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用于稳定锂金属电池的高韧性滑动交联凝胶聚合物电解质。

Highly Tough Slide-Crosslinked Gel Polymer Electrolyte for Stable Lithium Metal Batteries.

作者信息

Deng Xuetian, Chen Jing, Jia Xin, Da Xinyu, Zhao Yuanjun, Gao Yiyang, Gao Yang, Kong Xiangpeng, Ding Shujiang, Gao Guoxin

机构信息

School of Chemistry, Xi'an Jiaotong University, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, State Key Laboratory of Electrical Insulation and Power Equipment, Xi'an, 710049, P. R. China.

Department of Chemical and Biomolecular Engineering, National, University of Singapore, 21 Lower Kent Ridge Road, Singapore, 119077.

出版信息

Angew Chem Int Ed Engl. 2024 Oct 21;63(43):e202410818. doi: 10.1002/anie.202410818. Epub 2024 Sep 6.

Abstract

Gel polymer electrolytes (GPEs) hold great promise for the practical application of lithium metal batteries. However, conventional GPEs hardly resists lithium dendrites growth and maintains long-term cycling stability of the battery due to its poor mechanical performance. Inspired by the slide-ring structure of polyrotaxanes (PRs), herein we developed a dynamic slide-crosslinked gel polymer electrolyte (SCGPE) with extraordinary stretchability of 970.93 % and mechanical strength of 1.15 MPa, which is helpful to buffer the volume change of electrodes and maintain mechanical integrity of the battery structure during cycling. Notably, the PRs structures can provide fast ion transport channels to obtain high ionic conductivity of 1.73×10 S cm at 30 °C. Additionally, the strong polar groups in SCGPE restrict the free movement of anions to achieve high lithium-ion transference number of 0.71, which is favorable to enhance Li transport dynamics and induce uniform Li deposition. Benefiting from these features, the constructed Li|SCGPE-3|LFP cells exhibit ultra-long and stable cycle life over 1000 cycles and high-capacity retention (89.6 % after 1000 cycles). Even at a high rate of 16 C, the cells deliver a high capacity of 79.2 mAh g. The slide-crosslinking strategy in this work provides a new perspective on the design of advanced GPEs for LMBs.

摘要

凝胶聚合物电解质(GPEs)在锂金属电池的实际应用中具有巨大潜力。然而,传统的GPEs由于其较差的机械性能,几乎无法抵抗锂枝晶的生长并维持电池的长期循环稳定性。受聚轮烷(PRs)滑环结构的启发,在此我们开发了一种动态滑交联凝胶聚合物电解质(SCGPE),其具有970.93%的非凡拉伸性和1.15 MPa的机械强度,这有助于缓冲电极的体积变化并在循环过程中保持电池结构的机械完整性。值得注意的是,PRs结构可以提供快速离子传输通道,在30 °C时获得1.73×10 S cm的高离子电导率。此外,SCGPE中的强极性基团限制了阴离子的自由移动,以实现0.71的高锂离子迁移数,这有利于增强Li传输动力学并诱导均匀的Li沉积。受益于这些特性,构建的Li|SCGPE - 3|LFP电池在超过1000次循环中表现出超长且稳定的循环寿命以及高容量保持率(1000次循环后为89.6%)。即使在16 C的高倍率下,电池仍能提供79.2 mAh g的高容量。这项工作中的滑交联策略为用于锂金属电池的先进GPEs设计提供了新的视角。

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