Deriving the kinetic parameters for Pt-silicide formation from temperatureramped in situ ellipsometric measurements

Citation
T. Stark et al., Deriving the kinetic parameters for Pt-silicide formation from temperatureramped in situ ellipsometric measurements, THIN SOL FI, 358(1-2), 2000, pp. 73-79
Citations number
21
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
THIN SOLID FILMS
ISSN journal
00406090 → ACNP
Volume
358
Issue
1-2
Year of publication
2000
Pages
73 - 79
Database
ISI
SICI code
0040-6090(20000110)358:1-2<73:DTKPFP>2.0.ZU;2-L
Abstract
Single-wavelength ellipsometry is employed to monitor in situ the reaction of 23 nm platinum layers with Si(100) to form platinum silicides during hea ting at constant rates up to 100 K/min. A previous study showed that by the use of 'Kissinger' plots the activation energy of the intermediate silicid e phase Pt2Si and that of the final PtSi can be determined with an accuracy of 50 meV. It is the purpose of the present paper to extend the study one step further and obtain also the pre-exponential growth factor by directly modeling the evolution of the ellipsometric data as they were obtained duri ng the temperature ramp. To do so, the chemical composition of the reaction products and the thickness of the formed layers were identified at crucial stages of the reaction via RES. Additionally, the optical constants of the constituent phases Pt, Pt2Si and PtSi were calculated from spectroscopic e llipsometry measurements in the range from 1.5 to 4.5 eV. With this input i nformation the evolution of the ellipsometric angles during the reaction of Pt and Si were modeled quantitatively. The analysis yields good fits to th e data for different ramp rates with activation energies of 1.50 and 1.70 e V and reaction coefficients of 37 and 27 cm(2)/s for the Pt/Si to Pt2Si and Pt2Si to PtSi formation, respectively. A significant improvement of the fi t is obtained when the activation energies are allowed to be distributed ab out their mean value with a width of 47 meV. This distribution takes inhomo geneities in the reaction process into account and leads to a broadening of the reaction fronts. (C) 2000 Elsevier Science S.A. All rights reserved.