With regard to the development of single atom catalysts
(SACs),
non-noble metal–organic layers combine a large functional variability
with cost efficiency. Here, we characterize reacted layers of melamine
and melem molecules on a Cu(111) surface by noncontact atomic force
microscopy (nc-AFM), X-ray photoelectron spectroscopy (XPS) and ab
initio simulations. Upon deposition on the substrate and subsequent
heat treatments in ultrahigh vacuum (UHV), these precursors undergo
a stepwise dehydrogenation. After full dehydrogenation of the amino
groups, the molecular units lie flat and are strongly chemisorbed
on the copper substrate. We observe a particularly extreme interaction
of the dehydrogenated nitrogen atoms with single copper atoms located
at intermolecular sites. In agreement with the nc-AFM measurements
performed with an O-terminated copper tip on these triazine- and heptazine-based
copper nitride structures, our ab initio simulations confirm a pronounced
interaction of oxygen species at these N–Cu–N sites.
To investigate the related functional properties of our samples regarding
the oxygen reduction reaction (ORR), we developed an electrochemical
setup for cyclic voltammetry experiments performed at ambient pressure
within a drop of electrolyte in a controlled O2 or N2 environment. Both copper nitride structures show a robust
activity in irreversibly catalyzing the reduction of oxygen. The activity
is assigned to the intermolecular N–Cu–N sites of the
triazine- and heptazine-based copper nitrides or corresponding oxygenated
versions (N–CuO–N, N–CuO2–N).
By combining nc-AFM characterization on the atomic scale with a direct
electrochemical proof of performance, our work provides fundamental
insights about active sites in a technologically highly relevant reaction.