Boron-hydrogen complexes in crystalline silicon

C. P. Herrero, M. Stutzmann, and A. Breitschwerdt
Phys. Rev. B 43, 1555 – Published 15 January 1991
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Abstract

Boron-hydrogen complexes and the diffusion of hydrogen in boron-doped silicon are analyzed by means of Raman-scattering and infrared-reflection spectroscopies. At temperatures lower than 200 °C, the hydrogen diffusion is controlled by a trapping at the acceptor sites, which becomes negligible at higher temperatures. Changes in the zone-center optical phonon of silicon and in the vibrational local modes of boron occur after hydrogen passivation. H and B local modes are studied as a function of temperature and external uniaxial stress. The analysis of the H-vibrational modes under stress reveals a nontrigonal symmetry of B-H complexes at 100 K, and a high mobility of hydrogen in these complexes. Our results are compared with different models proposed in the literature. We find that they are compatible with a ‘‘bond-minimum’’ site for hydrogen at low temperatures; however, under stress and at high temperatures, off-bond positions of H are proposed. We also analyze the stability of the boron-hydrogen complexes, and deduce a dissociation energy of 0.6 eV.

  • Received 16 May 1990

DOI:https://doi.org/10.1103/PhysRevB.43.1555

©1991 American Physical Society

Authors & Affiliations

C. P. Herrero, M. Stutzmann, and A. Breitschwerdt

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

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Issue

Vol. 43, Iss. 2 — 15 January 1991

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