Core-shell structured Si@Cu nanoparticles segregated in graphene-carbon nanotube networks enable high reversible capacity and rate capability of anode for lithium-ion batteries

Abstract

The volume expansion of Si electrodes and the poor conductivity of Si as well as the repeated rupture of solid electrolyte interface (SEI) lead to the rapid capacity decay of Si-based anode Li-ion batteries. The rational design of anode materials for the above problems is considered an effective solution. In this work, core-shell structured Si@Cu nanoparticles segregated in graphene-carbon nanotube networks (Si@Cu/CNT/rGO) is constructed by one-step hybrid and reduction self-assembly strategy. First, metallic copper was coated on silicon nanoparticles to improve the reaction kinetics of the cell during operation. The flexible reduced graphene oxide and rigid carbon nanotube are designed as a network structure for increasing the electrical conductivity and mechanical strength of the electrode material. This design not only provides sufficient buffering space for the volume change during cell operation, but also improves the electron migration effect of the composite Si@Cu/CNT/rGO. Thanks to this design, the composite electrode maintains a high lithium storage capacity of 1915.5 mAh/g (130 cycles) and 1486.7 mAh/g (200 cycles) after charging and discharging at 100 mA g−1 and 1000 mA g−1, respectively.