Tailoring the topological surface state in ultrathin α -Sn(111) films

We report on the electronic structure of α -Sn films in the very low thickness regime grown on InSb(111)A. High-resolution low photon energy angle-resolved photoemission spectroscopy allows for the direct observation of the linearly dispersing two-dimensional (2D) topological surface state (TSS) th...

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Main Authors: Rogalev, VA, Reis, F, Adler, F, Bauernfeind, M, Erhardt, J, Kowalewski, A, Scholz, MR, Dudy, L, Duffy, LB, Hesjedal, T, Hoesch, M, Bihlmayer, G, Schäfer, J
Format: Journal article
Published: American Physical Society 2019
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author Rogalev, VA
Reis, F
Adler, F
Bauernfeind, M
Erhardt, J
Kowalewski, A
Scholz, MR
Dudy, L
Duffy, LB
Hesjedal, T
Hoesch, M
Bihlmayer, G
Schäfer, J
author_facet Rogalev, VA
Reis, F
Adler, F
Bauernfeind, M
Erhardt, J
Kowalewski, A
Scholz, MR
Dudy, L
Duffy, LB
Hesjedal, T
Hoesch, M
Bihlmayer, G
Schäfer, J
author_sort Rogalev, VA
collection OXFORD
description We report on the electronic structure of α -Sn films in the very low thickness regime grown on InSb(111)A. High-resolution low photon energy angle-resolved photoemission spectroscopy allows for the direct observation of the linearly dispersing two-dimensional (2D) topological surface state (TSS) that exists between the second valence band and the conduction band. The Dirac point of this TSS was found to be 200 meV below the Fermi level in 10-nm-thick films, which enables the observation of the hybridization gap opening at the Dirac point of the TSS for thinner films. The crossover to a quasi-2D electronic structure is accompanied by a full gap opening at the Brillouin-zone center, in agreement with our density functional theory calculations. We further identify the thickness regime of α -Sn films where the hybridization gap in the TSS coexists with the topologically nontrivial electronic structure and one can expect the presence of a one-dimensional helical edge state.
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spelling oxford-uuid:56781c64-b577-4ef2-abb3-da30894972dc2022-03-26T16:50:34ZTailoring the topological surface state in ultrathin α -Sn(111) filmsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:56781c64-b577-4ef2-abb3-da30894972dcSymplectic Elements at OxfordAmerican Physical Society2019Rogalev, VAReis, FAdler, FBauernfeind, MErhardt, JKowalewski, AScholz, MRDudy, LDuffy, LBHesjedal, THoesch, MBihlmayer, GSchäfer, JWe report on the electronic structure of α -Sn films in the very low thickness regime grown on InSb(111)A. High-resolution low photon energy angle-resolved photoemission spectroscopy allows for the direct observation of the linearly dispersing two-dimensional (2D) topological surface state (TSS) that exists between the second valence band and the conduction band. The Dirac point of this TSS was found to be 200 meV below the Fermi level in 10-nm-thick films, which enables the observation of the hybridization gap opening at the Dirac point of the TSS for thinner films. The crossover to a quasi-2D electronic structure is accompanied by a full gap opening at the Brillouin-zone center, in agreement with our density functional theory calculations. We further identify the thickness regime of α -Sn films where the hybridization gap in the TSS coexists with the topologically nontrivial electronic structure and one can expect the presence of a one-dimensional helical edge state.
spellingShingle Rogalev, VA
Reis, F
Adler, F
Bauernfeind, M
Erhardt, J
Kowalewski, A
Scholz, MR
Dudy, L
Duffy, LB
Hesjedal, T
Hoesch, M
Bihlmayer, G
Schäfer, J
Tailoring the topological surface state in ultrathin α -Sn(111) films
title Tailoring the topological surface state in ultrathin α -Sn(111) films
title_full Tailoring the topological surface state in ultrathin α -Sn(111) films
title_fullStr Tailoring the topological surface state in ultrathin α -Sn(111) films
title_full_unstemmed Tailoring the topological surface state in ultrathin α -Sn(111) films
title_short Tailoring the topological surface state in ultrathin α -Sn(111) films
title_sort tailoring the topological surface state in ultrathin α sn 111 films
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