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The metallic electrode is encased in an alumina closed tube.
Metallic electrode is regarded as another important factor that may impact the device performance by varying the contact resistance.
As we have stated above, the nature of charges in the area between DNA and metallic electrode is strongly bounded dipoles.
In a comprehensive view, the nanopillar-type patterned metallic electrode is suggested to be applied in the present organic solar cell system, since its optimal design has a moderate filling ratio, which is much easier to process than its counterpart.
We noticed, also, that in the frequency range f < 1 Hz the conduction by bound charges and dipoles at the interface between DNA and metallic electrode is inferior to all the other conductivities.
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This shows that charges located at the boundary between DNA and metallic electrode are homogeneously distributed.
When a temperature gradient ΔT between the two metallic electrodes is presented, a spin-dependent thermoelectric voltage ΔV ↑emerges.
The coupling strength between the quantum dots and the metallic electrodes is taken as the energy unit.
However, the conductance order of the single-molecule junctions with different metallic electrodes is caused by the different coupling efficiency between the metallic electrodes and the anchoring group, and also the molecular energy levels and Fermi energy level of the electrodes [8, 9].
By using this approach, single-molecule junctions with carboxylic acid binding to different metallic electrodes were systematically investigated [9, 24].
ZnO nanowires on interdigitated metallic electrodes were observed by field emission scanning electron microscopy (FE-SEM, JEOL JSM-7000F).
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