Ma Yunsheng, Kobal Ivan, Matsushima Tatsuo
Catalysis Research Center, Hokkaido University, Sapporo 001-0021 Japan.
J Phys Chem B. 2005 Jan 20;109(2):689-91. doi: 10.1021/jp0448043.
The angular and velocity distributions of desorbing products were analyzed in the course of a catalyzed N2O + CO reaction on Pd(110). The reaction proceeded steadily above 450 K, and the N2 desorption merely collimated sharply along 45 degrees off the surface normal toward the [001] direction. It is proposed that this peculiar N2 desorption is induced by the decomposition of adsorbed N2O oriented along the [001] direction. On the basis of the observation of similar inclined N2 desorption in both NO + CO and N2O + CO reactions, the N2 formation via the intermediate N2Oa dissociation was confirmed in catalytic NO reduction.
在Pd(110)上催化N2O + CO反应过程中,对解吸产物的角度和速度分布进行了分析。该反应在450 K以上稳定进行,N2解吸仅沿与表面法线成45度角的方向急剧准直,朝向[001]方向。有人提出,这种特殊的N2解吸是由沿[001]方向取向的吸附N2O的分解引起的。基于在NO + CO和N2O + CO反应中都观察到类似的倾斜N2解吸,通过中间N2Oa解离形成N2在催化NO还原中得到了证实。