http://www.cnr.it/ontology/cnr/individuo/prodotto/ID265977
NH3-NO Coadsorption System on Pt(111). II. Intermolecular Interaction (Articolo in rivista)
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- NH3-NO Coadsorption System on Pt(111). II. Intermolecular Interaction (Articolo in rivista) (literal)
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- 2013-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/jp406069q (literal)
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Andrea Cepellotti, Angelo Peronio, Stefano Marchini, Nasiba Abdurakhmanova, Carlo Dri, Cristina Africh, Friedrich Esch, Giovanni Comelli, and Maria Peressi (2013)
NH3-NO Coadsorption System on Pt(111). II. Intermolecular Interaction
in Journal of physical chemistry. C; ACS, American chemical society, Washington, DC (Stati Uniti d'America)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Andrea Cepellotti, Angelo Peronio, Stefano Marchini, Nasiba Abdurakhmanova, Carlo Dri, Cristina Africh, Friedrich Esch, Giovanni Comelli, and Maria Peressi (literal)
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- http://pubs.acs.org/doi/abs/10.1021/jp406069q (literal)
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- Department of Physics, Università degli Studi di Trieste, via Alfonso Valerio 2, 34127 Trieste, Italy; Center of Excellence for Nanostructured Materials (CENMAT), Università degli Studi di Trieste, via Alfonso Valerio 2, 34127 Trieste, Italy; IOM-CNR Laboratorio TASC, Area Science Park, s.s. 14 km 163.5, Basovizza, 34149 Trieste, Italy; IOM-CNR DEMOCRITOS Theory@Elettra Group, Sincrotrone Trieste, Area Science Park, s.s. 14 km 163.5, Basovizza, 34149 Trieste, Italy; Consorzio Interuniversitario Nazionale per la Scienza e la Tecnologia dei Materiali (INSTM), Unità di ricerca di Trieste, piazzale Europa 1, 34128 Trieste, Italy (literal)
- Titolo
- NH3-NO Coadsorption System on Pt(111). II. Intermolecular Interaction (literal)
- Abstract
- Coadsorption of ammonia and nitric oxide on the (111) surface of platinum causes the mutual stabilization of the two adsorbed species, arranged in an ordered 2 × 2 mixed layer. Furthermore, their interaction leads also to stable, isolated triangular units, which we observe on the surface after annealing to 345 K. Having provided in the preceding article (10.1021/jp406068y) a detailed structural description of the NH3-NO mixed layer, we focus here on the stabilizing intermolecular interactions. By combining scanning tunneling microscopy (STM) experiments and density functional theory (DFT) calculations, we identify the isolated triangular units as formed by one NH3 and three NO molecules, and we characterize them in terms of structure, energetics, and charge rearrangement. Eventually, we investigate the nature of the chemical bond between the coadsorbed NH3 and NO both in the mixed layer and in the isolated triangular units, pointing out the essential role of the surface mediation in inducing attractive dipole-dipole interactions and the presence of hydrogen bonds. (literal)
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