Strategies to enhance Li+ transference number in liquid electrolytes for better lithium batteries

电解质 阳极 分离器(采油) 溶剂化 锂(药物) 过电位 离子 阴极 材料科学 化学工程 无机化学 化学 纳米技术 电化学 有机化学 物理化学 电极 热力学 物理 工程类 内分泌学 医学
作者
Pan Zhou,Xiaokun Zhang,Yong Xiang,Kai Liu
出处
期刊:Nano Research [Springer Science+Business Media]
卷期号:16 (6): 8055-8071 被引量:67
标识
DOI:10.1007/s12274-022-4833-1
摘要

Growing market demand from portable electronics to electric automobiles boosts the development of lithium-ion batteries (LIBs) with high energy density and rate performance. However, strong solvation effect between lithium ions (Li+) and solvent molecules in common electrolytes limits the mobility of Li+ ions in electrolytes. Consequently, anions dominate the charge conduction in electrolytes, and in most cases, the value of Li+ transference number (T+) is between 0.2 and 0.4. A low T+ will aggravate concentration polarization in the process of charging and discharging, especially at high rate, which not only increases the overpotential but also intensifies side reactions, along with uneven deposition of lithium (Li) and the growth of lithium dendrites when lithium metal is used as anode. In this review, promising strategies to improve T+ in liquid electrolytes would be summarized. The migration of Li+ ions is affected directly by the types and concentration of lithium salts, solvents, and additives in bulk electrolytes. Besides, Li+ ions will pass through the separator and solid electrolyte interphase (SEI) when transferring between anodes and cathodes. With this in mind, we will classify and summarize threads of enhancing T+ from five aspects: lithium salts, solvents, additives, separators, and SEI based on different mechanisms, including covalently bonding, desolvation effect, Lewis acid-base interaction, electrostatic interaction, pore sieving, and supramolecular interaction. We believe this review will present a systematic understanding and summary on T+ and point out some feasible threads to enhance battery performance by enhancing T+.
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