| The increasingly severe environmental problems caused by the widespread use of fossil energy have motivated the rapid development of lithium-ion batteries with high energy density and environmental sustainability,and developing high-performance electrodes for lithium-ion batteries has gained great research effort in recent years.TiO2is one of the most attractive choices due to its low cost,environmental friendliness,high safety,and good stability.However,the low conductivity and theoretical specific capacity of TiO2limit its practical application.Based on the good stability of TiO2,we constructed three kinds of nanostructured TiO2 composites,considering elaborate design of the composition and structure in this thesis.Various material measurements are used to systematically investigate the physical and chemical performance,preparation process and improved lithium storage performance of the TiO2 composites.Firstly,the modification of V2O5 nanosheet cathode with TiO2 as the structural auxiliary component was studied.A facile and controllable liquid-phase self-assemble strategy was proposed to uniformly decorate V2O5 nanosheets with TiO2 and Ag nanoparticles simultaneously,resulting in novel Ag-TiO2/V2O5 composites.The influence of solvent on the self-assembly process was explored,and the poor solvent THF for V2O5nanosheets is the key to the success of self-assembly.It should be stressed that our strategy boasts precise control over the loading density of the nanoparticles on the nanosheets.The introduction of Ag improves the conductivity,and TiO2 nanoparticles can effectively isolate the V2O5 nanosheets from restacking,shorten the Li+diffusion pathway,and increase the contact area between electrode and electrolyte,thus providing more electrochemically active sites.Consequently,the resulting Ag-TiO2/V2O5 composites exhibit improved lithium storage performance over neat V2O5 nanosheets.A high reversible capacity of 266 mAh g-1 is achieved at a current density of 100 mA g-1 after100 cycles.Based on the good cycling stability of TiO2 anode,hierarchical CNT@TiO2@Mn3O4nanostructures composed of 2D TiO2 nanosheets,1D carbon nanotubes and 0D Mn3O4nanoparticles were constructed by combining solvothermal with above mentioned self-assembly method.In this composite,each component plays a unique,indispensable role.2D TiO2 nanosheets being flexible in nature are able to inhibit the aggregation of the Mn3O4 nanoparticles as well as buffer their volume variation suffered during the charging/discharging process.1D CNTs serve not only as a backbone to improve conductivity,but also maintain material structural stability.0D Mn3O4 nanoparticles contribute an extraordinarily high theoretical capacity and are capable of physically isolating the TiO2 nanosheets,which is favorable for the contact of active materials and electrolyte.The resulting CNT@TiO2@Mn3O4 composites exhibit enhanced cycle and rate performances,delivering a reversible capacity as high as 516 mAh g-1 at 500 mA g-1after 300 cycles,and 251 mAh g-1at 2000 mA g-1 after 600 cycles.Considering the enhancement in lithium storage performance of the hierarchically assembled composites,Fe3O4 nanoparticles were assembled on TiO2 nanosheets to prepare TiO2@Fe3O4,which were mixed with CNTs and then filtered to prepare TiO2@Fe3O4/CNT composite films.Highly conductive CNTs are cross-linked with each other to form three-dimensional porous conductive network for fast electron transport,and effectively disperse TiO2@Fe3O4,avoiding their agglomeration as well as preserving the advantages of two-dimensional structure.Fe3O4 nanoparticles uniformly distributed on the surface of TiO2 nanosheets,provide high capacity and isolate the nanosheets from restacking.TiO2 nanosheets with good flexibility not only alleviate the large volume change of Fe3O4 upon cycling,but also limit the agglomeration of the nanoparticles.The composite films were wet-transferred onto copper foil and directly used as binder-free anodes for lithium-ion batteries,showing improved rate performance.After 1000 cycles at 5000 mA g-1,a reversible specific capacity of 225 mAh g-1 could be remained. |