The reduction in noble metal content for efficient oxygen evolution catalysis is a crucial aspect towards the large scale commercialisation of polymer electrolyte membrane electrolyzers. Since catalytic stability and activity are inversely related, long service lifetime still demands large amounts of low-abundant and expensive iridium. In this manuscript we elaborate on the concept of maximizing the utilisation of iridium for the oxygen evolution reaction. By combining different tin oxide based support materials with liquid atomic layer deposition of iridium oxide, new possibilities are opened up to grow thin layers of iridium oxide with tuneable noble metal amounts. In-situ, time-and potential-resolved dissolution experiments reveal how the stability of the substrate and the catalyst layer thickness directly affect the activity and stability of deposited iridium oxide. Based on our results, we elaborate on strategies how to obtain stable and active catalysts with maximized iridium utilisation for the oxygen evolution reaction and demonstrate how the activity and durability can be tailored correspondingly. Our results highlight the potential of utilizing thin noble metal films with earth abundant support materials for future catalytic applications in the energy sector.
A remarkably simple characterization of glassy carbonsupported films of graphite, graphene oxide, and chemically converted graphene using Fe(CN) 3{ 6 / Fe(CN) 4{ 6 and O 2 as redox probes3
A successful
market introduction of electrocatalytically produced
hydrogen peroxide (H2O2) requires catalysts
that are highly selective, active, and economically suitable. Here,
we present important insights into tuning the selectivity toward H2O2 and elaborate on the opportunities opened for
high catalytic performance. Especially the metal loading, the accompanied
interparticle distance, and catalyst–support interaction were
identified as key contributors for high selectivity and activity.
We focused on the design of model catalysts with different Pd loadings
and distinct interparticle distances and their dependency on the selectivity
toward H2O2. The gained understandings can be
used as guidelines for the development of highly active and selective
catalysts while simultaneously reducing the noble metal loading and
the associated costs.
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