Wettability of Amorphous Diamond-Like Carbons Deposited on Si and PMMA in Pulse-Modulated Plasmas

被引:2
作者
Sung, Ta-Lun [1 ]
Yang, Jason Hsiao-Chun [2 ]
Teii, Kungen [2 ]
Teii, Shinriki [1 ,3 ]
Liu, Chung-Ming [1 ]
Tseng, Wan-Yu [4 ]
Lin, Li-Deh [4 ]
Ono, Shigeru [5 ]
机构
[1] Lunghwa Univ Sci & Technol, Dept Chem & Mat Engn, Tao Yuan 33306, Taiwan
[2] Kyushu Univ, Dept Appl Sci Elect & Mat, Kasuga, Fukuoka 8168580, Japan
[3] Musashi Inst Technol, Tokyo 1588557, Japan
[4] Natl Taiwan Univ, Dept Dent, Taipei 100, Taiwan
[5] Tokyo City Univ, Dept Elect & Elect Engn, Tokyo 1588557, Japan
关键词
Amorphous carbon; biomedical coating; chemical vapor deposition (CVD); diamond-like carbon (DLC); optical emission; polymethyl methacrylate (PMMA); pulse; wettability; CHEMICAL-VAPOR-DEPOSITION; C-H FILMS; BIOCOMPATIBILITY; POLYMERS;
D O I
10.1109/TPS.2012.2196057
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
Pulse-modulated direct-current methane plasmas are used to deposit amorphous diamond-like carbon films on Si and dentistry-use polymethyl methacrylate (PMMA) substrates as a function of the negative pulse voltage applied to the substrate (V-max). The films on PMMA show a transition from diamond-like to more graphitic carbon in the Raman spectra with increasing V-max, dissimilar to those on Si. This is attributed to easy deformation of PMMA, leading to the low compressive stress of the films (1 to 2 GPa). The contact angle of water for the films on both Si and PMMA is large, ranging from 79 degrees to 94 degrees almost independent of V-max, confirming that the films are hydrophobic despite the difference in carbon bonding state. The large dispersion component (41-43 mJ/m(2)) of the surface free energy of the films measured from the contact angle of water and 1-bromonaphthalene indicates the high mass density of the films. The small polar component (0.2-3.5 mJ/m(2)) is attributed to hydrogen saturation of the surface sites forming nonpolar C-H bonds and, thus, responsible for the hydrophobic behavior.
引用
收藏
页码:1837 / 1842
页数:6
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