Abstract
A series of sharp new infrared-absorption bands produced by high-energy-electron irradiation in phosphorus- and arsenic-doped float-zone-refined silicon is reported. In P-doped silicon, the dominant band is at 1150 ${\mathrm{cm}}^{\ensuremath{-}1}$, with associated weaker bands at 1310, 970, 1000, 1025, 1040, and 1450 ${\mathrm{cm}}^{\ensuremath{-}1}$. In As-doped silicon, the corresponding bands are at 1260 ${\mathrm{cm}}^{\ensuremath{-}1}$ and 1480, 1080, 1110, 1135, 1160, and 1650 ${\mathrm{cm}}^{\ensuremath{-}1}$. The spectra recover in both materials at \ensuremath{\sim}140\ifmmode^\circ\else\textdegree\fi{}C. Uniaxial-stress studies of these bands in oriented single crystals with polarized light are described. The results cannot be fit to the usual "piezospectrospic" classification of Kaplyanskii and Runciman. A model is presented which identifies the spectra as electronic transitions from the orbital singlet ground state of a single anistropic donor defect to a manifold of bound large-orbit effective-mass excited states. Extension of the Kaplyanskii classification to include the accidental degeneracy inherent in the effective-mass excited states in silicon explains the stress results. The symmetry of the defect is deduced to be monoclinic II. It is deduced that one or more group-V atoms are involved in the defect, but a microscopic identification of the defect is not possible.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.