Low thermal budget surface preparation for selective epitaxy a study on process robustness

Citation
Sm. Celik et Mc. Ozturk, Low thermal budget surface preparation for selective epitaxy a study on process robustness, J ELCHEM SO, 146(4), 1999, pp. 1557-1564
Citations number
31
Categorie Soggetti
Physical Chemistry/Chemical Physics","Material Science & Engineering
Journal title
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
ISSN journal
00134651 → ACNP
Volume
146
Issue
4
Year of publication
1999
Pages
1557 - 1564
Database
ISI
SICI code
0013-4651(199904)146:4<1557:LTBSPF>2.0.ZU;2-8
Abstract
The robustness of a low thermal budget surface preparation method for selec tive silicon epitaxial growth has been investigated. After the HF dip, the stability of hydrogen passivation on Si(100) in deionized water and air has been studied. No significant increase was observed in oxygen and carbon co verage for deionized water rinse times varying from 10 to 1000 a. On wafers exposed to air for up to 10,000 s, carbon coverage on Si(100) stayed at th e same level, whereas the oxygen coverage increased steadily. An in situ cl ean at 800 degrees C for 10 s reduced the interfacial oxygen below the seco ndary ion mass spectroscopy detection levels on wafers that had been contam inated by exposure to air for up to 1000 s. In situ cleaning was studied in ambients with different partial pressures of intentionally introduced oxyg en and nitrogen backgrounds. Oxygen was removed from Si(100) during the in situ clean for nitrogen partial pressures up to 1 x 10(-6) Torr. When the o xygen partial pressure is sufficiently high (1 X 10(-6) Torr), oxide remova l was not complete after in situ cleaning. There was no observable increase in the surface roughness for samples annealed in oxygen partial pressure u p to 1 x 10(-5) Ton Hydrogen passivation was removed from the substrates an d the surfaces were exposed to vacuum at room temperature for different tim es. After 10,000 a, the oxygen coverage was less than 2% of a monolayer. Th e carbon contamination on the surface was instantaneous and no additional c arbon accumulation on the surface was observed up to 10,000 s. There was no apparent increase in the defect density for these wait times. (C) 1999 The Electrochemical Society. S0013-4651(98)05-084-4. All rights reserved.