2009
DOI: 10.1016/j.apsusc.2008.10.040
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The effect of hydrogen peroxide on polishing removal rate in CMP with various abrasives

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Cited by 50 publications
(28 citation statements)
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“…4 and support the identification of the broad peak centered at ϳ300 nm with Ce 3+ and that at ϳ270 nm peak with Ce 4+ . Hence, the inescapable conclusion is that Ce 3+ adsorbs and binds to silica surfaces, 13,22,24 consistent with the role of Ce 3+ species that was proposed by Kelsall, 4 Wang et al, 6 and Manivannan and Ramanathan, 25 and there is no such interaction between Ce 4+ and silica surfaces.…”
Section: Absorbance (A U)mentioning
confidence: 65%
“…4 and support the identification of the broad peak centered at ϳ300 nm with Ce 3+ and that at ϳ270 nm peak with Ce 4+ . Hence, the inescapable conclusion is that Ce 3+ adsorbs and binds to silica surfaces, 13,22,24 consistent with the role of Ce 3+ species that was proposed by Kelsall, 4 Wang et al, 6 and Manivannan and Ramanathan, 25 and there is no such interaction between Ce 4+ and silica surfaces.…”
Section: Absorbance (A U)mentioning
confidence: 65%
“…These results are in accordance with earlier data [4][5][6][7] and support the more complicated nitride polishing mechanism in which the nitride is hydrolyzed to suboxide and then this suboxide is removed during polishing. 11,12 Additional factors such as H-bonding, hydrophobic/ hydrophilic interaction, basicity, and site blocking can also affect the polishing process. [5][6][7] Perhaps this explains why a simple correlation between the structure and even the COF value on one hand and the RR on the other is not as good as that for the oxide removal.…”
Section: Resultsmentioning
confidence: 99%
“…In this pH range, the oxide and nitride RRs decreased with an increase in DOC. In another report, Manivannan and Ramanathan 77 showed that the addition of H 2 O 2 to ceria slurries caused a drastic reduction in oxide and nitride RRs in the pH range of 7-10. Both these sets of results could be explained if Ce 3+ is the active site, which would be converted to Ce 4+ (assumed to be less active) at higher DOC or by the addition of H 2 O 2 .…”
Section: Ecs Journal Of Solid State Science and Technology 4 (11) P5mentioning
confidence: 99%