催化作用
材料科学
联想代换
化学工程
氧化还原
纳米技术
结合属性
多相催化
密度泛函理论
水煤气变换反应
饱和(图论)
化学
活化能
原位
纳米结构
纳米颗粒
作者
Huiryung Heo,Jeong-Un Jang,Jungseob So,Dong‐Yeun Koh
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-02-25
卷期号:16 (5): 5168-5183
被引量:1
标识
DOI:10.1021/acscatal.6c00375
摘要
Mixed-oxide catalysts show distinct catalytic behavior through crucial structural interactions among oxides and metals. While extensive research has focused on the individual roles of each oxide, the structural interactions in the mixed state and their role in catalytic mechanisms remain underexplored. To understand how mixed oxides alter catalytic behavior, we studied a suite of Cu-dispersed CeO 2 –Al 2 O 3 catalysts in the reverse water gas shift (RWGS) reaction. Structural analyses revealed that beyond a certain ceria loading, further addition led to negligible nanostructural ceria evolution, marking the saturation of additional CeO 2 –Al 2 O 3 interfacial structure formation and a corresponding plateau in catalytic performance. This finding indicates that catalytic activity is governed by the formation of CeO 2 –Al 2 O 3 interfaces that stabilize active Cu species rather than by the total ceria loading. While ceria is well-known for its redox activity due to oxygen-vacancy properties, this study suggests that it also promotes the associative pathway through synergistic interactions with adjacent alumina domains, offering insights into reaction pathways in mixed-oxide catalysts. Overall, this study demonstrates that the CeO 2 –Al 2 O 3 interface dictates both catalytic activity and mechanistic preference in the RWGS reaction, providing a design principle for developing interfacially engineered, mixed-oxide-supported catalysts for efficient CO 2 conversion.
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