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不同长度和时间尺度下催化固体中空间异质性的化学成像。

Chemical imaging of spatial heterogeneities in catalytic solids at different length and time scales.

作者信息

Weckhuysen Bert M

机构信息

Inorganic Chemistry and Catalysis group Debye Institute for Nanomaterials Science, Utrecht University, Sorbonnelaan 16, 3584 CA Utrecht, The Netherlands.

出版信息

Angew Chem Int Ed Engl. 2009;48(27):4910-43. doi: 10.1002/anie.200900339.

Abstract

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 (microm to mm), catalyst grains (nm to microm), and active sites and metal (oxide) particles (A 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.

摘要

了解多相催化剂中的时空梯度对于合理设计新型且更具可持续性的催化过程至关重要。导致空间和时间依赖性现象的非均质性在不同长度尺度上出现;也就是说,在催化反应器(毫米到米)、催化剂体(微米到毫米)、催化剂颗粒(纳米到微米)以及活性位点和金属(氧化物)颗粒(埃到纳米)的层面上。本综述记录了用于在这四个长度尺度上对催化过程中的空间非均质性进行成像的空间和时间分辨光谱方法的最新进展。将特别强调磁共振、光学和基于同步加速器的方法的使用,它们在提供空间分辨率(一维和二维成像)和深度剖析(三维成像)方面的能力,以及它们的时间分辨应用、单分子和纳米颗粒检测的潜力以及在反应条件下使用的情况。综述最后展望了催化活性的光谱标记、无标记光谱、纳米尺度断层扫描以及相关微观方法的未来前景。

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