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In this manuscript, we describe a biocompatible organic electrode system, comprising poly(3,4-ethylenedioxythiophene) (PEDOT) microelectrode arrays on indium tin oxide (ITO) glass, that can be used to regulate the neuron type, location, polarity, and outgrown length of neuron-like cells (PC-12). We fabricated a PEDOT microelectrode array with four different sizes (flat; 20, 50, and 100 μm) through electrochemical polymerization. Extracellular matrix proteins absorbed well on these organic electrodes; cells absorbed selectively on the organic electrodes when we used polyethylene oxide/polypropylene oxide/polyethylene oxide triblock copolymers (PEO/PPO/PEO, Pluronic™ F108) as the anti-adhesive coating. In this system, the neurite polarities and neuron types could be manipulated by varying the width of the PEDOT microelectrode arrays. On the unpatterned PEDOT electrode, PC-12 cells were randomly polarized, with approximately 80% having multi-polar cell types. In contrast, when we cultured PC-12 cells on the 20 μm wide PEDOT line array, the neurites aligned along the direction of the organic electrodes, with the percentage of uni- and bipolar PC-12 cells increasing to greater than 90%. The outgrowth of neurites on the microelectrodes was promoted by ∼60% with an applied electrical stimulation. Therefore, these electroactive PEDOT microelectrode arrays have potential for use in tissue engineering related to the development and regeneration of mammalian nervous systems. [ABSTRACT FROM AUTHOR]

A series of π-conjugated bis-terpyridyl ligands (M1–M3) bearing various benzodiazole cores and their corresponding main-chain Ru(ii) metallo-polymers were designed and synthesized. The formation of metallo-polymers were confirmed by NMR, relative viscosity, and UV-visible titration measurements. The effects of electron donor and acceptor interactions on their thermal, optical, electrochemical, and photovoltaic properties were investigated. Due to the strong intramolecular charge transfer (ICT) interaction and metal to ligand charge transfer (MLCT) in Ru(ii)-containing polymers, the absorption spectra covered a broad range of 260–750 nm with the optical band gaps of 1.77–1.63 eV. In addition, due to the broad sensitization areas of the metallo-polymers, their bulk heterojunction (BHJ) solar cell devices containing [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) as an electron acceptor exhibited a high short-circuit current (Jsc). An optimum PVC device based on the blended polymer P1 : PCBM = 1 : 1 (w/w) achieved the maximum power conversion efficiency (PCE) value up to 0.45%, with Voc= 0.61 V, Jsc= 2.18 mA cm−2, and FF= 34.1% (under AM 1.5 G 100 mW cm−2), which demonstrated a novel family of conjugated polyelectrolytes with the highest PCE value comparable with BHJ solar cells fabricated from ionic polythiophene and C60. [ABSTRACT FROM AUTHOR]

The influence of solvent on the electrochemical property and conductivity of PEDOT has been investigated by electrochemical and physical characterizations. The PEDOT treated with different solvents reveals a different reversibility of ionic transport and cycling stability, which is associated with the conformational rearrangement from aggregated to linear polymer chains, as evidenced from atomic force microscopy (AFM). The conductivity of the PEDOT thin film can also be enhanced while the degree of linear polymer chains is higher. The application of highly conductive PEDOT thin film as a buffer layer in the polymer photovoltaic devices was realized. A PCE of 4.27% for photovoltaic devices based on P3HT–PCBM under simulated sun light is achieved by using a PEDOT thin film treated with DMSO. [ABSTRACT FROM AUTHOR]

Building on the success of organic electronic devices, such as light-emitting diodes and field-effect transistors, procedures for fabricating non-volatile organic memory devices are now being explored. Here, we demonstrate a novel organic memory device fabricated by solution processing. Programmable electrical bistability was observed in a device made from a polystyrene film containing gold nanoparticles and 8-hydroxyquinoline sandwiched between two metal electrodes. The as-prepared device, which is in a low-conductivity state, displays an abrupt transition to a high-conductivity state under an external bias of 2.8 V. These two states differ in conductivity by about four orders of magnitude. Applying a negative bias of 1.8 V causes the device to return to the low-conductivity state. The electronic transition is attributed to the electric-field-induced charge transfer between the gold nanoparticles and 8-hydroxyquinoline. The transition from the low- to the high-conductivity state takes place in nanoseconds, and is non-volatile, indicating that the device may be used for low-cost, high-density memory storage. [ABSTRACT FROM AUTHOR]

In this Letter, ambipolar transport properties of a bilayer of In2O3 and a pentacene heterostructure have been realized. While In2O3 thin film transistors exhibited a n-channel behavior, pentacene presumed p-channel characteristics on bare SiO2/p-Si substrates. However, when a bilayer of In2O3/pentacene was realized on the gate dielectrics, the hybrid structure exhibited both n- and p-channel conductions, depicting an ambipolar transistor behavior. When two identical ambipolar transistors were integrated to establish an inverter structure, a voltage gain of 10 was obtained. The results indicate that these heterostructures can be utilized for the complementary circuits. [ABSTRACT FROM AUTHOR]

Thin film transistors (TFTs) of indium oxide (In2O3) and tin oxide (SnO2) were fabricated on SiO2 gate dielectric using reactive evaporation process. Structural investigation of the films revealed that In2O3 films were polycrystalline in nature with preferred (222) orientation and SnO2 films exhibited amorphous nature. The x-ray photoelectric spectroscopy measurements suggest that SnO2 films were oxygen rich and presume mixed oxidation states of Sn, namely Sn2+ and Sn4+. While the In2O3 based TFTs possess n-type channel conduction, SnO2 based TFTs exhibited anomalous p-type conductivity. Integration of these n- and p-type devices resulted in complementary inverter with a gain of 11. [ABSTRACT FROM AUTHOR]

In this article, we report the fabrication of SnO2 thin film transistors (TFTs) fabricated by reactive evaporation. Different from the previous reports, the fabricated TFTs exhibit p-type conductivity in its undoped form. The postdeposition annealing temperature was tuned to achieve p-channel SnO2 TFTs. The on/off ratio and the field-effect mobility were ∼103 and 0.011 cm2/V s, respectively. To demonstrate inverter circuit, two devices with different threshold voltages were combined and an output gain of 2.8 was achieved. The realization of p-channel oxide TFTs would open up new challenges in the area of transparent electronics. [ABSTRACT FROM AUTHOR]

Grazing-incidence x-ray diffraction and atomic force microscopy were performed on bulk heterojunction regioregular poly(3-hexylthiophene) (RR-P3HT) [6,6]-phenyl-C71-butyric acid methyl esters spin-cast films with different film processing conditions to correlate the crystalline nanostructure of P3HT with the corresponding solar cell performance. The increase in long wavelength absorption for solvent annealed films is related to highly conjugated crystal structure of RR-P3HT phase-separated in the active layer. Upon thermal annealing, the solvent annealed 50-nm-thick device shows high solar cell performance with fill factor up to 73% and power conversion efficiency of 3.80%. [ABSTRACT FROM AUTHOR]

The authors demonstrate the operation of an organic single-crystal complementary circuit in the form of a simple inverter. The device is constructed from a high mobility p-type organic single-crystal transistor of tetramethylpentacene (TMPC) and a n-type single-crystal transistor of N,N′-di[2,4-difluorophenyl]-3,4,9,10-perylenetetracarboxylic diimide (PTCDI). Field-effect mobilities of up to 1.0 cm2/V s are reported for TMPC devices, while a mobility of 0.006 cm2/V s is reported for a n-type PTCDI single-crystal device. Considering that organic single-crystal inverters have not yet been explored, they are representative of potential candidates for use in high-performance complementary circuits. [ABSTRACT FROM AUTHOR]

We compare organic donor/acceptor heterojunction photovoltaic devices based on copper phthalocyanine (CuPc) as the donor and [6,6]-phenyl C60 butyric acid methyl ester (PCBM) or buckminsterfullerene (C60) as the acceptor. The effect of the two acceptors on open-circuit voltage and short-circuit current density is studied. Improved interface properties, optimal energy level matching, and more balanced charge transport are believed to be the reasons for better performance of CuPc/PCBM heterojunction device, in terms of photocurrent and fill factor. The energy conversion efficiency of the devices under AM1.5G solar illumination at 130 mW/cm2 is improved to 1.18%, up from 0.74%. [ABSTRACT FROM AUTHOR]

Recently, electrical bistability was demonstrated in polymer thin films incorporated with metal nanoparticles [J. Ouyang, C. W. Chu, C. R. Szmanda, L. P. Ma, and Y. Yang, Nat. Mater. 3, 918 (2004)]. In this letter, we show the evidence that electrons are the dominant charge carriers in these bistable devices. Direct integration of bistable polymer layer with a light-emitting polymer layer shows a unique light-emitting property modulated by the electrical bistability. A unique negative differential resistance induced by the charged gold nanoparticles is observed due to the charge trapping effect from the nanoparticles when interfaced with the light-emitting layer. [ABSTRACT FROM AUTHOR]

Polymer-based photovoltaic cells have been fabricated by inserting a thin, transparent, transition metal oxide layer between the transparent anode (indium tin oxide) and the polymer layer. Two different transition metal oxides, namely vanadium oxide and molybdenum oxide, were used and the device performance was compared. The surface of the oxide films and the interface between the polymer and the oxide was studied with the help of atomic force microscopy. The effect of the thickness of the oxide layer on electrical characteristics of the device was also studied and optimized thickness was achieved to give high power conversion efficiency of 3.3% under simulated AM1.5G illumination of 100 mW/cm2. [ABSTRACT FROM AUTHOR]

An effective connecting structure for tandem organic light-emitting devices is reported. The connecting structure consists of a thin metal layer as the common electrode, a hole-injection layer containing MoO3 on one side of the common electrode, and an electron-injection layer involving Cs2CO3 on the other side. Such a connecting structure permits efficient opposite hole and electron injection into two adjacent emitting units and gives tandem devices superior electrical and optical performances. Furthermore, the present connecting structure involves no sputtering or handling of reactive metals during device fabrication and can be prepared purely by thermal evaporation, thus rendering device processing more feasible. [ABSTRACT FROM AUTHOR]

We demonstrate bilayer source-drain (S-D) electrodes for organic thin film transistors (OTFT). The bilayer consists of a transition metal oxide (MoO3,WO3, or V2O5) layer and a metal layer. The metal oxide layer, directly contacting the organic semiconducting layer, serves as the charge-injection layer. The overcoated metal layer is responsible for the conduction of charge carriers. We found that the metal oxide layer coupled between pentacene and metal layers played an important role in improving the field-effect transistor characteristics of OTFTs. Devices with the bilayer S-D electrodes showed enhanced hole-injection compared to those with only metal electrode. High field-effect mobility of 0.4 cm2/V s and on/off current ratios of 104 were obtained in the pentacene based TFTs using the bilayer S-D electrodes at a gate bias of -40 V. The improvement is attributed to the reduction in the contact barrier and the prevention of metal diffusion into the organic layer and/or unfavorable chemical reaction between the organic layer and the metal electrode. [ABSTRACT FROM AUTHOR]

We report organic solar cells fabricated with small-molecule organic semiconductor tetracene/C60 heterojunction as the photoactive layer. The external power conversion efficiency of the devices under AM 1.5 solar illumination at 100 mW/cm2 (1 sun) is 2.3±0.5% with relatively high open-circuit voltage (Voc=0.58±0.06 V) compared to most of the other small-molecular donor-acceptor (D-A) heterojunction solar cells reported so far. Using atomic force microscopy and x-ray diffraction we found that tetracene thin films consist of submicron-sized grains with rough surface and well defined molecular order. Therefore, using high mobility polycrystalline tetracene thin films for D-A heterojunction devices dramatically increases area of tetracene and C60 interface for exciton diffusion to reduce the recombination. [ABSTRACT FROM AUTHOR]

Flexible indium tin oxide (ITO)-free poly(3-hexylthiophene):[6,6]-phenyl C61-butyric acid methyl ester (P3HT:PC61BM) solar cells with a spin-coated silver nanowire transparent electrode are demonstrated. The solution-processed silver nanowire thin film not only exhibits high transmission (∼87%), but also shows low sheet resistance Rs (∼25 Ω/sq). For solar cells with a conventional structure, the power conversion efficiency (PCE) of devices based on silver nanowires can reach around 2.29%. For the inverted structure, the PCE of devices can reach 3.39%. Conventional and inverted flexible ITO-based P3HT:PC61BM solar cells are also fabricated as a reference for comparison. For both types of solar cells, the PCE of ITO-free devices is very close that of an ITO-based polymer solar cell. [ABSTRACT FROM AUTHOR]

Gold nanoparticle-decorated graphene oxides (AuNP-GOs) have been incorporated into inverted organic photovoltaic devices (OPVs) as anode interlayers. The OPVs fabricated with AuNP-GOs exhibited significant improvement in both the short-circuit current and fill factor compared to a reference device fabricated with neat GOs. We attribute the improvement in the efficiency of the device to the plasmonic effects of the AuNP-GO nanocomposites, which induced local enhancement of the electromagnetic field. More importantly, the inverted OPVs also exhibited better reliability after the use of AuNP-GO nanocomposites. [ABSTRACT FROM AUTHOR]

Abstract Gels prepared from low-molecular-weight gelators (LMWGs) represent versatile soft materials. Self-assembly of LMWGs forms nanofibers and above critical gelation concentrations, the entanglement of which leads to self-supporting gels. Owing to the dynamic properties of the self-assembly process, stimuli-responsive LMWGs have prospered in the last decade. In addition, incorporating multiple LMWGs into one system brings the opportunity to achieve sophisticated designs and functions. This review covers recent advances in the field of supramolecular gels, from stimuli-responsive gelators to multicomponent systems that are self-sorting and/or co-assembling.

Two-dimensional transition metal dichalcogenides (TMDCs) such as molybdenum sulfide MoS2 and tungsten sulfide WSe2 have potential applications in electronics because they exhibit high on-off current ratios and distinctive electro-optical properties. Spatially connected TMDC lateral heterojunctions are key components for constructing monolayer p-n rectifying diodes, light-emitting diodes, photovoltaic devices, and bipolar junction transistors. However, such structures are not readily prepared via the layer-stacking techniques, and direct growth favors the thermodynamically preferred TMDC alloys. We report the two-step epitaxial growth of lateral WSe2-MoS2 heterojunction, where the edge of WSe2 induces the epitaxial MoS2 growth despite a large lattice mismatch. The epitaxial growth process offers a controllable method to obtain lateral heterojunction with an atomically sharp interface. [ABSTRACT FROM AUTHOR]

This paper describes the design, assembly, fabrication, and evaluation of artificial molecular machines with the goal of implementing their internal nanoscale movements within nanoelectromechanical systems in an efficient manner. These machines, a unique class of switchable molecular compounds in the shape of bistable [2]rotaxanes, exhibit internal relative mechanical motions of their ring and dumbbell components as a result of optical, chemical, or electrical signals. As such, they hold promise as nanoactuation materials. Although micromechanical devices that utilize the force produced by switchable [3]rotaxane molecules have been demonstrated, the current prototypical devices require a mechanism that minimizes the degradation associated with the molecules in order for bistable rotaxanes to become practical actuators. We propose a modified design in which electricity, instead of chemicals, is employed to stimulate the relative movements of the components in bistable [3]rotaxanes. As an initial step toward the assembly of a wholly electrically powered actuator based on molecular motion, closely packed Langmuir-Blodgett films of an amphiphilic, bistable [2]rotaxane have been characterized and an in situ Fourier transform infrared spectroscopic technique has been developed to monitor molecular signatures in device settings. [ABSTRACT FROM AUTHOR]