科研之友
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摘要
A simple, one-step method is employed to produce, at room temperature, a single layer of an organic-inorganic nanocomposite containing non-aggregated lead sulphide (PbS) quantum dots (QDs) embedded in a 130 nm thick solution processed film of the organic semiconductor 6PcH2 (metal-free, non-peripherally substituted octahexyl phthalocyanine) on indium tin oxide. The mean size of PbS QDs is found from x-ray diffraction and transmission electron microscopy techniques to be much smaller than the Bohr radius. Further evidence of the quantum confinement effect is provided by a blue shift in the absorption spectrum and the increased band gap of 1.95 eV with respect to bulk PbS. The current-voltage characteristics of the hybrid and pristine 6PcH2 films, both in a sandwich configuration with the aluminium top electrode, exhibit bistable switching type hysteresis. The on-off ratio of the nanocomposite device is at least three orders of magnitude higher than that for 6PcH2 organic films, while both devices operate at a very low bias voltage of 0.5 V. The inclusion of the PbS QDs into the 6PcH2 film enhances the conductivity by nearly two orders of magnitude over that of a comparable pristine 6PcH2 film due to the formation of a charge transfer complex with PbS QDs and 6PcH2 acting as acceptors and donors of electrons, respectively.
- 出版日期2015-9
