Amade R, Heitjans P, Indris S, Finger M, Haeger A, Hesse D
Institut für Physikalische Chemie und Elektrochemie, University of Hannover, Callinstrasse 3-3a, 30167 Hannover, Germany.
Phys Chem Chem Phys. 2006 Feb 14;8(6):777-82. doi: 10.1039/b514867g. Epub 2005 Dec 22.
The electrical photoconductivity and conductivity at (and near) the surface of a TiO(2) single crystal (rutile) was studied in a range of temperatures between 300 and 573 K and under different ambient gases (oxygen and nitrogen) by means of impedance spectroscopy. The long times required (many hours) to reach steady state photoconductivity can be explained by the reduction of the material upon illumination. At about 475 K a maximum is observed in the equilibrium photoconductivity and a minimum in the rate constants of the rise and decay after switching on and off, respectively, the light. After switching off the light a fast decay takes place during the first milliseconds followed by a slow exponential decay. The first one is related to recombination through defects, while the latter is due to re-oxidation processes of the material. The results are correlated with measurements of photocatalytic activity.
通过阻抗谱研究了TiO₂单晶(金红石)在300至573K温度范围内以及在不同环境气体(氧气和氮气)下表面(及近表面)的光电导率和电导率。达到稳态光电导率所需的长时间(数小时)可通过光照下材料的还原作用来解释。在约475K时,平衡光电导率出现最大值,而在分别打开和关闭光后,上升和衰减速率常数出现最小值。关闭光后,在最初的几毫秒内会发生快速衰减,随后是缓慢的指数衰减。前者与通过缺陷的复合有关,而后者是由于材料的再氧化过程。这些结果与光催化活性的测量结果相关联。