Mechanism of enhanced wettability of nanocrystalline diamond films by plasma treatment

被引:19
|
作者
Yang, J. H. C. [1 ]
Teii, K. [1 ]
机构
[1] Kyushu Univ, Interdisciplinary Grad Sch Engn Sci, Dept Appl Sci Elect & Mat, Kasuga, Fukuoka 8168580, Japan
基金
日本学术振兴会;
关键词
Nanocrystalline diamond; Nanodiamond; Diamond-like carbon; Wettability; Surface free energy; Contact angle; Oxygen; Biomedical coating; DOPED ULTRANANOCRYSTALLINE DIAMOND; CHEMICAL-VAPOR-DEPOSITION; SURFACE FREE-ENERGY; AMORPHOUS-CARBON; GRAPHITE; XPS;
D O I
10.1016/j.tsf.2012.06.041
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The mechanism of wetting behavior of nanocrystalline diamond films is examined in terms of surface free energy, morphology, and bonding characteristics. The films are prepared by microwave plasma-enhanced chemical vapor deposition using Ar-rich/N-2/CH4 and Ar-rich/H-2/CH4 mixtures, followed by microwave hydrogen and oxygen plasma exposures separately. Contact angle measurement with water, ethylene glycol, and formamide reveals that both the as-deposited and hydrogen plasma treated films are hydrophobic, while the oxygen plasma treated film is extremely hydrophilic such that the contact angle is reduced down to almost zero degree. Fourier transform infrared spectroscopy reveals that the hydrogen atoms are dominantly bonded to diamond and amorphous sp(3)-bonded carbon, and they are removed by the oxygen plasma treatment. For the oxygen plasma treated film, the mean value of oxygen concentration for the top surface to bulk (similar to 1 mu m) measured by energy-dispersive X-ray spectroscopy is similar to 10 at.%, while that for the top several monolayers surface measured by X-ray photoelectron spectroscopy is much higher at similar to 37 at.%, indicating a higher degree of oxidation toward the surface. The carbon bonding state in the oxidized layer is disordered by incorporation of a large amount of oxygen in form of polar C-O bonds, which is accountable for a greater polar component of the apparent surface free energy and stronger dipole-dipole interactions. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:6566 / 6570
页数:5
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