Insight into the Impact of Electrolyte on Passivation of Lithium-Sulfur Cathodes

Abstract

One of the remaining challenges for lithium-sulfur batteries toward practical application is early cathode passivation by the insulating discharge product: Li2S. To understand how to best mitigate passivation and minimize related performance loss, a kinetic Monte-Carlo model for Li2S crystal growth from solution is developed. The key mechanisms behind the strongly different natures of Li2S layer growth, structure, and morphology for salts with different (DN) are revealed. LiTFSI electrolyte in dimethyl ether leads to lateral Li2S growth on carbon and fast passivation because it increases the Li2S precipitation-to-dissolution probability on carbon relative to Li2S. In contrast, LiBr electrolyte has a higher DN and yields a particle-like structure due to a significantly higher precipitation-to-dissolution probability on Li2S compared to carbon. The resulting large number of Li2S sites further favors particle growth, leading to low passivation. This study is able to identify the key parameters of the electrolyte and substrate material to tune Li2S morphology and growth to pave the way for optimized performance.,A kinetic Monte-Carlo model is developed to understand how to best mitigate passivation in lithium-sulfur batteries. The study reveals key mechanisms behind Li2S layer growth, structure, and morphology for salts with different Gutmann Donor Numbers. This study identifies key parameters to optimize Li2S morphology and growth for improved battery performance. image,