Experimental and Theoretical Characterization of Rh Single Atoms Supported on ?-Al2O3 with Varying Hydroxyl Contents during NO Reduction CO

Oxide-supported Rh catalysts are important compo-nents of commercial three-way catalysts for pollution abatement. Despite their universal application, many mysteries remain about the active structure of Rh on oxide supports as these materials often contain a mixture of nanoparticles and single-atom Rh species on the same support, even after aging. Probe molecule Fourier transform infrared (FTIR) spectroscopy in this work shows that atomically dispersed Rh on gamma-Al2O3 prefer to strongly bind CO when exposed to NO and CO mixtures and that light-off of NO reduction occurs at temperatures similar to CO desorption, suggesting that the first and rate-determining step in NO-CO reactions may be the desorption of CO from single-atom Rh dicarbonyl complexes, Rh(CO)2. Two sets of symmetric and asymmetric stretching frequencies associated with distinct Rh(CO)2 species are observed in FTIR spectra at 2084/ 2010 and 2094/2020 cm-1. During temperature ramps, the latter pair of bands at 2094/2020 cm-1 converts to the 2084/2010 cm-1 bands at 463 K before all symmetric and asymmetric bands disappear at 573 K. Bands then appear in the range of 1975-1985 cm-1 associated with Rh monocarbonyl, Rh(CO), species upon the disappearance of the 2084/2010 cm-1 bands, suggesting that CO desorbs sequentially from Rh(CO)2 by forming Rh(CO) intermediates. Combined DFT and FTIR experiments suggest that local OH coverage on the gamma-Al2O3 surface distinguishes the two Rh(CO)2 species: the higher frequency species resides on a less hydroxylated region and migrates to a more hydroxylated region at higher temperatures, causing the CO vibrational frequency to decrease by & SIM;10 cm-1. CO desorption occurs from this Rh(CO)2 structure with high local OH coverage, consistent with the DFT predicted trend of CO binding energies. Because of the coincidence of CO desorption with the light-off of NO reduction, local support hydroxylation of atomically dispersed Rh1/gamma-Al2O3 catalysts likely affects both the Rh structure after CO desorption and the kinetics of NO reduction, studies of which are enabled by the Rh(CO)2 model developed here.