材料科学
分离器(采油)
锂(药物)
氟化锂
阴极
氧化物
化学
化学工程
单层
电极
无机化学
电解质
纳米技术
冶金
物理化学
内分泌学
工程类
物理
热力学
医学
作者
Yujing Liu,Huadong Yuan,Yao Wang,Chi Jiang,Cong Ma,Ouwei Sheng,Gongxun Lu,Xiong Wen Lou
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-02-17
卷期号:375 (6582): 739-745
被引量:498
标识
DOI:10.1126/science.abn1818
摘要
High–energy density lithium (Li) metal batteries (LMBs) are promising for energy storage applications but suffer from uncontrollable electrolyte degradation and the consequently formed unstable solid-electrolyte interphase (SEI). In this study, we designed self-assembled monolayers (SAMs) with high-density and long-range–ordered polar carboxyl groups linked to an aluminum oxide–coated separator to provide strong dipole moments, thus offering excess electrons to accelerate the degradation dynamics of carbon-fluorine bond cleavage in Li bis(trifluoromethanesulfonyl)imide. Hence, an SEI with enriched lithium fluoride (LiF) nanocrystals is generated, facilitating rapid Li + transfer and suppressing dendritic Li growth. In particular, the SAMs endow the full cells with substantially enhanced cyclability under high cathode loading, limited Li excess, and lean electrolyte conditions. As such, our work extends the long-established SAMs technology into a platform to control electrolyte degradation and SEI formation toward LMBs with ultralong life spans.
科研通智能强力驱动
Strongly Powered by AbleSci AI