One-dimensional molecular nanostructures interacting with two-dimensional metals

Abstract

Electrons confined within the 2D layer of metals grown on silicon substrates exhibit exotic properties due to strong correlation effects. Their properties, such as their 2D superconductivity, have been frequently subjected to possible tuning by doping using charge transfer from adsorbed layers. Doping relies on adding electrons or holes to the system and the resulting shift of the Fermi level EF in the otherwise robust surface electronic structure. This strategy has not been sufficiently controlled in the case of an indium double layer grown on the Si(111) surface. This study provides an alternative approach relying on spatially periodic modification of the surface electronic structure of the 2D metal. Derivatives of diketopyrrolopyrroles (DPP) are used for the growth of perfectly ordered 1D-like molecular superstructures on top of the In double layer, imaged by scanning tunneling microscopy. The integral changes of electronic structure are measured by angle-resolved photoelectron spectroscopy and density functional theory calculations show local modification of the surface states near EF by the adsorbed molecules. This study demonstrates that the surface electronic states can be controllably patterned, using a proper bonding scheme. It is anticipated that the combination of the original 2D superconductor and the 1D-like patterning will motivate further research.

Graphical abstract: One-dimensional molecular nanostructures interacting with two-dimensional metals

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Article information

Article type
Communication
Submitted
02 Dec 2024
Accepted
07 Feb 2025
First published
12 Feb 2025
This article is Open Access
Creative Commons BY license

Nanoscale Horiz., 2025, Advance Article

One-dimensional molecular nanostructures interacting with two-dimensional metals

P. Kocán, B. Pieczyrak, S. Umachi, M. Cigánek, P. Sobotík, I. Ošťádal, L. Jurczyszyn, J. Krajčovič and K. Sakamoto, Nanoscale Horiz., 2025, Advance Article , DOI: 10.1039/D4NH00622D

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