High-quality ordered growth and characterization of organic systems is an important requirement to understand the physical properties underlying the new organic-molecule based electronic devices. In this work, pentacene (C22H14) is ultra-high-vacuum deposited in situ on the (1 × 2)-reconstructed surface of Au(110), at different substrate temperatures. Low-energy electron diffraction reveals a two-dimensional (2D) ordered phase, showing the presence of a (1×3) pentacene-induced long-range periodicity, for room-temperature deposition. High-resolution UV photoelectron spectroscopy investigations for pentacene adsorption at room- and low- (80 K) temperature, bring to light the new interface electronic levels and the molecular orbital evolution. Higher substrate temperature (370 K) during adsorption induces higher pentacene mobility, thus improving long-range ordering. Atomic force microscopy images at higher coverage show the presence of pentacene stripes, grown on top of the first 2D ordered layer, with a preferred orientation perpendicular to the substrate [1-10] direction. © 2003 Elsevier Science B.V. All rights reserved.

Growth morphology and electronic structure of 2D ordered pentacene on the Au(1 1 0)-(1 × 2) surface / Corradini, V.; Menozzi, C.; Cavallini, M.; Biscarini, F.; Betti, M. G.; Mariani, C.. - In: SURFACE SCIENCE. - ISSN 0039-6028. - 532-535:(2003), pp. 249-254. (Intervento presentato al convegno 7th International Conference on Nanometer-Scale Science and Technology and 21st European Conference on Surface Science tenutosi a Malmo, swe nel 2002) [10.1016/S0039-6028(03)00167-5].

Growth morphology and electronic structure of 2D ordered pentacene on the Au(1 1 0)-(1 × 2) surface

Biscarini F.;
2003

Abstract

High-quality ordered growth and characterization of organic systems is an important requirement to understand the physical properties underlying the new organic-molecule based electronic devices. In this work, pentacene (C22H14) is ultra-high-vacuum deposited in situ on the (1 × 2)-reconstructed surface of Au(110), at different substrate temperatures. Low-energy electron diffraction reveals a two-dimensional (2D) ordered phase, showing the presence of a (1×3) pentacene-induced long-range periodicity, for room-temperature deposition. High-resolution UV photoelectron spectroscopy investigations for pentacene adsorption at room- and low- (80 K) temperature, bring to light the new interface electronic levels and the molecular orbital evolution. Higher substrate temperature (370 K) during adsorption induces higher pentacene mobility, thus improving long-range ordering. Atomic force microscopy images at higher coverage show the presence of pentacene stripes, grown on top of the first 2D ordered layer, with a preferred orientation perpendicular to the substrate [1-10] direction. © 2003 Elsevier Science B.V. All rights reserved.
2003
7th International Conference on Nanometer-Scale Science and Technology and 21st European Conference on Surface Science
Malmo, swe
2002
532-535
249
254
Corradini, V.; Menozzi, C.; Cavallini, M.; Biscarini, F.; Betti, M. G.; Mariani, C.
Growth morphology and electronic structure of 2D ordered pentacene on the Au(1 1 0)-(1 × 2) surface / Corradini, V.; Menozzi, C.; Cavallini, M.; Biscarini, F.; Betti, M. G.; Mariani, C.. - In: SURFACE SCIENCE. - ISSN 0039-6028. - 532-535:(2003), pp. 249-254. (Intervento presentato al convegno 7th International Conference on Nanometer-Scale Science and Technology and 21st European Conference on Surface Science tenutosi a Malmo, swe nel 2002) [10.1016/S0039-6028(03)00167-5].
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1247678
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 51
  • ???jsp.display-item.citation.isi??? 53
social impact