School of Engineering, Brown University, Providence, Rhode Island 02912, United States.
G. W. Woodruff School of Mechanical Engineering and School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
J Am Chem Soc. 2023 Feb 1;145(4):2473-2484. doi: 10.1021/jacs.2c11807. Epub 2023 Jan 23.
Electrolytes, consisting of salts, solvents, and additives, must form a stable solid electrolyte interphase (SEI) to ensure the performance and durability of lithium(Li)-ion batteries. However, the electric double layer (EDL) structure near charged surfaces is still unsolved, despite its importance in dictating the species being reduced for SEI formation near a negative electrode. In this work, a newly developed model was used to illustrate the effect of EDL on SEI formation in two essential electrolytes, the carbonate-based electrolyte for Li-ion batteries and the ether-based electrolyte for batteries with Li-metal anodes. Both electrolytes have fluoroethylene carbonate (FEC) as a common additive to form the beneficial F-containing SEI component (, LiF). However, the role of FEC drastically differs in these electrolytes. FEC is an effective SEI modifier for the carbonate-based electrolyte by being the only F-containing species entering the EDL and being reduced, as the anion (PF) will not enter the EDL. For the ether-based electrolyte, both the anion (TFSI) and FEC can enter the EDL and be reduced. The competition of the two species within the EDL due to the surface charge and temperature leads to a unique temperature effect observed in prior experiments: the FEC additive is more effective in modulating SEI components at a low temperature (-40 °C) than at room temperature (20 °C) in the ether-based electrolyte. These collective quantitative agreements with experiments emphasize the importance of incorporating the effect of the EDL in multicomponent electrolyte reduction reactions in simulations/experiments to predict/control the formation of the SEI layer.
电解质由盐、溶剂和添加剂组成,必须形成稳定的固体电解质界面相(SEI),以确保锂离子电池的性能和耐久性。然而,尽管在决定负极附近形成 SEI 的还原物种方面很重要,但带电表面附近的双电层(EDL)结构仍然未得到解决。在这项工作中,使用新开发的模型说明了 EDL 对两种重要电解质(锂离子电池的碳酸盐电解质和具有 Li 金属阳极的电池的醚基电解质)中 SEI 形成的影响。这两种电解质都使用氟代碳酸乙烯酯(FEC)作为常见的添加剂来形成有益的含 F SEI 成分(LiF)。然而,FEC 在这两种电解质中的作用有很大的不同。FEC 是碳酸盐基电解质中有效的 SEI 改性剂,因为它是唯一进入 EDL 并被还原的含 F 物质,而阴离子(PF)不会进入 EDL。对于醚基电解质,阴离子(TFSI)和 FEC 都可以进入 EDL 并被还原。由于表面电荷和温度,两种物质在 EDL 内的竞争导致了先前实验中观察到的独特的温度效应:在醚基电解质中,FEC 添加剂在低温(-40°C)下比在室温(20°C)下更有效地调节 SEI 成分。这些与实验的集体定量一致性强调了在模拟/实验中考虑 EDL 对多组分电解质还原反应的影响的重要性,以预测/控制 SEI 层的形成。