Author:
Mouroux A.,Zhang S.-L.,Kaplan W.,Nygren S.,Östling M.,Petersson C. S.
Abstract
AbstractThe formation of TiSi2 from deposited Ti layers on Si and the subsequent transformation of TiSi 2 from the C49 to the C54 phase have long been of concern, particular for the silicide formation on heavily doped, narrow polycrystalline Si lines. In this work, phase formation during rapid thermal annealing of Ti/Mo bilayers sequentially deposited on blanket Si wafers and on narrow polycrystalline Si lines (0.6 μm width) is studied. The Mo layer is always 0.5 nm thick, and the Ti either 45 nm or 60 nm. It is shown that the initial physical separation of Ti from Si by the interposed Mo layer leads to complete prevention of the formation of the C49 phase. Instead, a Mo-bearing silicide phase of hexagonal structure forms first, and the C54 phase nucleates and then grows on top of it via Si diffusion through the growing silicide layers. The significance of this finding is that the usual sequence for the formation of TiSi2,. e. the C49 phase forms as a result of the Ti-Si interaction and the C54 phase forms as the product of phase transformation, is altered by the interposition of a thin refractory metal layer, here Mo. The difficulties involved in nucleation and growth of the C54 phase are then overcome, yet by a different approach than the usually employed ones which rely on ion implantation to enhance the formation of the C49 phase and the subsequent transformation to the C54 phase.
Publisher
Springer Science and Business Media LLC
Reference19 articles.
1. Kinetics and Mechanism of the C49 to C54 Titanium Disilicide Polymorphic Transformation
2. Kinetics and nucleation model of the C49 to C54 phase transformation in TiSi2 thin films on deep‐sub‐micron n+ type polycrystalline silicon lines
3. A kinetic study of the C49 to C54 TiSi2conversion using electrical resistivity measurements on single narrow lines
4. 14. Standard JCPDS diffraction pattern 35–785 (face-centered orthorhombic TiSi2), JCPDSInternational Center for Diffraction Data, PDF-2 Database, 12 Campus Boulevard, Newton Square, PA 19073–3273, USA.
5. 13. Standard JCPDS diffraction pattern 6–607 (hexagonal (Ti0.4Mo0.6)Si2) and pattern 7–331 (hexagonal (Ti0.8Mo0.2)Si2), JCPDS-International Center for Diffraction Data, PDF-2 Database, 12 Campus Boulevard, Newton Square, PA 19073–3273, USA.
Cited by
13 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献