Abstract

Quantum dots are known to confine electrons within their structure. Whenever they periodically aggregate into arrays and cooperative interactions arise, novel quantum properties suitable for technological applications show up. Control over the potential barriers existing between neighboring quantum dots is therefore essential to alter their mutual crosstalk. Here we show that precise engineering of the barrier width can be experimentally achieved on surfaces by a single atom substitution in a haloaromatic compound, which in turn tunes the confinement properties through the degree of quantum dot intercoupling. We achieved this by generating self-assembled molecular nanoporous networks that confine the two-dimensional electron gas present at the surface. Indeed, these extended arrays form up on bulk surface and thin silver films alike, maintaining their overall interdot coupling. These findings pave the way to reach full control over two-dimensional electron gases by means of self-assembled molecular networks.

Highlights

  • Quantum dots are known to confine electrons within their structure

  • Coupled Quantum dots (QDs) give rise to bonding and anti-bonding continuum states when set in arrays[19]

  • The fundamental energy is established by the bonding state and the overall bandwidth is limited by the anti-bonding ones

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Summary

Introduction

Quantum dots are known to confine electrons within their structure. Whenever they periodically aggregate into arrays and cooperative interactions arise, novel quantum properties suitable for technological applications show up. Control of the potential barriers between neighboring QDs is essential to alter the crosstalk (interaction) between the existing units and engineer twodimensional electron gases (2DEG)[8,9,10,11,12,13,14,15] These self-assembled two-dimensional (2D) nanoporous networks are periodic extensions of quantum corrals[7, 16] that induce confinement of scattered surface 2DEG electrons inside its nanocavities[8,9,10,11,12,13,14,15]. The communication between neighboring QDs is investigated following the 2DEG modification through a combination of scanning tunneling microscopy/spectroscopy (STM/STS), angle resolved photoemission spectroscopy (ARPES) and extended model calculations

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