催化作用
材料科学
金属
惰性
氧化物
色散(光学)
多相催化
化学工程
反应性(心理学)
氢
过渡金属
钯
催化剂载体
程序升温还原
无机化学
纳米技术
化学
冶金
有机化学
替代医学
病理
工程类
物理
光学
医学
作者
Ja Hun Kwak,Libor Kovařík,János Szanyi
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2013-07-17
卷期号:3 (9): 2094-2100
被引量:376
摘要
Because of their heterogeneous nature, supported metal catalysts always contain metal centers in a rather broad dispersion range, and the presence of even atomically dispersed metals has been reported on oxide supports. The role of the atomically dispersed metal centers in the overall catalytic performances of these supported metal catalysts, however, has not been addressed to date. In this study, temperature programmed reaction and scanning transmission electron microscopy experiments were applied to show the fundamentally different reactivity patterns exhibited by Pd metal in atomically dispersed and traditional 3D clusters in the demanding reaction of CO2 reduction. The requirement for two different catalyst functionalities in the reduction of CO2 with hydrogen on Pd/Al2O3 and Pd/MWCNT catalysts was also substantiated. The results obtained clearly show that the oxide support material, even when it is considered inert like Al2O3, can function as a critical, active component of complex catalyst systems.
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