Institut für Chemie und Biochemie der FU Berlin, Takustr. 3, D-14195 Berlin, Germany.
Chemphyschem. 2010 May 17;11(7):1344-63. doi: 10.1002/cphc.200900769.
The peculiar catalytic activity of Au-supported titanium dioxide surfaces in the CO oxidation reaction has been a focus of interest for more than twenty years. Herein, recent data concerning preparation and structural characterisation of planar catalyst model systems consisting of single-crystalline titania and/or gold nanoparticles deposited thereon is presented and reviewed. We first expand on the deposition and growth of TiO(2) films on selected metal host surfaces and then consider the deposition of Au nanoparticles on these surfaces, including information on their geometric and electronic structures. The second issue is the interaction of these materials with carbon monoxide (one of the essential ingredients of the CO oxidation reaction) which serves as a probe molecule and monitor of the chemical activity of the model catalyst samples. Concerted efforts relating the structural and chemical properties of the respective binary materials (titania support plus deposited gold) can help to tackle and finally resolve the still open problems concerning the high activity of Au-TiO(2) catalysts in the CO oxidation reaction.
负载金的二氧化钛表面在 CO 氧化反应中具有特殊的催化活性,这一特性引起了人们 20 多年的关注。本文介绍并综述了近年来关于由单晶二氧化钛和/或负载其上的金纳米粒子组成的平面催化剂模型系统的制备和结构特性的最新数据。我们首先扩展了在选定的金属基底表面上沉积和生长 TiO(2)薄膜的内容,然后考虑了在这些表面上沉积 Au 纳米粒子的情况,包括有关其几何和电子结构的信息。第二个问题是这些材料与一氧化碳(CO 氧化反应的基本成分之一)的相互作用,一氧化碳作为探针分子和模型催化剂样品化学活性的监测器。协调努力将相应二元材料(二氧化钛载体加上沉积的金)的结构和化学性质联系起来,有助于解决和最终解决关于 Au-TiO(2)催化剂在 CO 氧化反应中高活性的仍然存在的问题。