engineerable properties by modulating vectored non-covalent interactions.

摘要：The CoCrFeNiMn high entropy alloy was produced by homogenization, cold rolling and recrystallization. The effects of thermomechanical processing on microstructures and tensile properties at different temperatures were investigated using X-ray diffractometry（XRD）, optical microscopy（OM）, scanning electron microscopy（SEM） and multi-functional testing machine. The results show that dendritic structures in cast alloy evolve into equiaxed grains after being recrystallized, with single face-centered cubic（FCC） phase detected. The most refined alloys, stemming from the highest rolling ratio（40%）, exhibit the highest strength due to the grain boundary strengthening, while the variation of elongation with temperature shows a concave feature. For the coarse-grained alloys, both the ductility and work hardening ability decrease monotonically with increasing temperature. Serrated flow observed at intermediate temperatures is attributed to the effective pinning of dislocations, which manifests the occurrence of dynamic strain hardening and results in the deterioration in ductility. Besides, dimples on the fracture surfaces indicate the typical ductile rupture mode.

摘要：具有电化学变色功能的柔性电池在智能电子领域显示出巨大的应用潜力.然而,具有可视化电量预警功能的镍锌电池目前尚未见报道.在此,我们设计了一种用于柔性镍锌电池的电致变色镍钴氢氧化物/镍/氧化铟锡(NiCo BH/Ni/ITO)柔性电极.通过优化Ni层厚度,电极在电流密度为0.1 mA cm^(-2)时,着色效率为59.89 cm^(2)C^(-1),容量为7.15μA h cm^(-2).相应组装的电致变色镍锌电池功率密度为160μW cm^(-2)时,能量密度为12.69μW h cm^(-2),优于部分文献报道的透明柔性超级电容器和电致变色电池.值得注意的是,组装的镍锌电池在充放电过程中显示出可逆的颜色变化,提供了一种可视化监测电池剩余电量的新功能.

摘要：Catalytic hydrogenation is a vital industrial means to produce value-added fuels and fine chemicals,however, requiring highly efficient catalysts, especially the nonprecious ones. To date, the majority of high-performance industrial hydrogenation catalysts are made of precious metals-based materials, and any given catalyst could only be used to catalyze one or few specific reactions. Herein, we exemplify a crystal phase engineering approach to empower Ni nanoparticles(NPs) with superb intrinsic catalytic activities toward a wide spectrum of hydrogenation reactions. A facile pyrolysis approach is used to directly convert a Ni-imidazole MOF precursor into hexagonal close-packed(hcp)-phased Ni NPs on carbon support. The as-synthesized hcp-phased Ni NPs exhibit unprecedented hydrogenation catalytic activities in pure water towards nitro-, aldehyde-, ketone-, alkene-and N heterocyclic-compounds, outperforming the face-centered cubic(fcc)-Ni counterpart and the reported transition metalsbased catalysts. The density functional theory calculations unveil that the presence of hcp-Ni boosts the intrinsic catalytic hydrogenation activity by coherently enhancing the substrate adsorption strength and lowering the reaction barrier energy of the rate-determining step. We anticipate that the crystal phase engineering design approach unveiled in this work would be adoptable to other types of reactions.

摘要：Co87Nb10Zr3,Co76Nb19Zr5,Co64Nb26Zr10 and Co64Nb16Zr20 amorphous films were deposited on noncrystalline glass substrates by DC unbalanced magnetron sputtering. The compositions of amorphous films were tailored in the light of the individual deposition rate of Co,Nb and Zr. The amorphous films with the anticipated composition were prepared by means of co-sputtering Co,Nb and Zr targets simultaneously. It is indicated that there is interaction among three targets during co-sputtering. The morphology and composition of the films were observed by SEM,AFM and EDS. The structure and magnetic property were measured by XRD and physical property measurement system(PPMS) . The coercivity changes with the composition,varying from 240 to 1 600 A/m. After vacuum isothermal annealing at temperatures of 475,500,525 and 550 ℃ for 15 and 30 min,respectively,it is found that high Nb content is beneficial to improving thermal stability of amorphous films. The crystallized films have the mean grain size of 2-19 nm.

摘要：Microstructures and mechanical properties of dual-phase AlxCrMnFeCoNi (x=0.4, 0.5, 0.6, at.%) alloys were investigated. Thermomechanical processing leads to a microstructural evolution from cast dendritic structures to equiaxed ones, consisting of face-centered cubic (fcc) and body-centered cubic (bcc) phases in the two states. The volume fraction of bcc phase increases and the size of fcc grain decreases with increasing Al content, resulting in remarkably improved tensile strength. Specifically, the serrated flow occurring at the medium temperatures varies from type A+B to B+C or C as the testing temperature increases. The average serration amplitude of these Al-containing alloys is larger than that of CoCrFeNiMn alloy due to the enhanced pinning effect. The early small strain produces low-density of dislocation arrays and bowed dislocations in fcc grains while the dislocation climb and shearing mechanism dominate inside bcc grains. The cross-slip and kinks of dislocations are frequently observed and high-density-tangled dislocations lead to dislocation cells after plastic deformation with a high strain.

摘要：Valveless piezoelectric pump is widely used in the medical,however,there is a general and difficult problem to be solved:Low vortex and large flow rate are not compatible,resulting in the blood prone to thrombosis during blood *** this paper,a new valveless piezoelectric(PZT)pump with streamlined flow tubes(streamlined pump)is *** design method and the working principle of the pump are *** velocity streamlines are simulated,and the results demonstrate that there are no obvious vortexes in the flow tube of the streamlined *** prototype pumps(two cone pumps and three streamlined pumps)are designed and fabricated to perform flow rate and flow resistance *** experimental results illustrate that the maximum flow rate of the streamlined pump is 142 mL/min,which is 179%higher than that of the cone piezoelectric pump,demonstrating that the streamlined pump has a large flow rate *** research provides an inspiration for future research on simple structure,low vortex and large flow rate volume-type pumps,and also provides a useful solution for thrombosis preventing.

摘要：Noble metal-free electrocatalysts with high activity are highly desirable for the large-scale application of hydrogen evolution reaction(HER). Mo_(2) C-based nanomaterials have been proved as a promising alternative to noble metal-based electrocatalysts owing to the Pt-resembled d-band density and optimal intermediates-adsorption ***, the aggregation and excessive growth of crystals often occur during their high-temperature synthesis procedure, leading to low catalytic utilization. In this study, the ultrafine Mo_(2) C/Mo_(2) N heterostructure with large surface and interface confined in the N-doped carbon nanofibers(NCNFs) was obtained by a melamine-assisted method. The synergistic effect of Mo_(2) C/Mo_(2) N heterostructure and plenty active sites exposed on the surface of ultrafine nanocrystals improves the electrocatalytic activity. Meanwhile, the N-CNFs ensure fast charge transfer and high structural stability during reactions. Moreover, the in-situ synthesis method strengthens the interfacial coupling interactions between Mo_(2)C/Mo_(2) N heterostructure and N-CNFs, further enhancing the electronic conductivity and electrocatalytic activity. Owing to these advantages, Mo_(2)C/Mo_(2) N@N-CNFs exhibit excellent HER performance with a low overpotential of 75 mV at a current density of 10 mV cm^(-2) in alkaline solution, superior to the single-phased Mo_(2)C counterpart and recently reported Mo_(2)C/Mo_(2) N-based catalysts. This study highlights a new effective strategy to design efficient electrocatalysts via integrating heterostructure, nanostructure and carbon modification.