The effects of Cc incorporation into ZrO2 on the catalytic performance of Cu/ZrO2 for the hydrogenation of CO were investigated. A Ce0.3Zr0.7O2 solid solution was synthesized by forced hydrolysis at low pH. After calcination at 873 K, X-ray diffraction and Raman spectroscopy characterization indicated that the Ce0.3Zr0.7O2 had a t(II) crystal structure. It was found that 1.2 wt% Cu/Ce0.3Zr0.7O2 exhibited H? The consumption peaks at low temperature (<473 K) during H-2-TPR, indicating that a significant fraction (similar to 70%) of Ce4+ is reduced to Ce3+ 1.2 wt% Cu/Ce0.3Zr0.7O2 is 2.7 times more active for methanol synthesis than 1.2 wt% Cu/m-ZrO2 at 3.0 MPa at temperatures between 473 and 523 K and exhibits a higher selectivity to methanol. In situ infrared spectroscopy shows that. analogous to Cu/m-ZrO2, the primary surface species on Cu/Ce0.3Zr0.7O2 during CO hydrogenation are formate and methoxide species. A shift in the band position of the bridged methoxide species indicated that some of these groups were bonded to both Zr4+ and Ce3+ cations. For both catalysts, the rate-limited step for methanol synthesis is the reductive elimination of methoxide species. The higher rate of methanol synthesis on Cu/Ce0.3Zr0.7O2 relative to Cu/m-ZrO2 was due primarily to a similar to 2.4 times higher apparent rate constant, k(app), for methoxide hydrogenation, which is attributed to the higher surface concentration of H atoms on the former catalyst. The increased capacity of the Ce-containing catalyst is attributed to interactions of H atoms with Ce-O pairs present at the surface of the oxide phase. (c) 2005 Elsevier Inc. All rights reserved.