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光致超亲水性:TiO2 表面光致接触角随时间变化的动力学研究。

Photoinduced superhydrophilicity: a kinetic study of time dependent photoinduced contact angle changes on TiO2 surfaces.

机构信息

Engineering Department, Lancaster University, Lancaster LA1 4YR, United Kingdom.

出版信息

Langmuir. 2012 Dec 21;28(51):17647-55. doi: 10.1021/la3026649. Epub 2012 Dec 10.

DOI:10.1021/la3026649
PMID:23189964
Abstract

Transparent TiO(2) thin films were prepared on quartz substrates via a reverse micelle, sol-gel, spin-coating technique. The time dependence of the TiO(2) film photoinduced superhydrophilicity (PISH) was measured by goniometric observation of the contact angle, θ, of sessile water drops at the film surfaces. In these measurements, the TiO(2) substrate was illuminated by 315 nm light and drops were sequentially applied at a range of illumination times. Using a model for the wetting of heterogeneous surfaces derived by Israelachvili and Gee, these measurements were used to calculate the time dependence of f(2), the fractional surface coverage of the TiO(2) surface by adventitious contaminating organics (Israelachvili, J. N.; Gee, M. L. Contact angles on chemically heterogeneous surfaces. Langmuir 1989, 5, 288). Extending this model to include a Langmuir-Hinshelwood based kinetic analysis of f(2) as a function of time allowed for calculation of an expected value for θ immediately prior to illumination, that is, at illumination time t = 0. Such expected values of θ at t = 0 were calculated using two possible values of θ(1), the contact angle on a pristine unilluminated homogeneous TiO(2) surface: (i) θ(1) = 4° as suggested by, inter alia, Zubkov et al. (Zubkov, T.; Stahl, D.; Thompson, T. L.; Panayotov, D.; Diwald, O.; Yates, J. T. Ultraviolet Light-Induced Hydrophilicity Effect on TiO(2)(110)(1 × 1). Dominant Role of the Photooxidation of Adsorbed Hydrocarbons Causing Wetting by Water Droplets. J. Phys. Chem. B2005, 109, 15454); and (ii) where θ(1) = 25°, as suggested by Fujishima et al., representative of a more hydrophobic homogeneous TiO(2) surface that reconstructs upon exposure to ultraband gap illumination into a hydrophilic surface where θ(1) → 0° (Fujishima, A.; Zhang, X.; Tryk, D. A. TiO(2) photocatalysis and related surface phenomena Surf. Sci. Rep.2008, 63, 515). Analysis of data from our experiments and from selected literature sources demonstrates better agreement between these calculated and experimental values of θ at t = 0 when θ(1) is taken to be 4°, implying that an uncontaminated TiO(2) surface is inherently hydrophilic. The results of this study are discussed in the context of the current debate over the origin of the photoinduced superhydrophilic effect.

摘要

通过反胶束、溶胶-凝胶、旋涂技术在石英衬底上制备了透明 TiO(2) 薄膜。通过测量水在膜表面上的静止液滴接触角 θ 的接触角,测量了 TiO(2) 薄膜光致超亲水性 (PISH) 的时间依赖性。在这些测量中,用 315nm 光照射 TiO(2) 基底,并在一系列照射时间内依次施加液滴。使用 Israelachvili 和 Gee 推导的用于描述异质表面润湿的模型,这些测量用于计算 f(2) 的时间依赖性,f(2) 是 TiO(2) 表面上偶然污染有机物的表面覆盖率分数(Israelachvili,J. N.;Gee,M. L. 化学异质表面的接触角。朗缪尔 1989, 5, 288)。将该模型扩展到包括作为时间函数的 f(2) 的 Langmuir-Hinshelwood 动力学分析,允许计算照射时间 t = 0 之前即立即照射时 θ 的预期值。在 t = 0 时,使用两个可能的 θ(1) 值计算 θ 的这种预期值,θ(1) 是原始未照射的均匀 TiO(2) 表面上的接触角:(i)θ(1) = 4°,如 Zubkov 等人建议的那样(Zubkov,T.;Stahl,D.;Thompson,T. L.;Panayotov,D.;Diwald,O.;Yates,J. T. 光氧化吸附碳导致水液滴润湿的紫外光诱导亲水性效应。J. Phys. Chem. B2005, 109, 15454);和 (ii)θ(1) = 25°,如 Fujishima 等人建议的那样,代表暴露于超带隙照射下会重构为亲水表面的更疏水的均匀 TiO(2) 表面,其中 θ(1)→0°(Fujishima,A.;Zhang,X.;Tryk,D. A. TiO(2) 光催化及相关表面现象 Surf. Sci. Rep.2008, 63, 515)。分析我们实验的数据和来自选定文献来源的数据表明,当 θ(1) 取 4°时,这些计算值与实验值之间的 θ 在 t = 0 时的吻合更好,这意味着未污染的 TiO(2) 表面本质上是亲水的。在讨论光致超亲水性效应的起源时,讨论了这项研究的结果。

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