Current-voltage characteristics of a homologous series of polycyclic aromatic hydrocarbons

被引:48
作者
Boehme, Thilo
Simpson, Christopher D.
Muellen, Klaus
Rabe, Juergen P.
机构
[1] Humboldt Univ, Dept Phys, D-12489 Berlin, Germany
[2] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词
cyclodehydrogenation; hydrocarbons; nanotechnology; polycycles; scanning tunneling microscopy;
D O I
10.1002/chem.200601249
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel alkyl-substituted polycyclic aromatic hydrocarbon (PAH) with D-2h symmetry and 78 carbon atoms in the aromatic core (C78) was synthesized, thereby completing a homologous series of soluble PAH compounds with increasing size of the aromatic pi system (42, 60, and 78 carbon atoms). The optical band gaps were determined by UV/Vis and fluorescence spectroscopy in solution. Scanning tunneling microscopy (STM) and spectroscopy (STS) revealed diode-like current versus voltage (I-V) characteristics through individual aromatic cores in monolayers at the interface between the solution and the basal plane of graphite. The asymmetry of the current-voltage (I-V) characteristics increases with the increasing size of the aromatic core, and the concomitantly decreasing HOMO-LUMO gap. This is attributed to resonant tunneling through the HOMO of the adsorbed molecule, and an asymmetric position of the molecular species in the tunnel junction. Consistently, submolecularly resolved STM images at negative substrate bias are in good agreement with the calculated pattern for the electron densities of the HOMOs. The analysis provides the basis for tailoring rectification with a single molecule in an STM junction.
引用
收藏
页码:7349 / 7357
页数:9
相关论文
共 57 条
  • [1] [Anonymous], 1998, ANGEW CHEM INT EDIT
  • [2] AN EASILY OPERABLE SCANNING TUNNELING MICROSCOPE
    BESOCKE, K
    [J]. SURFACE SCIENCE, 1987, 181 (1-2) : 145 - 153
  • [3] BINNIG G, 1982, HELV PHYS ACTA, V55, P726
  • [4] The simple principle of decomposition of aromatic hydrogen carbons and their absorption spectra (Aromatic hydrogen carbons, 20. Announcement).
    Clar, E
    [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1936, 69 : 607 - 614
  • [5] CLAR E, 1978, TETRAHEDRON, V34, P3219, DOI 10.1016/0040-4020(78)87020-3
  • [6] Clar E., 1964, POLYCYCLIC HYDROCARB
  • [7] Effects of molecular geometry on the STM image contrast of methyl- and bromo-substituted alkanes and alkanols on graphite
    Claypool, CL
    Faglioni, F
    Matzger, AJ
    Goddard, WA
    Lewis, NS
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (44): : 9690 - 9699
  • [8] Functional group identification in scanning tunneling microscopy of molecular adsorbates
    Cyr, DM
    Venkataraman, B
    Flynn, GW
    Black, A
    Whitesides, GM
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (32) : 13747 - 13759
  • [9] Synthesis of large polycyclic aromatic hydrocarbons:: Variation of size and periphery
    Dötz, F
    Brand, JD
    Ito, S
    Gherghel, L
    Müllen, K
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (32) : 7707 - 7717
  • [10] Molecular organization of bis-urea substituted thiophene derivatives at the liquid/solid interface studied by scanning tunneling microscopy
    Gesquière, A
    Abdel-Mottaleb, MMS
    De Feyter, S
    De Schryver, FC
    Schoonbeek, F
    van Esch, J
    Kellogg, RM
    Feringa, BL
    Calderone, A
    Lazzaroni, R
    Brédas, JL
    [J]. LANGMUIR, 2000, 16 (26) : 10385 - 10391