Li Zheng, Hou Li-Peng, Yao Nan, Li Xi-Yao, Chen Zi-Xian, Chen Xiang, Zhang Xue-Qiang, Li Bo-Quan, Zhang Qiang
Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, P. R. China.
Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, 100081, P. R. China.
Angew Chem Int Ed Engl. 2023 Oct 23;62(43):e202309968. doi: 10.1002/anie.202309968. Epub 2023 Sep 15.
Lithium-sulfur (Li-S) batteries are promising due to ultrahigh theoretical energy density. However, their cycling lifespan is crucially affected by the electrode kinetics of lithium polysulfides. Herein, the polysulfide solvation structure is correlated with polysulfide electrode kinetics towards long-cycling Li-S batteries. The solvation structure derived from strong solvating power electrolyte induces fast anode kinetics and rapid anode failure, while that derived from weak solvating power electrolyte causes sluggish cathode kinetics and rapid capacity loss. By contrast, the solvation structure derived from medium solvating power electrolyte balances cathode and anode kinetics and improves the cycling performance of Li-S batteries. Li-S coin cells with ultra-thin Li anodes and high-S-loading cathodes deliver 146 cycles and a 338 Wh kg pouch cell undergoes stable 30 cycles. This work clarifies the relationship between polysulfide solvation structure and electrode kinetics and inspires rational electrolyte design for long-cycling Li-S batteries.
锂硫(Li-S)电池因其超高的理论能量密度而颇具前景。然而,它们的循环寿命受到多硫化锂电极动力学的关键影响。在此,多硫化物溶剂化结构与长循环Li-S电池的多硫化物电极动力学相关。源自强溶剂化能力电解质的溶剂化结构会引发快速的阳极动力学和快速的阳极失效,而源自弱溶剂化能力电解质的溶剂化结构则会导致缓慢的阴极动力学和快速的容量损失。相比之下,源自中等溶剂化能力电解质的溶剂化结构平衡了阴极和阳极动力学,并改善了Li-S电池的循环性能。具有超薄锂阳极和高硫负载阴极的Li-S硬币电池可实现146次循环,一个338 Wh kg的软包电池可稳定循环30次。这项工作阐明了多硫化物溶剂化结构与电极动力学之间的关系,并为长循环Li-S电池的合理电解质设计提供了思路。