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@ARTICLE{Bhm:903986,
author = {Böhm, Daniel and Beetz, Michael and Gebauer, Christian and
Bernt, Maximilian and Schröter, Jonas and Kornherr,
Matthias and Zoller, Florian and Bein, Thomas and
Fattakhova-Rohlfing, Dina},
title = {{H}ighly conductive titania supported iridium oxide
nanoparticles with low overall iridium density as {OER}
catalyst for large-scale {PEM} electrolysis},
journal = {Applied materials today},
volume = {24},
issn = {2352-9407},
address = {Amsterdam [u.a.]},
publisher = {Elsevier},
reportid = {FZJ-2021-05556},
pages = {101134 -},
year = {2021},
abstract = {To enable future large-scale generation of hydrogen via
proton exchange membrane (PEM) electrolysis, utilization of
scarce iridium-based catalysts required for the oxygen
evolution reaction (OER) has to be significantly lowered. To
address this question, the facile synthesis of a highly
active TiO2 supported iridium oxide based OER catalyst with
reduced noble metal content and an Ir-density of the
catalyst powder as low as 0.05–0.08 gIr cm-3 is described
in this work. A high surface area corrosion-resistant
titania catalyst support homogeneously coated with a 1-2 nm
thin layer of amorphous IrOOHx is oxidized in molten NaNO3
between 350-375°C. This procedure allows for a controllable
phase transformation and crystallization to form a layer of
interconnected IrO2 nanoparticles of ≈2 nm on the surface
of the TiO2 support. The increase in crystallinity is
thereby accompanied by a significant increase in
conductivity of up to 11 S cm-1 for a 30 $wt\%$ Ir loaded
catalyst. Oxidized samples further display a significantly
increased stability with less detectable Ir dissolution
under OER conditions. With a mass-based activity of 59 A g-1
at an overpotential of 300 mV, the electrocatalytic activity
is maintained at the level of the highly active amorphous
IrOOHx phase used as precursor and outperforms it at higher
current densities through the increased conductivity. MEA
measurements with catalyst loadings of 0.2-0.3 mg cm-2
further confirm the high catalytic activity and initial
stability at industrially relevant current densities. The
introduced synthesis approach therefore shows a path for the
fabrication of novel highly active and atom-efficient oxide
supported catalysts with complex nanostructures and thin
homogenous nanoparticle coatings that allows a future
large-scale application of PEM electrolysis technology
without restrictions by the natural abundance of iridium.},
cin = {IEK-1},
cid = {I:(DE-Juel1)IEK-1-20101013},
pnm = {1231 - Electrochemistry for Hydrogen (POF4-123)},
pid = {G:(DE-HGF)POF4-1231},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000697464800001},
doi = {10.1016/j.apmt.2021.101134},
url = {https://juser.fz-juelich.de/record/903986},
}