摘要：Lithium(Li) metal is widely considered as a promising anode for next-generation lithium metal batteries(LMBs) due to its high theoretical capacity and lowest electrochemical potential. However, the uncontrollable formation of Li dendrites has prevented its practical application. Herein, we propose a kind of multifunctional electrolyte additives(potassium perfluorinated sulfonates) from the multi-factor principle for electrolyte additive molecular design(EDMD) view to suppress the Li dendrite growth. The effects of these additives are revealed through experimental results, molecular dynamics simulations and firstprinciples calculations. Firstly, K^(+)can form an electrostatic shield on the surface of Li anode to prevent the growth of Li dendrites. Secondly, potassium perfluorinated sulfonates can improve the activity of electrolytes as co-conductive salts, and lower the electro-potential of Li nucleation. Thirdly, perfluorinated sulfonate anions not only can change the Li^(+)solvation sheath structure to decrease the desolvation energy barrier and increase the ion migration rate, but also can be partly decomposed to form the superior solid electrolyte interphase(SEI). Benefited from the synergistic effects, an outstanding cycle life over250 h at 1 m A cm^(-2) is achieved in symmetric Li||Li cells. In particular, potassium perfluorinated sulfonate additives(e.g., potassium perfluorohexyl sulfonate, denoted as K+PFHS) can also contribute to the formation of high-quality cathode electrolyte interphase(CEI). As a result, Li||LiNi_(0.6)Mn_(0.2)Co_(0.2)O_(2) full cells exhibit significantly enhanced cycling stability. This multi-factor principle for EDMD offers a unique insight on understanding the electrochemical behavior of ion-type electrolyte additives on both the Li metal anode and high-voltage cathode.

摘要：Ligands containing NH groups often show special *** this paper,a well-defined dinuclear Cu（II） complex bearing an unsymmetrical bipyridine-pyrazole-amine ligand was synthesized by the condensation of N–H to release *** sodium L-ascorbate as a reductant,the binuclear complex showed excellent activity in 1,3-dipolar cycloaddition reactions between alkynes and azides to obtain 1,4-disubstituted triazoles in 95%–99% isolated yields.

摘要：Due to obvious advantages,such as light weight,easy folding and deployment and high accuracy of optical imaging,the membrane diffraction large space telescope has currently been one of the hot research *** of the influence of external disturbance and attitude adjustment,the large space telescope will occur a certain degree of vibration inevitably,affecting the imaging accuracy of the space telescope for ***,to satisfy the requirement of imaging accuracy,it is necessary for the space telescope to adopt appropriate vibration control *** this paper,the active vibration control of the large space telescope is studied using cables as active *** that cables can work under tension but not under pression and the tensile capacity is limited,the unilateral and saturated characteristics of cable actuators are taken into account during control design in this ***,the dynamic model of the membrane diffraction space telescope is established using the finite element method(FEM).Secondly,in combination with the linear quadratic regulator(LQR)and the bang-bang regulator,a piecewise cost function is used to design the active vibration control ***,the controllability criterion and the genetic algorithm(GA)are adopted to determine the optimal positions of cable ***,the validity of the proposed control method is verified by numerical *** results indicate that the vibration of the space telescope can be suppressed effectively using the proposed control method,and the imaging requirements of the telescope may be realized using the least cable actuators,whose minimum quantity and position distribution are determined in this paper.

摘要：With the rapid development of portable devices and internet of things,the requirement of system wearability and integration accelerates the investigation of flexible multifunctional *** this study,we developed an integrated flexible sensing system with four nanowire-based sensors and a Ni microwire-based temperature *** four nanowirebased sensors are three kinds of photodetectors responding to lights with different wavelengths and a gas *** to the large surface volume ratio and considerable sub wavelength effect,all the nanowire-based sensors show good sensing response and excellent linear relationship between sensitivity and *** as-fabricated flexible sensing system can simultaneously detect environmental parameters,including temperature change,light intensities from UV-Visible to near infrared regions,and harmful gas *** flexible multifunctional sensing system therefore opens up a new way for the emerging portable and wearable electronics.

摘要：The decentralized production of H_(2)O_(2) via a twoelectron oxygen reduction reaction(2e^(-)ORR)has emerged as a promising alternative to the energy-intensive anthraquinone(AQ)***,its practical application requires 2eORR electrocatalysts with high activity and ***,we report the synthesis of metallic Ni nanoparticles anchored on bacterial cellulose-derived carbon fibers(Ni-NPs/BCCF)via a facile impregnation-pyrolysis method as efficient electrocatalysts for 2 e-ORR to H_(2)O_(2).By tuning the amount of Ni precursor,the best electrocatalytic performance toward 2 eORR was achieved for Ni-NPs/BCCF-20.7,affording a high H_(2)O_(2) selectivity of ~90% and an onset potential of 0.75 V *** hydrogen electrode(RHE)in an alkaline ***-NPs/BCCF-20.7 achieved the largest H_(2)O_(2) yield rate of 162.7±13.7 mmol gcat^(-1)h^(-1) and the highest Faradaic efficiency of 93.9%±4.2% at 0.2 and 0.5 V *** from the bulk ORR system,*** calculations revealed the more favorable"end-on"adsorption configuration of molecular oxygen on the exposed Ni(111)plane,which can effectively suppress the O-O bond dissociation,resulting in high selectivity for H_(2)O_(2) generation.

摘要：Production o f aromatics from lignin has attracted much attention. Because of the coexistence of C-O and C-C bonds and their complex combinations in the lignin macromolecular network, a plausible roadmap for developing a lignin catalytic decomposition process could be developed by exploring the transformation mechanisms of various model compounds. Herein, decomposition of a lignin model compound, 2-phenoxyacetophenone （2-PAP）, was investigated over several ce-sium-exchanged polyoxometalate （Cs-POM） catalysts. Decomposition of 2-PAP can follow two dif-ferent mechanisms： an active hydrogen transfer mechanism or an oxonium cation mechanism. The mechanism for most reactions depends on the competition between the acidity and redox proper-ties of the catalysts. The catalysts of POMs perform the following functions： promoting active hy-drogen liberated from ethanol and causing formation of and then temporarily stabilizing oxonium cations from 2-PAP. The use of Cs-PMo, which with strong redox ability, enhances hydrogen libera-tion and promotes liberated hydrogen transfer to the reaction intermediates. As a consequence, complete conversion of 2-PAP （〉99%） with excellent selectivities to the desired products （98.6% for phenol and 91.1% for acetophenone） can be achieved.

摘要：Metal-organic-framework （MOF）-based materials with novel physicochemical properties have emerged as promising catalysts for various hydrogenation reactions. In addition to metal clusters and multifunctional organic ligands, MOF-based catalysts can incorporate other functional species, and thus provide various active sites for hydrogenation processes. The structural properties of the catalysts play significant roles in enhancing the interactions among the reactants, products, and catalytic sites, which can be rationally designed. Because of the synergistic effects between the ac-tive sites and the structural properties, MOF-based catalysts can achieve higher activities and selec- tivities in hydrogenation reactions than can be obtained using traditional heterogeneous catalysts. This review provides an overview of recent developments in MOF-based catalysts in the hydro-genation of alkenes, alkynes, nitroarenes, cinnamaldehyde, furfural, benzene, and other compounds. Strategies for improving the catalytic performances of MOF-based catalysts are discussed as well as the different active sites and structural properties of the catalysts.

摘要：β-Glucuronidase(GUS)plays a key role in tumor initiation,metastasis,and progression,and thus,has been proposed as a promising cancer *** this study,we designed an enzyme-activatable near-infrared(NIR)fluorescent probe(DCM-βGlcA)for the rapid and accurate detection of GUS activity in vitro,in vivo and ex *** DCM-βGlcA was prepared by linking a glucuronic acid residue to dicyanomethylene-4 H-pyran(DCM).This probe exhibited significant light-up NIR fluorescent signals at 680 nm after reacting with GUS and the Stokes shift could reach 150 *** DCM-βGlcA showed a high sensitivity toward GUS and an excellent linear relationship at concentrations ranging between 0 and 4 U L^(-1)(R^(2)=0.9974)with the limit of detection as low as 0.19 U L^(-1).We used the DCM-βGlcA to identify GUS serum levels in both cancer patients and healthy individuals with a similar accuracy as that of an enzyme-linked immunosorbent assay(ELISA)while being easier and faster to ***,the DCM-βGlcA was used for tracking endogenous GUS in living cells,thereby discriminating GUSoverexpressed liver cancer from normal ***,the DCM-βGlcA was able to detect and image endogenous GUS in liver cancer tissue and tumor-bearing mouse *** findings demonstrate the potential of the DCM-βGlcA as a promising tool for detecting and monitoring GUS activity in preclinical applications.

摘要：Regulating the selectivity of catalysts in selective hydrogenation reactions at the atomic level is highly desirable but remains a grand challenge. Here we report a simple and practical strategy to synthesize a monolithic single-atom catalyst(SAC) with isolated Pd atoms supported on bulk nitrogen-doped carbon foams(Pd-SAs/CNF). Moreover, we demonstrate that the single-atom Pd sites with unique electronic structure endow Pd-SAs/CNF with an isolated site effect, leading to excellent activity and selectivity in 4-nitrophenylacetylene semi-hydrogenation reaction. In addition, benefiting from the great integrity and excellent mechanical strength, monolithic Pd-SAs/CNF catalyst is easy to separate from the reaction system for conducting the subsequent recycling. The cyclic test demonstrates the excellent reusability and stability of monolithic Pd-SAs/CNF *** discovery of isolated site effect provides a new approach to design highly selective catalysts. And the development of monolithic SACs provides new opportunities to advance the practical applications of single-atom catalysts.

摘要：We propose a novel optical polarizer based on an asymmetric dual-core photonic crystal fiber(PCF) with triangular lattice *** fiber is designed as that the effective indices of modes in the two cores are matched at one polarized state but mismatched at another polarized *** a result,one of the polarization states is coupled to the other core and transferred into a high-order *** transmission properties of the polarizer are investigated by the semi-vectorial beam propagation method(SV-BPM).Numerical results demonstrate that a device length of 11.3 mm shows extinction ratio as low as-20 dB with bandwidth as great as 80 nm ranging from 1.51 mm to 1.59 mm.