2012
DOI: 10.1016/j.tsf.2012.06.041
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Mechanism of enhanced wettability of nanocrystalline diamond films by plasma treatment

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Cited by 18 publications
(11 citation statements)
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“…After 72 h, the polar component and surface free energy of 304CuSS were still 1.5 mJ m À2 and 1.3 mJ m À2 lower than those of 304SS, respectively. Thus we can draw a conclusion that the polar component was the main factor that changed within the immersion time, and the polar component of the surface of 304CuSS was lower than that of the surface of 304SS [54,55] .…”
Section: Surface Free Energymentioning
confidence: 84%
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“…After 72 h, the polar component and surface free energy of 304CuSS were still 1.5 mJ m À2 and 1.3 mJ m À2 lower than those of 304SS, respectively. Thus we can draw a conclusion that the polar component was the main factor that changed within the immersion time, and the polar component of the surface of 304CuSS was lower than that of the surface of 304SS [54,55] .…”
Section: Surface Free Energymentioning
confidence: 84%
“…It was believed [54] that the wettability of a material depended upon the surface free energy, and the increase of the polar component contributed to the increase of the wettability. The lower the polar component was, the less likely the surface to be wet-out.…”
Section: Surface Free Energymentioning
confidence: 99%
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“…7 This technique was used to investigate the interaction of the diamond surface with several small molecules. 11 This change alters the adhesion 12 and the orientation 13 of organic molecules on the diamond and the change in orientation can additionally change the positions of the molecular orbitals in the film. 8 Whether an efficient and direct charge transfer occurs depends on the alignment of the highest occupied molecular orbital and the lowest unoccupied molecular orbital of the molecules with respect to the conduction band minimum (CBM), valence band maximum (VBM) and the Fermi level of the diamond.…”
mentioning
confidence: 99%
“…The A 1 tensor is diagonal and moreover for these calculations the approximation A 1[33] = 0 can be used since A 1[33] { A 1 [11] = A 1 [22] for phthalocyanines. In a general case, the integration must include the distribution function of the molecular orientations.…”
mentioning
confidence: 99%