首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Photodegradation mode of stearic acid crystal on heterogeneous anatase/amorphous titania films observed by differential interference contrast microscopy
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Photodegradation mode of stearic acid crystal on heterogeneous anatase/amorphous titania films observed by differential interference contrast microscopy

机译:差动干涉对比显微镜观察异质锐钛矿/非晶二氧化钛膜上硬脂酸晶体的光降解模式

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Reflected-light differential interference contrast microscopy was used to observe the disappearance of stearic acid crystal (B-polymorph) deposited onto a heterogeneous anatase/amorphous titania film upon ultraviolet light exposure. Microstructural studies of the films demonstrate the formation of anatase microdomains with sub-micrometric size randomly distributed throughout the amorphous surface of the film. The microscopy images reveal that the disappearance of stearic acid crystal is initiated in the immediate vicinity of these microdomains located within the crystal or close to its edges. The stearic acid disappearance proceeds via lateral growth and coalescence of pits in shape of flattened-hexagons showing a preferential orientation with respect to the stearic acid crystal symmetry. This latter fact, which is observed for the first time to the best of our knowledge, is explained by the dependence on crystallographic orientation of the progression rate of the pit edges. To justify the observed photodegradation mode, we first invoke the ultraviolet-induced formation of radical species at the anatase microdomains and their diffusion towards the pits edges. Then, the geometry and the preferential orientation of the pits are discussed in terms of anisotropy of intermolecular interactions within the crystal. These results suggest that the energy barrier seen by the radical species reaching the pit edges is correlated to the crystallographic orientation with consequences on the reaction kinetics. (C) 2016 Elsevier B.V. All rights reserved.
机译:使用反射光微分干涉对比显微镜观察紫外线照射后沉积在异质锐钛矿/非晶态二氧化钛薄膜上的硬脂酸晶体(B-多晶型物)的消失。薄膜的微结构研究表明形成了锐钛矿微区,其亚微米级尺寸随机分布在整个薄膜的非晶态表面。显微镜图像显示,硬脂酸晶体的消失始于位于晶体内或靠近其边缘的这些微区的紧邻区域。硬脂酸消失通过扁平六边形形状的凹坑的侧向生长和聚结而进行,相对于硬脂酸晶体对称性,这些凹坑显示出优先的取向。据我们所知,这是第一次被观察到的事实,这是由对凹坑边缘行进速度的晶体学取向的依赖性所解释的。为了证明观察到的光降解模式是正确的,我们首先在锐钛矿微区调用紫外光诱导的自由基种类的形成,并向凹坑边缘扩散。然后,根据晶体内分子间相互作用的各向异性讨论了凹坑的几何形状和优先取向。这些结果表明,自由基种类到达凹坑边缘所看到的能垒与晶体取向相关,从而影响反应动力学。 (C)2016 Elsevier B.V.保留所有权利。

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