溶剂
磷酸三甲酯
材料科学
电解质
石墨
阳极
溶剂化
无机化学
化学工程
溶解
水溶液
相间
溶剂效应
支撑电解质
有机化学
深共晶溶剂
电化学
化学稳定性
溶解度
碳纤维
电池(电)
磷酸盐
作者
Xinan Yan,Kean Chen,Zhongxue Chen,Xinping Ai,Yuliang Cao
标识
DOI:10.1002/aenm.202505287
摘要
ABSTRACT Graphite anodes have severe compatibility issues with most non‐aqueous electrolytes, which is known as a critical bottleneck hindering the advancement of lithium‐ion batteries (LIBs). The reduction of non‐aqueous solvents on graphite anodes involves complex processes, mainly including solvent co‐intercalation and decomposition. While much research focuses on solvent decomposition and the related solid electrolyte interphase (SEI) formation, investigations into solvent co‐intercalation are limited to solvents with high reductive stability (i.e., ethers). Herein, we demonstrate that reversible solvent co‐intercalation is an universal side reaction threatening the stability of the graphite anode. Besides ether‐based solvents, the reversible co‐intercalation into graphite can be achieved by three commonly used functional solvents, Trimethyl phosphate (TMP), Triethyl phosphate (TEP), and Tetramethylene sulfone (TMS). By systematically analyzing these reversible solvent co‐intercalation reactions, the solvating power of the solvent and Li + solvation structure were found to be the two critical factors determining the onset voltage of solvent cointercalation. The approaches to effectively protecting graphite from solvent cointercalation were also discussed. This work provides new insights into the understanding of electrolyte||graphite anode interface and shed lights into the development of high‐performance electrolytes for LIBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI