Tailoring surface-supported water-melamine complexes by cooperative H-bonding interactions.

The water-splitting photo-catalysis by carbon nitride heterocycles has been the subject of recent theoretical investigations, revealing a proton-coupled electron transfer (PCET) reaction from the H-bonded water molecule to the CN-heterocycle. In this context, a detailed characterization of the water-catalyst binding configuration becomes mandatory in order to validate and possibly improve the theoretical modeling. To this aim, we built a well-defined surface-supported water/catalyst interface by adsorbing water under ultra-high vacuum (UHV) conditions on a monolayer of melamine grown on the Cu(111) surface. By combining X-ray photoemission (XPS) and absorption (NEXAFS) spectroscopy we observed that melamine adsorbed onto copper is strongly tilted off the surface, with one amino group dangling to the vacuum side. The binding energy (BE) of the corresponding N 1s component is significantly higher compared to other N 1s contributions and displays a clear shift to lower BE as water is adsorbed. This finding along with density functional theory (DFT) results reveals that two adjacent melamine molecules concurrently work for stabilizing the H-bonded water-catalyst complex: one melamine acting as a H-donor via the amino-N (NH⋯OHH) and another one as a H-acceptor via the triazine-N (C[double bond, length as m-dash]N⋯HOH).