C60 as an Atom Trap to Capture Co Adatoms
Author(s) -
Peng Yang,
Dongzhe Li,
Vincent Repain,
Cyril Chacon,
Yann Girard,
Sylvie Rousset,
Alexander Smogunov,
Yannick J. Dappe,
Cyrille Barreteau,
Jérôme Lagoute
Publication year - 2015
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/jp512723c
Subject(s) - scanning tunneling microscope , molecule , density functional theory , scanning tunneling spectroscopy , cluster (spacecraft) , atom (system on chip) , spectroscopy , chemistry , chemical physics , trapping , electrochemical scanning tunneling microscope , substrate (aquarium) , materials science , molecular physics , atomic physics , nanotechnology , computational chemistry , physics , embedded system , ecology , oceanography , organic chemistry , quantum mechanics , computer science , geology , biology , programming language
International audienceC$_{60}$ molecules were used to trap Co adatoms and clusters on a Au(111) surface using atomic/molecular manipulation with a scanning tunneling microscope. Two manipulation pathways (successive integration of single Co atoms in one molecule or direct integration of a Co cluster) were found to efficiently allow the formation of complexes mixing a C$_{60}$ molecule with Co atoms. Scanning tunneling spectroscopy reveals the robustness of the π states of C$_{60}$ that are preserved after Co trapping. Scanning tunneling microscopy images and density functional theory calculations reveal that dissociated Co clusters of up to nine atoms can be formed at the molecule−substrate interface. These results open new perspectives in the interactions between metal adatoms and molecules, for applications in metal−organic devices
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