Chemical Imaging of Spatial Heterogeneities in Catalytic Solids at Different Length and Time Scales

被引:285
作者
Weckhuysen, Bert M. [1 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, Inorgan Chem & Catalysis Grp, NL-3584 CA Utrecht, Netherlands
关键词
heterogeneous catalysis; in situ spectroscopy; nanoparticles; single-molecule spectroscopy; zeolites; METAL-OXIDE CATALYSTS; IN-SITU SPECTROSCOPY; MAGNETIC-RESONANCE MICROSCOPE; RAMAN SCATTERING MICROSCOPY; X-RAY SPECTROMICROSCOPY; TO-OLEFIN CONVERSION; INFRARED-SPECTROSCOPY; HIGH-THROUGHPUT; OXIDATIVE DEHYDROGENATION; FLUORESCENCE MICROSCOPY;
D O I
10.1002/anie.200900339
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Knowledge of spatiotemporal gradients in heterogeneous catalysts is of paramount importance for the rational design of new and more sustainable catalytic processes. Heterogeneities resulting in space- and time-dependent phenomena occur at different length scales; that is, at the level of catalytic reactors (mm to m), catalyst bodies (μm to mm), catalyst grains (nm to μm), and active sites and metal (oxide) particles (Å to nm). This Review documents the recent advances in the development of space- and time-resolved spectroscopic methods for imaging spatial heterogeneities within catalytic processes at these four length scales. Particular emphasis will be on the use of magnetic resonance, optical, and synchrotron-based methods, their capabilities in providing spatial resolution (1D and 2D imaging) and depth profiling (3D imaging) as well as on their time-resolved application, potential for single-molecule and nanoparticle detection, and use under reaction conditions. The Review ends with future prospects on spectroscopic markers for catalytic activity, label-free spectroscopy, tomography at the nanoscale, and correlative microscopic approaches. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:4910 / 4943
页数:34
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