Natural and actual valence-band discontinuities in the a-Si/a-Si1xCx:H system: A photoemission study

R.-C. Fang and L. Ley
Phys. Rev. B 40, 3818 – Published 15 August 1989
PDFExport Citation

Abstract

We have measured core-level and valence-band spectra of a-Si1xCx and a-Si1xCx:H (0≤x≤1), alloys of 2H-SiC, and of the a-Si/a-Si1xCx and a-Si/a-Si1xCx:H interfaces. From these measurements we determine the valence-band offsets at the interface ΔEv, the overlayer-induced band bending, and the ‘‘natural’’ band discontinuities ΔEv0. The latter quantity is defined as the difference in the valence-band maximum of a-Si and a-Si1xCx:H when both are referred to the chemically unshifted Si 2p core-level component. It is found that ΔEv0 agrees with ΔEv for x<0.5 both for the hydrogenated and for dehydrogenated (annealed at 650°) alloy interfaces. In this range ΔEv is rather insensitive to x and amounts to 0.8 (with H) and 0.3 eV (without H), respectively. Above x=0.5, ΔEv rises in both cases linearly with x and reaches values of 2.0 (with H) and 1.5 eV (without H), respectively. These values are smaller than expected for the ‘‘natural’’ offsets and the differences can be accounted for by invoking an interface dipole density of 3.4×1014 eÅ/cm2 or a charge transfer of about 0.01 electrons per atom pair across the interface from silicon to the more electronegative Si1xCx or Si1xCx:H.

  • Received 3 April 1989

DOI:https://doi.org/10.1103/PhysRevB.40.3818

©1989 American Physical Society

Authors & Affiliations

R.-C. Fang and L. Ley

  • Max-Planck-Institut für Festkörperforschung, Heisenbergstrasse 1, Postfach 80 06 65, D-7000 Stuttgart 80, Federal Republic of Germany

References (Subscription Required)

Click to Expand
Issue

Vol. 40, Iss. 6 — 15 August 1989

Reuse & Permissions
Access Options
Author publication services for translation and copyediting assistance advertisement

Authorization Required


×
×

Images

×

Sign up to receive regular email alerts from Physical Review B

Log In

Cancel
×

Search


Article Lookup

Paste a citation or DOI

Enter a citation
×