Characteristics of floating gate device as analogue memory for neural networks

An effective controlling circuit for a floating-gate MOSFET analogue memory used in neural networks is described. It is possible to charge or discharge the floating gate storage with high resolution of more than 1% of full scale. The experimental results are described and discussed. An improved device structure is proposed for simplifying the controlling circuit.<>     

A self-convergence erase for NOR flash EEPROM using avalanche hotcarrier injection

A new erasing method for simple stacked gate NOR Flash EEPROM's is proposed and is applied to 2 M bit NOR Flash test array using 0.6 μm CMOS technology. Due to avalanche hot carrier injection after erasure by Fowler-Nordheim (F-N) tunneling current, the threshold voltages converge to a certain steady state. The steady state is a point of balance between the avalanche hot electron injection and the avalanche hot hole injection into the floating gate, and can be controlled easily by the channel doping and the applying control-gate voltage during convergence operation. The erasing method eliminates the problem of over-erased cells and realizes highly stable flash memory erasure     

Effect of TiO2 nanoparticles aggregation in silicate thin coating films on photocatalytic behavior for antifouling materials

Two types of disperser namely, a high speed agitation bead mill and a colloidal mill, were used for the dispersion behavior control of TiO₂ nanoparticles (20 nm in average primary diameter) in an aqueous suspension. A composite thin film raging in thickness from 90 to 400 nm was prepared from the coating suspension following the addition of a commercial ethyl silicate oligomer binder into the prepared suspension by means of a spray coating method. The mean aggregate size of TiO₂ nanoparticles in the aqueous suspension was found to be 80 nm and 290 nm in diameter, respectively, when using the agitated bead and colloidal milling methods. Large aggregates on the order of several hundred nanometers were found to remain in the suspension after colloidal milling. Further, a fine dispersion of TiO₂ nanoparticles in the thin film produced using the agitation bead milling process promoted the photocatalytic activity and enhanced transparency of the film for visible light. The aggregate structure of TiO₂ nanoparticles in an aqueous suspension was well maintained in the film prepared by a spray coating process.     

Growth and coarsening of g. p. Zones in Al- Zn alloys

The structural changes during the precipitation of G. P. zones in Al-Zn binary alloys have been investigated by means of anin situ small-angle scattering technique using synchrotron radiation. Defining a specific time, normalized by the half-completion time, the time-dependent evolution of the precipitation process can be divided into three periods, independent of alloy composition and quench-ing conditions. The structural and kinetic features of the first two periods have been analyzed in detail. The first stage represents a growing process of clusters with diffuse interface into the well-defined G. P. zones. The average size of these clusters increases, and the density decreases. The second stage corresponds to the Ostwald ripening process. This mechanism is described by utilizing a modified Lifshitz-Slyozov-Wagner theory.     

Plasma-initiated graft polymerization of water-soluble vinyl monomers onto hydrophobic films and its application to metal ion adsorbing films

Plasma-initiated graft polymerization of water-soluble vinyl monomers such as acrylic acid, 2-hydroxyethyl methacrylate and acrylamide was carried out onto polyethylene, polypropylene and poly(ethylene terephthalate) films. It was found that these monomers could be graft polymerized quite easily to 0.5%–670% of the mass of the dry films by exposing the films to a plasma for 90s, with subsequent post-polymerization at room temperature. Thus, polyethylene films capable of adsorbing and desorbing metal ions reversibly could be prepared by grafting the monomers described.     

Elimination Transformations for Associative–Commutative Rewriting Systems

To simplify the task of proving termination and AC-termination of term rewriting systems, elimination transformations have been vigorously studied since the 1990s. Dummy elimination, distribution elimination, general dummy elimination, and improved general dummy elimination are examples of elimination transformations. In this paper we clarify the essence of elimination transformations based on the notion of dependency pairs. We first present a theorem that gives a general and essential property for elimination transformations, making them sound with AC-termination. Based on the theorem, we design an elimination transformation called the argument filtering transformation. Next, we clarify the relation among various elimination transformations by comparing them with a corresponding restricted argument filtering transformation. Finally, we compare the AC-dependency pair method with the argument filtering transformation. Parts of this work were done while K. Kusakari was completing his Ph.D. thesis, “Termination, AC-Termination and Dependence Pairs of Term Rewriting Systems,” at Japan Advanced Institute of Science and Technology, School of Information Science (March, 2000). A preliminary version of parts of this article appeared in K. Kusakari, M. Nakamura, Y. Toyama, Argument filtering transformation, Proc. of Int. Conf. on Principles and Practice of Declarative Programming, LNCS 1702 (Springer-Verlag, 1999) pp.47–61.     

Location-free haptic interaction for large-area social applications

In this paper, we discuss the potential of force perception technologies for realizing hand-held devices in the field of social systems. We propose and develop an interactive force-sensation-based navigation system for waiters based on a force perception technology that we have proposed. The navigation system consists of our new hand-held haptic interface and a camera-based position and posture identification system. Since the proposed compact haptic interface does not require external grounding, it can be used outside the laboratory and does not interrupt human activity. We verify the feasibility of the system in trials where we collected the responses of system users.     

An ion-selective electrode for acetate based on a urea-functionalized porphyrin as a hydrogen-bonding ionophore

An ion-selective electrode for acetate based on (α,α,α,α)-5,10,15,20-tetrakis[2-(4-fluorophenylureylene)phenyl]porphyrin as an ionophore that has no metal center and forms hydrogen bonds to the analyte is described. At pH 7.0 (0.1 M HEPES-NaOH buffer), the electrode based on this ionophore and cationic sites (50 mol % relative to the ionophore) responds to acetate in a linear range from 1.58 × 10(-)(4) to 1.58 × 10(-)(2) M with a slope of -54.8 ± 0.8 mV/decade and a detection limit of (3.06 ± 1.15) × 10(-)(5) M. Selectivity coefficients determined with the separate solution method (SSM) indicate that interferences of hydrophobic inorganic anions are relatively small (log[Formula: see text] (SSM): NO(3)(-), +0.68; SCN(-), +0.60; NO(2)(-), +0.22; I(-), +0.20; ClO(4)(-), +0.12; Br(-), -0.13). Responses to anions that are good hydrogen bond acceptors, i.e., Cl(-), HSO(3)(-), and HCO(3)(-), were Nernstian and were weaker than the response to acetate (log[Formula: see text] (SSM): -0.54, -0.56, and -1.34, respectively). Negligibly small responses were observed for very hydrophilic anions, i.e., F(-), SO(4)(2)(-), and H(2)PO(4)(-)/HPO(4)(2)(-). While aliphatic carboxylates such as formate, propanoate, pyruvate, and lactate gave Nernstian responses similar to acetate, interferences of salicylate and benzoate were considerably decreased in comparison with electrodes based on cationic sites only. Concentrations of acetic acid in vinegar samples were determined by direct potentiometry and agreed with values determined by a standard enzymatic method.     

Stabilizing nanometer scale tip-to-substrate gaps in scanning electrochemical microscopy using an isothermal chamber for thermal drift suppression

The control of a nanometer-wide gap between tip and substrate is critical for nanoscale applications of scanning electrochemical microscopy (SECM). Here, we demonstrate that the stability of the nanogap in ambient conditions is significantly compromised by the thermal expansion and contraction of components of an SECM stage upon a temperature change and can be dramatically improved by suppressing the thermal drift in a newly developed isothermal chamber. Air temperature in the chamber changes only at ~.2 mK/min to remarkably and reproducibly slow down the drift of tip-substrate distance to ~0.4 nm/min in contrast to 5-150 nm/min without the chamber. Eventually, the stability of the nanogap in the chamber is limited by its fluctuation with a standard deviation of ±0.9 nm, which is mainly ascribed to the instability of a piezoelectric positioner. The subnanometer scale drift and fluctuation are measured by forming a ~20 nm-wide gap under the 12 nm-radius nanopipet tip based on ion transfer at the liquid/liquid interface. The isothermal chamber is useful for SECM and, potentially, for other scanning probe microscopes, where thermal-drift errors in vertical and lateral probe positioning are unavoidable by the feedback-control of the probe-substrate distance.