We have investigated the initial stages of vacuum-deposited sexithiophene (alpha-6T) adlayer formation on Au(111) vicinal surfaces at room temperature. The in situ scanning tunneling microscopy (STM) and photoemission spectroscopy (PES) reveal a step edge-driven growth of alpha-6T on the Au(111) vicinal surfaces that first leads to the formation of an ordered monolayer, comprising two phases with the molecular major axes aligned along the step edges. The monolayer formation is then followed by the appearance of a single-phase 2D superstructure at a two-monolayer coverage. The results highlight the potential of using vicinal metal surfaces as templates for generating organized organic nanostructures over macroscopic areas for applications in organic electronics and moletronics.
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http://dx.doi.org/10.1021/jp044921y | DOI Listing |
ACS Nano
January 2023
Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, People's Republic of China.
Epitaxial growth of wafer-scale monolayer semiconducting transition metal dichalcogenide single crystals is essential for advancing their applications in next-generation transistors and highly integrated circuits. Several efforts have been made for the growth of monolayer MoS single crystals on high-symmetry Au(111) and sapphire substrates, while more prototype growth systems still need to be discovered for clarifying the internal mechanisms. Herein, we report the epitaxial growth of unidirectionally aligned monolayer MoS domains and single-crystal films on low-symmetry Au(101) vicinal facets a facile chemical vapor deposition method.
View Article and Find Full Text PDFACS Nano
April 2020
Academy for Advanced Interdisciplinary Studies, Beijing Graphene Insititue, Peking University, Beijing 100871, People's Republic of China.
Two-dimensional (2D) semiconducting transition metal dichalcogenides (TMDs) have emerged as attractive platforms in next-generation nanoelectronics and optoelectronics for reducing device sizes down to a 10 nm scale. To achieve this, the controlled synthesis of wafer-scale single-crystal TMDs with high crystallinity has been a continuous pursuit. However, previous efforts to epitaxially grow TMD films on insulating substrates (, mica and sapphire) failed to eliminate the evolution of antiparallel domains and twin boundaries, leading to the formation of polycrystalline films.
View Article and Find Full Text PDFPhys Rev Lett
May 2010
Centre d'Investigaciò en Nanociència i Nanotecnologia, CIN2 (CSIC-ICN), Esfera UAB, Campus de Bellaterra, 08193-Barcelona, Spain.
The influence of structural defects, in the form of step lattices, on the spin polarization of the spin-orbit split Shockley surface state of Au(111) has been investigated. Spin- and angle-resolved photoemission data from three vicinal surfaces with different step densities are presented. The spin splitting is preserved in all three cases, and there is no reduction of the spin polarization of individual subbands, including the umklapp bands induced by the step lattice.
View Article and Find Full Text PDFJ Phys Condens Matter
September 2009
DIPC, Manuel Lardizábal 4, E-20018 San Sebastián, Spain.
Vicinal Au(111) surfaces exhibit periodic faceting within a wide range of miscut angles. There, the system segregates two alternating phases with different step lattice constants d(w) and d(n). Using a curved crystal surface that allows a smooth variation of the surface orientation, we have studied, as a function of the miscut angle, the evolution of Au(111) faceted structures by scanning tunneling microscopy, and their electronic surface states by angle-resolved photoemission.
View Article and Find Full Text PDFLangmuir
March 2008
Université Paris Diderot, Interfaces, Traitements, Organisation et Dynamique des Systèmes, CNRS UMR 7086, Paris, France.
We investigate the influence of the native staircase nanostructure of a Au(111) vicinal surface upon the self-assembly of alkylthiols. Through a comparison with standard alkylthiol SAMs deposited on Au(111) flat surfaces, we show that on the vicinal surface the octanethiol monolayer (OT SAM) reproduces the nanopatterned staircase structure, giving rise to a new kind of molecular layer self-ordered on the nanometer scale. The SAM's structure is determined by UHV STM and PM-IRRAS measurements and exhibits a specific behavior relative to the nanostructured substrate.
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