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Phys. Rev. B 78, 045303 (2008) [5 pages]

Spin-dependent processes at the crystalline Si-SiO2 interface at high magnetic fields

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D. R. McCamey1,*, G. W. Morley2, H. A. Seipel1, L. C. Brunel3, J. van Tol3, and C. Boehme1,†
1Department of Physics, University of Utah, 115 South 1400 East, Room 201, Salt Lake City, Utah 84112, USA
2London Centre for Nanotechnology and Department of Physics and Astronomy, 17-19 Gower Street, London WC1H 0AH, United Kingdom
3Center for Interdisciplinary Magnetic Resonance, National High Magnetic Field Laboratory, Florida State University, Tallahassee, Florida 32310, USA

Received 24 May 2008; published 2 July 2008

An experimental study on the nature of spin-dependent excess charge-carrier transitions at the interface between (111)-oriented phosphorous-doped ([P]≈1015 cm−3) crystalline silicon and silicon dioxide at high magnetic field (B0≈8.5 T) is presented. Electrically detected magnetic-resonance (EDMR) spectra of the hyperfine split 31P donor-electron transitions and paramagnetic interface defects were conducted at temperatures in the range of 3 K≤T≤12 K. The results at these previously unattained (for EDMR) magnetic-field strengths reveal the dominance of spin-dependent processes that differ from the previously well investigated recombination between the 31P donor and the Pb state, which dominates at low magnetic fields. While magnetic resonant current responses due to 31P and Pb states are still present, they do not correlate and only the Pb contribution can be associated with an interface process due to spin-dependent tunneling between energetically and physically adjacent Pb states. This work provides an experimental demonstration of spin-dependent tunneling between physically adjacent and identical electronic states as proposed by Kane Nature (London) 393 133 (1998)] for readout of donor qubits.

© 2008 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevB.78.045303
DOI:
10.1103/PhysRevB.78.045303
PACS:
76.30.−v, 71.55.Cn, 73.40.Qv

*dane.mccamey@physics.utah.edu

boehme@physics.utah.edu