Center for Research on Interface Structure and Phenomena, Department of Chemical Engineering, Yale University, New Haven, CT 06520-8286, USA.
Adv Mater. 2010 Jul 20;22(26-27):2854-69. doi: 10.1002/adma.200903927.
Advances in scanning probe microscopies (SPM) have allowed the mechanisms and rates of adsorption, diffusion and reactions on surfaces to be characterized by directly observing the motions of the individual atoms and molecules involved. The importance of oxides as thermal and photocatalysts, chemical sensors, and substrates for epitaxial growth has motivated dynamical SPM studies of oxide surfaces and their formation. Work on the TiO(2) (110) surface is reviewed as an example of how dynamic SPM studies have revealed unexpected interactions between adsorbates and defects that influence macroscopic reaction rates. Studies following diffusion, adsorption and phase transitions on bulk and surface oxides are also discussed. A perspective is provided on advanced SPM techniques that hold great promise for yielding new insights into the mechanisms and rates of elemental processes that take place either during oxidation or on oxide surfaces, with particular emphasis on methods that extend the time and chemical resolution of dynamical SPM measurements.
扫描探针显微镜(SPM)技术的进步使得通过直接观察相关的单个原子和分子的运动,来研究表面的吸附、扩散和反应的机制和速率成为可能。氧化物作为热催化剂和光催化剂、化学传感器以及外延生长的衬底的重要性,激发了对氧化物表面及其形成的动态 SPM 研究。本文以 TiO(2)(110)表面为例,综述了动态 SPM 研究如何揭示影响宏观反应速率的吸附物和缺陷之间的意外相互作用。本文还讨论了关于体相和表面氧化物上扩散、吸附和相变的研究。本文提供了对先进 SPM 技术的展望,这些技术有望为理解氧化或氧化物表面上元素过程的机制和速率提供新的见解,特别强调了能够提高动态 SPM 测量的时间和化学分辨率的方法。