Efficiency enhancement in blue organic light emitting diodes with a composite hole transport layer based on poly(ethylenedioxythiophene):poly(styrenesulfonate) doped with TiO2 nanoparticles

Blue color organic/polymeric light emitting diodes are very important because they can be used for tri-color display applications, fluorescence imaging, and exciting yellow phosphor for generating white light for general illumination. But the efficiency of blue organic/polymeric light emitting diodes is considerably low due to their large band gap that requires higher energy for effective emission. In this paper we report the enhancement in polyfluorene blue organic light emitting diodes with a polymer nano-composite hole transport layer. Blue light emitting diode based on polyfluorene as an emissive layer and poly(3,4 ethylenedioxythiophene):poly(styrenesulfonate)–titanium dioxide nanocomposite as the hole transport layer were fabricated and studied. Different concentrations of titanium dioxide nanoparticles were doped in poly(3,4 ethylenedioxythiophene):poly(styrenesulfonate) in the hole transport layer and the performance of the devices were studied. Significant enhancement in the blue peak at 430 nm of polyfluorene has been observed with increase in concentration of TiO₂ nanoparticles in the hole transport layer. The turn on voltage of the device has also been found to improve significantly with the incorporation of titanium dioxide nanoparticles in the hole transport layer. The optimized concentration of titanium dioxide in the hole transport layer for most efficient device has been found to 15 wt.%.     

Synthesis of Bi and Gd doped ZnB2O4 for evaluation as potential materials in luminescent display applications

A series of Bi³⁺ and Gd³⁺ doped ZnB₂O₄ phosphors were synthesized with solid state reaction technique. X-ray diffraction technique was employed to study the structure of prepared samples. Excitation and emission spectra were recorded to investigate the luminescence properties of phosphors. The doping of Bi³⁺ or Gd³⁺ with a small amount (no more than 3 mol%) does not change the structure of prepared samples remarkably. Bi³⁺ in ZnB₂O₄ can emit intense broad-band purplish blue light peaking at 428 nm under the excitation of a broad-band peaking at 329 nm. The optimal doping concentration of Bi³⁺ is experimentally ascertained to be 0.5 mol%. The decay time of Bi³⁺ in ZnB₂O₄ changes from 0.88 to 1.69 ms. Gd³⁺ in ZnB₂O₄ can be excited with 254 nm ultraviolet light and yield intense 312 nm emission. The optimal doping concentration of Gd³⁺ is experimentally ascertained to be 5 mol%. The decay time of Gd³⁺ in ZnB₂O₄ changes from 0.42 to 1.36 ms.     

Correlation between cell growth rate and glucose consumption determined by electrochemical monitoring

The electrochemical monitoring of glucose consumption is relevant for cell biology studies because of its wide detection range, high sensitivity and easy implementation. Whereas the glucose consumption and cell growth rate can be tightly correlated, they should also be cell population density dependent. In this work, we fabricated high sensitive enzyme electrodes for accurate monitoring of glucose consumption of cells in different growth stages. The performance of the fabricated device was firstly evaluated by cyclic voltammetry (CV) with p-benzoquinone (PBQ) as redox mediator, showing a linear response over a wide detection range (0.3-60 mM), a high sensitivity (1.61 ± 0.10 μA mM⁻¹ mm⁻² (n = 5)) and a low detection limit (80 μM). Then, daily glucose consumptions of NIH 3T3 cells in 24-well plates were determined for a period of 7 days. The results could be compared to the cell population growth curve, showing a close correlation but different behavior. We found that the increase of the glucose consumption took place prior the cell number increase but the glucose consumption per cell decreases linearly in the exponential growth stage of cells.     

Fabrication of ultraviolet photoconductive sensor using a novel aluminium-doped zinc oxide nanorod-nanoflake network thin film prepared via ultrasonic-assisted sol-gel and immersion methods

Unique and novel thin films with aluminium (Al)-doped zinc oxide (ZnO) nanostructures consisting of nanorod-nanoflake networks were prepared for metal-semiconductor-metal (MSM)-type ultraviolet (UV) photoconductive sensor applications. These nanostructures were grown on a glass substrate coated with a seed layer using a combination of ultrasonic-assisted sol-gel and immersion methods. The synthesised ZnO nanorods had diameters varying from 10 to 40 nm. Very thin nanoflake structures were grown vertically and horizontally on top of the nanorod array. The thin film had good ZnO crystallinity with a root mean square roughness of approximately 13.59 nm. The photocurrent properties for the Al-doped ZnO nanorod-nanoflake thin films were more than 1.5 times greater than those of the seed layer when the sensor was illuminated with 365 nm UV light at a density of 5 mA/cm². The responsivity of the device was found to be dependent on the bias voltage. We found that similar photocurrent curves were produced over eight cycles, which indicated that the UV sensing capability of the fabricated sensor was highly reproducible. Our results provide a new approach for utilising the novel structure of Al-doped ZnO thin films with a nanorod-nanoflake network for UV sensor applications. To the best of our knowledge, UV photoconductive sensors using Al-doped ZnO thin films with a nanorod-nanoflake network have not yet been reported.     

Preparation and characterization of unimorph actuators based on piezoelectric Pb(Zr0.52Ti0.48)O3 materials

This paper describes the preparation and characterization of unimorph actuators for deformable mirrors, based on Pb(Zr_0.52Ti_0.48)O₃ (PZT52) thin film. As comparison, two different designs, where the PZT layer in the unimorph actuators was driven by either interdigitated electrodes (IDT-mode) or parallel plate electrodes (d₃₁-mode), were investigated. The actuators utilize a unimorph membrane (diaphragm) structure consisting of an active PZT piezoelectric layer and a passive SiO₂/Si composite layer. To fabricate the diaphragm structures, n-type (1 0 0) silicon-on-insulator (SOI) wafers with 1 μm thermal SiO₂ were used as substrates (for d₃₁-mode actuators, the upper Si part of SOI need to be heavily doped and used as bottom electrodes simultaneously). Sol-gel derived PZT piezoelectric layers with PbTiO₃ (PT) bufferlayer in total of 0.86 μm were then fabricated on them, and 0.15 μm Al reflective layers were deposited and patterned into top electrode geometries, subsequently. The diaphragms were released using orientation-dependent wet etching (ODE) with 5-10 μm residual silicon layers. The complete unimorph actuators comprise 4 × 4 discrete units (4 mm² in size) with patterned PZT films for parallel plate configuration or 3 × 3 individual pixels (2 mm in IDT diameter) with continuous PZT films in graphic region for IDT configuration. The measurement results indicated that both of the two configurations can generate considerable deflections at low voltage. The measured maximum central deflections at 15 V were approximately 2.5 μm and 2.8 μm, respectively. The intrinsic strain conditions shaping the deflection profiles for the diaphragm actuators were also analyzed. In this paper, the behaviors of clamped parallel plate configuration without a diaphragm were also evaluated.     

Effect of La2CuO4 electrode area on potentiometric NOx sensor response and its implications on sensing mechanism

The intent of this work is to look at the effects of varying the La₂CuO₄ electrode area and the asymmetry between the sensing and counter electrode in a solid state potentiometric sensor with respect to NO_x sensitivity. NO₂ sensitivity was observed at 500-600 °C with a maximum sensitivity of ∼22 mV/decade [NO₂] observed at 500 °C for the sensor with a La₂CuO₄ electrode area of ∼30 mm². The relationship between NO₂ sensitivity and area is nearly parabolic at 500 °C, decreases linearly with increasing electrode area at 600 °C, and was a mixture of parabolic and linear behavior 550 °C. NO sensitivity varied non-linearly with electrode area with a minima (maximum sensitivity) of ∼−22 mV/decade [NO] at 450 °C for the sensor with a La₂CuO₄ electrode area of 16 mm². The behavior at 400 °C was similar to that of 450 °C, but with smaller sensitivities due to a saturation effect. At 500 °C, NO sensitivity decreases linearly with area.We also used electrochemical impedance spectroscopy (EIS) to investigate the electrochemical processes that are affected when the sensing electrode area is changed. Changes in impedance with exposure to NO_x were attributed to either changes in La₂CuO₄ conductivity due to gas adsorption (high frequency impedance) or electrocatalysis occurring at the electrode/electrolyte interface (total electrode impedance). NO₂ caused a decrease in high frequency impedance while NO caused an increase. In contrast, NO₂ and NO both caused a decrease in the total electrode impedance. The effect of area on both the potentiometric and impedance responses show relationships that can be explained through the mechanistic contributions included in differential electrode equilibria.     

Spectrophotometric sensor system based on a liquid waveguide capillary cell for the determination of titanium: Application to natural waters, sunscreens and a lake sediment

An analytical procedure for the spectrophotometric determination of titanium at trace levels was developed. The procedure involves the use of a multi-pumping flow system (MPFS) coupled with a liquid waveguide capillary cell (LWCC) with 1.0 m path length, 550 μm i.d. and 250 μL internal volume, which enabled to enhance the sensitivity of the determination and thus avoid complex and time-consuming pre-concentration steps. The determination is based on the colorimetric reaction of titanium with chromotropic acid. The limit of detection (3σ) was 0.4 μg/L and a linear response up to 100 μg/L with a sample throughput of 46 h⁻¹, and a low reagent consumption/effluent production was achieved. The developed procedure was applied to natural waters, sunscreen formulations and one certified lake sediment sample.     

Micromachined catalytic combustible hydrogen gas sensor

An integrated catalytic combustion H₂ sensor has been fabricated by using MEMS technology. Both the sensing elements and the reference elements could be integrated into the suspended micro heaters connected in a suitable circuit such as a Wheatstone configuration with low power consumption. Two sensitive elements and two reference sensors were integrated together onto a single chip. The size of chip was 5.76 mm² and the catalytic combustion sensor showed high response to H₂ at operating voltage of 1 V. The response and recovery times to 1000 ppm H₂ were 0.36 s and 1.29 s, respectively.     

Effect of surface defects on biosensing properties of TiO2 nanotube arrays

In this paper, highly ordered titania nanotube (TNT) arrays fabricated by anodization were annealed at different temperatures in CO to create different concentrations of surface defects. The samples were characterized by SEM, XRD and XPS. The results showed different concentrations of Ti³⁺ defects were doped in TNT arrays successfully. Furthermore, after co-immobilized with horseradish peroxidase (HRP) and thionine chloride (Th), TNT arrays was employed as a biosensor to detect hydrogen peroxide (H₂O₂) using an amperometric method. Cyclic voltammetry results and UV-Vis absorption spectra presented that with an increase of Ti³⁺ defects concentration, the electron transfer rate and enzyme adsorption amount of TNT arrays were improved largely, which could be ascribed to the creation of hydroxyl groups on TNT surface due to dissociative adsorption of water by Ti³⁺ defects. Annealing in CO at 500 °C appeared to be the most favorable condition to achieve desirable nanotube array structure and surface defects density (0.27%), thus the TNT arrays showed the largest adsorption amount of enzyme (9.16 μg/cm²), faster electron transfer rate (1.34 × 10⁻³ cm/s) and the best response sensitivity (88.5 μA/mM l⁻¹).     

Enhanced room temperature response of SnO2 thin film sensor loaded with Pt catalyst clusters under UV radiation for LPG

The room temperature response characteristics of SnO₂ thin film sensor loaded with platinum catalyst clusters are investigated for LPG under the exposure of ultraviolet radiation. The SnO₂-Pt cluster sensor structures have been prepared using rf sputtering. Combined effect of UV radiation exposure (λ = 365 nm) and presence of Pt catalyst clusters (10 nm thick) on SnO₂ thin film sensor surface is seen to lead to an enhanced response (4.4 × 10³) for the detection of LPG (200 ppm) at room temperature whereas in the absence of UV illumination a comparable response (∼5 × 10³) could be obtained but only at an elevated temperature of 220 °C. The present study therefore investigates the effect of UV illumination on LPG sensing characteristics of SnO₂ sensors loaded with Pt clusters of varying thickness values. Results indicate the possibility of utilizing the sensor structure with novel dispersal of Pt catalyst clusters on SnO₂ film surface for efficient detection of LPG at room temperature under the illumination of UV radiations.     

The study of the photo-response characteristics of organic photosensors integrated with pentacene based thin film transistors

We have investigated the photo-response characteristics of organic photosensors (OPS) integrated with pentacene based thin film transistors (TFTs). The fabricated device configuration is PEN/ITO/PEDOT:PSS/(poly(3-hexylethiophene)/phenyl-C61-butryic acid methyl ester) (P3HT/PCBM)/Al and PDMS/Au/(poly-4-vinyphenol) (PVP)/pentacene/Au. In order to study the effect of the applied voltage to the pentacene-TFT on the OPS, each device is connected in series. The response current is tuned dependant on the gate-source voltage and the anode-source voltage. The change of the photo induced ON current in the integrated device is measured under light illuminations ranging from 50 mW/cm² to 500 mW/cm²; the corresponding photo-response (ΔI/I₀) of the devices varied from 0.16 to 1.9. We found that the photo-response characteristic is high at the low anode-source voltage and high gate-source voltage.     

Development of molecularly imprinted electrochemical sensor with titanium oxide and gold nanomaterials enhanced technique for determination of 4-nonylphenol

4-Nonylphenol (4-NP) was reported to affect the health of wildlife and humans through altering endocrine function. A novel electrochemical sensor for sensitive and fast determination of 4-NP was developed. Titanium oxide (TiO₂) nanoparticles and gold nanoparticles (AuNPs) were introduced for the enhancement of electron conduction and sensitivity. 4-NP-imprinted functionalized AuNPs composites with specific binding sites for 4-NP was modified on electrode. The resulting electrodes were characterized by cyclic voltammetry (CV). Rebinding experiments were carried out to determine the specific binding capacity and selective recognition. The linear range was over the range from 4.80 × 10⁻⁴ to 9.50 × 10⁻⁷ mol L⁻¹, with the detection limit of 3.20 × 10⁻⁷ mol L⁻¹ (S/N = 3). The sensor was successfully employed to detect 4-NP in real samples.     

Sensitive amperometric determination of chemical oxygen demand using Ti/Sb-SnO2/PbO2 composite electrode

A novel Ti/Sb-SnO₂/PbO₂ composite electrode was fabricated for COD determination. The new electrode configuration improved the sensitivity of the amperometric method apparently. Effects of common experimental parameters, such as applied potential, pH and concentration of the electrolyte on its analytical performance were investigated. A linear range of 0.5-200 mg L⁻¹ COD and a detection limit (a signal-to-noise ratio of 3) of 0.3 mg L⁻¹ were achieved under optimized conditions. The experiments for detecting COD in model samples and real samples were carried out to evaluate the electrode's performance. The obtained results were in good agreement with those determined by the standard dichromate method, with a relative error less than 12%.     

High sensitive simultaneous determination of hydroquinone and catechol based on graphene/BMIMPF6 nanocomposite modified electrode

A novel nanocomposite, comprising of graphene sheet (GS) and ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF₆), was developed on the glassy carbon electrode (GCE) for the simultaneous determination of hydroquinone and catechol in 0.10 M acetate buffer solution (pH 5.0). At the GS/BMIMPF₆/GCE, both hydroquinone and catechol can cause a pair of quasi-reversible and well-defined redox peaks. In comparison with bare GCE and GS modified electrode, GS/BMIMPF₆/GCE showed larger peak currents, which was related to the higher specific surface area of graphene and high ionic conductivity of BMIMPF₆. Under the optimized condition, the cathodic peak current were linear over ranges from 5.0 × 10⁻⁷ M to 5.0 × 10⁻⁵ M for hydroquinone and from 5.0 × 10⁻⁷ M to 5.0 × 10⁻⁵ M for catechol, with the detection limits of 1.0 × 10⁻⁸ M and 2.0 × 10⁻⁸ M, respectively. The proposed method was successfully applied to the simultaneous determination of hydroquinone and catechol in artificial sample, and the results are satisfactory.     

Low power highly sensitive platform for gas sensing application

This paper reports a low power miniaturized MEMS based integrated gas sensor with 36.84 % sensitivity (ΔR/R₀) for as low as 4 ppm (NH₃) gas concentration. Micro-heater based gas sensor device presented here consumes very low power (360 °C at 98 mW/mm²) with platinum (Pt) micro-heater. Low powered micro-heater is an essential component of the metal oxide based gas sensors which are portable and battery operated. These micro-heaters usually cover less than 5 % of the gas sensor chip area but they need to be thermally isolated from substrate, to reduce thermal losses. This paper elaborates on design aspects of micro fabricated low power gas sensor which includes ‘membrane design’ below the microheater; the ‘cavity-to-active area ratio’; effect of silicon thickness below the silicon dioxide membrane; etc. using FEM simulations and experimentation. The key issues pertaining to process modules like fragile wafer handling after bulk micro-machining; lift-off of platinum and sensing films for the realization of heater, inter-digitated-electrodes (IDE) and sensing film are dealt with in detail. Low power platinum microheater achieving 700 °C at 267 mW/mm² are fabricated. Temperature calculations are based on experimentally calculated thermal coefficient of resistance (TCR) and IR imaging. Temperature uniformity and localized heating is verified with infrared imaging. Reliability tests of the heater device show their ruggedness and repeatability. Stable heater temperature with standard deviation (σ) of 0.015 obtained during continuous powering for an hour. Cyclic ON–OFF test on the device indicate the ruggedness of the micro-heater. High sensitivity of the device for was observed for ammonia (NH₃), resulting in 40 % response for ~4 ppm gas concentration at 230 °C operating temperature.     

Temperature sensor based on the Er green upconverted emission in a fluorotellurite glass

The temperature dependence of the green upconverted emission from the two thermally coupled ²H_11/2 and ⁴S_3/2 levels of the Er³⁺ ion in a fluorotellurite glass has been analyzed as a function of the optically active ion concentration in order to check its availability as a temperature sensor. The infrared-to-green upconverted emission have been observed by the naked eyes after a cw laser diode excitation at 800 nm. The fluorescence intensity ratio between the thermally coupled emitting levels as well as the temperature sensitivity has been experimentally obtained up to 540 K. A better behaviour as a temperature sensor has been obtained for the less Er³⁺ concentrated glass with a maximum sensitivity of 54 × 10⁻⁴ K⁻¹ at 540 K, one of the highest found in rare-earth doped transparent materials.     

Micromachined infrared pneumatic detector for gas sensor

We present a micromachined IR detector based on the principle of a pneumatic cell and suited as an IR detector in a miniaturised gas sensor. The detector basically consists of a sealed cavity, in which the heat generated by absorbed IR light results in an increased gas pressure. This pressure rise is detected capacitively. The theoretical performance of a 1 mm² micromachined device is calculated, and it is shown that a detectivity of 3.6·10⁹ cm. Hz^1/2/W can be expected. Moreover, a pneumatic gas leak is proposed to avoid thermal drift. Using conventional Silicon micromachining techniques, a prototype was fabricated which confirmed the principle of operation., The experimental results are compared to the theory.     

TiO2 nanofibers fixed in a microfluidic device for rapid determination of chemical oxygen demand via photoelectrocatalysis

Large arrays of one-dimensional uniform-sized TiO₂ nanofibers (TNFs) were prepared through a template-free method, and used as a working electrode in a transparent microfluidic device made from poly (dimethyl siloxane) (PDMS) to perform efficient photoelectrocatalysis for rapid and undefiled determination of chemical oxygen demand (COD). Photoelectrochemical measurements were used to evaluate the response of TNFs to the intensity of exciting light and the applied potential bias. The photoelectrocatalysis of TNFs in PDMS-based microfluidic device exhibited excellent performance for determination of COD. The practical limit of determination of 0.95 mg/L COD with a working range of 0-250 mg/L was achieved. The relative standard deviation (RSD) was 1.85% for 10 repeated measurements of 0.3 mmol/L glucose with COD value of 57.6 mg/L.     

Critical thermodynamic evaluation and optimization of the MnO–SiO2–“ TiO2 ”–“ Ti2O3 ” system

A complete review, critical evaluation, and thermodynamic optimization of phase equilibrium and thermodynamic properties of the MnO–SiO₂–“ TiO₂”–“ Ti₂O₃” systems at 1 bar pressure are presented. The molten oxide phase was described by the Modified Quasichemical Model. The Gibbs energies of the manganosite, spinel, pyrophanite and pseudobrookite and rutile solid solutions were taken from the previous study. A set of optimized model parameters for the molten oxide phase was obtained which reproduces all available reliable thermodynamic and phase equilibrium data within experimental error limits from 25 ^°C to above the liquidus temperatures over the entire range of compositions and oxygen partial pressure in the range of pO₂ from 10⁻²⁰ bar to 10⁻⁷ bar. Complex phase relationships in these systems have been elucidated, and discrepancies among the data have been resolved. The database of model parameters can be used along with software for Gibbs energy minimization in order to calculate any phase diagram section or thermodynamic properties.     

Fabrication of microfluidic devices for packaging CMOS MEMS impedance sensors

This work presents a polydimethylsiloxane (PDMS) microfluidic device for packaging CMOS MEMS impedance sensors. The wrinkle electrodes are fabricated on PDMS substrates to ensure a connection between the pads of the sensor and the impedance instrument. The PDMS device can tolerate an injection speed of 27.12 ml/h supplied by a pump. The corresponding pressure is 643.35 Pa. The bonding strength of the device is 32.44 g/mm². In order to demonstrate the feasibility of the device, the short circuit test and impedance measurements for air, de-ionized water, phosphate buffered saline (PBS) at four concentrations (1, 2 × 10⁻⁴, 1 × 10⁻⁴, and 6.7 × 10⁻⁵ M) were performed. The experimental results show that the developed device integrated with a sensor can differentiate various samples.