The efficient fixation/utilization Of CO2 has been pursued by chemists for decades. In this work, the catalytic kinetics Of CO2 fixation to methanol over a binary catalyst Cu/ZrO2 is investigated by first principles kinetic Monte Carlo simulation. A Cu/ZrO2 interface model is first established and the reaction network Of CO2 hydrogenation is explored. In the Cu/ZrO2 system two reaction channels to methanol are identified (i) a reverse water-gas shift reaction Via CO2 decomposition to CO and (ii) the well-regarded mechanism via a formate intermediate. The theoretical selectivity is determined to be 85% for methanol and 15% for CO. The removal of the oxidative species is kinetically slow. As a result, 87% of the interface sites are covered by these oxidative species, which oxidize the interface Cu. We show that the binding strength of 0 atom at the interface is a critical parameter determining the activity and selectivity of the catalyst. (C) 2009 Elsevier Inc. All rights reserved.