催化作用
掺杂剂
化学
水煤气变换反应
离解(化学)
无机化学
化学工程
立方氧化锆
人口
氧化还原
材料科学
物理化学
兴奋剂
陶瓷
人口学
工程类
有机化学
社会学
光电子学
生物化学
作者
Miriam González‐Castaño,Svetlana Ivanova,M.Á. Centeno,Theophiles Ioanides,Harvey Arellano‐García,J.A. Odriozola
摘要
By evaluating the functional modifications induced by Zr and Fe as dopants in Pt/CeO2-MOx/Al2O3 catalysts (M = Fe and Zr), the key features for improving water gas shift (WGS) performance for these systems have been addressed. Pt/ceria intrinsic WGS activity is often related to improved H2 surface dynamics, H2O absorption, retentions and dissociation capacities which are influenced greatly by the support nature. Two metals, iron and zirconia, were chosen as ceria dopants in this work, either in separate manner or combined. Iron incorporation resulted in CO-redox properties and oxygen storage capacities (OSC) improvement but the formation of Ce-Fe solid solutions did not offer any catalytic benefit, while the Zr incorporation influenced in a great manner surface electron densities and shows higher catalytic activity. When combined both metals showed an important synergy evidenced by 30% higher CO conversions and attributed to greater surface electron densities population and therefore absorption and activity. This work demonstrates that for Pt/ceria catalysts OSC enhancement does not necessarily imply a catalytic promotion.
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