| As a new type of intercalation/deintercalation anode material,Li3VO4shows high energy density and high safety compared with commercial graphite and Li4Ti5O12 anode materials,demonstrating great research and application value.However,it is a great challenge to tune the morphology of Li3VO4 owing to its strong hydrophilia,which results in unsatisfactory electrochemical performance.This paper aims to explore the synthesis of Li3VO4 via solvothermal method,and to improve the performance of Li3VO4 by combining it with conductive components.A mixed solution of ethylene glycol and deionized water(volume ratio1:1)was choosed as solvent,on the basis of preliminary experimental exploration.The main contents of this paper are as follows:Li3VO4 particles and Li3VO4/reduced graphene oxide(rGO)composite material was firstly synthesized via a solvent thermal approach at 90℃and atmosphere pressure.It is found that the introduction of graphene oxide not only effectively improves the conductivity of Li3VO4,but also inhibits the aggregation of Li3VO4 particles.As a result,the electronic conductivity and lithium ion diffusion of the Li3VO4/rGO are distinctly improved.The Li3VO4/rGO exhibits excellent electrochemical performance as anode for lithium ion batteries.When cycling at a specific current of 0.15 A g-1,the Li3VO4/rGO delivers initial charge/discharge capacity of 500.5/751.3 m Ah g-1.After 200 cycles,high discharge capacity of410.7 m Ah g-1 is still remained.The facile and the normal-pressure synthesis is easy to scale up,which is beneficial to its practical use.Li3VO4/rGO composite material was successfully prepared under high-temperature and high-pressure solvothermal environment in an autocave.The electrochemical performance of the Li3VO4/rGO could be optimized by tuning the reaction temperature.The obtained Li3VO4/rGO composite shows initial charge/discharge capacity of 629.8/847 m Ah g-1 at 0.15 A g-1,maintaining of 522.9/526.5 m Ah g-1 after 300 cycles.When increasing the current from0.15 to 0.3,0.75,1.5 and 1.5 m Ah g-1,the discharge capacity decreases from 526.4 to 448.2,370.1,314.2 and 261.9 m Ah g-1,respectively.After two periods of rate performance testing,the discharge capacity could revert to 486.1 m Ah g-1,showing excellent stability.The synthesis and electrochemical performance optimization of Li3VO4 via solvothermal method provide a new approach for the design of high-performance Li3VO4 materials.Li3VO4-MXene/N composite material was successfully synthesized via a solvothermal environment by introducing MXene as conductive material and hexamethylenetetramine as the source for N doping.The MXene/N could significantly improve the charge transfer and lithium ion diffusion in the composite,inducing high pseudocapacitive charge storage and excellent electrochemical performance.The initial charge/discharge capacity of the Li3VO4-MXene/N composite is 535.8/797.3 m Ah g-1 at 0.15 A g-1,respectively.After 200 cycles,the charge/discharge capacity still retains of 463.8/465.3 m Ah g-1.The high pseudocapacitance contribution caused by N-doped MXene provides a reference for the design of high-performance Li3VO4 anode materials.The excellent electrochemical performance of the Li3VO4-MXene/N makes it great potential in lithium-ion batteries. |