Ruthenium catalysts supported on TiO 2 have been shown to have competitive activity and selectivity for the methanation of CO 2 . In particular, a catalyst using pre-formed RuO 2 nanoparticles deposited on the TiO 2 support, showed competitive performances in a previous study. Here, ambient-pressure X-ray photoelectron spectroscopy was employed to determine the chemical state of this catalyst under reaction conditions. The active state of ruthenium is shown to be the metallic one. Surface adsorbates were monitored in the steady state, and CH x species were found to be favored over adsorbed carbon monoxide upon temperature increase.