A combined experimental and computational study on the adsorption and reactions of NO on rutile TiO2.

In this work we combined computational density functional theory with experimental infrared spectroscopy to determine the adsorbate structure of NO and its reaction products N(2)O(2), N(2)O, and NO(2) on rutile TiO(2). These reactions are important for the photo-catalytic reduction of NO in exhaust gas, but yet little is known about the mechanisms or the intermediates involved. The combination of high-quality ultrahigh vacuum FTIRS data with large scale embedded cluster calculations using an accurate hybrid density functional rendered it possible to identify and assign unambiguously vibrational frequencies for nine species which are formed upon adsorption and reaction of NO on rutile TiO(2). Some of them have been observed for the first time. As a result of the quantum chemical calculations we can report for all adsorbates accurate structures and binding energies.