Silatronix has developed and synthesized an entirely new class of OS molecules with superior thermal, chemical, and electrochemical properties. The leading candidate from this new class is OS3 which showcases greatly enhanced stability and performance attributes in Li-ion batteries. Specifically, OS3 provides benefits such as lower anode and cathode impedance and reduced gas generation in multiple Li-ion chemistries.
The role of the Li+ solvation structure in the determination of electrolyte performance, including the formation, stability, and performance of the SEI layer, has been investigated using multiple analytical techniques. These techniques include FTIR spectroscopy, Raman spectroscopy4, NMR spectroscopy3, and electrospray ionization mass spectrometry (ESI-MS)5.
In this work, we focus on understanding the unique role that OS3 plays in the Li+ solvation sheath with NMR spectroscopy using multiple nuclei to simultaneously probe the anion, cation, and solvent environments. Data collected for electrolytes containing solvents with a variety of functional groups finds that the NMR response to Li+ coordination is identical for multiple solvents with the same coordinating functionality (e.g., carbonate, nitrile, etc). Therefore, the solvation behavior of multiple solvents in complex electrolytes can be deconvoluted and individually understood. The strong participation of OS solvents in the Li+ solvation sheath, including the displacement of strong carbonate solvents such as EC. has been demonstrated in multiple electrolytes using NMR spectroscopy and ESI-MS.
*RJH and RW have a financial interest in the outcome of this work.
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