Tuning the Coordination Environment of Rh Single Atoms on Highly Dispersed Reducible Oxides for Enhanced Reverse Water–Gas Shift Performance

Controlling the dynamic mobility of catalyst surface active sites and their interactions with the surrounding environment is critical in generating active surfaces that directly influence catalytic activity and selectivity. Here, we report a strategy for tailoring the dispersion and electronic environment of single-atom Rh catalysts by decorating the alumina support with highly dispersed (HD) cerium and molybdenum oxides. The resulting catalysts exhibit markedly different behaviors in the Reverse Water–Gas Shift (RWGS) reaction. In particular, Rh/MoO x (HD)/Al 2 O 3 maintains atomically dispersed Rh even at elevated temperatures (up to 400 °C), achieving CO selectivity of up to 100% and resisting sintering via the formation of a newly developed structure featuring Rh single atoms embedded in MoO x clusters. In situ spectroscopy and microscopy analyses confirm the stabilization of Rh and the dynamic evolution of the Rh–Mo coordination under the reaction conditions. Our findings highlight the power of support modification in steering active site structure and activity, offering a pathway toward enhanced performance and tunable single-atom catalysts for CO 2 valorization.