氧化还原
阳极
电化学
电解质
硫醇
锂(药物)
电池(电)
溶解
材料科学
离子
化学工程
化学
金属锂
锂离子电池
无机化学
金属
电极
有机化学
物理化学
内分泌学
工程类
功率(物理)
物理
医学
量子力学
作者
Chao Li,Cheng Zhang,Kuaibing Wang,Fei Yu,Jian Xie,Qichun Zhang
标识
DOI:10.1016/j.cej.2021.133234
摘要
With the reversible two-electron redox reaction, dicarboxylates have been widely employed as advanced anodes for lithium-ion batteries. However, dicarboxylate-based anodes always displayed limited capacities, low rate performances, and poor long-cycle abilities due to their inevitable dissolution in the electrolyte. Here, to address the above-motioned issues, a functional multi-thiol-supported dicarboxylate-based metal–organic framework, namely Fe-TTTP, is synthesized and employed as a promising anode for lithium-ion batteries based on the redox-active Iron (III) ions and organic dicarboxylate ligands. Benefiting from its chemical structure with multiple redox metal-centers, high theoretical specific capacity, and insolubility, Fe-TTTP gains superior electrochemical performances, including a high reversible (charge) capacity of 950 mAh g−1 at 50 mA g−1, excellent rate performance (95 mAh g−1 up to 10000 mA g−1, 1.1 min for each cycle), and extraordinary cycling stability (310 ± 20 mAh g−1 for 5000 cycles at 2000 mA g−1).
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