Solid-state NMR spectroscopy is an
important technique for probing
the structure and local dynamics of materials at the molecular level.
For example, 1H double quantum (DQ) NMR is a well-established
probe of local dynamics. Here, this concept has been extended to characterize
fluorinated ionomer materials for the first time. 19F DQ
recoupling NMR experiments are applied to investigate the site-specific
local dynamics of the polymer electrolyte material, Nafion 117, under
various conditions with respect to temperature and hydration level.
The initial rise of the normalized double quantum (nDQ) build-up curves
generated from NMR dipolar recoupling experiments is compared as a
measure of the motionally averaged 19F–19F dipolar couplings for spectroscopically resolved domains of the
polymers. Since the side-chain and backbone fluorines can be distinguished
by their chemical shifts, it was possible to demonstrate a difference
between the side-chain and backbone local dynamics profiles. The side
chain is shown to be more sensitive toward the temperature and relative
humidity (%RH) changes, and generally the side chain exhibits greater
local dynamics as compared to the hydrophobic backbone, which is consistent
with subsegmental motion known as β-relaxation. Elevated temperature
and increased relative humidity give rise to increased local dynamics,
which is reflected by the slower initial increase of the nDQ build-up
curves. This NMR technique has been validated as a comparative analysis
tool, suitable for a range of perfluorinated ionomers.