Contact resistance and threshold voltage extraction in n -channel organic thin film transistors on plastic substrates

n-channel organic thin film transistors were fabricated on polyethylene naphthalate substrates. The first part of the paper is devoted to a critical analysis of eight methods to extract the threshold voltage from the transfer characteristic in the linear regime. Next, to improve electron injection and reduce contact resistance, self-assembled monolayers (SAMs) were deposited on the gold source and drain electrodes. The subsequent modification on the current-voltage characteristics of the transistors is analyzed by the transfer line method, using a threshold-voltage-corrected gate voltage. The improved performance of the device obtained with some of the SAM treatments is attributed to both a better morphology of the semiconductor film, resulting in an increased channel mobility, and to easier electron injection, which manifests itself through a lowering of the contact resistance. Interestingly, the modulation of the contact resistance exactly follows an opposite behavior to what reported in the case of p -channel devices, which brings further evidence for that charge injection is tuned by the direction and magnitude of the dipole moment of the SAM. © 2009 American Institute of Physics

Vertical Transport in Spin Coated Ultra Thin Polycrystalline Pentacene Organic Stacks

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In vivo gene transfer into the ocular ciliary muscle mediated by ultrasound and microbubbles.

This study aimed to assess application of ultrasound (US) combined with microbubbles (MB) to transfect the ciliary muscle of rat eyes. Reporter DNA plasmids encoding for Gaussia luciferase, β-galactosidase or the green fluorescent protein (GFP), alone or mixed with 50% Artison MB, were injected into the ciliary muscle, with or without US exposure (US set at 1 MHz, 2 W/cm(2), 50% duty cycle for 2 min). Luciferase activity was measured in ocular fluids at 7 and 30 days after sonoporation. At 1 week, the US+MB treatment showed a significant increase in luminescence compared with control eyes, injected with plasmid only, with or without MB (×2.6), and, reporter proteins were localized in the ciliary muscle by histochemical analysis. At 1 month, a significant decrease in luciferase activity was observed in all groups. A rise in lens and ciliary muscle temperature was measured during the procedure but did not result in any observable or microscopic damages at 1 and 8 days. The feasibility to transfer gene into the ciliary muscle by US and MB suggests that sonoporation may allow intraocular production of proteins for the treatment of inflammatory, angiogenic and/or degenerative retinal diseases

Vertical Transport in Spin Coated Ultra Thin Polycrystalline Pentacene Organic Stacks

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Transfer of the shared epitope through microchimerism in women with rheumatoid arthritis

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