From atomistic to collective dynamics: Bridging gaps in gas-phase electron microscopy for catalysis

被引:3
|
作者
Hansen, Thomas Willum [1 ]
Willinger, Marc [2 ]
机构
[1] Tech Univ Denmark, Natl Ctr Nano Fabricat & Characterizat, Lyngby, Denmark
[2] Tech Univ Munich, TUM Sch Nat Sci, Dept Chem, Garching, Germany
关键词
Transmission electron microscopy (TEM); Scanning electron microscopy (SEM); Catalysis; In situ; Operando; Kinetics; DENSITY-FUNCTIONAL THEORY; IN-SITU; KINETIC OSCILLATIONS; METHANOL SYNTHESIS; SELF-ORGANIZATION; NANOPARTICLES; OXIDATION; BEHAVIOR; COOXIDATION; CHEMISTRY;
D O I
10.1557/s43577-023-00596-3
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Catalysis is a highly complex phenomenon involving fundamental processes on multiple length scales. The full-scale complexity of catalysis is only poorly understood, and how atomic-scale processes influence long-range order in the materials is not well documented experimentally. The result is that we still, to a large degree, develop new catalysts on the basis of iterative trial-and-error approaches. Elucidating the link between atomic-scale structural dynamics, feedback mechanisms, and collective behavior could be the key to a deeper understanding and further optimization of catalysts and processes. From imaging of quasi-static low-energy configurations through gas-phase-induced state switching to observation of complex nonequilibrium dynamics and oscillatory behavior, electron microscopy has provided novel insights over several length and time scales and has meanwhile matured from a service tool for catalyst researchers to a driving force in catalysis research. Here, we discuss new insights provided by novel instrumentation and the extension from in situ to operando investigations, enabling the study of mechanisms and kinetics of catalytic processes.
引用
收藏
页码:842 / 851
页数:10
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