| Lithium vanadate(Li3VO4)has been regarded as a potential anode material for lithium ion batteries owing to its ideal discharge potential(~0.5-1.0 V vs.Li+/Li)and high theoretical capacity(592 m Ah g-1,with three Li+intercalation).However,the poor conductivity of Li3VO4and the difficulty in adjusting its morphology and structure due to hydrophilia restrict its electrochemical performance.Vanadium oxides exhibit diverse morphologies and facile synthesis methods,and has been studied as a raw material for synthesizing Li3VO4.Herein,vanadium oxides with special morphologies are used as templates to regulate the morphology of Li3VO4.Moreover,the electronic conductivity and electrochemical performance of Li3VO4is further improved via carbon combination.As a result,Li3VO4/C composite with high capacity and long cycle stability are obtained.The specific research contents and results are as follows:V2O5 microspheres were used as templates to tune the morphology of Li3VO4,and polyvinylpyrrolidone(PVP)was used as carbon source.After pyrolysis at high temperature,Li3VO4/C microspheres with high conductivity could be obtained.The microsphere structure can effectively shorten the diffusion path of lithium ions,thus enhancing the electrochemical performance of Li3VO4/C microspheres.The discharge capacity of the Li3VO4/C microspheres can maintain at 488 m Ah g-1 after 200 cycles at a current density of 0.2 A g-1.The capacity of the Li3VO4/C microspheres can be completely recovered after four periods of ratecapability testing.The microsphere structure induces high pseudocapacitive charge storage,which significantly improves the reaction kinetics of the Li3VO4/C microspheres.Carbon-coated Li3VO4/C nanorods were prepared by morphology inheritance approach,using VO2 nanorods as templates.The uniform size and the specific rod-like morphology of the Li3VO4/C nanorods significantly improve the electron and Li+transport in the composites.The Li3VO4/C nanorods exhibit high pseudocapacitive charge storage capacity and excellent rate performance.The discharge/charge capacities of the Li3VO4/C nanorods are 562/559 m Ah g-1after 200 cycles at a current density of 0.2 A g-1.The rate performance of the Li3VO4/C nanorods was tested at various current densities of 0.2,0.5,1.0,2.0 and 5.0 A g-1.After four periods of rate capability testing,the discharge capacity could be restored to 518 m Ah g-1.Stable cycling could also be achieved over 1000 cycles at a high current density of 2.0 A g-1.By using V2O3/C fiber obtained via electrospinning as template,mixing with lithium source and sintering,Li3VO4/C nanofibers were successfully prepared.The long distance and continuous electron transport path and the large specific surface area of the nanofibers provide fast paths for charge transfer in electrochemical process.Pores among fibers can alleviate the volume vatiation upon lithium ion intercalation/deintercalation,thus obtaining stable mechanical properties and long cycle life.The initial discharge/charge capacity of the Li3VO4/C nanofiber is 801.5/553.4 m Ah g-1 at a current density of 0.2 A g-1,maintaining of 558.9/563.2m Ah g-1 after 200 cycles.After five periods rate capability testing from 0.2 to 4.0 A g-1,the capacity of the Li3VO4/C nanofibers can be completely recovered.The synthesis of Li3VO4/C composites from the lithiation of vanadium oxides and carbon combination provide are viable for the design of Li3VO4 with special morphology.This method is expandable and referential for the synthesis of Li3VO4 anode materials with special morphology. |