Published January 6, 2012 | Version v1
Journal article

Nuclear magnetic resonance investigation of dynamics in poly(ethylene oxide)-based lithium polyether-ester-sulfonate ionomers

  • 1. Pennsylvania State University, University Park, PA (United States)
  • 2. Pacific Northwest Lab., Richland, WA (United States). Environmental Molecular Sciences Lab.

Description

Nuclear magnetic resonance (NMR) spectroscopy has been utilized to investigate the dynamics of poly(ethylene oxide)-based lithium sulfonate ionomer samples that have low glass transition temperatures. 1H and 7Li spin-lattice relaxation times (T1) of the bulk polymer and lithium ions, respectively, were measured and analyzed in samples with a range of ion contents. The temperature dependence of T1 values along with the presence of minima in T1 as a function of temperature enabled correlation times and activation energies to be obtained for both the segmental motion of the polymer backbone and the hopping motion of lithium cations. Similar activation energies for motion of both the polymer and lithium ions in the samples with lower ion content indicate that the polymer segmental motion and lithium ion hopping motion are correlated in these samples, even though their respective correlation times differ significantly. A divergent trend is observed for correlation times and activation energies of the highest ion content sample with 100% lithium sulfonation due to the presence of ionic aggregation. Details of the polymer and cation dynamics on the nanosecond timescale are discussed and complement the findings of X-ray scattering and Quasi Elastic Neutron Scattering experiments

Availability note (English)

Available from: DOI:10.1063/1.3669449 ; DOE Accepted Manuscript full text, or the publishers Best Available Version will be available free of charge after the embargo period from OSTI using http://www.osti.gov/pages/biblio/1076446

Additional details

Publishing Information

Journal Title
Journal of Chemical Physics
Journal Volume
136
Journal Issue
1
Journal Page Range
39 p.
ISSN
0021-9606

Optional Information

Contract/Grant/Project number
FG02-07ER46409
Funding organization
USDOE Office of Science (United States)
Secondary number(s)
OSTIID--1076446