偶极子
接口(物质)
跨度(工程)
化学物理
化学
材料科学
分子
纳米技术
有机化学
工程类
土木工程
吉布斯等温线
作者
Xinyi Liu,Shuang Wu,Zhimeng Hao,Long Shang,Mao Xia Guo,Jinze Hou,Siyuan Shao,Haixia Li,Yixin Li,Yong Lü,Kai Zhang,Zhenhua Yan,Jun Chen
标识
DOI:10.1002/ange.202416731
摘要
Sulfurized polyacrylonitrile (SPAN) is recognized as a promising organic cathode for long‐lifespan lithium metal batteries. Nevertheless, the irreversible cleavage/formation of multiple sulfur‐sulfur (S‐S) bonds of SPAN within conventional ether‐based electrolytes results in loss of active S species, severe capacity fading and shuttle effects. Herein, we propose a new electrolyte based on dipropyl ether (PE) solvent for Li‐SPAN batteries. Benefiting from the particular chain‐coordination structure and weak dipole interactions with Li+ and active species, the resulting electrolyte not only achieves low desolvation energy barrier and high Li+ transference number, but also displays stable electrolyte‐electrode interface (EEI). Consequently, the full cells utilizing this electrolyte exhibit good cyclability, outstanding capacity retention and superior extreme‐temperature (‐50°C to 50 °C) performance. Furthermore, the Ah‐scale pouch cell with lean electrolyte (2.5 g Ah‐1) achieves record cycle stability with 96.5% capacity retention after 75 cycles, which deliver an initial specific energy density of 150 Wh kg‐1 (based on the weight of the entire cell). Impressively, this strategy demonstrates universality in a series of organic electrodes employing with PE‐based electrolytes. This work highlights the strategy for modulating the dipole interaction at EEI for long‐lifespan Li‐organic batteries at extreme conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI