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表面羟基化诱导的静电力使石英表面的水膜变厚。

Surface Hydroxylation-Induced Electrostatic Forces Thicken Water Films on Quartz.

作者信息

Cihan Abdullah, Zarzycki Piotr, Hao Zhao

机构信息

Energy Geosciences Division, Lawrence Berkeley National Laboratory, Berkeley, California94720,United States.

出版信息

Langmuir. 2024 Jul 23;40(29):15099-15106. doi: 10.1021/acs.langmuir.4c01461. Epub 2024 Jul 12.

Abstract

Aqueous films on mineral surfaces control the physical, chemical, and biological transport processes in the atmosphere, soil, and rocks. Despite the importance of thin films for various research and engineering fields, there are still unanswered questions regarding the roles of the different forces affecting the nature of water films. One of these, the focus of this study, is the development of abnormally thick water films on quartz surfaces. In this study, we developed a density-functional-theory-based model to describe the time-dependent evolution of water films and identify the governing forces responsible for thickening films. We simulated the diffusion of water vapor from ambient air toward mineral surfaces and the formation and thickening of water films at various relative humidity values. Our model predicts an abnormal water film thickness on a hydroxylated quartz surface compared to a surface free of hydroxylation, which explains experimental observations. We further used the model to understand the key interaction forces at different stages of water film formation and thickening. Our model suggests that the attractive hydrogen bonding and van der Waals forces initiate a seed layer of water, and the electrostatic forces, generated by the hydroxylated and thus charged surface, lead to the thickening of water films. This generalizable model can provide insights into the peculiarities of water film development on various mineral surfaces.

摘要

矿物表面的水膜控制着大气、土壤和岩石中的物理、化学及生物传输过程。尽管薄膜在各个研究和工程领域都很重要,但关于影响水膜性质的不同作用力的作用,仍存在一些未解决的问题。其中之一,也是本研究的重点,是石英表面异常厚水膜的形成。在本研究中,我们开发了一个基于密度泛函理论的模型,以描述水膜随时间的演变,并确定导致水膜增厚的主导作用力。我们模拟了水蒸气从周围空气向矿物表面的扩散以及在不同相对湿度值下水膜的形成和增厚。我们的模型预测,与无羟基化的表面相比,羟基化石英表面的水膜厚度异常,这解释了实验观察结果。我们进一步使用该模型来理解水膜形成和增厚不同阶段的关键相互作用力。我们的模型表明,有吸引力的氢键和范德华力引发了水的种子层,而羟基化且带电的表面产生的静电力导致水膜增厚。这个可推广的模型可以深入了解各种矿物表面水膜形成的特殊性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe7a/11270996/1ef3d9c1d712/la4c01461_0001.jpg

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