posted on 2018-06-06, 00:00authored byJun Rao, R. Vijayaraghavan, Xiaoen Wang, Yundong Zhou, Patrick C. Howlett, Douglas R. MacFarlane, Maria Forsyth, Haijin Zhu
The
organic ionic plastic crystal (OIPC) family of electrolyte
materials has provided a universal material platform for many electrochemical
devices such as all-solid-state lithium ion batteries and medium-temperature
(T = 120∼180 °C) fuel cells. These OIPC
materials usually benefit from being compounded with various matrix
materials which not only provide mechanical support but also dramatically
affect the ion transport within the composites by forming a percolated
interfacial region and/or changing the solid-state structure and dynamics
of the bulk phase. Therefore, a fundamental understanding of the influence
of the matrix on the ion dynamics of the OIPCs is crucial. In this
work composite membranes based on protic organic ionic plastic crystal
(POIPC) 1-(N,N-dimethylammonium)-2-(ammonium)ethane
triflate ([DMEDAH2][Tf]2) and poly(vinylidene
difluoride) (PVDF) have been prepared and characterized systematically.
Particular attention has been paid to the influence of PVDF nanofibers
on the thermal properties, phase behavior, ionic conduction, and molecular
dynamics of the OIPC ions. We found that the presence of PVDF nanofibers
reduces the mobility of the OIPC molecules at the interfacial region,
while in the meantime it also dramatically changes the crystalline
structure and ion dynamics of the bulk OIPC phase. Solid-state NMR
revealed both lower mobile component content and significantly reduced
molecular dynamics in the composites. This result is highly consistent
with the DSC data which show a notably higher melting enthalpy for
the composite. Combination of DSC, solid-state NMR, and FTIR techniques
consistently explained the fundamental mechanisms of the decreased
ionic conductivity of the OIPC/PVDF composite material. Variable-temperature
synchrotron XRD results suggest that thermal history plays an important
role in modifying the POIPC crystal structure and symmetry, and the
addition of PVDF nanofibers tends to stabilize the metastable phase
of the POIPC material. This work highlights the importance of understanding
the OIPC–matrix interactions and the resultant interface when
designing future solid-state electrolytes.