Substrate-induced cooperative effects in water adsorption from density functional calculations

Article

关键词: INITIO MOLECULAR-DYNAMICS;    HYDROGEN-BOND NETWORKS;    AUGMENTED-WAVE METHOD;    AB-INITIO;    METAL-SURFACES;    LIQUID WATER;    CLUSTERS;    RU(0001);    SPECTROSCOPY;    DISSOCIATION;   

DOI  :  10.1103/PhysRevB.82.125432

来源: SCIE

【 摘 要 】

Density functional theory calculations are used to investigate the role of substrate-induced cooperative effects on the adsorption of water on a partially oxidized transition-metal surface, O(2x2)/Ru(0001). Focusing particularly on the dimer configuration, we analyze the different contributions to its binding energy. A significant reinforcement of the intermolecular hydrogen bond (H bond), also supported by the observed frequency shifts of the vibration modes, is attributed to the polarization of the donor molecule when bonded to the Ru atoms in the substrate. This result is further confirmed by our calculations for a water dimer interacting with a small Ru cluster, which clearly show that the observed effect does not depend critically on fine structural details and/or the presence of coadsorbates. Interestingly, the cooperative reinforcement of the H bond is suppressed when the acceptor molecule, instead of the donor, is bonded to the surface. This simple observation can be used to rationalize the relative stability of different condensed structures of water on metallic substrates.

【 授权许可】

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