Charge injection and transport properties of large area organic junctions based on aryl thin films covalently attached to a multilayer graphene electrode.


Journal

Nanoscale advances
ISSN: 2516-0230
Titre abrégé: Nanoscale Adv
Pays: England
ID NLM: 101738708

Informations de publication

Date de publication:
15 Jan 2019
Historique:
received: 25 07 2018
accepted: 25 09 2018
entrez: 22 9 2022
pubmed: 26 9 2018
medline: 26 9 2018
Statut: epublish

Résumé

The quantum interaction between molecules and electrode materials at molecule/electrode interfaces is a major ingredient in the electron transport properties of organic junctions. Driven by the coupling strength between the two materials, it results mainly in the broadening and energy shift of the interacting molecular orbitals. Using new electrode materials, such as the recently developed semi-conducting two-dimensional nanomaterials, has become a significant advancement in the field of molecular/organic electronics that opens new possibilities for controlling the interfacial electronic properties and thus the charge injection properties. In this article, we report the use of atomically thin two-dimensional multilayer graphene films as the base electrode in organic junctions with a vertical architecture. The interfacial electronic structure dominated by the covalent bonding between bis-thienyl benzene diazonium-based molecules and the multilayer graphene electrode has been probed by ultraviolet photoelectron spectroscopy and the results are compared with those obtained on junctions with standard Au electrodes. Room temperature injection properties of such interfaces have also been explored by electron transport measurements. We find that, despite strong variations of the density of states, the Fermi energy and the injection barriers, both organic junctions with Au base electrodes and multilayer graphene base electrodes show similar electronic responses. We explain this observation by the strong orbital coupling occurring at the bottom electrode/bis-thienyl benzene molecule interface and by the pinning of the hybridized molecular orbitals.

Identifiants

pubmed: 36132450
doi: 10.1039/c8na00106e
pii: c8na00106e
pmc: PMC9473172
doi:

Types de publication

Journal Article

Langues

eng

Pagination

414-420

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

There are no conflicts to declare.

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Auteurs

Clément Barraud (C)

MPQ UMR 7162, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France Clement.barraud@univ-paris-diderot.fr.

Matthieu Lemaitre (M)

MPQ UMR 7162, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France Clement.barraud@univ-paris-diderot.fr.

Roméo Bonnet (R)

MPQ UMR 7162, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France Clement.barraud@univ-paris-diderot.fr.

Jacko Rastikian (J)

MPQ UMR 7162, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France Clement.barraud@univ-paris-diderot.fr.

Chloé Salhani (C)

MPQ UMR 7162, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France Clement.barraud@univ-paris-diderot.fr.

Stéphanie Lau (S)

ITODYS UMR 7086, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France pascal.martin@univ-paris-diderot.fr.

Quyen van Nguyen (Q)

ITODYS UMR 7086, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France pascal.martin@univ-paris-diderot.fr.
Department of Advanced Materials Science and Nanotechnology, University of Science and Technology of Hanoi, Vietnam Academy of Science and Technology 18 Hoang Quoc Viet CauGiay Hanoi Vietnam.

Philippe Decorse (P)

ITODYS UMR 7086, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France pascal.martin@univ-paris-diderot.fr.

Jean-Christophe Lacroix (JC)

ITODYS UMR 7086, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France pascal.martin@univ-paris-diderot.fr.

Maria Luisa Della Rocca (ML)

MPQ UMR 7162, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France Clement.barraud@univ-paris-diderot.fr.

Philippe Lafarge (P)

MPQ UMR 7162, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France Clement.barraud@univ-paris-diderot.fr.

Pascal Martin (P)

ITODYS UMR 7086, Université Paris Diderot, Sorbonne Paris Cité, CNRS F-75013 Paris France pascal.martin@univ-paris-diderot.fr.

Classifications MeSH