A multi-functional electrolyte for lithium-ion batteries

Date
2016
Authors
Westhoff, Kevin A., author
Bandhauer, Todd M., advisor
Bradley, Thomas H., committee member
Prieto, Amy L., committee member
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Abstract
Thermal management of lithium-ion batteries (LIBs) is paramount for multi-cell packs, such as those found in electric vehicles, to ensure safe and sustainable operation. Thermal management systems (TMSs) maintain cell temperatures well below those associated with capacity fade and thermal runaway to ensure safe operation and prolong the useful life of the pack. Current TMSs employ single-phase liquid cooling to the exterior surfaces of every cell, decreasing the volumetric and gravimetric energy density of the pack. In the present study, a novel, internal TMS that utilizes a multi-functional electrolyte (MFE) is investigated, which contains a volatile co-solvent that boils upon heat absorption in small channels in the positive electrode of the cell. The inert fluid HFE-7000 is investigated as the volatile co-solvent in the MFE (1 M LiTFSI in 1:1 HFE-7000/ethyl methyl carbonate by volume) for the proposed TMS. In the first phase of the study, the baseline electrochemical performance of the MFE is determined by conductivity, electrochemical stability window, half and full cell cycling with lithium iron phosphate (LiFePO4), lithium titanate oxide (Li4Ti5O12), and copper antimonide (Cu2Sb), and impedance spectroscopy measurements. The results show that the MFE containing HFE-7000 has comparable stability and cycling performance to a conventional lithium-ion electrolyte (1 M LiPF6 in 3:7 ethylene carbonate/diethyl carbonate by weight). The MFE-containing cells had higher impedance than carbonate-only cells, indicating reduced passivation capability on the electrodes. Additional investigation is warranted to refine the binary MFE mixture by the addition of solid electrolyte interphase (SEI) stabilizing additives. To validate the thermal and electrochemical performance of the MFE, Cu2Sb and LiFePO4 are used in a full cell architecture with the MFE in a custom electrolyte boiling facility. The facility enables direct viewing of the vapor generation within the channel in the positive electrode and characterizes the galvanostatic electrochemical performance. Test results show that the LiFePO4/Cu2Sb cell is capable of operation even when a portion of the more volatile HFE-7000 is continuously evaporated under an extreme heat flux, proving the concept of a MFE. The conclusions presented in this work inform the future development of the proposed internal TMS.
Description
2016 Summer.
Includes bibliographical references.
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