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用于锂金属电池动态再生的磁取向纳米片夹层

Magnetically oriented nanosheet interlayer for dynamic regeneration in lithium metal batteries.

作者信息

Ju Zhengyu, Zheng Tianrui, Zhang Bowen, Dolocan Andrei, Marschilok Amy C, Takeuchi Esther S, Takeuchi Kenneth J, Yu Guihua

机构信息

Materials Science and Engineering Program and Walker Department of Mechanical Engineering, The University of Texas at Austin, Austin, TX 78712.

Texas Materials Institute, University of Texas at Austin, Austin, TX 78712.

出版信息

Proc Natl Acad Sci U S A. 2024 Oct 29;121(44):e2413739121. doi: 10.1073/pnas.2413739121. Epub 2024 Oct 23.

Abstract

Lithium (Li) metal has been recognized as a promising anode to advance the energy density of current Li-based batteries. However, the growth of the solid-electrolyte interphase (SEI) layer and dendritic Li microstructure pose significant challenges for the long-term operation of Li metal batteries (LMBs). Herein, we propose the utilization of a suspension electrolyte with dispersed magnetically responsive nanosheets whose orientation can be manipulated by an external magnetic field during cell operation for realizing in situ regeneration in LMBs. The regeneration mechanism arises from the redistribution of the ion flux and the formation of an inorganic-rich SEI for uniform and compact Li deposition. With the magnetic-field-induced regeneration process, we show that a Li||Li symmetric cell stably operates for 350 h at 2 mA cm and 2 mA h cm, ~5 times that of the cell with the pristine electrolyte. Furthermore, the cycling stability can be significantly extended in the Li||NMC full cell of 3 mA h cm, showing a capacity retention of 67% after 500 cycles at 1C. The dynamic Li metal regeneration demonstrated here could bring useful design considerations for reviving the operating cells for achieving high-energy, long-duration battery systems.

摘要

锂(Li)金属已被公认为是一种有前景的负极材料,可提高当前锂基电池的能量密度。然而,固体电解质界面(SEI)层的生长和锂枝晶微结构对锂金属电池(LMBs)的长期运行构成了重大挑战。在此,我们提出利用一种含有分散的磁响应纳米片的悬浮电解质,其取向可在电池运行期间通过外部磁场进行操控,以实现LMBs中的原位再生。再生机制源于离子通量的重新分布以及形成富含无机物的SEI,从而实现均匀且致密的锂沉积。通过磁场诱导的再生过程,我们展示了一个锂||锂对称电池在2 mA cm²和2 mA h cm²的条件下稳定运行350小时,这大约是使用原始电解质的电池的5倍。此外,在3 mA h cm²的锂||NMC全电池中,循环稳定性可显著延长,在1C下500次循环后容量保持率为67%。此处展示的动态锂金属再生可为恢复运行中的电池以实现高能、长续航电池系统带来有益的设计思路。

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