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"Doping" of Polyyne with an Organometallic Fragment Leads to Highly Conductive Metallapolyyne Molecular Wire.
Tanaka, Yuya; Kato, Yuya; Tada, Tomofumi; Fujii, Shintaro; Kiguchi, Manabu; Akita, Munetaka.
Afiliação
  • Tanaka Y; Laboratory for Chemistry and Life Science, Institute of Innovative Research , Tokyo Institute of Technology , Yokohama 226-8503 , Japan.
  • Kato Y; Laboratory for Chemistry and Life Science, Institute of Innovative Research , Tokyo Institute of Technology , Yokohama 226-8503 , Japan.
  • Tada T; Materials Research Center for Element Strategy , Tokyo Institute of Technology , Yokohama 226-8503 , Japan.
  • Fujii S; Department of Chemistry, School of Science , Tokyo Institute of Technology , Ookayama, Tokyo 152-8551 , Japan.
  • Kiguchi M; Department of Chemistry, School of Science , Tokyo Institute of Technology , Ookayama, Tokyo 152-8551 , Japan.
  • Akita M; Laboratory for Chemistry and Life Science, Institute of Innovative Research , Tokyo Institute of Technology , Yokohama 226-8503 , Japan.
J Am Chem Soc ; 140(32): 10080-10084, 2018 08 15.
Article em En | MEDLINE | ID: mdl-29962208
ABSTRACT
Exploration of highly conductive molecules is essential to achieve single-molecule electronic devices. The present paper describes the results on single-molecule conductance study of polyyne wires doped with the organometallic Ru(dppe)2 fragment, X-(C≡C) n-Ru(dppe)2-(C≡C) n-X. The metallapolyyne wires end-capped with the gold fragments (X = AuL) are subjected to single-molecule conductance measurements with the STM break junction technique, which reveal the high conductance (10-3-10-2 G0; n = 2-4) with the low attenuation factor (0.25 Å-1) and the low contact resistance (33 kΩ). A unique "'doping'" effect of Ru(dppe)2 fragment was found to lead to the high performance as suggested by the hybrid density functional theory-nonequilibrium green function calculation.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article