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锂硫电池中咖啡因快速结合多硫化物的傅里叶变换红外光谱研究

FTIR Spectroscopy Study on Rapid Polysulfide Binding via Caffeine in Lithium-Sulfur Batteries.

作者信息

Yim Taber, Pereira Rhyz, Nedsaengtip Jantakan, Fafarman Aaron T, Kalra Vibha

机构信息

Department of Chemical and Biological Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States.

Smith School of Chemical and Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.

出版信息

J Phys Chem Lett. 2024 Dec 12;15(49):12164-12170. doi: 10.1021/acs.jpclett.4c02789. Epub 2024 Dec 2.

Abstract

Lithium-sulfur batteries are limited by the high mobility of polysulfides in the electrolyte, which allows them to migrate from the cathode to the lithium anode. This is known as polysulfide shuttling and simultaneously diminishes the active material and poisons the anode. Various cathode additives have been shown empirically to mitigate this problem, although the mechanism is not often ascertained experimentally. Herein, we demonstrate for the first time that the small molecule additive caffeine reduces the polysulfide shuttling current in a lithium-sulfur battery and decreases the capacity fade in galvanostatic cycling experiments. Using Fourier transform infrared (FTIR) spectroscopy, we identify reversible shifts in the carbonyl stretching frequencies of caffeine that are strongly correlated with the onset of polysulfide formation during both discharging and charging. These spectroscopic shifts are consistent with a polar-polar interaction between polysulfides and the carbonyl groups of caffeine, leading to the observed decrease in polysulfide mobility.

摘要

锂硫电池受到电解质中多硫化物高迁移率的限制,这使得它们能够从阴极迁移到锂阳极。这被称为多硫化物穿梭,同时会减少活性材料并使阳极中毒。尽管该机制通常未通过实验确定,但根据经验已证明各种阴极添加剂可缓解此问题。在此,我们首次证明小分子添加剂咖啡因可降低锂硫电池中的多硫化物穿梭电流,并在恒电流循环实验中减少容量衰减。使用傅里叶变换红外(FTIR)光谱,我们确定了咖啡因羰基伸缩频率的可逆变化,这些变化与放电和充电过程中多硫化物形成的开始密切相关。这些光谱变化与多硫化物和咖啡因羰基之间的极性 - 极性相互作用一致,导致观察到的多硫化物迁移率降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19e4/11648080/042a794b23cf/jz4c02789_0001.jpg

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