Analyzing the Case for Bifunctional Catalysis

被引:62
作者
Andersen, Mie [1 ,2 ]
Medford, Andrew J. [3 ,4 ]
Norskov, Jens K. [3 ,4 ]
Reuter, Karsten [1 ,2 ,3 ,4 ]
机构
[1] Tech Univ Munich, Chair Theoret Chem, Lichtenbergstr 4, D-85747 Garching, Germany
[2] Tech Univ Munich, Catalysis Res Ctr, Lichtenbergstr 4, D-85747 Garching, Germany
[3] Stanford Univ, Dept Chem Engn, SUNCAT Ctr Interface Sci & Catalysis, Stanford, CA 94305 USA
[4] SLAC Natl Accelerator Lab, SUNCAT Ctr Interface Sci & Catalysis, 2575 Sand Hill Rd, Menlo Pk, CA 94025 USA
关键词
bifunctional catalysis; computational chemistry; diffusion; reaction mechanisms; transition metals; TRANSITION-METAL OXIDE; SCALING RELATIONS; ADSORPTION; SURFACES; SENSITIVITY; OXIDATION; SPILLOVER; EVOLUTION; DESIGN; WATER;
D O I
10.1002/anie.201601049
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Bifunctional coupling of two different catalytic site types has often been invoked to explain experimentally observed enhanced catalytic activities. We scrutinize such claims with generic scaling-relation-based microkinetic models that allow exploration of the theoretical limits for such a bifunctional gain for several model reactions. For sites at transition-metal surfaces, the universality of the scaling relations between adsorption energies largely prevents any improvements through bifunctionality. Only the consideration of systems that involve the combination of different materials, such as metal particles on oxide supports, offers hope for significant bifunctional gains.
引用
收藏
页码:5210 / 5214
页数:5
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