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On-Surface Synthesis and Evolution of Self-Assembled Poly(p-phenylene) Chains on Ag(111): A Joint Experimental and Theoretical Study.
Ivanovskaya, Viktoria V; Zobelli, Alberto; Basagni, Andrea; Casalini, Stefano; Colazzo, Luciano; de Boni, Francesco; de Oteyza, Dimas G; Sambi, Mauro; Sedona, Francesco.
Afiliación
  • Ivanovskaya VV; Dipartimento di Scienze Chimiche, Università degli Studi di Padova, 35131Padova, Italy.
  • Zobelli A; Université Paris-Saclay, CNRS, Laboratoire de Physique des Solides, 91405Orsay, France.
  • Basagni A; Dipartimento di Scienze Chimiche, Università degli Studi di Padova, 35131Padova, Italy.
  • Casalini S; Dipartimento di Scienze Chimiche, Università degli Studi di Padova, 35131Padova, Italy.
  • Colazzo L; Center for Quantum Nanoscience, Institute for Basic Science (IBS), Seoul03760, Republic of Korea.
  • de Boni F; Ewha Womans University, Seoul03760, Republic of Korea.
  • de Oteyza DG; Dipartimento di Scienze Chimiche, Università degli Studi di Padova, 35131Padova, Italy.
  • Sambi M; Nanomaterials and Nanotechnology Research Center (CINN), CSIC-UNIOVI-PA, 33940El Entrego, Spain.
  • Sedona F; Dipartimento di Scienze Chimiche, Università degli Studi di Padova, 35131Padova, Italy.
J Phys Chem C Nanomater Interfaces ; 127(1): 393-402, 2023 Jan 12.
Article en En | MEDLINE | ID: mdl-36660099
The growth of controlled 1D carbon-based nanostructures on metal surfaces is a multistep process whose path, activation energies, and intermediate metastable states strongly depend on the employed substrate. Whereas this process has been extensively studied on gold, less work has been dedicated to silver surfaces, which have a rather different catalytic activity. In this work, we present an experimental and theoretical investigation of the growth of poly-p-phenylene (PPP) chains and subsequent narrow graphene ribbons starting from 4,4″-dibromo-p-terphenyl molecular precursors deposited at the silver surface. By combing scanning tunneling microscopy (STM) imaging and density functional theory (DFT) simulations, we describe the molecular morphology and organization at different steps of the growth process and we discuss the stability and conversion of the encountered species on the basis of calculated thermodynamic quantities. Unlike the case of gold, at the debromination step we observe the appearance of organometallic molecules and chains, which can be explained by their negative formation energy in the presence of a silver adatom reservoir. At the dehydrogenation temperature, the persistence of intercalated Br atoms hinders the formation of well-structured graphene ribbons, which are instead observed on gold, leading only to a partial lateral coupling of the PPP chains. We numerically derive very different activation energies for Br desorption from the Ag and Au surfaces, thereby confirming the importance of this process in defining the kinetics of the formation of molecular chains and graphene ribbons on different metal surfaces.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Phys Chem C Nanomater Interfaces Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Phys Chem C Nanomater Interfaces Año: 2023 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos