journal article·2008-11-25

Probing Charge Transport of Ruthenium-Complex-Based Molecular Wires at the Single-Molecule Level

Ke Liu, Xianhong Wang, Fosong Wang

ACS Nano· Volume 2· Issue 11
Publisher page

Abstract

A ruthenium(II) bis(sigma-arylacetylide)-complex-based molecular wire functionalized with thiolacetyl alligator clips at both ends (OPERu) was used to fabricate gold substrate-molecular wire-conductive tip junctions. To elucidate the ruthenium-complex-enhanced charge transport, we conducted a single-molecule level investigation using the technique-combination method, where electronic decay constant, single-molecular conductance, and barrier height were obtained by scanning tunneling microscopy (STM) apparent height measurements, STM break junction measurements, and conductive probe-atomic force microscopy (CP-AFM) measurements, respectively. A quantitative comparison of OPERu with the well-studied pi-conjugated molecular wire oligo(1,4-phenylene ethynylene) (OPE) indicated that the lower electronic decay constant as well as the higher conductance of OPERu resulted from its lower band gap between the highest occupied molecular orbital (HOMO) and the gold Fermi level. The small offset of 0.25 eV was expected to be beneficial for the long-range charge transport of molecular wires. Moreover, the observed cross-platform agreement proved that this technique-combination method could serve as a benchmark for the detailed description of charge transport through molecular wires.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Quantum and electron transport phenomena · Surface and Thin Film Phenomena

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People’s Republic of China

Graduate School of the Chinese Academy of Science, Beijing 100039, People’s Republic of China

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