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Towards π-wires on a semiconductor surface: Benzyne on Si(001).
Glaser, T; Tripp, M; Luy, J-N; Tonner-Zech, R; Koert, U; Dürr, M.
Afiliação
  • Glaser T; Institut für Angewandte Physik and Zentrum für Materialforschung, Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 16, D-35392, Giessen, Germany.
  • Tripp M; Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Straße 4, D-35032, Marburg, Germany.
  • Luy JN; Wilhelm-Ostwald-Institut für Physikalische und Theoretische Chemie, Universität Leipzig, Linnéstraße 2, D-04103, Leipzig, Germany.
  • Tonner-Zech R; Wilhelm-Ostwald-Institut für Physikalische und Theoretische Chemie, Universität Leipzig, Linnéstraße 2, D-04103, Leipzig, Germany.
  • Koert U; Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Straße 4, D-35032, Marburg, Germany.
  • Dürr M; Institut für Angewandte Physik and Zentrum für Materialforschung, Justus-Liebig-Universität Giessen, Heinrich-Buff-Ring 16, D-35392, Giessen, Germany.
Chemphyschem ; 23(23): e202200404, 2022 12 05.
Article em En | MEDLINE | ID: mdl-36166680
Towards the goal of covalently bound molecular wires on silicon, the adsorption of benzyne on Si(001) was studied by means of scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), and density functional calculations (DFT). The benzyne molecule is found to adsorb preferentially via the strained triple bond on one dimer of the Si(001) surface which results in an intact π system covalently bound to the surface. With increasing coverage, the molecules primarily adsorb along the dimer rows; on stepped surfaces, these molecular wires are all oriented in the same direction.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Silício / Microscopia de Tunelamento Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Silício / Microscopia de Tunelamento Idioma: En Ano de publicação: 2022 Tipo de documento: Article