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Quasi one-dimensional band dispersion and surface metallization in long-range ordered polymeric wires.

Identifieur interne : 002341 ( PubMed/Curation ); précédent : 002340; suivant : 002342

Quasi one-dimensional band dispersion and surface metallization in long-range ordered polymeric wires.

Auteurs : Guillaume Vasseur [France] ; Yannick Fagot-Revurat [France] ; Muriel Sicot [France] ; Bertrand Kierren [France] ; Luc Moreau [France] ; Daniel Malterre [France] ; Luis Cardenas [Canada] ; Gianluca Galeotti [Canada] ; Josh Lipton-Duffin [Canada] ; Federico Rosei [Canada] ; Marco Di Giovannantonio [Italie] ; Giorgio Contini [Italie] ; Patrick Le Fèvre [France] ; François Bertran [France] ; Liangbo Liang [États-Unis] ; Vincent Meunier [États-Unis] ; Dmitrii F. Perepichka [Canada]

Source :

RBID : pubmed:26725974

Abstract

On-surface covalent self-assembly of organic molecules is a very promising bottom-up approach for producing atomically controlled nanostructures. Due to their highly tuneable properties, these structures may be used as building blocks in electronic carbon-based molecular devices. Following this idea, here we report on the electronic structure of an ordered array of poly(para-phenylene) nanowires produced by surface-catalysed dehalogenative reaction. By scanning tunnelling spectroscopy we follow the quantization of unoccupied molecular states as a function of oligomer length, with Fermi level crossing observed for long chains. Angle-resolved photoelectron spectroscopy reveals a quasi-1D valence band as well as a direct gap of 1.15 eV, as the conduction band is partially filled through adsorption on the surface. Tight-binding modelling and ab initio density functional theory calculations lead to a full description of the band structure, including the gap size and charge transfer mechanisms, highlighting a strong substrate-molecule interaction that drives the system into a metallic behaviour.

DOI: 10.1038/ncomms10235
PubMed: 26725974

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Le document en format XML

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<div type="abstract" xml:lang="en">On-surface covalent self-assembly of organic molecules is a very promising bottom-up approach for producing atomically controlled nanostructures. Due to their highly tuneable properties, these structures may be used as building blocks in electronic carbon-based molecular devices. Following this idea, here we report on the electronic structure of an ordered array of poly(para-phenylene) nanowires produced by surface-catalysed dehalogenative reaction. By scanning tunnelling spectroscopy we follow the quantization of unoccupied molecular states as a function of oligomer length, with Fermi level crossing observed for long chains. Angle-resolved photoelectron spectroscopy reveals a quasi-1D valence band as well as a direct gap of 1.15 eV, as the conduction band is partially filled through adsorption on the surface. Tight-binding modelling and ab initio density functional theory calculations lead to a full description of the band structure, including the gap size and charge transfer mechanisms, highlighting a strong substrate-molecule interaction that drives the system into a metallic behaviour.</div>
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<Year>2016</Year>
<Month>04</Month>
<Day>25</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>07</Month>
<Day>23</Day>
</DateRevised>
<Article PubModel="Electronic">
<Journal>
<ISSN IssnType="Electronic">2041-1723</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>7</Volume>
<PubDate>
<Year>2016</Year>
<Month>Jan</Month>
<Day>04</Day>
</PubDate>
</JournalIssue>
<Title>Nature communications</Title>
<ISOAbbreviation>Nat Commun</ISOAbbreviation>
</Journal>
<ArticleTitle>Quasi one-dimensional band dispersion and surface metallization in long-range ordered polymeric wires.</ArticleTitle>
<Pagination>
<MedlinePgn>10235</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1038/ncomms10235</ELocationID>
<Abstract>
<AbstractText>On-surface covalent self-assembly of organic molecules is a very promising bottom-up approach for producing atomically controlled nanostructures. Due to their highly tuneable properties, these structures may be used as building blocks in electronic carbon-based molecular devices. Following this idea, here we report on the electronic structure of an ordered array of poly(para-phenylene) nanowires produced by surface-catalysed dehalogenative reaction. By scanning tunnelling spectroscopy we follow the quantization of unoccupied molecular states as a function of oligomer length, with Fermi level crossing observed for long chains. Angle-resolved photoelectron spectroscopy reveals a quasi-1D valence band as well as a direct gap of 1.15 eV, as the conduction band is partially filled through adsorption on the surface. Tight-binding modelling and ab initio density functional theory calculations lead to a full description of the band structure, including the gap size and charge transfer mechanisms, highlighting a strong substrate-molecule interaction that drives the system into a metallic behaviour.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Vasseur</LastName>
<ForeName>Guillaume</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Institut Jean Lamour, UMR 7198, Université de Lorraine/CNRS, BP 70239, F-54506 Vandoeuvre-les-Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fagot-Revurat</LastName>
<ForeName>Yannick</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>Institut Jean Lamour, UMR 7198, Université de Lorraine/CNRS, BP 70239, F-54506 Vandoeuvre-les-Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sicot</LastName>
<ForeName>Muriel</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Institut Jean Lamour, UMR 7198, Université de Lorraine/CNRS, BP 70239, F-54506 Vandoeuvre-les-Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Kierren</LastName>
<ForeName>Bertrand</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Institut Jean Lamour, UMR 7198, Université de Lorraine/CNRS, BP 70239, F-54506 Vandoeuvre-les-Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Moreau</LastName>
<ForeName>Luc</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Institut Jean Lamour, UMR 7198, Université de Lorraine/CNRS, BP 70239, F-54506 Vandoeuvre-les-Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Malterre</LastName>
<ForeName>Daniel</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>Institut Jean Lamour, UMR 7198, Université de Lorraine/CNRS, BP 70239, F-54506 Vandoeuvre-les-Nancy, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Cardenas</LastName>
<ForeName>Luis</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Centre Énergie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique, 1650 Boulevard Lionel-Boulet, Varennes, Quebec, Canada J3X 1S2.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>IRCELYON, Institut de Recherches sur la Catalyse et l'Environnement de Lyon, Villeurbanne 69626, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Galeotti</LastName>
<ForeName>Gianluca</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Centre Énergie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique, 1650 Boulevard Lionel-Boulet, Varennes, Quebec, Canada J3X 1S2.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lipton-Duffin</LastName>
<ForeName>Josh</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Centre Énergie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique, 1650 Boulevard Lionel-Boulet, Varennes, Quebec, Canada J3X 1S2.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute for Future Environments, Queensland University of Technology (QUT), 2 George Street, Brisbane, Queensland 4001, Australia.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Rosei</LastName>
<ForeName>Federico</ForeName>
<Initials>F</Initials>
<AffiliationInfo>
<Affiliation>Centre Énergie, Matériaux et Télécommunications, Institut National de la Recherche Scientifique, 1650 Boulevard Lionel-Boulet, Varennes, Quebec, Canada J3X 1S2.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Institute for Fundamental and Frontier Science, University of Electronic Science and Technology of China, Chengdu 610054, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Di Giovannantonio</LastName>
<ForeName>Marco</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Instituto di Struttura della Materia, CNR, Via Fosso del Cavaliere 100, 00133 Roma, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Contini</LastName>
<ForeName>Giorgio</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>Instituto di Struttura della Materia, CNR, Via Fosso del Cavaliere 100, 00133 Roma, Italy.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Physics Department, University of Rome 'Tor Vergata', Via della Ricerca Scientifica 1, I-00133 Roma, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Le Fèvre</LastName>
<ForeName>Patrick</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Synchrotron SOLEIL, L'Orme des Merisiers, Saint-Aubin, BP 48, F-91192 Gif sur Yvette, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Bertran</LastName>
<ForeName>François</ForeName>
<Initials>F</Initials>
<AffiliationInfo>
<Affiliation>Synchrotron SOLEIL, L'Orme des Merisiers, Saint-Aubin, BP 48, F-91192 Gif sur Yvette, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Liang</LastName>
<ForeName>Liangbo</ForeName>
<Initials>L</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0003-1199-0049</Identifier>
<AffiliationInfo>
<Affiliation>Department of Physics, Applied Physics, and Astronomy, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Meunier</LastName>
<ForeName>Vincent</ForeName>
<Initials>V</Initials>
<AffiliationInfo>
<Affiliation>Department of Physics, Applied Physics, and Astronomy, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Perepichka</LastName>
<ForeName>Dmitrii F</ForeName>
<Initials>DF</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec, Canada H3A 0B8.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2016</Year>
<Month>01</Month>
<Day>04</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>Nat Commun</MedlineTA>
<NlmUniqueID>101528555</NlmUniqueID>
<ISSNLinking>2041-1723</ISSNLinking>
</MedlineJournalInfo>
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