Tunable energy and mass renormalization from homothetic Quantum dot arrays

Fuente: arXiv
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Autores principales: Li, Ignacio Piquero-Zulaica Jun, El-Fattah, Zakaria M. Abd, Solianyk, Leonid, Gallardo, Iker, Monjas, Leticia, Hirsch, Anna K. H., Arnau, Andres, Ortega, J. Enrique, Stohr, Meike, Lobo-Checa, Jorge
Formato: Preprint
Publicado: 2019
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author Li, Ignacio Piquero-Zulaica Jun
El-Fattah, Zakaria M. Abd
Solianyk, Leonid
Gallardo, Iker
Monjas, Leticia
Hirsch, Anna K. H.
Arnau, Andres
Ortega, J. Enrique
Stohr, Meike
Lobo-Checa, Jorge
author_facet Li, Ignacio Piquero-Zulaica Jun
El-Fattah, Zakaria M. Abd
Solianyk, Leonid
Gallardo, Iker
Monjas, Leticia
Hirsch, Anna K. H.
Arnau, Andres
Ortega, J. Enrique
Stohr, Meike
Lobo-Checa, Jorge
contents Quantum dot arrays in the form of molecular nanoporous networks are renown for modifying the electronic surface properties through quantum confinement. Here we show that, compared to the pristine surface state, the fundamental energy of the confined states can exhibit downward shifts accompanied by a lowering of the effective masses simultaneous to the appearance of tiny gaps at the Brillouin zone boundaries. We observed these effects by angle resolved photoemission for two self-assembled homothetic (scalable) Co-coordinated metal-organic networks. Complementary scanning tunneling spectroscopy measurements confirmed these findings. Electron plane wave expansion simulations and density functional theory calculations provide insight into the nature of this phenomenon, which we assign to metal-organic overlayer-substrate interactions in the form of adatom-substrate hybridization. The absence to date of the experimental band structure resulting from single adatom metal-coordinated nanoporous networks has precluded the observation of the significant surface state renormalization reported here, which we infer are general of low interacting and well-defined adatom arrays.
format Preprint
id arxiv_https___arxiv_org_abs_1910_06876
institution arXiv
publishDate 2019
record_format arxiv
spellingShingle Tunable energy and mass renormalization from homothetic Quantum dot arrays
Li, Ignacio Piquero-Zulaica Jun
El-Fattah, Zakaria M. Abd
Solianyk, Leonid
Gallardo, Iker
Monjas, Leticia
Hirsch, Anna K. H.
Arnau, Andres
Ortega, J. Enrique
Stohr, Meike
Lobo-Checa, Jorge
Chemical Physics
Mesoscale and Nanoscale Physics
Quantum Physics
Quantum dot arrays in the form of molecular nanoporous networks are renown for modifying the electronic surface properties through quantum confinement. Here we show that, compared to the pristine surface state, the fundamental energy of the confined states can exhibit downward shifts accompanied by a lowering of the effective masses simultaneous to the appearance of tiny gaps at the Brillouin zone boundaries. We observed these effects by angle resolved photoemission for two self-assembled homothetic (scalable) Co-coordinated metal-organic networks. Complementary scanning tunneling spectroscopy measurements confirmed these findings. Electron plane wave expansion simulations and density functional theory calculations provide insight into the nature of this phenomenon, which we assign to metal-organic overlayer-substrate interactions in the form of adatom-substrate hybridization. The absence to date of the experimental band structure resulting from single adatom metal-coordinated nanoporous networks has precluded the observation of the significant surface state renormalization reported here, which we infer are general of low interacting and well-defined adatom arrays.
title Tunable energy and mass renormalization from homothetic Quantum dot arrays
topic Chemical Physics
Mesoscale and Nanoscale Physics
Quantum Physics
url https://arxiv.org/abs/1910.06876