Nonvolatile flexible organic bistable devices fabricated utilizing CdSe/ZnS nanoparticles embedded in a conducting poly N-vinylcarbazole polymer layer

The bistable effects of CdSe/ZnS nanoparticles embedded in a conducting poly N-vinylcarbazole (PVK) polymer layer by using flexible poly-vinylidene difluoride (PVDF) and polyethylene terephthalate (PET) substrates were investigated. Transmission electron microscopy (TEM) images revealed that CdSe/ZnS nanoparticles were formed inside the PVK polymer layer. Current-voltage (I-V) measurement on the Al/[CdSe/ZnS?nanoparticles+?PVK]/ITO/PVDF and Al/[CdSe/ZnS nanoparticles+?PVK ]/ITO/PET structures at 300?K showed a nonvolatile electrical bistability behavior with a flat-band voltage shift due to the existence of the CdSe/ZnS nanoparticles, indicative of trapping, storing and emission of charges in the electronic states of the CdSe nanoparticles. A bistable behavior for the fabricated organic bistable device (OBD) structures is described on the basis of the I-V results. These results indicate that OBDs fabricated by embedding inorganic CdSe/ZnS nanoparticles in a conducting polymer matrix on flexible substrates are prospects for potential applications in flexible nonvolatile flash memory devices.     

Operating mechanisms of organic bistable devices containing ZnO nanoparticles embedded in a poly-4-vinyl-phenol layer

Scanning electron microscopy images showed that self-assembled ZnO nanoparticles were created inside a poly-4-vinyl-phenol (PVP) layer. Current-voltage (I-V) measurements on the Al/ZnO nanoparticles embedded in a PVP layer/indium tin oxide (ITO)/glass device fabricated by using a simple spin coating method at 300 K showed an electrical hysteresis behavior, indicative of an essential feature for a bistable device. The data fitting results of the I-V curves showed that the carrier transport mechanisms at low and high voltages were attributed to the space charge limited current and the Fowler-Nordheim tunneling processes, respectively. Possible operating mechanisms for the memory effects in the Al/ZnO nanoparticles embedded in a PVP layer/ITO devices are described on the basis of the I-V results.     

Electrical bistabilities and memory mechanisms of organic bistable devices fabricated utilizing SnO2 nanoparticles embedded in a poly(methyl methacrylate) layer

Organic bistable devices fabircated utilizing SnO2 nanoparticles embedded in a poly(methyl methacrylate) (PMMA) polymer layer were formed by using a spin coating method. Transmission electon microscopy images and photoluminescence spectra showed that synethized SnO2 nanoparticles were randomly distributed in the dibutyl ehter solution. Current-voltage (I-V) measurements on the Al/SnO2 nanoparticles embedded in PMMA layer/ITO devices at 300 K showed current bistability due to the existence of SnO2 nanoparticles. Current-time (I-t) results showed the memory retention characteristic of the device. Carrier transport mechanisms of the device are described on the basis of the I-V experimental results and electronic structures.     

Charging and discharging of single conjugated-polymer nanoparticles

Despite intense, long-term interest in organic semiconductors from both an applied and fundamental perspective, key aspects of the electronic properties of these materials remain poorly defined. A particularly challenging problem is the molecular nature of positive charge carriers, that is, holes or oxidized species in organics. Here, the unique ability of single-molecule spectroelectrochemistry (SMS-EC) to unravel complex electrochemical process in heterogeneous media is used to study the oxidation of nanoparticles of the conjugated polymer poly(9,9-dioctylfluorene-co-benzothiadiazole). A reversible hole-injection charging process has been observed that occurs primarily by initial injection of shallow (untrapped) holes, but soon after the injection, a small fraction of the holes becomes deeply trapped. Good agreement between experimental data and simulations strongly supports the presence of deep traps in the studied nanoparticles and highlights the ability of SMS-EC to study energetics and dynamics of deep traps in organic materials at the nanoscale.     

Unipolar bistable switching of organic non-volatile memory devices with poly(styrene-co-styrenesulfonic acid Na)

We demonstrated unipolar organic bistable memory devices with 8 x 8 cross-bar array type structure. The active material for the organic non-volatile memory devices is poly(styrene-co-styrenesulfonic acid Na) (PSSANa). From the electrical measurements of the PSSANa organic memory devices, we observed rewritable unipolar switching behaviors with a stable endurance and narrow cumulative probability. Also the PSSANa memory devices exhibited a uniform cell-to-cell switching with a high ON/OFF ratio of approximately 10(5) and good retention time of approximately 10(4) seconds without significant degradation.     

Synthesis and optical characterization of ZnO nanoparticles capped with 2-aminothiols

ZnO nanoparticles were synthesized by precipitation method. To reduce the agglomeration among small ZnO nanoparticles, an efficient surface modification method was proposed using 2-aminothiols as a capping agent. The effect of capping reagent is investigated on optoelectronics properties of ZnO. The capping of ZnO with 2-aminothiol leads to the shift in fluorescence intensity and also effected the UV–vis spectra of ZnO. The strategy exposed new dimensions to fine tune the fluorescence signatures of the ZnO.     

Dielectric characteristics of poly(N-vinylcarbazole) and its nanocomposites with ZnO and acetylene black

Dielectric constant and dielectric loss parameters of poly(N-vinylcarbazole) homopolymer and several nanocomposites of poly(N-vinylcarbazole) with ZnO were studied as a function of frequency. In the low frequency range (0–20 kHz) the dielectric constant values of the base polymer varied from ∼30 to ∼2, and the same for the composite varied from 8500 to 2000 (4.54), 5000 to 1000 (2.63) and 2000 to 500 (1.17), the figures in parenthesis denoting the ratio of ZnO:PNVC in the nanocomposites. Likewise, dielectric loss parameters were found to be (7–10 × 10⁻³) for the homopolymer and 4.0, 2.5 and 1.25 for the three PNVC–ZnO composites respectively. Notably, a mechanical mixture of ZnO and PNVC (1.17) exhibited much lower dielectric constant (400–25) and loss parameters (0.14–0.065). These features imply polarization was differently affected depending on factors such as grain size and grain-boundary interfaces being formed in these systems. Tan δ–temperature variation for the composites revealed the occurrence of a maximum between 60 and 70 °C. These features signified dipole group loss in the composite. Dielectric constant of a conducting nanocomposite of poly(N-vinylcarbazole) with acetylene black revealed very low negative value tending to zero at high frequency.     

Room temperature optical and magnetic properties of polyvinylpyrrolidone capped ZnO nanoparticles

Defect induced room temperature ferromagnetic properties of polyvinylpyrrolidone (PVP) capped nanocrystalline ZnO samples have been studied. Crystal phase and the lattice parameter of the synthesized nanocrystalline samples have been determined from X-ray diffraction spectra (XRD) and high-resolution transmission electron micrographs (HR-TEM). Room temperature photoluminescence (PL) spectrum for the bare ZnO sample shows a strong band at ~ 379 nm and another band at ~ 525 nm. The PL spectra also revealed that the number of oxygen vacancies in the uncapped sample is more than the PVP capped sample. Both sample exhibit ferromagnetic property at room temperature when annealed at 500 °C for 3 h, due to the formation of adequate oxygen vacancy related defects. The saturation magnetization for the annealed PVP capped sample is found to be larger compared to that for the uncapped sample.     

Electron transfer properties of organic dye-sensitized solar cells based on indoline sensitizers with ZnO nanoparticles

Two indoline dyes, coded D149 and D205, were used as the sensitizers of ZnO dye-sensitized solar cells (DSCs) with optimal energy conversion efficiencies of more than 5%, under AM 1.5 full sunlight illumination (100?mW?cm( - 2)). Higher interfacial charge transfer rate and retardant fluorescence decay confirmed from transient fluorescence illustrated that D205-sensitized ZnO DSCs could possess better electron transport than D149-sensitized ZnO DSCs. The enhancement of V(oc) and J(sc) for D205-sensitized ZnO DSCs was ascribed to the effective suppression of electron recombination by extending the alkyl chain on the terminal rhodanine moiety from ethyl to octyl. The evidence of enhanced electron diffusion coefficient was further shown by electrochemical impedance spectroscopy (EIS).     

Optoelectronic characteristics of inorganic/organic hybrid device based on poly(N-vinylcarbazole)/ cadmium selenide thin films

Inorganic/organic hybrid light-emitting diodes were easily fabricated with a thin film containing water-soluble cadmium selenide nanocrystals and poly(N-vinylcarbazole) as an emitting layer by a spin-coating method. The cadmium selenide nanocrystals were synthesized in aqueous solution with L-cysteine hydrochloride as the stabilizer and were transferred from the aqueous solution into chloroform by a cationic surfactant cetyltrimethyl ammonium bromide. A broad emission spanning the whole visible wavelength range was obtained from the inorganic/organic hybrid devices whether poly(N-vinylcarbazole) was present in the devices or not, and the electroluminescence intensity of the devices increased as the applied voltages increased. However, an obvious blue-shift of the wavelength was observed with the increasing applied voltages in the device with poly(N-vinylcarbazole). Accordingly, the emission color of the device made with poly(N-vinylcarbazole) could be tuned from white to blue by varying the applied voltages, but the emission color of the device made without poly(N-vinylcarbazole) was almost constrained in the white region. This can be attributed to a limited contribution of poly(N-vinylcarbazole) emission to the electroluminescence spectra under the higher applied voltage. By comparing the electroluminescence intensity and the current-voltage characteristics of the devices made with and without poly(N-vinylcarbazole), the performance of the device with poly(N-vinylcarbazole) was improved greatly, which indicated that poly(N-vinylcarbazole) played an important role in the carrier injection and transportation in the device with poly(N-vinylcarbazole).     

Effect of glycerol on retention time and electrical properties of polymer bistable memory devices based on glycerol-modified PEDOT:PSS

The addition of glycerol to Poly(3,4-ethylenedioxythiophene):Poly(styrene sulfonate) (PEDOT:PSS) films affected the bipolar switching characteristics of nonvolatile polymer memory devices (PMDs). Increasing the glycerol/PEDOT:PSS ratio caused increase in the OFF-current of the PMDs, but did not affect the ON-current levels. This result demonstrates that highly-conductive current paths occur in the ON-state. The write-read-erase-read cycle test was operated > 10(5) times. And, the ON-retention time is largely dependent on the glycerol to PEDOT:PSS ratio and annealing temperature. In addition, AFM analysis on the G-PEDOT:PSS films to see how the surface morphology of G-PEDOT:PSS layer influences the retention time properties was carried out.     

Photocatalytic degradation of organic dyes with manganese-doped ZnO nanoparticles

Manganese-doped and undoped ZnO photocatalysts were synthesized via wet-chemical techniques. Doping of ZnO with manganese (Mn(2+)) was intended to create tail states within the band gap of ZnO. These can subsequently be used as efficient photocatalysts which can effectively degrade organic contaminants only with visible light irradiation. Photocatalysts prepared with these techniques, which were characterized with transmission electron microscopy (TEM), infrared spectroscopy (FTIR), photo-co-relation spectroscopy (PCS) and UV-vis-spectroscopy showed significant difference in the optical absorption of Mn-doped ZnO. Enhancement in optical absorption of Mn-doped ZnO indicates that it can be used as an efficient photocatalyst under visible light irradiation. The photo-reduction activities of photocatalysts were evaluated using a basic aniline dye, methylene blue (MB) as organic contaminant irradiated only with visible light from tungsten bulb. It was found that manganese-doped ZnO (ZnO:Mn(2+)) bleaches MB much faster than undoped ZnO upon its exposure to the visible light. The experiment demonstrated that the photo-degradation efficiency of ZnO:Mn(2+) was significantly higher than that of undoped ZnO and might also be better than the conventional metal oxide semiconductor such as TiO(2) using MB as a contaminant.     

Hybrid photovoltaic devices of polymer and ZnO nanofiber composites

Organic semiconductor-based photovoltaic devices offer the promise of a low-cost photovoltaic technology that could be manufactured via large-scale, roll-to-roll printing techniques. Existing organic photovoltaic devices have currently achieved solar power conversion efficiencies greater than 3%. Although encouraging, the reasons higher efficiencies have not been achieved are poor overlap between the absorption spectrum of the organic chromophores and the solar spectrum, non-ideal band alignment between the donor and acceptor species, and low charge carrier mobilities resulting from the disordered nature of organic semiconductors. To address the latter issues, we are investigating the development of nanostructured oxide/conjugated polymer composite photovoltaic (PV) devices. These composites can take advantage of the high electron mobilities attainable in oxide semiconductors and can be fabricated using low-temperature solution-based growth techniques. Additionally, the morphology of the composite can be controlled in a systematic way through control of the nanostructured oxide growth. ZnO nanostructures that are vertically aligned with respect to the substrate have been grown. Here we discuss the fabrication of such nanostructures and present results from ZnO nanofiber/poly(3-hexylthiophene) (P3HT) composite PV devices. The best performance with this cell structure produced an open circuit voltage (V_oc) of 440 mV, a short circuit current density (J_sc) of 2.2 mA/cm², a fill factor (FF) of 0.56, and a conversion efficiency (η) of 0.53%. Incorporation of a blend of P3HT and (6,6)-phenyl C₆₁ butyric acid methyl ester (PCBM) into the ZnO nanofibers produced enhanced performance with a V_oc of 475 mV, J_sc of 10.0 mA/cm², FF of 0.43, and η of 2.03%. The power efficiency is limited in these devices by the large fiber spacing and the reduced V_oc.     

A solid-state dye-sensitized solar cell based on a novel ionic liquid gel and ZnO nanoparticles on a flexible polymer substrate

This paper describes a new strategy to make a full solid-state, flexible, dye-sensitized solar cell (DSSC) based on novel ionic liquid gel, organic dye, ZnO nanoparticles and carbon nanotube (CNT) thin film stamped onto a polyethylene terephthalate (PET) substrate. The CNTs serve both as the charge collector and as scaffolds for the growth of ZnO nanoparticles, where the black dye molecules are anchored. It opens up the possibility of developing a continuous roll to roll processing for THE mass production of DSSCs.     

A transparent and flexible organic bistable memory device using parylene with embedded gold nanoparticles

In this work, we demonstrate the fabrication of a transparent and flexible memory device in the simple structure of metal/dielectric/metal (MIM). Here, the MIM structure consists of gold electrode/200 nm Parylene-C/20 nm gold nanoparticles/100 nm Parylene-C/indium-tin-oxide (ITO) coated polyethylene terephthalate (PET). The use of parylene as the dielectric layer is important to ensure that there is no thermal stress induced on the flexible ITO/PET substrate compare to other reported works using various organic dielectrics that require high temperature curing. In addition, parylene deposition does not disturb the drop-casted gold nanoparticles. Hence, the use of parylene will be the right step forward in the fabrication of mechanically flexible and optically transparent devices. Current versus voltage (I–V) plot shows the presence of hysteresis suggesting the charge storage capability as a memory device. In the I–V plot, three distinct regions based on the slope have been identified and the transport mechanisms are discussed and explained. The fabricated device shows similar behavior as write-once-read-many memory device and can be programmed with either positive or negative bias voltage. However, the memory device shows unstable current state when being bent under different curvature diameters.     

Effect of ZnO nanoparticles on the structure and ionic relaxation of poly(ethylene oxide)-LiI polymer electrolyte nanocomposites

The effect of ZnO nanoparticles on the structure and ionic relaxation of LiI salt doped poly(ethylene oxide) (PEO) polymer electrolytes has been investigated. X-ray diffraction, high resolution transmission electron microscopy and field emission scanning electron microscopy show that ZnO nanoparticles dispersed in the PEO-LiI polymer electrolyte reduce the crystallinity of PEO and increase relative smoothness of the surface morphology of the nanocomposite electrolyte. The electrical conductivity of the nanocomposites is found to increase due to incorporation of ZnO nanoparticles. We have shown that the structural modification due to insertion of ZnO nanoparticles results in the enhancement of the mobility i.e., the hopping rate of mobile Li+ ions and hence the ionic conductivity of PEO-LiI-ZnO nanocomposite electrolyte.     

Preparation and electrical properties of Ga-doped ZnO nanoparticles by a polymer pyrolysis method

In this article, preparation of Ga-doped zinc oxide (GZO) nanoparticles by a polymer pyrolysis method is reported. The pyrolysis behaviors of the polymer precursors prepared via the in situ polymerization of metal salts and acrylic acid are analyzed using thermalgravity-differential scanning calorimetry (TG-DSC) techniques. Then, the structural characteristics of the products are studied by X-ray diffraction (XRD) and transmission electron microscopy (TEM). It is revealed by the results that the GZO nanoparticles calcined at 600 °C show good crystallinity with the wurtzite structure. GZO nanoparticles doped with 4 mol% Ga have a mean particle size of 26 nm with spherical-like morphology. Electrical resistivity measurement shows that, before and after high temperature annealing under H₂ atmosphere, the resistivity of the GZO nanoparticles is decreased by one and four orders in magnitude, respectively, compared with the pure ZnO nanoparticles. In addition, due to its versatility, this in situ polymer pyrolysis method can be easily extended to synthesis of other n-type doped semiconductor, such as In and Al doped ZnO or Sb doped SnO₂.     

Charge trapping and luminance mechanisms of organic light-emitting devices with a 5,6,11,12-tetraphenylnaphthacene emission layer

The electrical and the optical properties of the organic light-emitting devices fabricated utilizing a 5,6,11,12-tetraphenylnaphthacene (rubrene) emission layer (EML) were investigated to clarify their charge trapping and luminance mechanisms. The increase in the thickness of the rubrene EML extended the width of the recombination zone, resulting in the enhancement of the efficiency and in the variation of the shoulder peak intensity of the electroluminescence spectra. The charge trapping and luminance mechanisms were affected by the total thickness of the rubrene layer, regardless of the existence of the barrier layers. The charge trapping and luminance mechanisms are described on the basis of the experimental results.     

Ag nanoparticles capped by a nontoxic polymer: Electrochemical and spectroscopic characterization of a novel nanomaterial for glucose detection

Modified electrodes with metal or metal oxides nanoparticles are particularly appealing to improve sensor performances and fabricate miniaturized devices, as required also in glucose detection. A Pt electrode modified by drop casting of a novel nanostructured film based on silver nanoparticles (Ag-NPs) capped in a commercial nontoxic polyvinyl alcohol (PVA) matrix is proposed here as a valid alternative to classical glucose (bio)sensors. The extensive electrochemical and spectroscopic characterization by X-ray Photoelectron Spectroscopy (XPS) of this advanced nanomaterial is presented to study its response to glucose and to investigate the chemical nature of deposited Ag.