A terbium(iii)-bis(phthalocyaninato) neutral complex was deposited on the rutile TiO2(110) surface, and their interaction was studied by Scanning Tunneling Microscopy (STM) and X-ray Photoelectron Spectroscopy (XPS). It was found that the TiO2 rutile surface favours the adsorption of isolated molecules adopting a lying down configuration with the phthalocyanine planes tilted by about 30° when they lie in the first layer. The electronic and chemical properties of the molecules on the surface were studied by XPS as a function of the TiO2(110) substrate preparation. This study evidences that strong molecule-substrate interactions are present and a charge transfer process occurs from the molecule to the surface.

Substrate mediated interaction of terbium(iii) double-deckers with the TiO2(110) surface / Serrano G.; Sorrentino A.L.; Poggini L.; Cortigiani B.; Goletti C.; Sessoli R.; Mannini M.. - In: PHYSICAL CHEMISTRY CHEMICAL PHYSICS. - ISSN 1463-9076. - STAMPA. - 23:(2021), pp. 12060-12067. [10.1039/d1cp00928a]

Substrate mediated interaction of terbium(iii) double-deckers with the TiO2(110) surface

Serrano G.
;
Sorrentino A. L.;Poggini L.
;
Cortigiani B.;Sessoli R.;Mannini M.
2021

Abstract

A terbium(iii)-bis(phthalocyaninato) neutral complex was deposited on the rutile TiO2(110) surface, and their interaction was studied by Scanning Tunneling Microscopy (STM) and X-ray Photoelectron Spectroscopy (XPS). It was found that the TiO2 rutile surface favours the adsorption of isolated molecules adopting a lying down configuration with the phthalocyanine planes tilted by about 30° when they lie in the first layer. The electronic and chemical properties of the molecules on the surface were studied by XPS as a function of the TiO2(110) substrate preparation. This study evidences that strong molecule-substrate interactions are present and a charge transfer process occurs from the molecule to the surface.
2021
23
12060
12067
Goal 9: Industry, Innovation, and Infrastructure
Serrano G.; Sorrentino A.L.; Poggini L.; Cortigiani B.; Goletti C.; Sessoli R.; Mannini M.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1254187
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