电解质
锂(药物)
离子
材料科学
锂离子电池的纳米结构
无机化学
化学工程
化学
电化学
工程类
物理化学
电极
有机化学
医学
内分泌学
作者
Qidi Wang,Jianlin Wang,Jouke R. Heringa,Xuedong Bai,Marnix Wagemaker
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-07-11
卷期号:9 (8): 3796-3806
标识
DOI:10.1021/acsenergylett.4c01358
摘要
One of the primary challenges to improving lithium-ion batteries lies in comprehending and controlling the intricate interphases. However, the complexity of interface reactions and the buried nature make it difficult to establish the relationship between the interphase characteristics and electrolyte chemistry. Herein, we employ diverse characterization techniques to investigate the progression of electrode–electrolyte interphases, bringing forward opportunities to improve the interphase properties by what we refer to as high-entropy solvation disordered electrolytes. Through formulating an electrolyte with a regular 1.0 M concentration that includes multiple commercial lithium salts, the solvation interaction with lithium ions alters fundamentally. The participation of several salts can result in a weaker solvation interaction, giving rise to an anion-rich and disordered solvation sheath despite the low salt concentration. This induces a conformal, inorganic-rich interphase that effectively passivates electrodes, preventing solvent co-intercalation. Remarkably, this electrolyte significantly enhances the performance of graphite-containing anodes paired with high-capacity cathodes, offering a promising avenue for tailoring interphase chemistries.
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