Rodriguez J A, Ma S, Liu P, Hrbek J, Evans J, Pérez M
Chemistry Department, Brookhaven National Laboratory, Upton, NY 11973, USA.
Science. 2007 Dec 14;318(5857):1757-60. doi: 10.1126/science.1150038.
The high performance of Au-CeO2 and Au-TiO2 catalysts in the water-gas shift (WGS) reaction (H2O + CO-->H2 + CO2) relies heavily on the direct participation of the oxide in the catalytic process. Although clean Au(111) is not catalytically active for the WGS, gold surfaces that are 20 to 30% covered by ceria or titania nanoparticles have activities comparable to those of good WGS catalysts such as Cu(111) or Cu(100). In TiO(2-x)/Au(111) and CeO(2-x)/Au(111), water dissociates on O vacancies of the oxide nanoparticles, CO adsorbs on Au sites located nearby, and subsequent reaction steps take place at the metal-oxide interface. In these inverse catalysts, the moderate chemical activity of bulk gold is coupled to that of a more reactive oxide.
金-二氧化铈(Au-CeO₂)和金-二氧化钛(Au-TiO₂)催化剂在水煤气变换(WGS)反应(H₂O + CO→H₂ + CO₂)中的高性能在很大程度上依赖于氧化物在催化过程中的直接参与。尽管纯净的金(111)对WGS没有催化活性,但被二氧化铈或二氧化钛纳米颗粒覆盖20%至30%的金表面具有与良好的WGS催化剂(如铜(111)或铜(100))相当的活性。在TiO(₂₋ₓ)/Au(111)和CeO(₂₋ₓ)/Au(111)中,水在氧化物纳米颗粒的氧空位上解离,CO吸附在附近的金位点上,随后的反应步骤在金属-氧化物界面发生。在这些逆催化剂中,块状金的适度化学活性与活性更高的氧化物的化学活性相耦合。