TY - JOUR
T1 - Detailed in-situ monitoring of film growth
T2 - application to TiSi2 chemical vapor deposition
AU - Mendicino, M. A.
AU - Seebauer, E. G.
N1 - Funding Information:
This research was supported by a National Science Foundation Presidential Young Investi- gator Award No. CTS 88-57037 and by Semiconductor Research Corporation under contract No. 92-SJ-190. We acknowledge a Hauser Undergraduate Scholarship for B. Sutanto, and X-ray diffraction measurements by Professor Les Allen.
PY - 1993/12
Y1 - 1993/12
N2 - An experimental approach for monitoring chemical vapor deposition is described that combines in-situ, real-time monitoring of deposition rate and gas composition together with transfer capabilities into ultrahigh vacuum for Auger analysis. This approach has been applied in the specific case of TiSi2 low-pressure deposition on Si using TiCl4 and SiH4. In the early stages of growth, Si for the growing film is supplied directly from the substrate. In later stages, Si arrives through SiH4 adsorption. The primary gas phase reaction products are H2, HCl, SiH3Cl and the radical species SiCl2. Removing surface contamination from the substrate is not sufficient to promote film nucleation; surface defects are apparently required as well. Steady-state multiplicity in the reaction rate is observed near 700°C for large SiH4:TiCl4 ratios.
AB - An experimental approach for monitoring chemical vapor deposition is described that combines in-situ, real-time monitoring of deposition rate and gas composition together with transfer capabilities into ultrahigh vacuum for Auger analysis. This approach has been applied in the specific case of TiSi2 low-pressure deposition on Si using TiCl4 and SiH4. In the early stages of growth, Si for the growing film is supplied directly from the substrate. In later stages, Si arrives through SiH4 adsorption. The primary gas phase reaction products are H2, HCl, SiH3Cl and the radical species SiCl2. Removing surface contamination from the substrate is not sufficient to promote film nucleation; surface defects are apparently required as well. Steady-state multiplicity in the reaction rate is observed near 700°C for large SiH4:TiCl4 ratios.
UR - http://www.scopus.com/inward/record.url?scp=0027813353&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027813353&partnerID=8YFLogxK
U2 - 10.1016/0022-0248(93)90148-P
DO - 10.1016/0022-0248(93)90148-P
M3 - Article
AN - SCOPUS:0027813353
SN - 0022-0248
VL - 134
SP - 377
EP - 385
JO - Journal of Crystal Growth
JF - Journal of Crystal Growth
IS - 3-4
ER -