Área de investigación | Química y Ciencia y Tecnología de los Materiales |
Título | Vibrational Frequencies of Cerium-Oxide-Bound CO: A Challenge for Conventional DFT Methods |
Tipo de publicación | Artículo de revista |
Año de publicación | 2020 |
Autores | Lustemberg, PG, Plessow, PN, Wang, Y, Yang, C, Nefedov, A, Studt, F, Woell, C, M. Ganduglia-Pirovano, V |
Revista | PHYSICAL REVIEW LETTERS |
Volumen | 125 |
Número | 25 |
Type of Article | Article |
Abstract | In ceria-based catalysis, the shape of the catalyst particle, which determines the exposed crystal facets, profoundly affects its reactivity. The vibrational frequency of adsorbed carbon monoxide (CO) can be used as a sensitive probe to identify the exposed surface facets, provided reference data on well-defined single crystal surfaces together with a definitive theoretical assignment exist. We investigate the adsorption of CO on the CeO2 (110) and (111) surfaces and show that the commonly applied DFT(PBE) + U method does not provide reliable CO vibrational frequencies by comparing with state-of-the-art infrared spectroscopy experiments for monocrystalline CeO2 surfaces. Good agreement requires the hybrid DFT approach with the HSE06 functional. The failure of conventional density-functional theory (DFT) is explained in terms of its inability to accurately describe the facet- and configuration-specific donation and backdonation effects that control the changes in the C-O bond length upon CO adsorption and the CO force constant. Our findings thus provide a theoretical basis for the detailed interpretation of experiments and open up the path to characterize more complex scenarios, including oxygen vacancies and metal adatoms. |
DOI | 10.1103/PhysRevLett.125.256101 |