Influence of bis(2,2,2-trifluoroethyl) carbonate flame retarding co-solvent on interfacial chemistry in carbonate ester lithium-ion battery electrolytes†

Mohammad Baghban Shemirani, Florian Gebert and Andrew J. Naylor
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Abstract

The development of flame-retarding battery electrolytes may be achieved by the inclusion of non-flammable solvents in existing conventional electrolyte formulations. Here the use of one such promising solvent, bis(2,2,2-trifluoroethyl) carbonate (TFEC), mixed with conventional lithium-ion battery solvents ethylene carbonate and ethyl methyl carbonate, achieves comparable or superior electrochemical performance to a state-of-the-art benchmark (up to 90% capacity retention between 5th and 200th cycle, compared with 76% for the benchmark). Further electrochemical analysis indicates comparable cell resistance and rate capability, though a TFEC content beyond 90 vol% leads to increased resistance and rapid capacity fading. This was found to be caused by lithium trapping in the graphite electrodes and formation of a thinner solid electrolyte interphase with a distinct chemistry, as determined by X-ray photoelectron spectroscopy. TFEC's low Li+-solvating ability likely significantly influences these electrolytes' physico-chemical and electrochemical behaviour.

Abstract Image

双(2,2,2-三氟乙基)碳酸酯阻燃共溶剂对碳酸酯锂离子电池电解质界面化学的影响
阻燃电池电解质的开发可以通过在现有的常规电解质配方中加入不可燃溶剂来实现。在这里,使用一种这样有前途的溶剂,二(2,2,2-三氟乙基)碳酸酯(TFEC),与传统的锂离子电池溶剂碳酸乙烯酯和甲基碳酸乙酯混合,实现了与最先进的基准相当或更好的电化学性能(在第5到200次循环之间高达90%的容量保留率,而基准为76%)。进一步的电化学分析表明,尽管TFEC含量超过90 vol%会导致电阻增加和容量快速衰减,但电池电阻和倍率能力相当。根据x射线光电子能谱的测定,这是由石墨电极中的锂捕获和形成具有独特化学性质的更薄的固体电解质界面引起的。TFEC的低Li+溶剂化能力可能会显著影响这些电解质的物理化学和电化学行为。
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