Hattori A, Kawahara T, Uemoto T, Suzuki F, Tada H, Ito S
Technical Research Laboratory, Kansai Research Center Nippon Sheet Glass Co., Ltd., 1, Kaidoshita, Konoike Itami, Hyogo, 664-8520, Japan
J Colloid Interface Sci. 2000 Dec 15;232(2):410-413. doi: 10.1006/jcis.2000.7166.
Wettability of sol-gel TiO(2) film surfaces has been studied by following the H(2)O contact angle (straight theta) as functions of illumination time and subsequent dark storage time. Upon illumination of the TiO(2) surface (lambda(ex)>300 nm), the value of straight theta rapidly decreased to reach approximately zero (photoprocess). When the resultant superhydrophilic sample was stored in the dark, the straight theta value increased slowly with increasing storage time (dark process). Ultrathin SiO(x) films were formed on the surface of TiO(2) by repeating chemisorption of 1,3,5,7-tetramethylcyclotetrasiloxane and its photooxidation. With increasing thickness of the SiO(x) monolayer coating, the rate for the dark process significantly decreased, while that for the photoprocess also decreased. Both X-ray photoelectron spectroscopic studies and product analyses during the photoprocess clarified that photocatalytic oxidation of organic adsorbates in air causes the superhydrophilicity of the TiO(2) surfaces. Copyright 2000 Academic Press.
通过跟踪水接触角(θ)随光照时间和随后的暗存储时间的变化,研究了溶胶 - 凝胶法制备的TiO₂薄膜表面的润湿性。在TiO₂表面光照(λ(ex)>300 nm)时,θ值迅速下降至接近零(光过程)。当所得的超亲水样品在黑暗中存储时,θ值随存储时间的增加而缓慢增加(暗过程)。通过重复1,3,5,7 - 四甲基环四硅氧烷的化学吸附及其光氧化,在TiO₂表面形成了超薄SiOₓ薄膜。随着SiOₓ单层涂层厚度的增加,暗过程的速率显著降低,而光过程的速率也降低。光电子能谱研究和光过程中的产物分析均表明,空气中有机吸附物的光催化氧化导致了TiO₂表面的超亲水性。版权所有2000年学术出版社。