Investigating miscibility and lithium ion transport in blends of poly(ethylene oxide) with a polyanion containing precisely-spaced delocalized charges

A novel precision single-ion conductor with phenylsulfonyl(trifluoromethylsulfonyl)imide lithium salt covalently bound to every fifth carbon of a polyethylene backbone, p5PhTFSI-Li, was synthesized via ring opening metathesis polymerization (ROMP) followed by post polymerization modification. The conversion of poly(4-phenylcyclopentene), bearing 94% sulfonate anions, to trifluoromethanesulfonimide (TFSI) anions was highly efficient (similar to 90%) as determined by F-19 NMR analysis and corroborated through other spectroscopic methods. The flexible hydrocarbon backbone combined with a bulky TFSI anion led to an observable glass transition temperature of 199 degrees C even at these high levels of ionization. A high thermal stability up to 375 degrees C was also observed. Blending of p5PhTFSI-Li with poly(ethylene oxide) at various compositions was performed to investigate electrochemical performance and transference numbers with respect to the lithium electrode using a combination of impedance and polarization methods. At 90 degrees C and a 50 : 50 wt% blend composition, this system displayed the highest reported conductivity (2.00 x 10(-4) S cm(-1)) of a system with a demonstrated lithium-ion transference number near unity. Such performance is also atypical of single ion conductors produced through post-polymerization modification, which we attribute to the high yield of TFSI conversion. Investigations into the complex miscibility and phase behavior of these blends at various compositions was also probed by a combination of microscopy and differential scanning calorimetry, which is discussed with reference to computational predictions of how charge correlations affect polymer blend phase behavior.