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Growth of Metal Phthalocyanine on Deactivated Semiconducting Surfaces Steered by Selective Orbital Coupling.
Wagner, Sean R; Huang, Bing; Park, Changwon; Feng, Jiagui; Yoon, Mina; Zhang, Pengpeng.
Afiliação
  • Wagner SR; Department of Physics and Astronomy, Michigan State University, East Lansing, Michigan 48824-2320, USA.
  • Huang B; Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
  • Park C; Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
  • Feng J; Department of Physics and Astronomy, Michigan State University, East Lansing, Michigan 48824-2320, USA.
  • Yoon M; Center for Nanophase Materials Sciences, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, USA.
  • Zhang P; Department of Physics and Astronomy, Michigan State University, East Lansing, Michigan 48824-2320, USA.
Phys Rev Lett ; 115(9): 096101, 2015 Aug 28.
Article em En | MEDLINE | ID: mdl-26371664
ABSTRACT
Using scanning tunneling microscopy and density functional theory, we show that the molecular ordering and orientation of metal phthalocyanine molecules on the deactivated Si surface display a strong dependency on the central transition-metal ion, driven by the degree of orbital hybridization at the heterointerface via selective p-d orbital coupling. This Letter identifies a selective mechanism for modifying the molecule-substrate interaction which impacts the growth behavior of transition-metal-incorporated organic molecules on a technologically relevant substrate for silicon-based devices.
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Base de dados: MEDLINE Idioma: En Revista: Phys Rev Lett Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Base de dados: MEDLINE Idioma: En Revista: Phys Rev Lett Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos