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@ARTICLE{Wagner:875401,
author = {Wagner, Maximilian and Lorenz, Oliver and Lohmann-Richters,
Felix and Varga, Aron and Abel, Bernd},
title = {{O}n the {R}ole of {L}ocal {H}eating on {C}athode
{D}egradation during the {O}xygen {R}eduction {R}eaction in
{S}olid {A}cid {F}uel {C}ells},
journal = {Sustainable energy $\&$ fuels},
volume = {4},
number = {10},
issn = {2398-4902},
address = {Cambridge},
publisher = {Royal Society of Chemistry},
reportid = {FZJ-2020-02010},
pages = {5284-5293},
year = {2020},
abstract = {Reliable, stable, and long-term performance is one of the
most important requirements for fuel cells in general.
Widespread application of intermediate temperature solid
acid fuel cells is still hindered by relatively fast
degradation. However, durability studies are both expensive
as well as, by their nature, time consuming and therefore
rarely performed. In this study, we propose a viable method
to investigate degradation pathways on a practical time
scale. Five different types of electrodes were fabricated
with varying geometrical complexity, but all containing
platinum as the electrocatalyst. By utilizing small amounts
of well-connected platinum as electrode catalyst,
outstanding mass normalized currents were achieved resulting
in accelerated cell degradation. Clearly observable effects
on the electrodes were characterized ex situ by scanning
electron microscopy and the electrochemical activity
measured in operando by the decline of the current density
at a constant cell voltage. After electrochemical
measurement, changes of the electrodes were almost
exclusively limited to the cathode side, where the
electrolyte CsH2PO4 penetrated the previously distinct
platinum layer originating from the current collector
fibers. The observed morphological changes decreased the
number of electrocatalytically active sites by covering the
platinum layer or isolating the current collectors. These
effects correlate both with the duration of the measurement
and the current density. At different potentials, an
asymptotic behavior of the cell performance was observed,
identifying current-induced localized heating as the main
degradation mechanism. Due to the high overpotential at the
cathode, hotspots close to the current collectors could
reach sufficient temperatures during cell operation to
facilitate a morphological change of the electrolyte. This
work gives a detailed analysis of the degradation mechanism
in platinum-based solid acid fuel cell electrodes, providing
valuable information for designing stable high-performance
electrodes.},
cin = {IEK-14},
ddc = {660},
cid = {I:(DE-Juel1)IEK-14-20191129},
pnm = {135 - Fuel Cells (POF3-135)},
pid = {G:(DE-HGF)POF3-135},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000573449300036},
doi = {10.1039/D0SE00842G},
url = {https://juser.fz-juelich.de/record/875401},
}