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用于实用锂硫电池的具有抗还原溶剂壳层的多硫化锂电解质结构

Electrolyte Structure of Lithium Polysulfides with Anti-Reductive Solvent Shells for Practical Lithium-Sulfur Batteries.

作者信息

Zhang Xue-Qiang, Jin Qi, Nan Yi-Ling, Hou Li-Peng, Li Bo-Quan, Chen Xiang, Jin Zhe-Hui, Zhang Xi-Tian, Huang Jia-Qi, Zhang Qiang

机构信息

Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, P. R. China.

Key Laboratory for Photonic and Electronic Bandgap Materials, Ministry of Education, School of Physics and Electronic Engineering, Harbin Normal University, Harbin, 150025, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2021 Jul 5;60(28):15503-15509. doi: 10.1002/anie.202103470. Epub 2021 Jun 4.

Abstract

The lithium-sulfur (Li-S) battery is regarded as a promising secondary battery. However, constant parasitic reactions between the Li anode and soluble polysulfide (PS) intermediates significantly deteriorate the working Li anode. The rational design to inhibit the parasitic reactions is plagued by the inability to understand and regulate the electrolyte structure of PSs. Herein, the electrolyte structure of PSs with anti-reductive solvent shells was unveiled by molecular dynamics simulations and nuclear magnetic resonance. The reduction resistance of the solvent shell is proven to be a key reason for the decreased reactivity of PSs towards Li. With isopropyl ether (DIPE) as a cosolvent, DIPE molecules tend to distribute in the outer solvent shell due to poor solvating power. Furthermore, DIPE is more stable than conventional ether solvents against Li metal. The reactivity of PSs is suppressed by encapsulating PSs into anti-reductive solvent shells. Consequently, the cycling performance of working Li-S batteries was significantly improved and a pouch cell of 300 Wh kg was demonstrated. The fundamental understanding in this work provides an unprecedented ground to understand the electrolyte structure of PSs and the rational electrolyte design in Li-S batteries.

摘要

锂硫(Li-S)电池被认为是一种很有前景的二次电池。然而,锂负极与可溶性多硫化物(PS)中间体之间持续的寄生反应会显著恶化工作中的锂负极。抑制寄生反应的合理设计因无法理解和调控多硫化物的电解质结构而受到困扰。在此,通过分子动力学模拟和核磁共振揭示了具有抗还原溶剂壳的多硫化物的电解质结构。溶剂壳的还原抗性被证明是多硫化物对锂反应性降低的关键原因。以二异丙醚(DIPE)作为共溶剂,由于溶剂化能力差,DIPE分子倾向于分布在外部溶剂壳中。此外,DIPE相对于传统醚类溶剂对锂金属更稳定。通过将多硫化物封装到抗还原溶剂壳中,抑制了多硫化物的反应性。因此,工作中的锂硫电池的循环性能得到显著改善,并展示了一个300 Wh kg的软包电池。这项工作中的基础认识为理解多硫化物的电解质结构以及锂硫电池中的合理电解质设计提供了前所未有的依据。

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