Abstract Based on a displacement reaction mechanism, Cu 2 Se is a good candidate for non-insertion-based cathode materials of rechargeable magnesium batteries. Nevertheless, its relatively low electronic conductivity leads to… Click to show full abstract
Abstract Based on a displacement reaction mechanism, Cu 2 Se is a good candidate for non-insertion-based cathode materials of rechargeable magnesium batteries. Nevertheless, its relatively low electronic conductivity leads to a poor rate capability and an unsatisfactory cycling performance. In this work, we firstly reported the improved electrochemical performance of Cu 2 Se cathode based on displacement reaction for Mg batteries triggered by a Li salt additive in a typical magnesium electrolyte 0.4 mol dm −3 (PhMgCl) 2 -AlCl 3 /THF. Cu 2 Se materials with different morphologies and particle sizes were synthesized by a solvothermal process and a hydrothermal method, respectively. Cu 2 Se with smaller particle sizes by the hydrothermal method exhibits a higher specific capacity (152.7 mAh g −1 first discharge capacity at 0.02 C) but poor cycling performance in 0.4 mol dm −3 (PhMgCl) 2 -AlCl 3 /THF electrolyte. LiCl was added in the magnesium electrolyte to promote the displacement reaction of the Cu 2 Se material. An initial discharge capacity of approximately 239.7 mAh g −1 with 48.4% capacity retention after 20 cycles at 0.1 C can be obtained for Cu 2 Se in 0.4 mol dm −3 (PhMgCl) 2 -AlCl 3 +1.0 mol dm −3 LiCl/THF electrolyte. Furthermore, the cycling performance and rate capability are enhanced by in situ homogeneously anchoring Cu 2 Se particles onto the surface of the reduced graphene oxide (rGO) nanosheets. Cu 2 Se/rGO composite with 10 wt% rGO exhibits 64.2% capacity retention after 20 cycles at 0.1 C, and a more than 120 mAh g −1 reversible capacity at 0.2 C in the hybrid Mg 2+ /Li + electrolyte.
               
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