LiF dissolution by anion-binding-agent in LiCFx battery systems: Lower ohmic and interfacial resistance.
Journal Article
·
OSTI ID:1427209
- Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)
In this paper we will discuss our preliminary thermal and electrochemical data aimed at developing a robust nonflammable Li-CFx cell capable of wide temperature operation. To accomplish this goal, we are evaluating a thermally stable solvent comprised of an anion binding agent (ABA) and lithium fluoride (LiF), typically at a 1:1 molar ratio. In conventional carbonate based electrolytes, ABA is soluble while LiF remains insoluble. However, the neutral ABA solubilizes LiF and forms a salt complex represented as Li+(ABAF-). We are exploiting this unique feature and apply this strategy to CFx chemistry to improve cell performance, due to the CFx cell chemistry generating LiF as discharge product. Continuous solvation of the salt mixture during discharge allows for utilization of electrolytes initially containing sub stoichiometric amount of LiF. The practical benefits are reduced cell weight, mitigation of electrode fouling, and consequently better low temperature performance. Electrolytes containing dimethyl methyl phosphonate (DMMP), 1M tris(pentafluorophenyl) borane (TPFB) and varying concentrations of LiF (1M; 0.5M and 0.1M) were prepared and characterized for ionic conductivity and voltage stability. In general, ionic conductivity decreases with decreasing LiF concentration. The room temperature conductivity for the DMMP 1M TPFB:1M LiF is ~ 9mS/cm and ~3mS/cm for the 1M TPFB:0.1M LiF. Unlike the conductivity, the electrochemical voltage stability did not vary substantially with LiF concentration and the electrolytes showed a stable voltage window in the range 0-3.5V vs. Li+/Li, which is substantially wider than the Li-CFx cell voltage. Flammability measurement performed at our thermal abuse facility demonstrated that the electrolyte was nonflammable. Discharge performance of CFx materials obtained from several vendors was evaluated in 2032 coin cells at room temperature. Experimental results demonstrate a reduction in ohmic resistance and interfacial resistance during discharge for a cell containing lower concentrations of added LiF compared to ABA. These observations are a direct demonstration that the unbound ABA in the electrolyte dissolves the LiF generated in the discharge reaction.
- Research Organization:
- Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)
- Sponsoring Organization:
- USDOE National Nuclear Security Administration (NNSA)
- DOE Contract Number:
- AC04-94AL85000
- OSTI ID:
- 1427209
- Report Number(s):
- SAND--2015-0872J; 565599
- Country of Publication:
- United States
- Language:
- English
Similar Records
Comparative studies of the electrochemical and thermal stability of two types of composite lithium battery electrolytes using boron-based anion receptors
Pushing the Theoretical Limit of Li-CFx Batteries: A Tale of Bi-functional Electrolyte
Comparative Studies of the Electrochemical and Thermal Stability of Composite Electrolytes for Lithium Battery Using Two Types of Boron-Based Anion Receptors
Journal Article
·
Fri Oct 01 00:00:00 EDT 1999
· Journal of the Electrochemical Society
·
OSTI ID:20001078
Pushing the Theoretical Limit of Li-CFx Batteries: A Tale of Bi-functional Electrolyte
Journal Article
·
Tue Dec 31 23:00:00 EST 2013
· Journal of the American Chemical Society
·
OSTI ID:1134170
Comparative Studies of the Electrochemical and Thermal Stability of Composite Electrolytes for Lithium Battery Using Two Types of Boron-Based Anion Receptors
Conference
·
Sun Oct 17 00:00:00 EDT 1999
·
OSTI ID:770777