Sang Cheol Kim, Jingyang Wang, Rong Xu, Pu Zhang, Yuelang Chen, Zhuojun Huang, Yufei Yang, Zhiao Yu, Solomon Oyakhire, Wenbo Zhang, Louisa Greenburg, Mun Sek Kim, David Boyle, Philaphon Sayavong, Yusheng Ye, Jian Qin, Zhenan Bao, Yi Cui
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引用次数: 0
摘要
电解质工程是提高电池性能的关键,尤其是锂金属电池。电解质的最新进展通过增强电极界面的电化学稳定性大大改善了可循环性,但同时实现高离子导电性仍然具有挑战性。在这里,我们报告了一种通过增加电解质中的分子多样性来增强锂金属电池的电解质设计策略,这本质上导致了高熵电解质(HEEs)。我们发现,在弱溶剂化电解质中,熵效应减少了离子聚集,同时保留了典型的富阴离子溶剂化结构,这是基于同步加速器的x射线散射和分子动力学模拟的特征。与传统的弱溶剂化电解质相比,具有较小尺寸簇的电解质的离子电导率提高了2倍,能够在无阳极LiNi0.6Mn0.2Co0.2 (NMC622) Cu袋电池中以高达2C (6.2 mA cm-2)的高电流密度稳定循环。通过在三种不同的弱溶剂化电解质体系中的性能改进,验证了该设计策略的有效性。
High Entropy Electrolytes for Practical Lithium Metal Batteries
Electrolyte engineering is crucial for improving battery performance, particularly for lithium metal batteries. Recent advances in electrolytes have greatly improved cyclability by enhancing electrochemical stability at the electrode interfaces, but concurrently achieving high ionic conductivity has remained challenging. Here we report an electrolyte design strategy for enhanced lithium metal batteries by increasing the molecular diversity in electrolytes, which essentially leads to high entropy electrolytes (HEEs). We find that in weakly solvating electrolytes, the entropy effect reduces ion clustering while preserving the characteristic anion-rich solvation structures, which is characterized by synchrotron-based X-ray scattering and molecular dynamics simulations. Electrolytes with smaller-sized clusters exhibit a 2-fold improvement in ionic conductivity compared to conventional weakly-solvating electrolytes, enabling stable cycling at high current densities up to 2C (6.2 mA cm-2) in anode-free LiNi0.6Mn0.2Co0.2 (NMC622) || Cu pouch cells. The efficacy of the design strategy is verified by performance improvements in three disparate weakly solvating electrolyte systems.