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用于富镍正极固态锂金属电池的具有整体定向通道的耐高压共价有机框架电解质

High-Voltage-Tolerant Covalent Organic Framework Electrolyte with Holistically Oriented Channels for Solid-State Lithium Metal Batteries with Nickel-Rich Cathodes.

作者信息

Niu Chaoqun, Luo Wenjia, Dai Chenmin, Yu Chengbing, Xu Yuxi

机构信息

School of Engineering, Westlake University, Hangzhou, 310024, China.

School of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu, 610500, China.

出版信息

Angew Chem Int Ed Engl. 2021 Nov 15;60(47):24915-24923. doi: 10.1002/anie.202107444. Epub 2021 Aug 18.

Abstract

By introducing lithiophilic groups and electrochemically stable quinolyl aromatic ring linkages, we prepared covalent organic frameworks (COFs) exhibiting a large band gap with an ultralow HOMO value (-6.2 eV under vacuum) and oxidative stability up to 5.6 V (versus Li /Li) as solid-state electrolytes (SSEs). The obtained flexible COF SSE thin films showed a holistically oriented arrangement along the (001) facet with remarkable ionic conductivity up to 1.5×10  S cm at 60 °C and excellent mechanical strength with a high Young's modulus of 10.5 GPa. Molecular dynamic simulations showed that lithium ions are transmitted in this COF SSE by directional hopping paths with fast drift velocity. The COF SSE film was used to assemble all-solid-state lithium metal batteries with nickel-rich cathodes (NMC811). The batteries demonstrated stable cycling performance over 400 cycles, high coulombic efficiency (>99 %), and could also withstand abuse tests, such as folding.

摘要

通过引入亲锂基团和具有电化学稳定性的喹啉基芳环连接,我们制备了共价有机框架(COF),其作为固态电解质(SSE)具有大的带隙、超低的最高占据分子轨道值(真空下为 -6.2 eV)以及高达5.6 V(相对于Li/Li)的氧化稳定性。所获得的柔性COF SSE薄膜沿(001)晶面呈现整体取向排列,在60°C时具有高达1.5×10⁻³ S cm⁻¹的显著离子电导率以及10.5 GPa的高杨氏模量所赋予的优异机械强度。分子动力学模拟表明锂离子通过具有快速漂移速度的定向跳跃路径在该COF SSE中传输。该COF SSE薄膜用于组装具有富镍阴极(NMC811)的全固态锂金属电池。这些电池在400次循环中表现出稳定的循环性能、高库仑效率(>99%),并且还能承受诸如折叠等滥用测试。

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