REACTION PATHWAYS AND SOURCES OF OH GROUPS IN LOW-TEMPERATURE REMOTE PECVD SILICON DIOXIDE THIN-FILMS

被引:29
|
作者
THEIL, JA [1 ]
TSU, DV [1 ]
LUCOVSKY, G [1 ]
机构
[1] N CAROLINA STATE UNIV,DEPT MAT SCI & ENGN,RALEIGH,NC 27695
关键词
Chemical vapor deposition; dielectric thin films; OH in silica; plasma enhanced chemical vapor deposition; silicon dioxide; SiO[!sub]2[!/sub; SiO[!sub]2[!/sub] ir spectroscopy;
D O I
10.1007/BF02651747
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Silicon oxides deposited by remote plasma-enhanced chemical-vapor deposition (Remote PECVD) can be grown under conditions which produce hydrogen-free SiO2, and under conditions which promote the incorporation of bonded-hydrogen in either SiH or SiOH groups, but generally not in both. In this paper, we investigate the relationship between the deposition conditions leading to OH incorporation, and other post-deposition pathway(s) by which OH can also be incorporated. Two ways by which OH can be incorporated into the oxides are by: (i)intrinsic pathways which are associated with the heterogeneous chemical reactions responsible for film growth; and (ii)extrinsic pathways which refer to incorporation after film deposition stops. The results of our experiments to date show no evidence to support the intrinsic process; all of the infrared (ir) detectable OH is shown to derive from post-deposition or extrinsic sources. We have found two distinct post-deposition sources, one from the deposition chamber ambient during cool-down and one from atmospheric moisture. Each of these sources has a particular spectroscopic signature. We show that OH incorporated from atmospheric moisture occurs as spatially correlated near-neighbor Si-OH groups, whereas OH groups incorporated in the deposition chamber ambient are randomly distributed in the SiO2 host material. © 1990 The Mineral,Metal & Materials Society,Inc.
引用
收藏
页码:209 / 217
页数:9
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