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Facet Free Selective Silicon Epitaxy by Rapid Thermal Chemical Vapor Deposition

Published online by Cambridge University Press:  10 February 2011

Katherine E. Violette
Affiliation:
Texas Instruments Incorporated, Silicon Technology Development Center, 13570 N. Central Expressway, M/S 3701, Dallas, TX 75243
Rick Wise
Affiliation:
Texas Instruments Incorporated, Silicon Technology Development Center, 13570 N. Central Expressway, M/S 3701, Dallas, TX 75243
Chih-Ping Chao
Affiliation:
Texas Instruments Incorporated, Silicon Technology Development Center, 13570 N. Central Expressway, M/S 3701, Dallas, TX 75243
Sreenath Unnikrishnan
Affiliation:
Texas Instruments Incorporated, Silicon Technology Development Center, 13570 N. Central Expressway, M/S 3701, Dallas, TX 75243
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Abstract

A facet-free, selective epitaxy process has been identified using the SiH2CI2 /HCI/H2 chemistry in a commercially available, single-wafer epitaxy reactor. The pre-epitaxy bake required a minimum of 900°C in order to obtain a clean silicon surface with reasonable throughput while preserving the integrity of the shallow trench isolation structures. The epitaxy growth rate ranged from as low as 130Å/rnin at 825°C, 10 torr to as high as 1500 Å/min at 875°C and 70 torr while the deposition rate of polysilicon on polysilicon differed significantly: at 10 torr, the epitaxy growth rate is greater by as much as 50%, and at 70 torr the polysilicon deposition rate is greater by as much as 40%. The facet suppression depended heavily on two things: the undercut beneath the polysilicon gate sidewall insulator and the process pressure. The undercut is believed to be responsible for suppressing the initial stage of facet formation, most probably by completely eliminating lateral overgrowth of the crystal. The process conditions then enable continued facet suppression perhaps by restricting the silicon surface mobility. The sidewall structure and process conditions combine to make a reliably facet-free selective epitaxy process

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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