溶剂化
电解质
碳酸乙烯酯
材料科学
锂(药物)
离子
溶剂
化学工程
化学物理
化学
物理化学
电极
有机化学
医学
工程类
内分泌学
作者
Chaeeun Song,Seung Hee Han,Youngwoo Choi,Hong Rim Shin,Min Kyu Kim,Chaewon Gong,Dongyan Chen,Jong‐Won Lee,Seungbum Hong,Nam‐Soon Choi
标识
DOI:10.1002/adma.202418773
摘要
Abstract The grain sizes of solid electrolyte interphase (SEI) and solvation structure of electrolytes can affect Li + ion transport across SEI and control the desolvation kinetics of solvated Li + ions during fast‐charging of Li‐ion batteries (LIBs). However, the impact of the geometric structure of SEI grains on the fast charging capability of LIBs is rarely examined. Here, the correlation between the SEI grain size and fast charging characteristics of cells is explored, and the desolvation kinetics is controlled by replacing the strongly binding ethylene carbonate (EC) solvent with a weakly binding nitrile‐based solvent under fast charging conditions. The evolution of small grains of SEI to provide sufficient paths for Li + ion supply can be achieved by the modification of solvation structure in the electrolyte. Additionally, the less resistive SEI composition and low viscosity of isoBN‐containing electrolyte enable a more rapid charging of LiNi 0.8 Co 0.1 Mn 0.1 O 2 /graphite full cells by facilitating the SEI crossing of Li + ions with less Li plating at a charging rate of 4 C at 25 °C. This work sheds light on solvation structure and interface engineering to enhance the fast charging cycle stability of LIBs for tailorable adoption in transportation sectors.
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