摘要：Ceramic electrolytes are important in ceramic-liquid hybrid electrolytes(CLHEs),which can effectively solve the interfacial issues between the electrolyte and electrodes in solid-state batteries and provide a highly efficient Li-ion transfer for solid–liquid Li metal *** the ionic transport mechanisms in CLHEs and the corresponding role of ceramic electrolytes is crucial for a rational design ***,the Li-ion transfer in the ceramic electrolytes of CLHEs was confirmed by tracking the 6Li and 7Li substitution behavior through solid-state nuclear magnetic resonance *** ceramic and liquid electrolytes simultaneously participate in Li-ion transport to achieve highly efficient Li-ion transfer in CLHEs.A spontaneous Li-ion exchange was also observed between ceramic and liquid electrolytes,which serves as a bridge that connects the ceramic and liquid electrolytes,thereby greatly strengthening the continuity of Li-ion pathways in CLHEs and improving the kinetics of Li-ion *** importance of an abundant solid–liquid interface for CLHEs was further verified by the enhanced electrochemical performance in LiFePO4/Li and LiNi0.8Co0.1Mn0.1O2/Li batteries from the generated *** work provides a clear understanding of the Li-ion transport pathway in CLHEs that serves as a basis to build a universal Li-ion transport model of CLHEs.

摘要：Advanced electromagnetic(EM)wave absorbing materials with strong absorption and broad bandwidth are important for military stealth and elimination of microwave pollution in consumers’*** organic framework(MOF)-derived metal/carbon hybrids with ordered structure are significantly urgent in this *** this contribution,we presented a design strategy of hollow cage-like or solid box-like magnetic/dielectric Fe/Co/C and dielectric Fe/Mn/C EM wave absorbing nanomaterials via pyrolyzing Prussian blue’s analogs with controllable topology and phase *** solid box-like Fe/Co/C and hollow cage-like Fe/Mn/C showed favorable absorption property with a broad effective absorption bandwidth(EAB)and a low reflection loss(RL).Especially,the EAB of 8.8 GHz at a thickness of 2.5 mm for solid box-like Fe/Co/C nanocomplex prepared at 900℃is a new record for this type of *** design and tuning strategy for EM wave absorbers derived from topology-controllable MOF is important for EM functional materials possessing great potential in military stealth and consumers’electronics.

摘要：Fe3O4 is a promising high-capacity anode material for lithium ion batteries, but challenges including short cycle life and low rate capability hinder its widespread implementation. In this work, a well-defined tubular structure constructed by carbon-coated Fe3O4 has been successfully fabricated with hierarchically porous structure, high surface area, and suitable thickness of carbon layer. Such purposely designed hybrid nanostructures have an enhanced electronic/ionic conductivity, stable electrode/electrolyte interface, and physical buffering effect arising from the nanoscale combination of carbon with Fe3O4, as well as the hollow, aligned and hierarchically porous architectures. When used as an anode material for a lithium-ion half cell, the carbon-coated hierarchical Fe3O4 nanotubes showed excellent cycling performance with a specific capacity of 1,020 mAh.g^-1 at 200 mA.g^-1 after 150 cycles, a capacity retention of ca. 103%. Even at a higher current density of 1,000 mA·g^-1, a capacity of 840 mAh·g^-1 is retained after 300 cycles with no capacity loss. In particular, a superior rate capability can be obtained with a stable capacity of 355 mAh.g^-1 at 8,000 mA·g^-1. The encouraging results indicate that hierarchically tubular hybrid nanostructures can have important implications for the development of high-rate electrodes for future rechargeable lithium ion batteries （LIBs）.

摘要：It is important for the determination of biologically and/or environmentally relevant species by utilization of fluorescent probes. Conventional fluorescent probes are subjected to the influence of aggregation-caused quenching that is limiting their application due to low selectivity as well as photobleaching. Additionally, quencher pairs are usually introduced in the design of these probes, which lead to the complex synthetic procedure. A novel class of fluorogens with aggregation-induced emission (AIE) characteristic provide a solution to address the dilemma. By taking advantage of the unique characteristic of AIE fluorogens, specific turn-on probes have been developed via combination with recognition components, exhibiting low background, good selectivity and outstanding photostability. This review focuses on the development of fluorescent probes with AIE characteristics via the bond cleavage as well as formation strategy.

摘要：This vertically self‐pillared(VSP)structure extends the application range of traditional porous materials with facile mass/ion transport and enhanced reaction ***,we prepare a single crystal metal‐organic framework(MOF),employing the ZIF‐67 structure as a proof of concept,which is constructed by vertically self‐pillared nanosheets(VSP‐MOF).We further converted VSP‐MOF into VSP‐cobalt sulfide(VSP‐CoS2)through a sulfidation *** plays an important role in almost all battery technologies;for metallic batteries,lithium anodes exhibit a high theoretical specific capacity,low density,and low redox ***,during the half‐cell reaction(Li++e=Li),uncontrolled dendritic Li penetrates the separator and solid electrolyte interphase *** employed as a composite scaffold for lithium metal deposition,there are many advantage to using this framework:1)the VSP‐CoS2 substrate provides a high specific surface area to dissipate the ion flux and mass transfer and acts as a pre‐catalyst,2)the catalytic Co center favors the charge transfer process and preferentially binds the Li+with the enhanced electrical fields,and 3)the VSP structure guides the metallic propagation along the nanosheet 2D orientation without the protrusive *** these features enable the VSP structure in metallic batteries with encouraging performances.

摘要：As a popular anode material for lithium-ion batteries,anatase TiO2 nanoparticles with exposed{001}facets usually exhibit exceptional lithium storage performance owing to more accessible sites and fast migration of lithium ions along the good crystalline ***,there are few researches on the lithium storage capability of TiO2 nanocrystals with other high-energy facets owing to lack of effective synthesis method for controlling crystal ***,anatase TiO2 nanocrystals with exposed{010}-and[111]-facets are successfully prepared by using the delaminated tetratitanate nanoribbons as *** electrochemical properties of these TiO2 nanocrystals with high-energy surfaces and the comparison with commercial TiO2 nanoparticles(P25)are *** is found that the cycle and rate performance of TiO2 nanocrystals is highly improved by reducing the particle size of ***,TiO2 nanocrystals with exposed{010}-and[111]-facets exhibit better lithium storage capacities in comparison with P25 without a specific facet though P25 has smaller particle size than these TiO2 nanocrystals,indicating that the exposed facets of TiO2 nanocrystals have an important impact on their lithium storage ***,the synthesis design of high-performance TiO2 materials applied in the next-generation secondary batteries should both consider the particle size and the exposed facets of nanocrystals.

摘要：Capsule catalysts composed of pre-shaped core catalysts and layer zeolites have been widely used in the tandem reactions where multiple continuous reactions are combined into one process. They show excellent catalytic performance in heterogeneous catalysis, including the direct synthesis of middle isoparaflins or dimethyl ether from syngas, as compared to the conventional hybrid catalysts. The present review highlights the recent development in the design of capsule catalysts and their catalytic applications in heterogeneous catalysis. The capsule catalyst preparation methods are introduced in detail, such as hydrothermal synthe- sis method, dual-layer method, physically adhesive method and single crystal crystallization method. Purthermore, several new applications of capsule catalysts in heterogeneous cat- alytic processes are presented such as in the direct synthesis of liquefied petroleum gas from syngas, the direct synthesis of para-xylene from syngas and methane dehydroaromatization. In addition, the development in the design of multifunctional capsule catalysts is discussed, which makes the capsule catalyst not just a simple combination of two dill）rent catalysts, but has some special functions such as changing the surface hydrophobic or acid properties of the core catalysts. Finally, the future perspectives of the design and applications of capsule catalysts in heterogeneous catalysis are provided.

摘要：Single-atom catalysts(SACs)have been widely used in heterogeneous catalysis owing to the maximum utilization of metal-active sites with controlled structures and well-defined *** tailored coordination with nitrogen atom,the metal-nitrogen(M-N)-based SACs have demonstrated interesting physical,optical and electronic properties and have become intense in photocatalysis and electrocatalysis in the past *** substantial efforts in constructing various M–N-based SACs,the principles for modulating the intrinsic photocatalytic and electrocatalytic performance of their active sites and catalytic mechanism have not been sufficiently ***,the present review intends to shed some light on recent research made in studying the correlation between intrinsic electronic structure,catalytic mechanism,single-metal atom(SMA)confinement and their photocatalytic and electrocatalytic activities(conversion,selectivity,stability and etc).Based on the analysis of fundamentals of M–N-based SACs,theoretical calculations and experimental investigations,including synthetic methods and characterization techniques,are both included to provide an integral understanding of the underlying mechanisms behind improved coordination structure and observed ***,the challenges and perspectives for constructing highly active M–N based photocatalysis and electrocatalysis SACs are *** particular,extensive technical and mechanism aspects are thoroughly discussed,summarized and analyzed for promoting further advancement of M-N-based SACs in photocatalysis and electrocatalysis.

摘要：Three-dimensional quantitative structure activity relationship （3D-QSAR） and docking studies of a series of arylthioindole derivatives as tubulin inhibitors against human breast cancer cell line MCF-7 have been carried out. An optimal 3D-QSAR model from the comparative molecular field analysis （CoMFA） for training set with significant statistical quality （R2=0.898） and predictive ability （q2=0.654） was established. The same model was further applied to predict pIC50 values of the compounds in test set, and the resulting predictive correlation coefficient R2（pred） reaches 0.816, further showing that this CoMFA model has high predictive ability. Moreover, the appropriate binding orientations and conformations of these compounds interacting with tubulin are located by docking study, and it is very interesting to find the consistency between the CoMFA field distribution and the 3D topology structure of active site of tubulin. Based on CoMFA along with docking results, some important factors improving the activities of these compounds were discussed in detail and were summarized as follows： the substituents R3-R5 （on the phenyl ring） with higher electronegativity, the substituent R6 with higher eleetropositivity and bigger bulk, the substituent R7 with smaller bulk, and so on. In addition, five new compounds with higher activities have been designed. Such results can offer useful theoretical references for experimental works.

摘要：The active sites of monodisperse transition metal Ni-clusters were anchored on carbon nitride(CN)by an in situ photoreduction deposition method to promote the efficient separation of photogenerated charges and achieve high-efficiency photocatalytic activity for hydrogen *** Ni-cluster/CN exhibited a photocatalytic hydrogen production rate of 16.5 mmol·h^(-1)·g^(-1) and a total turnover frequency(TOF(H_(2)))value of 461.14 h^(-1).X-ray absorption spectroscopy based on synchrotron radiation indicated that CN had two reaction centers to form stable interface interactions with monodispersed Ni-clusters,in which carbon can act as an electron acceptor,while nitrogen can act as an electron ***,the hybrid electronic structure of the Ni-cluster/CN system was constructed,which was favorable for photocatalytic activity for hydrogen *** in-depth understanding of the interfacial interaction between CN and Ni-clusters will have important reference significance on the mechanistic study of development based on the cocatalyst.