电池快速充电中位错-管道扩散的超快钠输运

Jae-Hwan Kim, Young-Hwan Lee, Jun-Hyoung Park, Byeong-Joo Lee, Young-Woon Byeon, Jae‐Chul Lee
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引用次数: 2

摘要

二次电池的充电过程总是与合金阳极的大体积膨胀有关,在许多情况下,在传播界面附近产生高压残余应力。这种现象导致阳极的倍率性能显著下降,不利于快速充电电池的发展。然而,对于Na-Sn电池系统,在界面附近产生的残余应力没有被储存,而是通过在Sn晶体中产生高密度位错来缓解。直接接触扩散实验表明,这些位错促进了Na的优先输运,并通过“位错-管道扩散”加速了Na向Sn晶体的超快扩散。在测量界面附近残余应力的分布和大小的同时,进行了进一步的分析,观察了原子尺度结构的演变。此外,结合经典分子动力学和第一性原理计算进行了多尺度模拟,以解释Na-Sn体系中观察到的超快扩散速率的结构起源。这些发现不仅解决了关于管道扩散和载流子离子扩散之间关系的知识空白,而且为快速充电电池中使用的阳极材料的适当选择提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrafast Na Transport into Crystalline Sn via Dislocation-Pipe Diffusion for Rapid Battery Charging
The charging process of secondary batteries is always associated with a large volume expansion of the alloying anodes, which in many cases, develops high compressive residual stresses near the propagating interface. This phenomenon causes a significant reduction in the rate performance of the anodes and is detrimental to the development of fast-charging batteries. However, for the Na-Sn battery system, the residual stresses that develop near the interface are not stored, but are relieved by the generation of high-density dislocations in crystalline Sn. Direct-contact diffusion experiments show that these dislocations facilitate the preferential transport of Na and accelerate the Na diffusion into crystalline Sn at ultrafast rates via "dislocation-pipe diffusion". Advanced analyses are performed to observe the evolution of atomic-scale structures while measuring the distribution and magnitude of residual stresses near the interface. In addition, multi-scale simulations that combined classical molecular dynamics and first-principles calculations are performed to explain the structural origins of the ultrafast diffusion rates observed in the Na-Sn system. These findings not only address the knowledge gaps regarding the relationship between pipe diffusion and the diffusivity of carrier ions but also provide guidelines for the appropriate selection of anode materials for use in fast-charging batteries.
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