Fluorocarbon films have low surface energy and can be used as antistiction coating for microelectromechanical systems. By using the passivation process in a deep reactive ion etcher, the fluorocarbon films can be deposited and integrated with other processes in the clean room. The properties such as wettability, surface energies, and thermal stability, have been investigated in detail. It has been found that the fluorocarbon films deposited have a static water contact angle of 109° and a surface energy around 14.5mJ∕m2, whereas as-received and as-deposited single silicon, poly silicon, and silicon nitride have a much lower water contact angle and a higher surface energy. The fluorocarbon films keep their good hydrophobicity up to 300°C, and the degradation temperature depends on the thickness of the fluorocarbon films. Decomposition happens at lower temperatures (100–300°C) even though the decomposition rate is quite slow without affecting the contact angle. The decomposition mechanism at low temperatures (less than 300°C) might be different from that at high temperatures. It has been shown that the fluorocarbon film deposited by a deep reactive ion etcher tool provides very high hydrophobicity, low surface energy, good thermal stability, and antiadhesion behavior for use in nanoimprinting lithography.Fluorocarbon films have low surface energy and can be used as antistiction coating for microelectromechanical systems. By using the passivation process in a deep reactive ion etcher, the fluorocarbon films can be deposited and integrated with other processes in the clean room. The properties such as wettability, surface energies, and thermal stability, have been investigated in detail. It has been found that the fluorocarbon films deposited have a static water contact angle of 109° and a surface energy around 14.5mJ∕m2, whereas as-received and as-deposited single silicon, poly silicon, and silicon nitride have a much lower water contact angle and a higher surface energy. The fluorocarbon films keep their good hydrophobicity up to 300°C, and the degradation temperature depends on the thickness of the fluorocarbon films. Decomposition happens at lower temperatures (100–300°C) even though the decomposition rate is quite slow without affecting the contact angle. The decomposition mechanism at low temperatures...
[1]
K. Tachibana,et al.
Characterization of porosity and dielectric constant of fluorocarbon porous films synthesized by using plasma-enhanced chemical vapor deposition and solvent process
,
2003
.
[2]
D. Kaelble,et al.
A Reinterpretation of Organic Liquid-Polytetrafluoroethylene Surface Interactions
,
1970
.
[3]
D. Nilsson,et al.
Fabrication of silicon molds for polymer optics
,
2003
.
[4]
P. Kohl,et al.
Plasma chemistry in fluorocarbon film deposition from pentafluoroethane/argon mixtures
,
1999
.
[5]
Kunihide Tachibana,et al.
Radical kinetics for polymer film deposition in fluorocarbon (C4F8, C3F6 and C5F8) plasmas
,
2000
.
[6]
K. Sasaki,et al.
Laser desorption time-of-flight mass spectrometry of fluorocarbon films synthesized by C4F8/H2 plasmas
,
2003
.
[7]
A. Adamson.
Physical chemistry of surfaces
,
1960
.
[8]
P. Favia,et al.
Morphological and structural study of plasma deposited fluorocarbon films at different thicknesses
,
2003
.
[9]
Anders Kristensen,et al.
Nanoimprint lithography in the cyclic olefin copolymer, Topas®, a highly ultraviolet-transparent and chemically resistant thermoplast
,
2004
.
[10]
M. Schmidt,et al.
A novel integrated MEMS process using fluorocarbon films deposited with a Deep Reactive Ion Etching (DRIE) tool
,
1999
.
[11]
M. Ishida,et al.
The property of plasma-polymerized fluorocarbon film in relation to CH4/C4F8 ratio and substrate temperature
,
2000
.
[12]
M. Ishida,et al.
A novel deposition technique for fluorocarbon films and its applications for bulk- and surface-micromachined devices
,
1998
.
[13]
D. K. Owens,et al.
Estimation of the surface free energy of polymers
,
1969
.
[14]
Carlos H. Mastrangelo,et al.
Elimination of post-release adhesion in microstructures using conformal fluorocarbon coatings
,
1997
.