Taming Solvent-Solute Interaction Accelerates Interfacial Kinetics in Low-Temperature Lithium-Metal Batteries

被引:128
|
作者
Jin, Cheng-Bin [1 ]
Yao, Nan [1 ]
Xiao, Ye [2 ]
Xie, Jin [1 ]
Li, Zeheng [1 ]
Chen, Xiang [1 ]
Li, Bo-Quan [2 ]
Zhang, Xue-Qiang [2 ]
Huang, Jia-Qi [2 ]
Zhang, Qiang [1 ]
机构
[1] Tsinghua Univ, Dept Chem Engn, Beijing Key Lab Green Chem React Engn & Technol, Beijing 100084, Peoples R China
[2] Beijing Inst Technol, Adv Res Inst Multidisciplinary Sci, Beijing 100081, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
interfacial kinetics; Li-metal batteries; low-temperature electrolytes; solvent-solute interaction; SOLID-ELECTROLYTE INTERPHASE; LI+-DESOLVATION; ION BATTERY; EFFICIENCY; GRAPHITE; LIFE;
D O I
10.1002/adma.202208340
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium (Li)-metal batteries promise energy density beyond 400 Wh kg(-1), while their practical operation at an extreme temperature below -30 degrees C suffers severe capacity deterioration. Such battery failure highly relates to the remarkably increased kinetic barrier of interfacial processes, including interfacial desolvation, ion transportation, and charge transfer. In this work, the interfacial kinetics in three prototypical electrolytes are quantitatively probed by three-electrode electrochemical techniques and molecular dynamics simulations. Desolvation as the limiting step of interfacial processes is validated to dominate the cell impedance and capacity at low temperature. 1,3-Dioxolane-based electrolyte with tamed solvent-solute interaction facilitates fast desolvation, enabling the practical Li|LiNi0.5Co0.2Mn0.3O2 cells at -40 degrees C to retain 66% of room-temperature capacity and withstand remarkably fast charging rate (0.3 C). The barrier of desolvation dictated by solvent-solute interaction environments is quantitatively uncovered. Regulating the solvent-solute interaction by low-affinity solvents emerges as a promising solution to low-temperature batteries.
引用
收藏
页数:9
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