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Unveiling the pentagonal nature of perfectly aligned single-and double-strand Si nano-ribbons on Ag(110)

Author

Listed:
  • Jorge I. Cerdá

    (Instituto de Ciencia de Materiales de Madrid, ICMM-CSIC)

  • Jagoda Sławińska

    (Instituto de Ciencia de Materiales de Madrid, ICMM-CSIC)

  • Guy Le Lay

    (Aix Marseille Université, CNRS, PIIM UMR 7345)

  • Antonela C. Marele

    (Universidad Autónoma de Madrid)

  • José M. Gómez-Rodríguez

    (Universidad Autónoma de Madrid
    Condensed Matter Physics Center (IFIMAC), Universidad Autónoma de Madrid
    Instituto Nicolás Cabrera, Universidad Autónoma de Madrid)

  • María E. Dávila

    (Instituto de Ciencia de Materiales de Madrid, ICMM-CSIC)

Abstract

Carbon and silicon pentagonal low-dimensional structures attract a great interest as they may lead to new exotic phenomena such as topologically protected phases or increased spin–orbit effects. However, no pure pentagonal phase has yet been realized for any of them. Here we unveil through extensive density functional theory calculations and scanning tunnelling microscope simulations, confronted to key experimental facts, the hidden pentagonal nature of single- and double-strand chiral Si nano-ribbons perfectly aligned on Ag(110) surfaces whose structure has remained elusive for over a decade. Our study reveals an unprecedented one-dimensional Si atomic arrangement solely comprising almost perfect alternating pentagons residing in the missing row troughs of the reconstructed surface. We additionally characterize the precursor structure of the nano-ribbons, which consists of a Si cluster (nano-dot) occupying a silver di-vacancy in a quasi-hexagonal configuration. The system thus materializes a paradigmatic shift from a silicene-like packing to a pentagonal one.

Suggested Citation

  • Jorge I. Cerdá & Jagoda Sławińska & Guy Le Lay & Antonela C. Marele & José M. Gómez-Rodríguez & María E. Dávila, 2016. "Unveiling the pentagonal nature of perfectly aligned single-and double-strand Si nano-ribbons on Ag(110)," Nature Communications, Nature, vol. 7(1), pages 1-7, December.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms13076
    DOI: 10.1038/ncomms13076
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