Sen Lv, Xingkai Ma, Siwen Ke, Yaoda Wang, Tianrui Ma, Shuai Yuan, Zhong Jin* and Jing-Lin Zuo*,
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引用次数: 0
摘要
阴极上多硫化物的穿梭和阳极上锂枝晶的不可控生长限制了锂硫(Li-S)电池的实际应用。本研究设计并合成了一种金属配位的三维共价有机框架(COF),该框架具有均匀分布的镍-双(二硫杂环戊烯)和富含 N 的三嗪中心(即 NiS4-TAPT),可作为锂-硫电池中硫阴极和锂阳极的双功能宿主。NiS4-TAPT 中丰富的镍中心和 N-位点可大大提高多硫化物的吸附和转化能力。同时,Ni-双(二硫烯)中心的存在可使锂阳极上的锂均匀成核,从而抑制锂枝晶的生长。这项工作证明了整合催化和吸附位点以优化宿主材料和氧化还原活性中间体之间化学相互作用的有效性,从而有可能促进用于高性能二次电池的金属配位 COF 材料的合理设计。
Metal-Coordinated Covalent Organic Frameworks as Advanced Bifunctional Hosts for Both Sulfur Cathodes and Lithium Anodes in Lithium–Sulfur Batteries
The shuttling of polysulfides on the cathode and the uncontrollable growth of lithium dendrites on the anode have restricted the practical application of lithium–sulfur (Li–S) batteries. In this study, a metal-coordinated 3D covalent organic framework (COF) with a homogeneous distribution of nickel–bis(dithiolene) and N-rich triazine centers (namely, NiS4-TAPT) was designed and synthesized, which can serve as bifunctional hosts for both sulfur cathodes and lithium anodes in Li–S batteries. The abundant Ni centers and N-sites in NiS4-TAPT can greatly enhance the adsorption and conversion of the polysulfides. Meanwhile, the presence of Ni–bis(dithiolene) centers enables uniform Li nucleation at the Li anode, thereby suppressing the growth of Li dendrites. This work demonstrated the effectiveness of integrating catalytic and adsorption sites to optimize the chemical interactions between host materials and redox-active intermediates, potentially facilitating the rational design of metal-coordinated COF materials for high-performance secondary batteries.
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