Perspective on the mechanism of mass transport-induced (tip-growing) Li dendrite formation by comparing conventional liquid organic solvent with solid polymer-based electrolytes

IF 2.9 Q2 ELECTROCHEMISTRY Journal of Electrochemical Science and Engineering Pub Date : 2023-08-09 DOI:10.5599/jese.1724
L. Stolz, M. Winter, J. Kasnatscheew
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Abstract

A major challenge of Li metal electrodes is the growth of high surface area lithium during Li deposition with a variety of possible shapes and growing mechanisms. They are reactive and lead to active lithium losses, electrolyte depletion and safety concerns due to a potential risk of short-circuits and thermal runaway. This work focuses on the mechanism of tip-growing Li dendrite as a particular high surface area lithium morphology. Its formation mechanism is well-known and is triggered during concentration polarization, i.e. during mass (Li+) transport limitations, which has been thoroughly investigated in literature with liquid electrolytes. This work aims to give a stimulating perspective on this formation mechanism by considering solid polymer electrolytes. The in-here shown absence of the characteristic “voltage noise” immediately after complete concentration polarization, being an indicator for tip-growing dendritic growth, rules out the occurrence of the particular tip-growing morphology for solid polymer electrolytes under the specific electrochemical conditions. The generally poorer kinetics of solid polymer electrolytes compared to liquid electrolytes imply lower limiting currents, i.e. lower currents to realize complete concen­tration polarization. Hence, this longer-lasting Li-deposition times in solid polymer electro­lytes are assumed to prevent tip-growing mechanism via timely enabling solid electrolyte interphase formation on fresh Li deposits, while, as stated in previous literature, in liquid electrolytes, Li dendrite tip-growth process is faster than solid electrolyte interphase forma­tion kinetics. It can be reasonably concluded that tip-growing Li dendrites are in general practically unlikely for both, (i) the lower conducting electrolytes like solid polymer electro­lytes due to enabling solid electrolyte interphase formation and (ii) good-conducting electro­lytes like liquids due to an impractically high current required for concentration polarization.
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通过比较传统液体有机溶剂和固体聚合物电解质对质量传递诱导(尖端生长)锂枝晶形成机制的看法
锂金属电极的一个主要挑战是在锂沉积过程中以各种可能的形状和生长机制生长高表面积锂。它们是反应性的,会导致活性锂的损失、电解质的消耗以及由于短路和热失控的潜在风险而引起的安全问题。本文重点研究了尖端生长的锂枝晶作为一种特殊的高表面积锂形态的机理。它的形成机制是众所周知的,是在浓度极化期间触发的,即在质量(Li+)输运限制期间,这在文献中已经用液体电解质进行了深入的研究。这项工作旨在通过考虑固体聚合物电解质,对这种形成机制给出一个刺激的观点。这里所示的完全浓度极化后立即没有特征性的“电压噪声”,这是枝晶尖生长的一个指标,排除了固体聚合物电解质在特定电化学条件下出现特定的尖生长形态。与液体电解质相比,固体聚合物电解质的动力学通常较差,这意味着较低的极限电流,即实现完全浓度极化的电流较低。因此,在固体聚合物电解质中,这种较长的锂沉积时间被认为是通过及时使新鲜锂沉积上的固体电解质间相形成来阻止尖端生长机制,而如先前文献所述,在液体电解质中,锂枝晶尖端生长过程比固体电解质间相形成动力学更快。可以合理地得出结论,尖端生长的Li枝晶通常在两种情况下都是不可能的,(i)低导电性电解质,如固体聚合物电解质,因为可以形成固体电解质间相;(ii)导电性良好的电解质,如液体,因为浓度极化所需的电流高得不切实际。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.60
自引率
27.30%
发文量
90
审稿时长
6 weeks
期刊最新文献
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