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具有醚官能化阴离子的聚合物电解质中负电荷迁移率的抑制

Suppressed Mobility of Negative Charges in Polymer Electrolytes with an Ether-Functionalized Anion.

作者信息

Zhang Heng, Chen Fangfang, Lakuntza Oier, Oteo Uxue, Qiao Lixin, Martinez-Ibañez Maria, Zhu Haijin, Carrasco Javier, Forsyth Maria, Armand Michel

机构信息

CIC Energigune, Parque Tecnológico de Álava, Albert Einstein 48, 01510, Miñano, Álava, Spain.

ARC Centre of Excellence for Electromaterials Science (ACES), Institute for Frontier Materials (IFM), Deakin University, Burwood, Victoria, 3125, Australia.

出版信息

Angew Chem Int Ed Engl. 2019 Aug 26;58(35):12070-12075. doi: 10.1002/anie.201905794. Epub 2019 Aug 5.

Abstract

Suppressing the mobility of anionic species in polymer electrolytes (PEs) is essential for mitigating the concentration gradient and internal cell polarization, and thereby improving the stability and cycle life of rechargeable alkali metal batteries. Now, an ether-functionalized anion (EFA) is used as a counter-charge in a lithium salt. As the salt component in PEs, it achieves low anionic diffusivity but sufficient Li-ion conductivity. The ethylene oxide unit in EFA endows nanosized self-agglomeration of anions and trapping interactions between the anions and its structurally homologous matrix, poly(ethylene oxide), thus suppressing the mobility of negative charges. In contrast to previous strategies of using anion traps or tethering anions to a polymer/inorganic backbone, this work offers a facile and elegant methodology on accessing selective and efficient Li-ion transport in PEs and related electrolyte materials (for example, composites and hybrid electrolytes).

摘要

抑制聚合物电解质(PEs)中阴离子物种的迁移率对于减轻浓度梯度和电池内部极化至关重要,从而提高可充电碱金属电池的稳定性和循环寿命。现在,一种醚官能化阴离子(EFA)被用作锂盐中的抗衡电荷。作为PEs中的盐成分,它实现了低阴离子扩散率但足够的锂离子电导率。EFA中的环氧乙烷单元赋予阴离子纳米级自聚集以及阴离子与其结构同源基质聚环氧乙烷之间的捕获相互作用,从而抑制负电荷的迁移率。与先前使用阴离子陷阱或将阴离子束缚到聚合物/无机主链的策略不同,这项工作提供了一种简便而巧妙的方法来实现PEs和相关电解质材料(例如复合材料和混合电解质)中选择性和高效的锂离子传输。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e841/6771960/4078c621b926/ANIE-58-12070-g003.jpg

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