Abstract
We have measured the effect of added salt on the chain dimensions of mixtures of poly(ethylene oxide) (PEO) and lithium bis(trifluoromethanesulfonyl)imide salt (LiTFSI) in the melt state through small-angle neutron scattering (SANS) experiments. Scattering profiles from blends of hydrogenated and deuterated PEO mixed with LiTFSI were measured as a function of salt concentration. Scattering profiles from pure deuterated PEO/LiTFSI mixtures were used for background-subtraction purposes. The densities of PEO/LiTFSI mixtures of varying salt concentrations were measured to calculate partial molar monomer volumes of PEO and LiTFSI to account for nonideal mixing. Kratky plots of the scattering profiles were used to calculate the salt concentration dependence of statistical segment length. At low salt concentrations, segment length decreases with increasing salt concentration, before increasing with increasing salt concentration in the high salt concentration regime. The random phase approximation was used to predict theoretical scattering profiles from the calculated segment lengths and partial molar volumes; there is excellent agreement between the theoretical and measured scattering profiles at all salt concentrations. There appears to be a correlation between chain dimensions and coordination between lithium ions and EO monomers. The scattering profiles of the pure deuterated PEO/LiTFSI mixtures suggested the presence of ion clusters of characteristic size of 0.6 nm at high salt concentrations.
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