Dodecacene generated on surface: reopening of the energy gap

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Abstract

The acene series represents a model system to investigate the intriguing electronic properties of extended π-electron structures in the one-dimensional limit, which are important for applications in electronics and spintronics and for the fundamental understanding of electronic transport. This article presents the on-surface generation of the longest acene obtained so far: dodecacene. Scanning tunneling spectroscopy gives access to the energy position and spatial distribution of its electronic states on the Au(111) surface. We observe that, after a progressive closing of the gap and a stabilization to about 1 eV at the length of decacene and undecacene, the energy gap of dodecacene unexpectedly increases to 1.4 eV. Considering the acene series as an exemplary general case, the paper discusses the evolution with length of the single tunneling resonances in comparison with ionization energy, electronic affinity, and optical gap

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This is the Accepted Manuscript version of an article published in its final version at https://doi.org/10.1021/acsnano.9b08456. This accepted version is deposited in this institutional repository in accordance with the American Chemical Society’s Green Open Access policy. Redistribution, commercial use, and the creation of derivative works are not permitted

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F. Eisenhut, T. Kühne, F. García, S. Fernández, E. Guitián, D. Pérez, G. Trinquier, G. Cuniberti, C. Joachim, D. Peña, F. Moresco. Dodecacene Generated on Surface: Reopening of the Energy Gap. ACS Nano 2020, 14, 1011–1017

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Discussion with J.P. Malrieu from the Laboratoire de Chimie et Physique Quantiques, IRSAMC-CNRS-UMR5626 is gratefully acknowledged. This work was funded by the European Union’s Horizon 2020 research and innovation program under the project MEMO, Grant Agreement No. 766864 and the project SPRING (Grant Agreement No. 863098). Support by the German Excellence Initiative via the Cluster of Excellence EXC1056 “Center for Advancing Electronics Dresden” (cfaed) is acknowledged. We thank the Agencia Estatal de Investigación (MAT2016-78293-C6-3-R and CTQ2016-78157-R), Xunta de Galicia (Centro singular de investigación de Galicia, accreditation 2016-2019, ED431G/09), and the Fondo Europeo de Desarrollo Regional (FEDER) for financial support. F.G. acknowledges the Juan de la Cierva Incorporación 2017 program

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This Accepted Manuscript is deposited in this institutional repository in accordance with the American Chemical Society’s Green Open Access policy. Redistribution, commercial use, and the creation of derivative works are not permitted.