石英晶体微天平
涂层
化学工程
图层(电子)
吸附
钛
动力学
聚合
材料科学
逐层
沉积(地质)
化学
有机化学
聚合物
复合材料
古生物学
物理
量子力学
沉积物
工程类
生物
作者
Sebastian Geißler,Alejandro Barrantes,Pentti Tengvall,Phillip B. Messersmith,Hanna Tiainen
出处
期刊:Langmuir
[American Chemical Society]
日期:2016-07-25
卷期号:32 (32): 8050-8060
被引量:83
标识
DOI:10.1021/acs.langmuir.6b01959
摘要
Polyphenols can form functional coatings on a variety of different materials through auto-oxidative surface polymerization in a manner similar to polydopamine coatings. However, the mechanisms behind the coating deposition are poorly understood. We report the coating deposition kinetics of the polyphenol tannic acid (TA) and the simple phenolic compound pyrogallol (PG) on titanium surfaces. The coating deposition was followed in real time over a period of 24 h using a quartz crystal microbalance with dissipation monitoring (QCM-D). TA coatings revealed a multiphasic layer formation: the deposition of an initial rigid layer was followed by the buildup of an increasingly dissipative layer, before mass adsorption stopped after approximately 5 h of coating time. The PG deposition was biphasic, starting with the adsorption of a nonrigid viscoelastic layer which was followed by layer stiffening upon further mass adsorption. Coating evaluation by ellipsometry and AFM confirmed the deposition kinetics determined by QCM-D and revealed maximum coating thicknesses of approximately 50 and 75 nm for TA and PG, respectively. Chemical characterization of the coatings and polymerized polyphenol particles indicated the involvement of both physical and chemical interactions in the auto-oxidation reactions.
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