电解质
电化学
硫化物
阴极
单排替反应
亲核细胞
溶解
化学
化学工程
离子键合
无机化学
离子液体
金属
复合数
碳纤维
电极
材料科学
离子
催化作用
物理化学
有机化学
复合材料
工程类
作者
Weiqin Wang,Yuanying Yang,Yanna NuLi,Jingjing Zhou,Jun Yang,Jiulin Wang
标识
DOI:10.1016/j.jpowsour.2019.227325
摘要
We fabricate in-situ carbon-encapsulated cuprous sulfide (Cu2[email protected]) composite through a metal-organic framework (MOF)-derived sulfurization method and compare its electrochemical performance as a displacement reaction cathode of hybrid Mg2+/Li+ batteries with 0.4 mol L−1 (PhMgCl)2-AlCl3+1.0 mol L−1 LiCl/THF nucleophilic hybrid electrolyte and 0.2 mol L−1 Mg(HMDS)2-(AlCl3)2–MgCl2+1.0 mol L−1 LiTFSI/DME non-nucleophilic hybrid electrolyte. Benefiting from the intrinsic property of Cu2S, well-defined hybrid porous structure and carbon encapsulation derived from MOFs, the Cu2[email protected] composite exhibits 399.2 mA h g−1 discharge capacity and the capacity maintains at approximately 150 mA h g−1 at 0.05 C after 50 cycles in the nucleophilic hybrid electrolyte. The mechanism investigation verifies that the formed Cu1.96S in the first discharge process succeeds to transform into MgS and Li2S, which results in the reversible displacement reaction dominantly occurring between Cu1.96S and Cu during subsequent cycles. When using the non-nucleophilic hybrid electrolyte, an enhanced cycling stability can be achieved due to the mitigation of ionic sulfide dissolution. The present work demonstrates the feasibility of building the structural design of low-cost displacement reaction cathode with more compatible electrolyte, and provides the potential of establishing practical hybrid Mg2+/Li+ batteries for energy storage.
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