钠钙玻璃和溶胶凝胶衍生硅酸锂薄膜在室温储存期间表面润湿性的变化

IF 2.3 4区 材料科学 Q2 MATERIALS SCIENCE, CERAMICS Journal of Sol-Gel Science and Technology Pub Date : 2024-08-31 DOI:10.1007/s10971-024-06523-5
Hiromitsu Kozuka, Yuta Miyao, Tomoaki Kato, Manato Miki
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引用次数: 0

摘要

在固体表面长时间保持水的润湿性通常很难实现。我们将钠钙玻璃板存放在装有带风扇过滤器的空气净化器的容器中,2 天后水接触角从 3°增加到 33°。在玻璃表面获得的 X 射线光电子能谱(XPS)光谱显示,碳氢化合物的数量在储存过程中有所增加,这表明碳氢化合物的吸附是储存过程中接触角增大的原因之一。接着,我们采用溶胶-凝胶法,在 Si(100)晶片上用硝酸锂-正硅酸四乙酯溶液制备了标称锂/硅摩尔比为 0.12-0.86 的硅酸锂薄膜。薄膜被储存在装有空气净化器的容器中,并测量了水接触角与储存时间的函数关系。通过对 Li/Si = 0.24 的薄膜进行 XPS 分析,发现尽管在储存期间薄膜表面的碳氢化合物数量有所增加,但 Li/Si ≥ 0.24 的薄膜在 10 天内的接触角仍低于 15°。通过场发射扫描电子显微镜(FE-SEM)和红外线(IR)吸收光谱分析,我们发现薄膜表面在储存过程中变得浑浊,这是碳酸锂沉淀的结果。我们认为,在测量接触角时,将水滴置于薄膜表面,碳酸锂沉淀上吸附的碳氢化合物可能会被冲走,这种碳氢化合物的清除可能会导致低接触角的长期存在。通过 XPS 进行的元素深度剖面分析表明,Li+ 离子在浸水过程中从薄膜中渗出,从而形成了二氧化硅薄膜。我们预计形成的二氧化硅薄膜是多孔的,因此会因毛细管效应而表现出持续的低水接触角。然而,该薄膜显示出较高的初始接触角,并在储存过程中进一步增大。折射率测量结果表明,二氧化硅薄膜出乎意料地相对致密,不具有多孔性和持续亲水性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Changes in the wettability of the surface of soda-lime glass and of sol-gel-derived lithium silicate thin films during storage at room temperature

Maintaining the water wettability for extended period is generally tough to achieve on solid surface. We stored a soda-lime glass plate in a container equipped with an air purifier with a fan filter, where the water contact angle increased from 3° to 33° in 2 days. X-ray photoelectron spectroscopic (XPS) spectra obtained on the glass surface showed that hydrocarbons increased in amount during storage, indicating their adsorption as one of the causes of the increased contact angle during storing. Next we prepared lithium silicate thin films with nominal Li/Si mole ratios of 0.12–0.86 on Si(100) wafers by sol-gel method from lithium nitrate-tetraethyl orthosilicate solutions. The films were stored in the container with the air purifier, and the water contact angle was measured as a function of storage time. The films of Li/Si ≥ 0.24 kept contact angles lower than 15° over 10 days although hydrocarbons increased in amount on the surface during storage, which was examined by XPS analysis on the film of Li/Si = 0.24. The film surface turned cloudy during storage, which we attributed to lithium carbonate precipitates by field emission scanning electron microscopy (FE-SEM) and infrared (IR) absorption spectroscopy. We thought that hydrocarbons adsorbed on lithium carbonate precipitates may be washed out when a water droplet is placed on the film surface in contact angle measurements, and that such hydrocarbon removal may lead to the long-term duration of the low contact angle. Elemental depth profile analysis by XPS showed that Li+ ions leach out from the film during soaking in water, resulting in the formation of a silica film. We expected the resulting silica film to be porous and hence to exhibit persistent low water contact angle due to capillary effect. However, the film showed higher initial contact angles, which further increased during storing. The silica film was unexpectedly relatively dense, which was revealed by refractive index measurements, not having porous nature with persistent hydrophilicity.

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来源期刊
Journal of Sol-Gel Science and Technology
Journal of Sol-Gel Science and Technology 工程技术-材料科学:硅酸盐
CiteScore
4.70
自引率
4.00%
发文量
280
审稿时长
2.1 months
期刊介绍: The primary objective of the Journal of Sol-Gel Science and Technology (JSST), the official journal of the International Sol-Gel Society, is to provide an international forum for the dissemination of scientific, technological, and general knowledge about materials processed by chemical nanotechnologies known as the "sol-gel" process. The materials of interest include gels, gel-derived glasses, ceramics in form of nano- and micro-powders, bulk, fibres, thin films and coatings as well as more recent materials such as hybrid organic-inorganic materials and composites. Such materials exhibit a wide range of optical, electronic, magnetic, chemical, environmental, and biomedical properties and functionalities. Methods for producing sol-gel-derived materials and the industrial uses of these materials are also of great interest.
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