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@ARTICLE{Schiavone:865997,
author = {Schiavone, Maria-Maddalena and Iwase, Hiroki and Takata,
Shin-ichi and Radulescu, Aurel},
title = {{T}he {M}ultilevel {S}tructure of {S}ulfonated
{S}yndiotactic-{P}olystyrene {M}odel {P}olyelectrolyte
{M}embranes {R}esolved by {E}xtended {Q}-{R}ange {C}ontrast
{V}ariation {SANS}},
journal = {Membranes},
volume = {9},
number = {11},
issn = {2077-0375},
address = {Basel},
publisher = {MDPI},
reportid = {FZJ-2019-05257},
pages = {136 - 158},
year = {2019},
abstract = {Membranes based on sulfonated synditoactic polystyrene
(s-sPS) were thoroughly characterized by contrast variation
small-angle neutron scattering (SANS) over a wide Q-range in
dry and hydrated states. Following special sulfonation and
treatment procedures, s-sPS is an attractive material for
fuel cells and energy storage applications. The film samples
were prepared by solid-state sulfonation, resulting in
uniform sulfonation of only the amorphous phase while
preserving the crystallinity of the membrane. Fullerenes,
which improve the resistance to oxidation decomposition,
were incorporated in the membranes. The fullerenes seem to
be chiefly located in the amorphous regions of the samples,
and do not influence the formation and evolution of the
morphologies in the polymer films, as no significant
differences were observed in the SANS patterns compared to
the fullerenes-free s-sPS membranes, which were investigated
in a previous study. The use of uniaxially deformed film
samples, and neutron contrast variation allowed for the
identification and characterization of different structural
levels with sizes between nm and μm, which form and evolve
in both the dry and hydrated states. The scattering length
density of the crystalline regions was varied using the
guest exchange procedure between different toluene
isotopologues incorporated into the sPS lattice, while the
variation of the scattering properties of the hydrated
amorphous regions was achieved using different H2O/D2O
mixtures. Due to the deformation of the films, the
scattering characteristics of different structures can be
distinguished on specific detection sectors and at different
detection distances after the sample, depending on their
size and orientation.},
cin = {JCNS-FRM-II / JCNS-1},
ddc = {570},
cid = {I:(DE-Juel1)JCNS-FRM-II-20110218 /
I:(DE-Juel1)JCNS-1-20110106},
pnm = {6215 - Soft Matter, Health and Life Sciences (POF3-621) /
6G15 - FRM II / MLZ (POF3-6G15) / 6G4 - Jülich Centre for
Neutron Research (JCNS) (POF3-623)},
pid = {G:(DE-HGF)POF3-6215 / G:(DE-HGF)POF3-6G15 /
G:(DE-HGF)POF3-6G4},
experiment = {EXP:(DE-MLZ)KWS2-20140101},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:31652905},
UT = {WOS:000501625200007},
doi = {10.3390/membranes9110136},
url = {https://juser.fz-juelich.de/record/865997},
}