ZnO Nanoparticle Layer Research Articles

Heterojunction of ZnO nanoparticle/PMMA and its ultraviolet electroluminescence.

A ZnO nanoparticle layer was synthesized by the sol-gel method on ITO glass. Devices with a ZnO nanoparticle layer/polymethylmethacrylate (PMMA) heterojunction structure were then fabricated and the room temperature electroluminescence (EL) spectra were studied. Under DC bias, ultraviolet (UV) EL at 390 nm from the ZnO band edge emission was observed, and defect-related emission of ZnO at 600 and 760 nm were also detected. The EL mechanisms are discussed in terms of the carrier tunneling process.

Fabrication of Well-Aligned ZnO Nanorods Using a Composite Seed Layer of ZnO Nanoparticles and Chitosan Polymer.

In this study, by taking the advantage of both inorganic ZnO nanoparticles and the organic material chitosan as a composite seed layer, we have fabricated well-aligned ZnO nanorods on a gold-coated glass substrate using the hydrothermal growth method. The ZnO nanoparticles were characterized by the Raman spectroscopic techniques, which showed the nanocrystalline phase of the ZnO nanoparticles. Different composites of ZnO nanoparticles and chitosan were prepared and used as a seed layer for the fabrication of well-aligned ZnO nanorods. Field emission scanning electron microscopy, energy dispersive X-ray, high-resolution transmission electron microscopy, X-ray diffraction, and infrared reflection absorption spectroscopic techniques were utilized for the structural characterization of the ZnO nanoparticles/chitosan seed layer-coated ZnO nanorods on a gold-coated glass substrate. This study has shown that the ZnO nanorods are well-aligned, uniform, and dense, exhibit the wurtzite hexagonal structure, and are perpendicularly oriented to the substrate. Moreover, the ZnO nanorods are only composed of Zn and O atoms. An optical study was also carried out for the ZnO nanoparticles/chitosan seed layer-coated ZnO nanorods, and the obtained results have shown that the fabricated ZnO nanorods exhibit good crystal quality. This study has provided a cheap fabrication method for the controlled morphology and good alignment of ZnO nanorods, which is of high demand for enhancing the working performance of optoelectronic devices.

Hydrothermal Growth of Vertically Aligned ZnO Nanorods Using a Biocomposite Seed Layer of ZnO Nanoparticles.

Well aligned ZnO nanorods have been prepared by a low temperature aqueous chemical growth method, using a biocomposite seed layer of ZnO nanoparticles prepared in starch and cellulose bio polymers. The effect of different concentrations of biocomposite seed layer on the alignment of ZnO nanorods has been investigated. ZnO nanorods grown on a gold-coated glass substrate have been characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) techniques. These techniques have shown that the ZnO nanorods are well aligned and perpendicular to the substrate, and grown with a high density and uniformity on the substrate. Moreover, ZnO nanorods can be grown with an orientation along the c-axis of the substrate and exhibit a wurtzite crystal structure with a dominant (002) peak in an XRD spectrum and possessed a high crystal quality. A photoluminescence (PL) spectroscopy study of the ZnO nanorods has revealed a conventional near band edge ultraviolet emission, along with emission in the visible part of the electromagnetic spectrum due to defect emission. This study provides an alternative method for the fabrication of well aligned ZnO nanorods. This method can be helpful in improving the performance of devices where alignment plays a significant role.

Investigation of luminescent properties of ZnO nanoparticles for their use as a down‐shifting layer on solar cells

AbstractCommercially available solar cells (e.g. CdS/CdTe, CIGS, c‐Si) have a spectrally narrow absorption band when compared to the solar emission spectrum. The UV‐wavelength response of a solar cell (SC) can be improved by the application of a luminescent down‐shifting layer (LDSL) on the SC front side, permitting the conversion of short‐wavelength photons to the longer wavelength photons better matching the SC’s absorption spectrum. The ideal down‐shifting material must possess a large Stokes shift and have a high luminescence quantum yield. We propose the use of the LDSL containing ZnO nanoparticles of less than 5 nm in diameter able to absorb UV light (λ < 400 nm), where the solar cell spectral response (SR) is low, and re‐emitting at longer wavelengths (λ > 425 nm), where the typical SC’s SR increases. ZnO nanoparticles were synthesized by a low energy cluster beam deposition (LECBD) technique and their luminescent properties were studied as a function of the oxygen partial pressure (OPP) applied during the deposition process. The stoichiometry and crystallinity of ZnO nanoparticles can be controlled via the adjustment of the OPP. It was also observed that there exists an optimal value of the oxygen pressure introduced during the LECBD process, which permits to obtain the highest visible photoluminescence emission, necessary for an efficient down‐shifting. The yield of the down‐shifting in ZnO nanoparticle layer was determined varying the excitation wavelength using the photoluminescence excitation technique.

Highly Efficient, Color-Pure, Color-Stable Blue Quantum Dot Light-Emitting Devices

For colloidal quantum dot light-emitting diodes (QD-LEDs), blue emissive device has always been inferior to green and red counterparts with respect to device efficiency, primarily because blue QDs possess inherently unfavorable energy levels relative to green and red ones, rendering hole injection to blue QDs from neighboring hole transport layer (HTL) inefficient. Herein, unprecedented synthesis of blue CdZnS/ZnS core/shell QDs that exhibit an exceptional photoluminescence (PL) quantum yield of 98%, extraordinarily large size of 11.5 nm with a shell thickness of 2.6 nm, and high stability against a repeated purification process is reported. All-solution-processed, multilayered blue QD-LEDs, consisting of an HTL of poly(9-vinlycarbazole), emissive layer of CdZnS/ZnS QDs, and electron transport layer of ZnO nanoparticles, are fabricated. Our best device displays not only a maximum luminance of 2624 cd/m(2), luminous efficiency of 2.2 cd/A, and external quantum efficiency of 7.1%, but also no red-shift and broadening in electroluminescence (EL) spectra with increasing voltage as well as a spectral match between PL and EL.

Sparking deposited ZnO nanoparticles as double-layered photoelectrode in ZnO dye-sensitized solar cell

The semiconducting layers of ZnO nanoparticles (ZN), ZnO powder (ZP) and ZnO nanopowder (ZNP) were designed and fabricated for double-layered semiconducting photoelectrode in dye-sensitized solar cells (DSSCs). The under-layer was ZN, which was prepared by simple and cost-effective sparking technique onto F-doped tin oxide (FTO) glass substrate and its thickness was controlled by number of sparking cycles for 0, 10, 25, 50 and 100 rounds under atmospheric pressure. Then, ZP or ZNP was screened on to ZN to form double-layered photoelectrode. Here, the DSSC structures were FTO/double-layered ZnO/Eosin Y/electrolyte/Pt counterelectrode. The best results of DSSCs were observed with Jsc of 4.71mA/cm2 and 5.56mA/cm2 and photoconversion efficiency of 1.11% and 1.14% at 50 sparking cycles for ZP and ZNP over-layers, respectively. The efficiency enhancement can be explained by combination effects of electron and light scattering. Moreover, the modified equation of short circuit current density was developed and effectively used to explain the efficiency enhancement.

Highly Efficient Blue–Green Quantum Dot Light-Emitting Diodes Using Stable Low-Cadmium Quaternary-Alloy ZnCdSSe/ZnS Core/Shell Nanocrystals

High-quality blue-green emitting ZnxCd(1-x)S(1-y)Se(y)/ZnS core/shell quantum dots (QDs) have been synthesized by a phosphine-free method. The quantum yields of as-synthesized ZnxCd(1-x)S(1-y)Se(y)/ZnS core/shell QDs can reach 50-75% with emissions between 450 and 550 nm. The emissions of such core/shell QDs are not susceptible to ligand loss through the photostability test. Blue-green light-emitting diodes (LEDs) based on the low-cadmium ZnxCd(1-x)S(1-y)Se(y)/ZnS core/shell QDs have been successfully demonstrated. Composite films of poly[9,9-dioctylfluorene-co-N-[4-(3-methylpropyl)]-diphenylamine] (TFB) and ZnO nanoparticle layers were chosen as the hole-transporting and the electron-transporting layers, respectively. Highly bright blue-green QD-based light-emitting devices (QD-LEDs) showing maximum luminance up to 10000 cd/m(2), in particular, the blue QD-LEDs show an unprecedentedly high brightness over 4700 cd/m(2) and peak external quantum efficiency (EQE) of 0.8%, which is the highest value ever reported. These results signify a remarkable progress in QD-LEDs and offer a practicable platform for the realization of QD-based blue-green display and lighting.

ZnO nanoparticles as a luminescent down-shifting layer for photosensitive devices

The optical properties of ZnO nanoparticles (NPs) fabricated by three different methods were studied by the UV-excited continuous wave photoluminescence in order to estimate their down-shifting (DS) efficiency. Such a luminescent layer modifies the incident solar radiation via emitting wavelengths better matching the spectral response of the underlying photosensitive device (photodiode), thereby increasing its efficiency. Some of the studied ZnO NPs were subsequently deposited on the front side of commercial silicon photodiodes and the external quantum efficiency (EQE) characteristics of the final devices were measured. Through comparison of the photodiode's EQE characteristics before and after the deposition of the ZnO NPs layer, it was concluded that for the photodiode with a low UV sensitivity (about 8%), the ZnO luminescent layer produces a down-shifting effect and the EQE in the UV and blue range improves by 16.6%, while for the photodiodes with a higher initial UV sensitivity (about 50%), the EQE in this range decreases with the ZnO layer thickness, due to the effects competing with DS, like the diminution of the ZnO layer transmittance and an increasing diffusion.

Electrochemical synthesis of a double‐layer film of ZnO nanosheets/nanoparticles and its application for dye‐sensitized solar cells

ABSTRACTA double‐layer film, consisting of an upper layer of ZnO nanosheets and a lower layer of ZnO nanoparticles (designated as ZnONS/NP), was synthesized for the photoanode of a dye‐sensitized solar cell (DSSC) by a one‐step potentiostatic electrodeposition on a conducting fluorine‐doped tin oxide substrate at 70 °C in a solution containing zinc nitrate and sodium acetate, followed by the pyrolysis of the film at 300 °C. The growth mechanism of the double‐layer nanostructure was studied by monitoring the morphological changes at various periods of electrodeposition. The effects of the concentration of acetate anion on the morphology of the double‐layer structure were also studied. The double‐layer film of ZnONS/NP showed a better self‐established light scattering property, compared with that of a thin film of ZnO nanoparticles, prepared without acetate anion. The concentration of an acetate anion in the electrolyte for the electrodeposition of the double‐layer film, the electrodeposition period, and the period for dye adsorption were optimized for obtaining the best performance for a DSSC with a photoanode consisting of the double layer. A metal‐free dye, coded as D149, was used in this research. A conversion efficiency of 4.65% was achieved for a DSSC (0.2376 cm2) with the photoanode, consisting of the double‐layer film, under 100 mW/cm2 illumination in the wavelength range of 400–800 nm. X‐ray diffraction patterns, thermo gravimetric curves, elemental analysis, scanning electron microscopic images, transmission electron microscopic image, transmission spectra, and electrochemical impedance spectra were used to explain observations. Copyright © 2012 John Wiley & Sons, Ltd.

Functionalised zinc oxide nanowire gas sensors: Enhanced NO2 gas sensor response by chemical modification of nanowire surfaces

Surface coating with an organic self-assembled monolayer (SAM) can enhance surface reactions or the absorption of specific gases and hence improve the response of a metal oxide (MOx) sensor toward particular target gases in the environment. In this study the effect of an adsorbed organic layer on the dynamic response of zinc oxide nanowire gas sensors was investigated. The effect of ZnO surface functionalisation by two different organic molecules, tris(hydroxymethyl)aminomethane (THMA) and dodecanethiol (DT), was studied. The response towards ammonia, nitrous oxide and nitrogen dioxide was investigated for three sensor configurations, namely pure ZnO nanowires, organic-coated ZnO nanowires and ZnO nanowires covered with a sparse layer of organic-coated ZnO nanoparticles. Exposure of the nanowire sensors to the oxidising gas NO2 produced a significant and reproducible response. ZnO and THMA-coated ZnO nanowire sensors both readily detected NO2 down to a concentration in the very low ppm range. Notably, the THMA-coated nanowires consistently displayed a small, enhanced response to NO2 compared to uncoated ZnO nanowire sensors. At the lower concentration levels tested, ZnO nanowire sensors that were coated with THMA-capped ZnO nanoparticles were found to exhibit the greatest enhanced response. ΔR/R was two times greater than that for the as-prepared ZnO nanowire sensors. It is proposed that the ΔR/R enhancement in this case originates from the changes induced in the depletion-layer width of the ZnO nanoparticles that bridge ZnO nanowires resulting from THMA ligand binding to the surface of the particle coating. The heightened response and selectivity to the NO2 target are positive results arising from the coating of these ZnO nanowire sensors with organic-SAM-functionalised ZnO nanoparticles.

Efficient laser induced consolidation of nanoparticulate ZnO thin films with reduced thermal budget

Layers of ZnO nanoparticles with thicknesses of about 40 nm were prepared on Si substrates. It was shown that UV laser irradiation is suitable for consolidation and significant densification of the ZnO particle layers under ambient conditions. Both experiments and simulations show that an underlying SiO2 particle layer has a beneficial effect in inhibiting heat transfer towards the substrate and thus enables the application of temperature-sensitive carrier substrates like polymer foils despite the extremely high melting temperature of ZnO.

High-Efficiency Inverted Polymer Solar Cells with Double Interlayer

We have studied the performance of normal and inverted bulk-heterojunction solar cells with an active layer composed of a blend of poly[(4,4'-bis(2-ethylhexyl)dithieno[3,2-b:2',3'-d]silole)-2,6-diyl-alt-(2,1,3-benzothiadiazole)-4,7-diyl] (PDTS-BTD) and {6,6}-phenyl-C71 butyric acid methyl ester (PC(71)BM). For inverted cells, a thin layer of ZnO nanoparticles and MoO(3) were used as interlayers for the bottom cathode and the top anode respectively. To enhance the device performance, a thin film of 4,4',4″-tris[N-(3-methylphenyl)-N-phenylamino]triphenylamine (MTDATA) was used along with MoO(3) as an anode interlayer to improve the hole extraction from the photoactive layer to the anode. The inverted polymer solar cells with double interlayer exhibit a higher power conversion efficiency of 6.45% compared to the conventional cell of 4.91% due to efficient charge extraction and favorable vertical morphology of active layer blend. Our ultraviolet photoemission spectroscopy results indicate that the formation of band bending due to interlayer leads to the enhancement in hole extraction.

Solution-processed, nanostructured hybrid solar cells with broad spectral sensitivity and stability

Hybrid organic-inorganic solar cells, as an alternative to all-organic solar cells, have received significant attention for their potential advantages in combining the solution-processability and versatility of organic materials with high charge mobility and environmental stability of inorganic semiconductors. Here we report efficient and air-stable hybrid organic-inorganic solar cells with broad spectral sensitivity based on a low-gap polymer poly[2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']-dithiophene)-alt-4,7-(2,1,3-benzothiadiazole)] (PCPDTBT) and spherical CdSe nanoparticles. The solvents used for depositing the hybrid PCPDTBT:CdSe active layer were shown to strongly influence the film morphology, and subsequently the photovoltaic performance of the resulted solar cells. Appropriate post-deposition annealing of the hybrid film was also shown to improve the solar cell efficiency. The inclusion of a thin ZnO nanoparticle layer between the active layer and the metal cathode leads to a significant increase in device efficiency especially at long wavelengths, due to a combination of optical and electronic effects including more optimal light absorption in the active layer and elimination of unwanted hole leakage into the cathode. Overall, maximum power conversion efficiencies up to 3.7 ± 0.2% and spectral sensitivity extending above 800 nm were achieved in such PCPDTBT:CdSe nanosphere hybrid solar cells. Furthermore, the devices with a ZnO nanoparticle layer retained ∼70% of the original efficiency after storage under ambient laboratory conditions for over 60 days without any encapsulation.

Enhanced performance of a flexible dye-sensitized solar cell with a composite semiconductor film of ZnO nanorods and ZnO nanoparticles

A composite thin film of only 6 μm, consisting of a first layer of ZnO nanorods (ZNRs) and a second layer of ZnO nanoparticles (ZNPs), was deposited on a flexible Ti foil. The structures and morphologies of the films of ZNRs, ZNPs, and their composite (hereafter ZNRs/ZNPs) were studied by X-ray diffraction (XRD) patterns, scanning electron microscopic (SEM) and transmission electron microscopy (TEM) images. The Ti foil with the composite film was used as the photoanode of a flexible dye-sensitized solar cell (DSSC); an indium doped tin oxide/polyethylene naphthalate (ITO/PEN) substrate with a thin layer of platinum was used as the counter electrode. A power conversion efficiency ( η) of 2.19% was achieved for the DSSC with ZNRs/ZNPs, through back-illumination, which is higher than that of the cell with only ZNPs (1.80%); the DSSC with bare ZNRs showed a very poor efficiency of 0.90%. Explanations are substantiated by electrochemical impedance spectra (EIS), laser-induced photo-voltage transients, and incident photon-to-electron conversion efficiency (IPCE) curves.

Effect of [OH–] Linkages on Luminescent Properties of ZnO Nanoparticles

Optical properties of ZnO nanoparticles prepared from a simple chemical method using sodium zincate bath show strong white light emission. X-ray absorption fine structure studies reveal a completely different local environment around Zn in these ZnO nanoparticles. The observed luminescence properties and local structural changes have been explained on the basis of a linkage between Zn and OH– ions in the surface layers of ZnO nanoparticles.

Stable and efficient quantum-dot light-emitting diodes based on solution-processed multilayer structures

Researchers demonstrate solution-processed light-emitting diodes based on a quantum-dot emissive layer between an organic hole-transport layer and an electron-transport layer of ZnO nanoparticles. The device achieves a luminance of 68,000 cd m−2 and power efficiencies of up to 8.2 lm W−1.

Electrodeposition of ZnO Nanostructures on Molecular Thin Films

Electrodeposition of highly crystalline ZnO nanostructures directly onto copper phthalocyanine and pentacene thin films, from aqueous solutions containing zinc nitrate and dissolved oxygen, has been successfully demonstrated for the first time using a two-step electrochemical deposition process. Importantly, surface activation of the molecular thin film substrates by depositing a thin layer of ZnO nanoparticles at high cathodic overpotentials prior to film growth was found to be crucial for achieving a dense coverage of ZnO nanostructures with uniform morphology. The mechanism for ZnO deposition via electroreduction of hydroxide precursor species (oxygen and NO3– ions) at the organic-electrolyte interface was shown to be analogous to that reported for conventional inorganic and metal electrodes. Comparison of cathodic current density-time curves, measured during deposition, with film orientation and morphology revealed that the cathodic current density and number of nucleation sites are key factors in det...

Hybrid polymer-CdSe solar cells with a ZnO nanoparticle buffer layer for improved efficiency and lifetime

We report the use of a solution-processed ZnO nanoparticle buffer layer in hybrid solar cells based on blends of poly(3-hexylthiophene) (P3HT) and CdSe quantum dots. Depending on the size of the CdSe nanocrystal, these devices exhibit 20–70% higher photocurrent output than similar devices without the ZnO nanoparticle layer, which is attributed to a combination of electronic and optical effects. With negligible change in open-circuit voltage and a small increase in the fill factor, the power conversion efficiency of these P3HT:CdSe hybrid solar cells was increased by 30–80% with incorporation of the ZnO nanoparticle layer. The presence of the ZnO nanoparticle layer also drastically improves the stability of these hybrid solar cells. Less than 40% loss in efficiency was observed for such devices after 70 days of exposure to the laboratory ambient without any type of encapsulation.

Properties of SiO2 and Si3N4 as gate dielectrics for printed ZnO transistors

In this article, the authors report on thin film transistors based on gas phase synthesized ZnO nanoparticles using low temperature deposited silicon dioxide and silicon nitride as gate dielectrics. For bottom gate transistors, the devices using silicon nitride as gate insulator show the lowest off-current for a given induced charge and the steepest subthreshold slope. The charge carrier mobility of around 3×10−3 cm2/V s and an Ion/Ioff ratio of around 105 are almost independent of the insulator material. In a double gated thin film transistor using low stress silicon nitride as a top gate insulator, transistor parameters are extracted for the identical semiconducting layer when the bottom and top gates are used. It is shown that the extracted charge carrier mobility is not inherent for the ZnO nanoparticle layer but rather an effective value for the device under investigation.

Probing Charge Carrier Density in a Layer of Photodoped ZnO Nanoparticles by Spectroscopic Ellipsometry

Changes in the optical constants of a layer of ZnO nanoparticles (5 nm diameter) induced by UV illumination in O2-free atmosphere are determined by using spectroscopic ellipsometry. The onset of op...