ABSTRACT:The electro-optical properties of lead zirconate titanate (PZT) thin films depend strongly on the quality and crystallographic orientation of the thin films. We demonstrate a novel method to grow highly textured PZT thin films on silicon using the chemical solution deposition (CSD) process. We report the use of ultrathin (5−15 nm) lanthanide (La, Pr, Nd, Sm) based intermediate layers for obtaining preferentially (100) oriented PZT thin films. X-ray diffraction measurements indicate preferentially oriented intermediate Ln 2 O 2 CO 3 layers providing an excellent lattice match with the PZT thin films grown on top. The XRD and scanning electron microscopy measurements reveal that the annealed layers are dense, uniform, crack-free and highly oriented (>99.8%) without apparent defects or secondary phases. The EDX and HRTEM characterization confirm that the template layers act as an efficient diffusion barrier and form a sharp interface between the substrate and the PZT. The electrical measurements indicate a dielectric constant of ∼650, low dielectric loss of ∼0.02, coercive field of 70 kV/cm, remnant polarization of 25 μC/cm 2 , and large breakdown electric field of 1000 kV/cm. Finally, the effective electro-optic coefficients of the films are estimated with a spectroscopic ellipsometer measurement, considering the electric field induced variations in the phase reflectance ratio. The electro-optic measurements reveal excellent linear effective pockels coefficients of 110 to 240 pm/V, which makes the CSD deposited PZT thin film an ideal candidate for Si-based active integrated nanophotonic devices.
We have measured the electrophoretic mobility of single, optically trapped colloidal particles, while gradually depleting the co-ions and counterions in the liquid around the particle by applying a dc voltage. This is achieved in a nonpolar liquid, where charged reverse micelles act as co-ions and counterions. By increasing the dc voltage, the mobility first increases when the concentrations of co-ions and counterions near the particle start to decrease. At sufficiently high dc voltage (around 2 V), the mobility reaches a saturation value when the co-ions and counterions are fully separated. The increase in mobility is larger when the equilibrium ionic strength is higher. The dependence of the experimental data on the equilibrium ionic strength and on the applied voltage is in good agreement with the standard theory of electrophoretic retardation, assuming that the bare particle charge remains constant. This method is useful for studying the electrophoretic retardation effect and charging mechanisms for nonpolar colloids, and it sheds light on previously unexplained particle acceleration in electronic ink devices.
Barium titanate (BaTiO3) thin films are prepared by conventional 2-methoxy ethanol-based chemical solution deposition. We report highly c-axis-oriented BaTiO3 thin films grown on silicon substrates, coated with a lanthanum oxynitrate buffer layer of 8.9 nm. The influence of the intermediate buffer layer on the crystallization of BaTiO3 film is investigated. The annealing temperature and buffer layer sintering conditions are optimized to obtain good crystal growth. X-ray diffraction measurements show the growth of highly oriented BaTiO3 thin films having a single perovskite phase with tetragonal geometry. The scanning electron microscopy and atomic force microscopy studies indicate the presence of smooth, crack-free, uniform layers, with densely packed crystal grains on the silicon surface. A BaTiO3 film of 150-nm thickness, deposited on a buffer layer of 7.2 nm, shows a dielectric constant of 270, remnant polarization (2Pr) of 5 μC/cm2, and coercive field (Ec) of 60 kV/cm.
We extend the one-dimensional space-charge limited current theory to a twodimensional geometry where current flows in a thin layer between two coplanar semi-infinite electrodes. It is shown that the surface charge density in the gap between the electrodes is the finite Hilbert transform of the in-plane component of the electric field. This enables us to derive analytical expressions for the field and charge density for single carrier injection and for photo-carrier extraction by solving a non-linear integral equation for the field. The analytical expressions have been verified by numerical calculations. For the in-plane geometry, the one-dimensional Mott-Gurney equationFor extraction of photo-generated carriers the one-dimensional J ⇠ g 3/4V 1/2 dependence is replaced by a K ⇠ g 2/3 V 2/3 dependence, where g is the generation rate of photo-carriers. We also extend these results to take into account trapping. We show experimental evidence obtained with an organic photoconductor confirming the predicted voltage, width and generation dependencies.
In this paper we investigate the performance of a transparent photoconductive sensor based on a double layer of organic materials (m-MTDAB / PTCBI) which are deposited on two interdigitated transparent ITO electrodes. The performance of the sensor is demonstrated with electro-optical measurements: the I(V) curves consist of two linear sections meeting at a knee voltage V t . Linear regression performed on the I(V) curves below V t show that the conductance is a power law of the luminance incident on the device. We present a model to describe the behaviour of the sensor below V t .We present measurements of I(t) for a transient illumination of the sensor. Plotting the inverse of the current as a function of time we find that the transient is consistent with the model for voltages below V t . For voltages above V t we find that the sensor behaves like a resistor in series with a space charge (SC) region. We present a local illumination experiment that confirms the existence of a SC region between the electrodes of the photoconductive sensor for V>V t . The space charge region is located near the cathode of the sensor.
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