2026-04-13T00:03:37Zhttps://recercat.cat/oai/request

oai:recercat.cat:2445/1277702025-11-19T20:34:31Zcom_2072_1057col_2072_478796col_2072_478917

00925njm 22002777a 4500 dc Piñero Vargas, Juan José author Ramírez, Pedro J. author Bromley, Stefan Thomas author Illas i Riera, Francesc author Viñes Solana, Francesc author Rodríguez, José A. author 2019-01-31T12:21:45Z 2019-11-15T06:10:18Z 2018-11-15 2019-01-31T12:21:46Z The catalyzed dissociation of molecular hydrogen on the surfaces of diverse materials is currently widely studied due to its importance in a broad range of hydrogenation reactions that convert noxious exhaust products and/or greenhouse gases into added-value greener products such as methanol. In the search for viable replacements for expensive late transition metal catalysts TiC has been increasingly investigated as a potential catalyst for H2 dissociation. Here, we report on a combination of experiments and density functional theory calculations on the well-defined TiC(001) surface revealing that multiple H and H2 species are available on this substrate, with different binding configurations and adsorption energies. Our calculations predict an initial occupancy of H atoms on surface C atom sites, which then enables the subsequent stabilization of H atoms on top of surface Ti atoms. Further H2 can be also molecularly adsorbed over Ti sites. These theoretical predictions are in full accordance with information extracted from X-ray photoemission spectroscopy and temperature-programmed desorption experiments. The experimental results show that at high coverages of hydrogen there is a reconstruction of the TiC(001) surface which facilitates the binding of the adsorbate. Hidrogenació Metalls de transició Catàlisi Química de superfícies Hydrogenation Transition metals Catalysis Surface chemistry Diversity of adsorbed hydrogen on the TiC (001) surface at high coverages