Title of article :
Role of polycation adsorption in poly-Si, SiO2 and Si3N4 removal during chemical mechanical polishing: Effect of polishing pad surface chemistry
Author/Authors :
Penta، نويسنده , , Naresh K. and Matovu، نويسنده , , John B. and Veera، نويسنده , , P.R. Dandu and Krishnan، نويسنده , , Sitaraman and Babu، نويسنده , , S.V.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
8
From page :
21
To page :
28
Abstract :
The dramatic differences in the effects of two different polishing pads (IC1000 and Politex) on the removal rates (RRs) of poly-Si, SiO2, and Si3N4 films during chemical mechanical polishing using aqueous abrasive-free solutions of a cationic polymer, poly(diallyldimethyl ammonium chloride) (PDADMAC), are described. For example, with a 250 ppm of aqueous PDADMAC solution, poly-Si RR is <1 nm/min with a Politex pad but is about 500 nm/min using an IC1000 pad. The difference in the RRs is attributed to differences in the strengths of PDADMAC-mediated bridging interactions between the pads and the substrates. Also, when the same 250 ppm of PDADMAC was used as an additive in either silica- or ceria-based dispersions, the RRs of both SiO2 and Si3N4 films were suppressed to less than 1 nm/min for both pads. Possible mechanisms for the observed differences in the RRs of poly-Si, SiO2, and Si3N4 on the two pads are discussed based on elemental analysis of the pads, X-ray photoelectron spectroscopy, and zeta potential measurements (of the pads in the absence and presence of PDADMAC). Also, the results of exposure to eosin Y, a dye that changes color on exposure to PDADMAC provided useful insights into the strength of the bridging attraction between the pads and PDADMAC.
Keywords :
Polishing pads , Bridging attraction , CMP , Poly-Si , PDADMAC , sio2 , Si3N4 , Eosin Y staining
Journal title :
Colloids and Surfaces A Physicochemical and Engineering Aspects
Serial Year :
2011
Journal title :
Colloids and Surfaces A Physicochemical and Engineering Aspects
Record number :
1940742
Link To Document :
بازگشت