TY - JOUR
T1 - Methodologies for Design, Characterization and Testing of Electrolytes that Enable Extreme Fast Charging of Lithium-Ion Cells
AU - Gao, Ningshengjie
AU - Kim, Sangwook
AU - Chinnam, Parameswara
AU - Dufek, Eric
AU - Colclasure, Andrew
AU - Jansen, Andrew
AU - Son, Seoung-Bum
AU - Bloom, Ira
AU - Dunlop, Alison
AU - Trask, Stephen
AU - Gering, Kevin
N1 - Publisher Copyright:
© 2021
PY - 2022/1
Y1 - 2022/1
N2 - Selection, testing and validation of electrolyte candidates for Li-ion cells are discussed, based on a 10-minute target for extreme fast charge (XFC). A combination of modeling and laboratory measurements create a timely and synergistic approach to identifying candidate electrolyte formulations. Multi-solvent systems provide a balanced set of properties, wherein lower molecular-weight solvents offer reduced viscosity, increased species diffusivity, and mitigation of concentration polarization at high charge rates. Carefully selected formulations can exhibit peak conductivity and usable conductivity range of two to three times that of the baseline EC-EMC (3:7, wt.) + LiPF6. Candidates are also chosen based on stability and longevity within the cell environment. Lab testing coincides with property predictions from the Advanced Electrolyte Model (AEM) and a macro-scale cell model. Cell testing utilized coin and pouch cells having NMC532 or NMC811 cathodes with graphite electrodes. Results indicate combinations of low-molecular weight solvents are key for fast-charge electrolytes as they extend the useful conductivity range to both low and higher salt concentrations, and possess higher self-diffusivities compared to conventional solvents. This reduces impacts from concentration polarization. The choice of electrolyte also influences the tendency for lithium metal deposition at the anode, as showcased by experimental and modeling results herein.
AB - Selection, testing and validation of electrolyte candidates for Li-ion cells are discussed, based on a 10-minute target for extreme fast charge (XFC). A combination of modeling and laboratory measurements create a timely and synergistic approach to identifying candidate electrolyte formulations. Multi-solvent systems provide a balanced set of properties, wherein lower molecular-weight solvents offer reduced viscosity, increased species diffusivity, and mitigation of concentration polarization at high charge rates. Carefully selected formulations can exhibit peak conductivity and usable conductivity range of two to three times that of the baseline EC-EMC (3:7, wt.) + LiPF6. Candidates are also chosen based on stability and longevity within the cell environment. Lab testing coincides with property predictions from the Advanced Electrolyte Model (AEM) and a macro-scale cell model. Cell testing utilized coin and pouch cells having NMC532 or NMC811 cathodes with graphite electrodes. Results indicate combinations of low-molecular weight solvents are key for fast-charge electrolytes as they extend the useful conductivity range to both low and higher salt concentrations, and possess higher self-diffusivities compared to conventional solvents. This reduces impacts from concentration polarization. The choice of electrolyte also influences the tendency for lithium metal deposition at the anode, as showcased by experimental and modeling results herein.
KW - advanced electrolyte model (AEM)
KW - cell transport model
KW - extreme fast charge
KW - lithium metal plating
KW - lithium-ion batteries
UR - http://www.scopus.com/inward/record.url?scp=85118502291&partnerID=8YFLogxK
U2 - 10.1016/j.ensm.2021.10.011
DO - 10.1016/j.ensm.2021.10.011
M3 - Article
AN - SCOPUS:85118502291
SN - 2405-8297
VL - 44
SP - 296
EP - 312
JO - Energy Storage Materials
JF - Energy Storage Materials
ER -