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首页> 外文期刊>Journal of power sources >Metal Organic Framework (MOF)-Derived carbon-encapsulated cuprous sulfide cathode based on displacement reaction for Hybrid Mg~(2+)/Li~+ batteries
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Metal Organic Framework (MOF)-Derived carbon-encapsulated cuprous sulfide cathode based on displacement reaction for Hybrid Mg~(2+)/Li~+ batteries

机译:基于有机置换Mg〜(2 +)/ Li〜+电池置换反应的金属有机骨架(MOF)衍生的碳包覆硫化亚铜阴极

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摘要

We fabricate in-situ carbon-encapsulated cuprous sulfide (Cu2S@C) 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 Cu2S@C 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.
机译:我们通过金属有机骨架(MOF)衍生的硫化方法制备了原位碳包裹的硫化亚铜(Cu2S @ C)复合材料,并比较了其作为0.4 mol L-混合Mg2 + / Li +电池的置换反应阴极的电化学性能。 1(PhMgCl)(2)-AlCl3 + 1.0 mol L-1 LiCl / THF亲核混合电解质和0.2 mol L-1 Mg(HMDS)(2)-(AlCl3)(2)-MgCl2 + 1.0 mol L-1 LiTFSI / DME非亲核混合电解质。得益于Cu2S的固有特性,明确定义的杂化多孔结构和来自MOF的碳封装,Cu2S @ C复合材料显示399.2 mA hg(-1)的放电容量,并且在200℃时的容量保持在大约150 mA hg(-1)。在亲核混合电解质中经过50个循环后的温度为0.05C。机理研究证实,在第一个放电过程中形成的Cu1.96S成功转化为MgS和Li2S,从而导致在随后的循环中,Cu1.96S和Cu之间主要发生可逆置换反应。当使用非亲核性混合电解质时,由于减轻了离子硫化物的溶解,可以实现增强的循环稳定性。本工作证明了用更兼容的电解质构建低成本置换反应阴极的结构设计的可行性,并为建立实用的储能混合Mg2 + / Li +混合电池提供了潜力。

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