When Electron Transfer Meets Electron Transport in Redox-Active Molecular Nanojunctions

被引:26
|
作者
Janin, Marion [1 ]
Ghilane, Jalal [1 ]
Lacroix, Jean-Christophe [1 ]
机构
[1] Univ Paris Diderot, NanoElectroChem Grp, ITODYS, UMR CNRS 7086, F-75205 Paris 13, France
关键词
CONDUCTANCE; FABRICATION; RESISTANCE; RECTIFICATION; JUNCTIONS; SWITCH; WIRES;
D O I
10.1021/ja3122125
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A scanning electrochemical microscope (SECM) was used to arrange two microelectrodes face-to-face separated by a micrometric gap. Polyaniline (PANI) was deposited electrochemically from the SECM tip side until it bridged the two electrodes. The junctions obtained were characterized by following the current through the PANI as a function of its electrochemical potential measured versus a reference electrode acting as a gate electrode in a solid-state transistor. PANI nano-junctions showed conductances below 100 nS in the oxidized state, indicating control of the charge transport within the whole micrometric gap by a limited number of PAN! wires. The SECM configuration makes it possible to observe in the same experiment and in the same current range the electron-transfer and electron-transport processes. These two phenomena are distinguished here and characterized by following the variation of the current with the bias voltage and the scan rate. The electron-transfer current changes with the scan rate, while the charge-transport current varies with the bias voltage. Finally, despite the initially micrometric gap, a junction where the conductance is controlled by a single oligoaniline strand is achieved.
引用
收藏
页码:2108 / 2111
页数:4
相关论文
共 50 条
  • [31] Aminotroponiminates as tunable, redox-active ligands: reversible single electron transfer and reductive dimerisation
    Lichtenberg, C.
    Krummenacher, I.
    CHEMICAL COMMUNICATIONS, 2016, 52 (65) : 10044 - 10047
  • [32] Molecular structure-property relationships for electron-transfer-rate attenuation in redox-active core dendrimers.
    Gorman, C
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U400 - U400
  • [33] Redox potentials along the redox-active low-barrier H-bonds in electron transfer pathways
    Saito, Keisuke
    Mandal, Manoj
    Ishikita, Hiroshi
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2020, 22 (44) : 25467 - 25473
  • [34] Utility of redox-active ligands for reversible multi-electron transfer in uranyl(vi) complexes
    Takeyama, Tomoyuki
    Tsushima, Satoru
    Takao, Koichiro
    INORGANIC CHEMISTRY FRONTIERS, 2023, 10 (14) : 4028 - 4044
  • [35] Electron transfer across the polarized interface between water and a hydrophobic redox-active ionic liquid
    Langmaier, Jan
    Trojanek, Antonin
    Samec, Zdenek
    ELECTROCHEMISTRY COMMUNICATIONS, 2010, 12 (10) : 1333 - 1335
  • [36] Vectorial photoinduced electron-transfer in tailored redox-active proteins and supramolecular nanoparticle arrays
    Willner, I
    Willner, B
    COORDINATION CHEMISTRY REVIEWS, 2003, 245 (1-2) : 139 - 151
  • [37] POLY 618-Homogeneous electron transfer between redox-active cluster core dendrimers
    Gorman, Christopher B.
    Hong, Young-Rae
    Sharma, Anil
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 234
  • [38] Extracellular Electron Transfer across Bacterial Cell Membranes via a Cytocompatible Redox-Active Polymer
    Nishio, Koichi
    Nakamura, Ryuhei
    Lin, Xiaojie
    Konno, Tomohiro
    Ishihara, Kazuhiko
    Nakanishi, Shuji
    Hashimoto, Kazuhito
    CHEMPHYSCHEM, 2013, 14 (10) : 2159 - 2163
  • [39] Effective Electron Transfer of Self-Assembled Redox-Active Peptide with an Affinity for Glucose Oxidase
    Taira, Shu
    Yokoyama, Kenji
    Kaneko, Daisaku
    Yamaguchi, Natsuki
    Endo, Tatsuro
    SENSORS AND MATERIALS, 2015, 27 (05) : 377 - 381
  • [40] Stimulation of Redox-Induced Electron Transfer by Interligand Hydrogen Bonding in a Cobalt Complex with Redox-Active Guanidine Ligand
    Lohmeyer, Lukas
    Schoen, Florian
    Kaifer, Elisabeth
    Himmel, Hans-Joerg
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021, 60 (18) : 10415 - 10422