Boosting sulfur-based cathode performance via confined reactions in covalent organic frameworks with polarized sites

Da Zhu, Li Sheng, Jin Wang, Li Wang, Hong Xu, Xiangming He
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引用次数: 2

Abstract

The widespread promotion of the sulfur-based cathode is continuously threatened by the dissolution or slow kinetic reactions of polysulfides, resulting in a deterioration of capacity and volume expansion. Herein, a hierarchical imine-based covalent organic framework (COFs) with AA stacking structure is constructed as a sulfur host matrix. The one-dimensional channels in COF are decorated with polarized methoxy groups which can confine and immobilize sulfur species through weak interactions, alleviating the shuttle effect during the battery tests. The composite electrode (COF@S) is fabricated through the melt-diffusion method in one-pot synthesis and exhibits a slow fading rate (0.20% each cycle) in a 0.5 C stability test. A promising mechanism for constructing the cathode composite is demonstrated in lithium-sulfur chemistry in this work.

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在具有极化位点的共价有机框架中通过限制反应提高硫基阴极性能
硫基阴极的广泛推广不断受到多硫化物溶解或缓慢动力学反应的威胁,导致容量和体积膨胀的恶化。本文构建了一种具有AA堆叠结构的分级亚胺基共价有机骨架(COFs)作为硫主体基质。COF中的一维通道用极化的甲氧基修饰,甲氧基可以通过弱相互作用限制和固定硫物种,缓解电池测试过程中的穿梭效应。复合电极(COF@S)通过熔融扩散法在一锅合成中制备,并在0.5 C稳定性试验。本工作在锂硫化学中证明了构建阴极复合材料的一种很有前途的机制。
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