Back to Search Start Over

Au-rich filamentary behavior and associated subband gap optical absorption in hyperdoped Si

Authors :
Massachusetts Institute of Technology. Department of Physics
Mailoa, Jonathan P
Buonassisi, T.
Yang, W.
Akey, A. J.
Smillie, L. A.
Johnson, B. C.
McCallum, J. C.
Macdonald, D.
Aziz, M. J.
Williams, J. S.
Massachusetts Institute of Technology. Department of Physics
Mailoa, Jonathan P
Buonassisi, T.
Yang, W.
Akey, A. J.
Smillie, L. A.
Johnson, B. C.
McCallum, J. C.
Macdonald, D.
Aziz, M. J.
Williams, J. S.
Source :
American Physical Society
Publication Year :
2018

Abstract

Au-hyperdoped Si, synthesized by ion implantation and pulsed laser melting, is known to exhibit a strong sub-band gap photoresponse that scales monotonically with the Au concentration. However, there is thought to be a limit to this behavior since ultrahigh Au concentrations (>1×10[superscript 20] cm[superscript −3]) are expected to induce cellular breakdown during the rapid resolidification of Si, a process that is associated with significant lateral impurity precipitation. This work shows that the cellular morphology observed in Au-hyperdoped Si differs from that in conventional, steady-state cellular breakdown. In particular, Rutherford backscattering spectrometry combined with channeling and transmission electron microscopy revealed an inhomogeneous Au distribution and a subsurface network of Au-rich filaments, within which the Au impurities largely reside on substitutional positions in the crystalline Si lattice, at concentrations as high as ∼3 at. %. The measured substitutional Au dose, regardless of the presence of Au-rich filaments, correlates strongly with the sub-band gap optical absorptance. Upon subsequent thermal treatment, the supersaturated Au forms precipitates, while the Au substitutionality and the sub-band gap optical absorption both decrease. These results offer insight into a metastable filamentary regime in Au-hyperdoped Si that has important implications for Si-based infrared optoelectronics.

Details

Database :
OAIster
Journal :
American Physical Society
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1037801072
Document Type :
Electronic Resource