Two-terminal electrical bistable devices have been fabricated using a sandwich structure of organic/ metal/organic as the active medium, sandwiched between two external electrodes. The nonvolatile electrical bistability of these devices can be controlled using a positive and a negative electrical bias alternatively. A forward bias may switch the device to a high-conductance state, while a reverse bias is required to restore it to a low-conductance state. In this letter, a model to explain this electrical bistability is proposed. It is found that the bistability is very sensitive to the nanostructure of the middle metal layer. For obtaining the devices with well-controlled bistability, the middle metal layer is incorporated with metal nanoclusters separated by thin oxide layers. These nanoclusters behave as the charge storage elements, which enable the nonvolatile electrical bistability when biased to a sufficiently high voltage. This mechanism is supported by the experimental data obtained from UV-visible absorption spectra, atomic force microscopy, and impedance spectroscopy.

Energy transfer and triplet exciton confinement in polymer/phosphorescent dopant systems have been investigated. Various combinations of host‐guest systems have been studied, consisting of two host polymers, poly(vinylcarbazole) (PVK) and poly[9,9‐bis(octyl)‐fluorene‐2,7‐diyl] (PF), blended with five different phosphorescent iridium complexes with different triplet energy levels. These combinations of hosts and dopants provide an ideal situation for studying the movement of triplet excitons between the host polymers and dopants. The excitons either can be confined at the dopant sites or can flow to the host polymers, subject to the relative position of the triplet energy levels of the material. For PF, because of its low triplet energy level, the exciton can flow back from the dopants to PF when the dopant has a higher triplet energy and subsequently quench the device efficiency. In contrast, efficient electrophosphorescence has been observed in doped PVK films because of the high triplet energy level of PVK. Better energy transfer from PVK to the dopants, as well as triplet exciton confinement on the dopants, leads to higher device performance than found in PF devices. Efficiencies as high as 16, 8.0, and 2.6 cd/A for green, yellow, and red emissions, respectively, can be achieved when PVK is selected as the host polymer. The results in this study show that the energy transfer and triplet exciton confinement have a pronounced influence on the device performance. In addition, this study also provides material design and selection rules for the efficient phosphorescent polymer light‐emitting diodes. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 2681–2690, 2003

The advantages of polymers are the fabrication and patterning of ultra-large-area coatings. In this paper, an approach which combines self-assembled polyelectrolytes, ink-jet printing, and electroless metal plating technologies for the fabrication of vertically integrated electronic circuits is successfully demonstrated. Through these processes, several layers of metal integrated circuits were deposited sequentially with polymer layers sandwiched between each layer of wires. Hence, one can build vertically integrated electronic components consisting of diodes, capacitors, resistors, and inductors with a relatively simple and low-cost technology.

We report the fabrication of a photoresponsive organic field-effect transistor (OFET) based on a stable, n-type organic semiconductor (F 16 CuPc) and low-temperature processable polymer gate dielectric. The device exhibited a photoswitching speed of much less than 10 ms and a photosensitivity of 1.5 mA/W at low optical power. Under illumination, the device produced a current gain (I light /I dark ) of 22 at V G ) 4 V. The drain current increased gradually with an increase in the illumination intensity, resulting in typical output FET characteristics. The multifunctions (photodetection, photoswitching, signal amplification) achieved by the single device can ensure very promising material for future optoelectronic applications.

Highly stable, reproducible, photosensitive organic field-effect transistors based on an n-type organic material, copper hexadecafluorophthalocyanine, and two different polymeric gate dielectrics has been reported and their performances have been compared by evaluating the surface/interface properties. The devices produced a maximum photocurrent gain (I(light)/I(dark)) of 79 at V(G) = 7 V and showed the potentiality as multifunctional optoelectronic switching applications depending upon the external pulses. The switching time of the transistor upon irradiation of light pulse, i.e., the photoswitching time of the device, was measured to be approximately 10 ms. On the basis of optical or combination of optical and electrical pulses, the electronic/optoelectronic properties of the device can be tuned efficiently. The multifunctions achieved by the single device can ensure very promising material for high density RAM and other optoelectronic applications. Furthermore, as the device geometry in the present work is not limited to rigid substrate only, it will lead to the development of flexible organic optoelectronic switch compatible with plastic substrates.

We report the formation of laterally stacked ambipolar crystal wire for high-mobility organic field-effect transistors (OFETs), along with a simple logic circuit through a solution process. A soluble pentacene derivative, 6,13-bis(triisopropylsilylethynyl)pentacene (Tips-pentacene), and N,N'-dioctyl-3,4,9,10-perylenedicarboximide (PTCDI-C8) were used as p-type and n-type organic semiconductors, respectively. The laterally stacked ambipolar crystal wire is made up of Tips-pentacene and PTCDI-C8 crystals in a structure of Tips-pentacene/PTCDI-C8/Tips-pentacene (TPT). The inner part of the crystal is made up of PTCDI-C8, and Tips-pentacene is present on both sides. These TPT crystals exhibit typical ambipolar charge transport behavior in organic electronic devices, which show very balanced hole and electron mobility as high as 0.23 cm(2)/V·s and 0.13 cm(2)/V·s, respectively. Static and dynamic operational stability of the device is investigated by measuring the device performance as a function of storage time and applying voltage pulse, respectively, and it shows good air stability. In addition, a simple logic circuit based on the TPT crystal wire has been fabricated, and the static and dynamic performance has been evaluated. The results indicate that the TPT crystals are potentially useful for miniaturized organic electronic devices.

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High quality, single crystalline, ordered arrays of a p-conjugated organic molecule, N,N 0 -dioctyl-3,4,9,10-perylene tetracarboxylic diimide (PTCDI-C 8 ), were grown by solution processing and used to fabricate a low-cost, high-performance organic phototransistor (OPT). The single crystalline nature of the microstructure was investigated using 2D-GIXD measurement. The organic field-effect transistor fabricated using periodic arrays of elongated crystals exhibited a photoresponsivity (P) of ca. 1 A W À1 and a photo to dark current ratio (I on /I off ) of 2.5 Â 10 3 at V G ¼ 12 V and a maximum P of ca. 7 A W À1 at the high gate bias regime (V G ¼ 50 V) with an optical power of ca. 7.5 mW cm À2 . With polymeric gate dielectric, the OPT exhibited very stable n-type characteristics both in the dark and under light illumination and showed reproducible photo-switching behavior. The dependence of the photocurrent on the gate/drain voltage and on illumination intensity provided an effective way to control the number of photo-carriers generated in the active material, enabling the precise tuning of the device's performance. Performance comparison between OPTs with ordered crystal arrays and thin films of PTCDI-C 8 confirmed that the material's intrinsic properties were better realized in the crystalline device, presumably because of higher charge carrier mobility and better charge transport capability. This one-step, solution-based, self-assembly fabrication of multifunctional (photodetection, photoswitching, signal amplification) optoelectronic devices has potential to aid the development of organic semiconductors with high-quality micro/nanostructures for large-scale application and lowcost optoelectronic devices.