4.6 Article

Static and dynamic electronic characterization of organic monolayers grafted on a silicon surface

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 18, Issue 5, Pages 3675-3684

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cp05943g

Keywords

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Funding

  1. NSF-CHE [1300180]
  2. Chateaubriand Fellowship
  3. Nanotwinning FP7 grant [NN294952]
  4. Self-Assembly of Organic/Inorganic Nanocomposite Materials'' program, Office of Science
  5. Office of Basic Energy Sciences (BES)
  6. Materials Sciences and Engineering (MSE) Division of the U.S. Department of Energy (DOE) [DE-AC02-05CH11231]
  7. Direct For Mathematical & Physical Scien
  8. Division Of Chemistry [1300180] Funding Source: National Science Foundation

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Organic layers chemically grafted on silicon offer excellent interfaces that may open up the way for new organic-inorganic hybrid nanoelectronic devices. However, technological achievements rely on the precise electronic characterization of such organic layers. We have prepared ordered grafted organic monolayers (GOMs) on Si(111), sometimes termed self-assembled monolayers (SAMs), by a hydrosilylation reaction with either a 7-carbon or an 11-carbon alkyl chain, with further modification to obtain amine-terminated surfaces. X-ray photoelectron spectroscopy (XPS) is used to determine the band bending (similar to 0.3 eV), and ultraviolet photoelectron spectroscopy (UPS) to measure the work function (similar to 3.4 eV) and the HOMO edge. Scanning tunneling microscopy (STM) confirms that the GOM surface is clean and smooth. Finally, conductive AFM is used to measure electron transport through the monolayer and to identify transition between the tunneling and the field emission regimes. These organic monolayers offer a promising alternative to silicon dioxide thin films for fabricating metal-insulator-semiconductor (MIS) junctions. We show that gold nanoparticles can be covalently attached to mimic metallic nano-electrodes and that the electrical quality of the GOMs is completely preserved in the process.

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