Lithium Tetrafluoroborate-Based Ester Electrolyte Formulations to Improve the Operating Temperature Range in NCM 622 || Graphite Li-Ion Batteries
Source abstract
Abstract
The use of alternative lithium salts, lithium tetrafluoroborate (LiBF 4 ), lithium difluoro(oxalato)borate, and lithium hexafluorophosphate (LiPF 6 ), in the ester/fluoroethylene carbonate electrolyte results in improved low-temperature performance at −20 °C compared to LiPF 6 in a carbonate-based electrolyte, but the room-temperature performance of the ester-based formulation has significant capacity fade due to the instability of the solid electrolyte interphase (SEI). Incorporation of electrolyte additives, lithium bis(oxalato)borate, lithium difluorophosphate, and lithium bis(trimethylsilyl) phosphate (LiTMSP), into lithium tetrafluoroborate (LiBF 4 ) ester-based electrolytes (methyl acetate/fluoroethylene carbonate-MA/FEC) has been investigated in graphite//LiNi 0.6 Co 0.2 Mn 0.2 O 2 cells to improve room-temperature cycling stability without diminishing low-temperature rate performance. The LiBF 4 -based ester electrolyte containing 1% LiTMSP delivers the highest reversible capacity at low temperature (−20 °C), while the room-temperature performance is significantly improved compared to that of the base ester-based electrolyte (LiBF 4 -MA) and almost comparable to that of the standard carbonate-based electrolyte. The improved electrochemical performance for 1% LiTMSP at −20 °C is due to the lower charge transfer resistance as supported by electrochemical impedance spectroscopy, and improved room-temperature performance can be ascribed to the generation of a stable phosphate-rich SEI on the graphite surface as revealed by X-ray photoelectron spectroscopy.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Battery Materials · Advanced Battery Materials and Technologies · Advanced Battery Technologies Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University of Rhode Island, Kingston, Rhode Island 02881, United States
Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, Maryland 20742, United States
Funding
Vehicle Technologies Office
References (35)
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