相间
电解质
锂(药物)
材料科学
溶解
电极
化学工程
碳酸丙烯酯
金属锂
快离子导体
导电体
碳酸锂
传质
盐(化学)
纳米技术
作者
Yehui Wu,Xihao Wang,Shengchuang Du,Tiansheng Bai,Huijie Tian,Qunhui Yuan,Wanbao Wu,Jiawen Huang,Guanhua Lin,Xingjun Liu,Deping Li,Lijie Ci,Jingyu Lu
标识
DOI:10.1038/s41467-026-76653-7
摘要
Abstract Constructing a robust, highly conductive solid electrolyte interphase is the key to unlock the high-rate potential of lithium negative electrodes for broad applications. Here we propose a simple yet effective strategy, by introducing a sulfur-containing compound and LiNO 3 as dual additives into a conventional carbonate electrolyte. As an example, 3-sulfolene is found to enhance the dissolution of LiNO 3 , and it works with NO 3 − to regulate the Li + -solvation structure and facilitate the formation of a robust while uniform solid electrolyte interphase rich in Li 3 N/Li 2 S/Li 2 O inorganics, enabling rapid Li + transfer and high interfacial stability. Consequently, Li | |LiFePO 4 cells achieve 81.7% capacity retention after 6,000 cycles at 80 C, while Li | |LiNi 0.8 Co 0.1 Mn 0.1 O 2 cells maintain 81.3% capacity after 500 cycles at 10 C. Moreover, two pouch cells with specific energy exceeding 500 Wh kg −1 (calculated based on total mass of the pouch cells) retain 92.1% and 91.8% of initial capacities after 143 and 149 cycles (charged at 0.1 C and discharged at 0.3 C), respectively. This work provides a general dual-additive strategy to promote the formation of an inorganic-rich solid electrolyte interphase for high-rate lithium negative electrodes.
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