金属锂
相间
阳极
超分子化学
锂(药物)
材料科学
金属
化学
纳米技术
无机化学
化学工程
电极
分子
有机化学
冶金
医学
物理化学
工程类
生物
遗传学
内分泌学
作者
Yongfeng Zhou,Jinghan Li,Yupo Xu,Wei You,Chengkai Hong,Shui Yu,Zhaofeng Ouyang,Zhaoming Zhang,Wei Yu,Hao Sun,Chunyang Yu,Wenfeng Jiang
标识
DOI:10.1002/ange.202505794
摘要
Supramolecular polymers (SPs) driven by host‐guest interactions have seen considerable advancements over the past decade, but the guest species involved are predominantly neutral molecules or cations. Strong and dependable macrocycle‐anion interactions for supramolecular polymerization are highly sought after, yet the functionalities of this class of SPs featuring negatively charged backbones remain largely unexplored. Here we report a novel host‐guest interaction between one tetraurea macrocycle and two organophosphate anions with high affinity (association constant Ka = 1.06 × 109 M−2). It can serve as noncovalent joints to efficiently link low‐molecular‐mass polyethylene oxide (PEO) diorganophosphates into long linear SPs. Being used as an interphase layer in anode‐free lithium (Li) metal batteries, the polymer material promotes Li+ absorption and desolvation through electrostatic attractions, and enables fast Li+ transport by the alternatingly arranged anionic linkages and PEO units in the polymer main chain. As a result, the SP layer homogenizes Li+ flux to achieve uniform Li deposition, and significantly improves the electrochemical performance of LiFePO4 full batteries by a factor of 285% with cycling stability over 200 cycles. These findings pave the way for a new family of anion‐based SPs with tunable architectures and compositions, and suggest their promising applications in future batteries.
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