多硫化物
化学
电解质
法拉第效率
锂(药物)
电化学
储能
能量密度
无机化学
化学工程
电极
工程物理
物理化学
工程类
内分泌学
功率(物理)
物理
医学
量子力学
作者
Gebrekidan Gebresilassie Eshetu,Xabier Júdez,Chunmei Li,Maria Martínez‐Ibáñez,Ismael Gracia,Олександр Бондарчук,Javier Carrasco,Lide M. Rodrı́guez-Martı́nez,Heng Zhang,Michel Armand
摘要
With a remarkably higher theoretical energy density compared to lithium-ion batteries (LIBs) and abundance of elemental sulfur, lithium sulfur (Li–S) batteries have emerged as one of the most promising alternatives among all the post LIB technologies. In particular, the coupling of solid polymer electrolytes (SPEs) with the cell chemistry of Li–S batteries enables a safe and high-capacity electrochemical energy storage system, due to the better processability and less flammability of SPEs compared to liquid electrolytes. However, the practical deployment of all solid-state Li–S batteries (ASSLSBs) containing SPEs is largely hindered by the low accessibility of active materials and side reactions of soluble polysulfide species, resulting in a poor specific capacity and cyclability. In the present work, an ultrahigh performance of ASSLSBs is obtained via an anomalous synergistic effect between (fluorosulfonyl)(trifluoromethanesulfonyl)imide anions inherited from the design of lithium salts in SPEs and the polysulfide species formed during the cycling. The corresponding Li–S cells deliver high specific/areal capacity (1394 mAh gsulfur–1, 1.2 mAh cm–2), good Coulombic efficiency, and superior rate capability (∼800 mAh gsulfur–1 after 60 cycles). These results imply the importance of the molecular structure of lithium salts in ASSLSBs and pave a way for future development of safe and cost-effective Li–S batteries.
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