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@ARTICLE{Scheepers:858358,
author = {Scheepers, Fabian and Stähler, Andrea and Stähler, Markus
and Carmo, Marcelo and Lehnert, Werner and Stolten, Detlef},
title = {{L}ayer {F}ormation from {P}olymer {C}arbon-{B}lack
{D}ispersions},
journal = {Coatings},
volume = {8},
number = {12},
issn = {2079-6412},
address = {Basel},
publisher = {MDPI},
reportid = {FZJ-2018-07245},
pages = {450 -},
year = {2018},
abstract = {It has been well-established that effects such as cracking
are observable when wet layers are dried. In particular, the
layer thickness, as well as the surface tension of the
liquid, is responsible for this behavior. The layer
formation of polymer electrolyte fuel cells and electrolyzer
electrodes, however, has not yet been analyzed in relation
to these issues, even though the effect of cracks on cell
performance and durability has been frequently discussed. In
this paper, water propanol polymer-containing carbon-black
dispersions are analyzed in situ with regard to their
composition during drying. We demonstrate that crack
behavior can be steered by slight variations in the initial
dispersion when the solvent mixture is near the dynamic
azeotropic point. This minor adjustment may strongly affect
the drying behavior, leading to either propanol or
water-enriched liquid phases at the end of the drying
process. If the evaporation of the solvent results in
propanol enrichment, the critical layer thickness at which
cracks occur will be increased by about $30\%$ due to a
decrease in the capillary pressure. Microscopic images
indicate that the crack area ratio and width depend on the
wet layer thickness and initial liquid phase composition.
These results are of much value for future electrode
fabrication, as cracks affect electrode properties.},
cin = {IEK-3},
ddc = {660},
cid = {I:(DE-Juel1)IEK-3-20101013},
pnm = {135 - Fuel Cells (POF3-135)},
pid = {G:(DE-HGF)POF3-135},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000455200300036},
doi = {10.3390/coatings8120450},
url = {https://juser.fz-juelich.de/record/858358},
}