Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy
- Autores
- Massimi, Lorenzo; Angelucci, Marco; Gargiani, Perluigi; Betti, Maria Grazia; Montoro, Silvia Susana; Mariani, Carlo
- Año de publicación
- 2014
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Iron-phthalocyanine and cobalt-phthalocyanine chains, assembled along the Au(110)-(1×2) reconstructed channels, present a strong interaction with the Au metallic states, via the central metal ion. X-ray photoemission spectroscopy from the metal-2p core-levels and valence band high-resolution ultraviolet photoelectron spectroscopy bring to light signatures of the interaction of the metalphthalocyanine single-layer with gold. The charge transfer from Au to the molecule causes the emerging of a metal-2p core level component at lower binding energy with respect to that measured in the molecular thin films, while the core-levels associated to the organic macrocycle (C and N 1s) are less influenced by the adsorption, and the macrocycles stabilize the interaction, inducing a strong interface dipole. Temperature Programmed Desorption experiments and photoemission as a function of temperature allow to estimate the adsorption energy for the thin-films, mainly due to the moleculemolecule van der Waals interaction, while the FePc and CoPc single-layers remain adsorbed on the Au surface up to at least 820 K. © 2014 AIP Publishing LLC.
Fil: Massimi, Lorenzo. Universita Di Roma. Departamento de Fisica; Italia
Fil: Angelucci, Marco. Universita Di Roma. Departamento de Fisica; Italia
Fil: Gargiani, Perluigi. Universita Di Roma. Departamento de Fisica; Italia
Fil: Betti, Maria Grazia. Universita Di Roma. Departamento de Fisica; Italia
Fil: Montoro, Silvia Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Santa Fe. Instituto de Física del Litoral; Argentina
Fil: Mariani, Carlo. Universita Di Roma. Departamento de Fisica; Italia - Materia
-
Metal-phthalocyanine
X-ray photoemission
Desorption
adsorption energy - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/9875
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Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energyMassimi, LorenzoAngelucci, MarcoGargiani, PerluigiBetti, Maria GraziaMontoro, Silvia SusanaMariani, CarloMetal-phthalocyanineX-ray photoemissionDesorptionadsorption energyhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1Iron-phthalocyanine and cobalt-phthalocyanine chains, assembled along the Au(110)-(1×2) reconstructed channels, present a strong interaction with the Au metallic states, via the central metal ion. X-ray photoemission spectroscopy from the metal-2p core-levels and valence band high-resolution ultraviolet photoelectron spectroscopy bring to light signatures of the interaction of the metalphthalocyanine single-layer with gold. The charge transfer from Au to the molecule causes the emerging of a metal-2p core level component at lower binding energy with respect to that measured in the molecular thin films, while the core-levels associated to the organic macrocycle (C and N 1s) are less influenced by the adsorption, and the macrocycles stabilize the interaction, inducing a strong interface dipole. Temperature Programmed Desorption experiments and photoemission as a function of temperature allow to estimate the adsorption energy for the thin-films, mainly due to the moleculemolecule van der Waals interaction, while the FePc and CoPc single-layers remain adsorbed on the Au surface up to at least 820 K. © 2014 AIP Publishing LLC.Fil: Massimi, Lorenzo. Universita Di Roma. Departamento de Fisica; ItaliaFil: Angelucci, Marco. Universita Di Roma. Departamento de Fisica; ItaliaFil: Gargiani, Perluigi. Universita Di Roma. Departamento de Fisica; ItaliaFil: Betti, Maria Grazia. Universita Di Roma. Departamento de Fisica; ItaliaFil: Montoro, Silvia Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Santa Fe. Instituto de Física del Litoral; ArgentinaFil: Mariani, Carlo. Universita Di Roma. Departamento de Fisica; ItaliaAmerican Institute Of Physics2014-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/9875Massimi, Lorenzo; Angelucci, Marco; Gargiani, Perluigi; Betti, Maria Grazia; Montoro, Silvia Susana; et al.; Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy; American Institute Of Physics; Journal Of Chemical Physics; 140; 6-2014; 2447041-24470480021-9606enginfo:eu-repo/semantics/altIdentifier/doi/10.1063/1.4883735info:eu-repo/semantics/altIdentifier/url/http://aip.scitation.org/doi/full/10.1063/1.4883735info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:36:18Zoai:ri.conicet.gov.ar:11336/9875instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:36:18.974CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy |
title |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy |
spellingShingle |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy Massimi, Lorenzo Metal-phthalocyanine X-ray photoemission Desorption adsorption energy |
title_short |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy |
title_full |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy |
title_fullStr |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy |
title_full_unstemmed |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy |
title_sort |
Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy |
dc.creator.none.fl_str_mv |
Massimi, Lorenzo Angelucci, Marco Gargiani, Perluigi Betti, Maria Grazia Montoro, Silvia Susana Mariani, Carlo |
author |
Massimi, Lorenzo |
author_facet |
Massimi, Lorenzo Angelucci, Marco Gargiani, Perluigi Betti, Maria Grazia Montoro, Silvia Susana Mariani, Carlo |
author_role |
author |
author2 |
Angelucci, Marco Gargiani, Perluigi Betti, Maria Grazia Montoro, Silvia Susana Mariani, Carlo |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Metal-phthalocyanine X-ray photoemission Desorption adsorption energy |
topic |
Metal-phthalocyanine X-ray photoemission Desorption adsorption energy |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Iron-phthalocyanine and cobalt-phthalocyanine chains, assembled along the Au(110)-(1×2) reconstructed channels, present a strong interaction with the Au metallic states, via the central metal ion. X-ray photoemission spectroscopy from the metal-2p core-levels and valence band high-resolution ultraviolet photoelectron spectroscopy bring to light signatures of the interaction of the metalphthalocyanine single-layer with gold. The charge transfer from Au to the molecule causes the emerging of a metal-2p core level component at lower binding energy with respect to that measured in the molecular thin films, while the core-levels associated to the organic macrocycle (C and N 1s) are less influenced by the adsorption, and the macrocycles stabilize the interaction, inducing a strong interface dipole. Temperature Programmed Desorption experiments and photoemission as a function of temperature allow to estimate the adsorption energy for the thin-films, mainly due to the moleculemolecule van der Waals interaction, while the FePc and CoPc single-layers remain adsorbed on the Au surface up to at least 820 K. © 2014 AIP Publishing LLC. Fil: Massimi, Lorenzo. Universita Di Roma. Departamento de Fisica; Italia Fil: Angelucci, Marco. Universita Di Roma. Departamento de Fisica; Italia Fil: Gargiani, Perluigi. Universita Di Roma. Departamento de Fisica; Italia Fil: Betti, Maria Grazia. Universita Di Roma. Departamento de Fisica; Italia Fil: Montoro, Silvia Susana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Santa Fe. Instituto de Física del Litoral; Argentina Fil: Mariani, Carlo. Universita Di Roma. Departamento de Fisica; Italia |
description |
Iron-phthalocyanine and cobalt-phthalocyanine chains, assembled along the Au(110)-(1×2) reconstructed channels, present a strong interaction with the Au metallic states, via the central metal ion. X-ray photoemission spectroscopy from the metal-2p core-levels and valence band high-resolution ultraviolet photoelectron spectroscopy bring to light signatures of the interaction of the metalphthalocyanine single-layer with gold. The charge transfer from Au to the molecule causes the emerging of a metal-2p core level component at lower binding energy with respect to that measured in the molecular thin films, while the core-levels associated to the organic macrocycle (C and N 1s) are less influenced by the adsorption, and the macrocycles stabilize the interaction, inducing a strong interface dipole. Temperature Programmed Desorption experiments and photoemission as a function of temperature allow to estimate the adsorption energy for the thin-films, mainly due to the moleculemolecule van der Waals interaction, while the FePc and CoPc single-layers remain adsorbed on the Au surface up to at least 820 K. © 2014 AIP Publishing LLC. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-06 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/9875 Massimi, Lorenzo; Angelucci, Marco; Gargiani, Perluigi; Betti, Maria Grazia; Montoro, Silvia Susana; et al.; Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy; American Institute Of Physics; Journal Of Chemical Physics; 140; 6-2014; 2447041-2447048 0021-9606 |
url |
http://hdl.handle.net/11336/9875 |
identifier_str_mv |
Massimi, Lorenzo; Angelucci, Marco; Gargiani, Perluigi; Betti, Maria Grazia; Montoro, Silvia Susana; et al.; Metal-phthalocyanine ordered layers on Au(110): Metal-dependent adsorption energy; American Institute Of Physics; Journal Of Chemical Physics; 140; 6-2014; 2447041-2447048 0021-9606 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1063/1.4883735 info:eu-repo/semantics/altIdentifier/url/http://aip.scitation.org/doi/full/10.1063/1.4883735 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Institute Of Physics |
publisher.none.fl_str_mv |
American Institute Of Physics |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844613137471373312 |
score |
13.070432 |