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Published on: December 20, 2016
High Concentration Hybrid Electrolytes Using Phosphonium Ionic Liquid Additives for Stable High-Energy Density Li-Ion
Mohammad Kahrizi1,2, Hiroyuki Ueda1,2, Tan Xing3
1Institute for Frontier Materials (IFM), Deakin University, 221 Burwood Highway, Burwood, Victoria 3125, Australia.
None:
This study explores a phosphonium ionic liquid additive in carbonate-based electrolytes that can improve the cycling stability of silicon/graphite (Si/Gr) and silicon (Si) anodes. The electrolytes consist of a carbonate solvent mixture (EC/EMC/DEC in a 1:1:1 weight ratio) combined with a 10% weight ratio of the ionic liquid additive, trimethyl(isobutyl)phosphonium bis(fluorosulfonyl)imide (P111i4FSI), in LiFSI concentrations of 1 M and 4 M. Si/Gr || LiFePO4 (LFP), Si || LFP, Li-metal || LiNi0.6Mn0.2Co0.2O2 (NMC622), and Si/Gr || NMC622 cells were evaluated through extended cycling tests. Voltage profiles, dQ/dE analyses, and scanning electron microscopy (SEM) demonstrate distinct failure mechanisms for the two anodes: solid electrolyte interphase (SEI) growth and limited lithium availability in Si/Gr anodes and severe structural cracking and pulverization in Si anodes due to volumetric expansion. X-ray photoelectron spectroscopy (XPS) revealed distinct SEI layer compositions. In the base electrolyte, higher lithium concentrations were detected at the surface and deeper SEI layers, attributed to higher Li2CO3 content. Conversely, in the SEI layers formed in the high concentration hybrid electrolyte (HCHE), the presence of phosphorus (from the ionic liquid's cation) and a higher amount of LiF within the SEI are commensurate with reduced side reactions and efficient lithium-ion transport. Therefore, a 3-fold improvement in the cell cycling stability was obtained, with Si/Gr anodes cycled at 450 mAh/g and 96% efficiency up to 185 cycles and Si anodes cycled at 1000 mAh/g and 99.1% efficiency up to 100 cycles.
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