Ion energy dependence of film properties for diamond-like carbon prepared with plasma-assisted deposition

2001 ◽  
Vol 16 (11) ◽  
pp. 3034-3037 ◽  
Author(s):  
Cao Zexian

Hydrogen-free diamondlike carbon films were prepared on Si(100) with electron cyclotron wave-resonance plasma, which serves to sputter the graphite target and to simultaneously bombard the growing surface. Direct penetration of postionized carbon atoms (up to 140 eV) in addition to the momentum transfer from Ar plasma facilities the formation of the Ta–C structure. Surface morphology, mechanical, and optical properties of the deposits were examined with respect to the ion energy. Atomic force microscope images revealed island morphology in deposits with a typical root-mean-square roughness of 20 nm. A maximum content of about 70% for the fourfold-bonded structure was estimated from the Raman profiles, giving rise to a micro hardness of 60 ± 5 GPa.

1997 ◽  
Vol 498 ◽  
Author(s):  
N. A. Morrison ◽  
S. Muhl ◽  
S. E. Rodil ◽  
W. I. Milne ◽  
J. Robertson ◽  
...  

ABSTRACTA compact electron cyclotron wave resonance (ECWR) source has been developed for the high rate deposition of hydrogenated tetrahedral amorphous carbon (ta-C:H). The ECWR provides growth rates of up to 900 A/mm and an independent control of the deposition rate and ion energy. The ta-C:H was deposited using acetylene as the source gas and was characterized in terms of its bonding, stress and friction coefficient. The results indicated that the ta-C:H produced using this source fulfills the necessary requirements for applications requiring enhanced tribological performance.


1989 ◽  
Vol 162 ◽  
Author(s):  
P. W. Pastel ◽  
W. J. Varhue

ABSTRACTDiamond-like carbon films have been deposited with a low temperature 2.45 GHz electron cyclotron resonance plasma enhanced chemical vapor deposition system. The bombarding ion energy was independently controlled with a RF bias to the substrate. The production rate of reactant species and the impinging ion energy are decoupled with this system. The optical band gap decreased from 2.7 to 1.2 eV as substrate bias was increased from 0 to -140 V.


1999 ◽  
Vol 337 (1-2) ◽  
pp. 71-73 ◽  
Author(s):  
N.A. Morrison ◽  
S.E. Rodil ◽  
A.C. Ferrari ◽  
J. Robertson ◽  
W.I. Milne

1996 ◽  
Vol 118 (2) ◽  
pp. 431-438 ◽  
Author(s):  
B. Wei ◽  
K. Komvopoulos

An experimental investigation of the surface topography, nanoindentation hardness, and nanowear characteristics of carbon thin films was conducted using atomic force and point contact microscopy. Hydrogenated carbon films of thickness 5, 10, and 25 nm were synthesized using a sputtering technique. Atomic force microscopy images obtained with silicon nitride tips of nominal radius less than 20 nm demonstrated that the carbon films possessed very similar surface topographies and root-mean-square roughness values in the range of 0.7–1.1 nm. Nanoindentation and nanowear experiments performed with diamond tips of radius equal to about 20 nm revealed a significant enhancement of the hardness and wear resistance with increasing film thickness. High-resolution surface imaging indicated that plastic flow was the dominant deformation process in the nanoindentation experiments. The carbon wear behavior was strongly influenced by variations in the film thickness, normal load, and number of scanning cycles. For a given film thickness, increasing the load caused the transition from an atomic-scale wear process, characterized by asperity deformation and fracture, to severe wear consisting of plowing and cutting of the carbon films. Both the critical load and scanning time for severe wear increased with film thickness. Below the critical load, the wear rate decreased with further scanning and the amount of material worn off was negligibly small, while above the critical load the wear rate increased significantly resulting in the rapid removal of carbon. The observed behavior and trends are in good qualitative agreement with the results of other experimental and contact mechanics studies.


2012 ◽  
Vol 112 (9) ◽  
pp. 093305 ◽  
Author(s):  
Vitezslav Stranak ◽  
Ann-Pierra Herrendorf ◽  
Steffen Drache ◽  
Martin Cada ◽  
Zdenek Hubicka ◽  
...  

1995 ◽  
Vol 117 (4) ◽  
pp. 594-601 ◽  
Author(s):  
B. Wei ◽  
K. Komvopoulos

An experimental investigation of the surface topography, nanoindentation hardness, and nanowear characteristics of carbon thin films was conducted using atomic force and point contact microscopy. Hydrogenated carbon films of thickness 5, 10, and 25 nm were synthesized using a sputtering technique. Atomic force microscopy images obtained with silicon nitride tips of nominal radius less than 20 nm demonstrated that the carbon films possessed very similar surface topographies and root-mean-square roughness values in the range of 0.7–1.1 nm. Nanoindentation and nanowear experiments performed with diamond tips of radius equal to about 20 nm revealed a significant enhancement of the hardness and wear resistance with increasing film thickness. High-resolution surface imaging indicated that plastic flow was the dominant deformation process in the nanoindentation experiments. The carbon wear behavior was strongly influenced by variations in the film thickness, normal load, and number of scanning cycles. For a given film thickness, increasing the load caused the transition from an atomic-scale wear process, characterized by asperity deformation and fracture, to severe wear consisting of plowing and cutting of the carbon films. Both the critical load and scanning time for severe wear increased with film thickness. Below the critical load, the wear rate decreased with further scanning and the amount of material worn off was negligibly small, while above the critical load the wear rate increased significantly resulting in the rapid removal of carbon. The observed behavior and trends are in good qualitative agreement with the results of other experimental and contact mechanics studies.


2000 ◽  
Vol 9 (3-6) ◽  
pp. 524-529 ◽  
Author(s):  
S. Rodil ◽  
N.A. Morrison ◽  
W.I. Milne ◽  
J. Robertson ◽  
V. Stolojan ◽  
...  

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