Learn about our response to COVID-19, including freely available research and expanded remote access support.

Synchrotron x-ray photoelectron spectroscopy study of hydrogen-terminated 6HSiC{0001} surfaces

N. Sieber, Th. Seyller, L. Ley, D. James, J. D. Riley, R. C. G. Leckey, and M. Polcik
Phys. Rev. B 67, 205304 – Published 6 May 2003
PDFExport Citation

Abstract

We report on highly resolved core-level and valence-band photoemission spectroscopies of hydrogenated, unreconstructed 6HSiC(0001) and (0001¯) using synchrotron radiation. In the C 1s core level spectra of 6HSiC(0001¯) a chemically shifted surface component due to C-H bonds is observed at a binding energy (0.47±0.02)eV higher than that of the bulk line. The Si 2p core-level spectra of SiC(0001) suggest the presence of a surface component as well but a clear identification is hindered by a large Gaussian width, which is present in all spectra and which is consistent with values found in the literature. The effect of thermal hydrogen desorption was studied. On 6HSiC(0001) the desorption of hydrogen at 700750°C is accompanied by a simultaneous transformation to the Si-rich (3×3)R30° reconstruction. On 6HSiC(0001¯) first signs of hydrogen desorption, i.e., the formation of a dangling bond state in the fundamental band gap of SiC, are seen at temperatures around 670°C while the (1×1) periodicity is conserved. At 950°C a (3×3) reconstruction is formed. The formation of these reconstructions on thermally hydrogenated 6HSiC(0001) and (0001¯) is discussed in the light of earlier studies of 6HSiC{0001} surfaces. It will be shown that by using the hydrogenated surfaces as a starting point it is possible to gain insight into how the (3×3)R30° and (3×3) reconstructions are formed on 6HSiC(0001) and 6HSiC(0001¯), respectively. This is due to the fact that only hydrogen-terminated 6HSiC{0001} surfaces possess a surface carbon to silicon ratio of 1:1.

  • Received 31 October 2002

DOI:https://doi.org/10.1103/PhysRevB.67.205304

©2003 American Physical Society

Authors & Affiliations

N. Sieber, Th. Seyller*, and L. Ley

  • Institut für Technische Physik, Lehrstuhl für Experimentalphysik, Universität Erlangen-Nürnberg, Erwin-Rommel-Strasse 1, 91058 Erlangen, Germany

D. James, J. D. Riley, and R. C. G. Leckey

  • Department of Physics, La Trobe University, Bundoora, Victoria 3083, Australia

M. Polcik

  • Fritz-Haber-Institut, Faradayweg 4-6, 14195 Berlin, Germany

  • *Corresponding author. Email address: thomas.seyller@physik.uni-erlangen.de

References (Subscription Required)

Click to Expand
Issue

Vol. 67, Iss. 20 — 15 May 2003

Reuse & Permissions
Access Options
APS and the Physical Review Editorial Office Continue to Support Researchers

COVID-19 has impacted many institutions and organizations around the world, disrupting the progress of research. Through this difficult time APS and the Physical Review editorial office are fully equipped and actively working to support researchers by continuing to carry out all editorial and peer-review functions and publish research in the journals as well as minimizing disruption to journal access.

We appreciate your continued effort and commitment to helping advance science, and allowing us to publish the best physics journals in the world. And we hope you, and your loved ones, are staying safe and healthy.

Ways to Access APS Journal Articles Off-Campus

Many researchers now find themselves working away from their institutions and, thus, may have trouble accessing the Physical Review journals. To address this, we have been improving access via several different mechanisms. See Off-Campus Access to Physical Review for further instructions.

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
×