Effective and Highly Selective CO Generation from CO2 Using a Polycrystalline α-Mo2C Catalyst

Present experiments show that synthesized polycrystalline hexagonal alpha-Mo2C is a highly efficient and selective catalyst for CO2 uptake and conversion to CO through the reverse water gas shift reaction. The CO2 conversion is similar to 16% at 673 K, with selectivity toward CO > 99%. CO2 and CO adsorption is monitored by DRIFTS, TPD, and microcalorimetry, and a series of DFT based calculations including the contribution of dispersion terms. The DFT calculations on most stable model surfaces allow for identifying numerous binding sites present on the catalyst surface, leading to a high complexity in measured and interpreted IR-and TPD-spectra. The computational results also explain ambient temperature CO2 dissociation toward CO as resulting from the presence of surface facets such as Mo2C(201)-Mo/C-displaying Mo and C surface atoms and Mo-terminated Mo2C(001)Mo. An ab initio thermodynamics consideration of reaction conditions, however, demonstrates that these facets bind CO2 and CO + O intermediates too strongly for a subsequent removal, whereas the Mo2C(101)-Mo/C exhibits balanced binding properties, serving as a possible explanation of the observed reactivity. In summary, results show that polycrystalline alpha-Mo2C is an economically viable, highly efficient, and selective catalyst for CO generation using CO2 as a feedstock.