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Waves On A Metal Surface And Quantum Corrals

Author

Listed:
  • M.F. CROMMIE

    (Department of Physics, Boston University, Boston, MA 02215, USA)

  • C.P. LUTZ

    (IBM Research Division, Almaden Research Center, 650 Harry Road, San Jose, CA 95120–6099, USA)

  • D.M. EIGLER

    (IBM Research Division, Almaden Research Center, 650 Harry Road, San Jose, CA 95120–6099, USA)

  • E.J. HELLER

    (Department of Physics and Harvard-Smithsonian Observatory, 17 Oxford Street, Harvard University, Cambridge, MA 02138, USA)

Abstract

Electrons occupying surface states on the close-packed faces of noble metals form a two-dimensional (2-d) nearly free electron gas. Because this system is accessible to the scanning tunneling microscope (STM), it provides a unique opportunity to study the local properties of low-dimensional electrons. OnCu(111)we have observed standing wave patterns in the surface local density of states due to the quantum mechanical interference of surface state electrons scattering off of step edges and adsorbates. We find that Fe adatoms strongly scatter the surface state and, as a result, are good building blocks for constructing atomic-scale barriers (“quantum corrals”) to confine the surface state electrons. The barriers are constructed by individually positioning Fe adatoms using the tip of a cold (4 K) STM. Tunneling spectroscopy performed inside of the corrals reveals discrete resonances, consistent with size quantization. A more quantitative understanding is obtained by accounting for the multiple scattering of surface state electrons with the corrals’ constituent adatoms. This scattering is characterized by a complex phase shift which can be extracted from the electronic density pattern inside a quantum corral.

Suggested Citation

  • M.F. Crommie & C.P. Lutz & D.M. Eigler & E.J. Heller, 1995. "Waves On A Metal Surface And Quantum Corrals," Surface Review and Letters (SRL), World Scientific Publishing Co. Pte. Ltd., vol. 2(01), pages 127-137.
  • Handle: RePEc:wsi:srlxxx:v:02:y:1995:i:01:n:s0218625x95000121
    DOI: 10.1142/S0218625X95000121
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