Theoretical analyses of chemical reactions for forming hydrocarbon-bridged SiOCH low-k Films in PECVD processes

N. Tajima, Y. Ohashi, S. Nagano, Y. Xu, S. Matsumoto, T. Kada, T. Ohno
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引用次数: 2

Abstract

The advantages of the SiOCH low-k films with hydrocarbon cross-links (hydrocarbon bridges) Si-Cn-Si have been reported recently. However, hydrocarbon cross-links are not produced so selectively by the PECVD method, since the hydrocarbon components tend to form terminal atom groups such as Si-CH3. For producing hydrocarbon cross-links effectively by the PECVD method, the polymerization reactions of SiOCH precursors in the PECVD process should be understood well. We have theoretically examined the bonding reactions of the atom groups of SiOCH compounds. By examining the reactions involving radicals and ions, it has been found that the radical species Si·, C·, and O· produce Si-O, C-Si, and O-Si bonds, respectively, while the ionic species produce Si-O bonds. These results suggest that the precursors should produce Si-Cn· radicals preferably for the effective production of the hydrocarbon cross-links.
PECVD工艺中烃类桥接SiOCH低钾膜形成化学反应的理论分析
烃类交联(烃类桥)Si-Cn-Si的SiOCH低钾膜的优点最近得到了报道。然而,PECVD方法不能选择性地产生碳氢化合物交联,因为碳氢化合物组分倾向于形成末端原子群,如Si-CH3。为了用PECVD方法有效地生产烃交联,必须了解PECVD过程中SiOCH前驱体的聚合反应。我们从理论上考察了SiOCH化合物原子基的成键反应。通过考察自由基和离子的反应,发现自由基Si·、C·和O·分别生成Si-O、C-Si和O-Si键,而离子型生成Si-O键。这些结果表明,前驱体应优先生成Si-Cn·自由基,以有效地生成烃类交联。
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