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Alberto Morgante

Researcher at University of Trieste

Publications -  150
Citations -  5094

Alberto Morgante is an academic researcher from University of Trieste. The author has contributed to research in topics: X-ray photoelectron spectroscopy & Photoemission spectroscopy. The author has an hindex of 34, co-authored 148 publications receiving 4748 citations. Previous affiliations of Alberto Morgante include AREA Science Park & Fritz Haber Institute of the Max Planck Society.

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Atomic-scale structure and catalytic reactivity of the RuO(2)(110) surface

TL;DR: The results provide atomic-scale verification of a general mechanism originally proposed by Mars and van Krevelen in 1954 and are likely to be of general relevance for the mechanism of catalytic reactions at oxide surfaces.
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X-ray Diffraction and Computation Yield the Structure of Alkanethiols on Gold(111)

TL;DR: The structure of self-assembled monolayers of long-chain alkyl sulfides on gold has been resolved by density functional theory–based molecular dynamics simulations and grazing incidence x-ray diffraction for hexanethiol and methylthiol and it is found that the sulfur atoms of the molecules bind at two distinct surface sites.
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Structure of a CH3S monolayer on Au(111) solved by the interplay between molecular dynamics calculations and diffraction measurements.

TL;DR: The authors' simulations find a dynamic equilibrium between bridge site adsorption and a novel structure where 2 CH3S radicals are bound to an Au adatom that has been lifted from the gold substrate, which is characterized by a large atomic roughness with both adatoms and vacancies.
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Zwitterionic self-assembly of l-methionine nanogratings on the Ag(111) surface

TL;DR: It is suggested that zwitterionic assembly of amino acids represents a general construction motif to achieve biomolecular nanoarchitectures on surfaces to control matter at the nanoscale.
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Defect states at the TiO2(110) surface probed by resonant photoelectron diffraction.

TL;DR: The charge distribution of the defect states at the reduced TiO(2)(110) surface is studied via a new method, the resonant photoelectron diffraction, and the defect charge is found to be shared by several surface and subsurface Ti sites with the dominant contribution on a specific subsurfaced site in agreement with density functional theory calculations.