Inorganic Chemistry and Catalysis Group, Debye Institute for NanoMaterials Science, Faculty of Science, Utrecht University, Universiteitsweg 99, 3584 CG Utrecht, The Netherlands.
Nat Chem. 2012 Nov;4(11):873-86. doi: 10.1038/nchem.1478. Epub 2012 Oct 23.
Recent years have witnessed the introduction of spatiotemporal spectroscopy for the characterization of catalysts at work at previously unattainable resolution and sensitivity. They have revealed that heterogeneous catalysts are more heterogeneous than often expected. Dynamic changes in the nature of active sites, such as their distribution and accessibility, occur both between and within particles. Scientists now have micro- and nanospectroscopic methods at hand to improve the understanding of catalyst heterogeneities and exploit them in catalyst design. Here we review the latest developments within this lively field. The trends include detection of single particles or molecules, super-resolution imaging, the transition from two- to three-dimensional imaging, selective staining, integration of spectroscopy with electron microscopy or scanning probe methods, and measuring under realistic reaction conditions. Such experimental approaches change the hitherto somewhat static picture of heterogeneous catalysis into one that acknowledges that catalysts behave almost like living objects--explaining why many characterization methods from the life sciences are being incorporated into catalysis research.
近年来,时空光谱学被引入到催化剂的表征中,其分辨率和灵敏度达到了前所未有的水平。研究表明,多相催化剂比人们通常预期的要更加复杂。活性位的性质(如分布和可及性)在颗粒之间和颗粒内部都发生动态变化。现在,科学家们已经掌握了微观和纳米光谱学方法,可以提高对催化剂不均匀性的理解,并在催化剂设计中加以利用。本文综述了这一活跃领域的最新进展。这些趋势包括对单个粒子或分子的检测、超分辨率成像、从二维成像到三维成像的转变、选择性染色、将光谱学与电子显微镜或扫描探针方法相结合,以及在实际反应条件下进行测量。这些实验方法将多相催化的迄今有些静态的图像转变为一种认识,即催化剂的行为几乎与活体一样——这解释了为什么许多来自生命科学的表征方法被纳入到催化研究中。