Publications by Year: 2004

2004

The deterministic and reliable singlemode fiber integration with spatial solitons through ultratight needs in photorefractives have been demonstrated. Efficient electro-optic beam handling was allowed where the fiber carried the information sequence and also delivered the photorefractively active control beam that configured the circuitry.

Item Citation: Journal of Applied Physics. April 1, 2004, Vol. 95 Issue 7, 3822-3824Accession Number: edsgcl.123305906; Publication Type: Academic Journal; Source: Journal of Applied Physics; Language: English; Publication Date: 20040401; Rights: Copyright 2004 Gale, Cengage Learning. All rights reserved.; Imprint: American Institute of Physics, Inc.

P Ben Ishai, CEM de Oliveira, Y Ryabov, Yu. Feldman, and AJ Agranat. 2004. “Glass-forming liquid kinetics manifested in a KTN: Cu crystal.” Physical Review B - Condensed Matter and Materials Physics, 70, 13, Pp. 132104-1-132104-4. Publisher's Version
Accession Number: edselc.2-52.0-37649030903; (Physical Review B - Condensed Matter and Materials Physics, October 2004, 70(13):132104-1-132104-4) Publication Type: Academic Journal; Rights: Copyright 2008 Elsevier B.V., All rights reserved.
A D’Ercole, E Palange, E DelRe, A Ciattoni, B Crosignani, and AJ Agranat. 2004. “Miniaturization and embedding of soliton-based electro-optically addressable photonic arrays..” Applied Physics Letters, 85, 14, Pp. 2679. Publisher's Version Abstract

We achieved the soliton-based miniaturized integration of electro-optic devices in a photorefractive paraelectric bulk crystal, by driving self-trapping through an external bias field in a top-sided electrode geometry. The ensuing spatially resolved electric field manifests a localized voltage-dependent region in which a quasi-uniform field leads to screening-like self-trapped waves at considerably low voltages without sample miniaturization, along with their electro-optic beam manipulation. By replicating the electrode structure, our achievements constitute the basic building block that paves the way to digitally addressable volume photonic manipulator arrays. [ABSTRACT FROM AUTHOR]Copyright of Applied Physics Letters is the property of American Institute of Physics and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

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CEM de Oliveira, G Orr, N Axelrold, and AJ Agranat. 2004. “Controlled composition modulation in potassium lithium tantalate niobate crystals grown by off-centered TSSG method.” J. Cryst. Growth 273 (1-2), Pp. 203 - 206. Publisher's Version Abstract
Off-centered top-seeded solution growth (TSSG) method is demonstrated as an effective and simple way to generate controlled composition modulation in potassium lithium tantalate niobate (KLTN) single crystals. The changes in concentration were measured by differential interference contrast (DIC) microscopy. Large length with periodic modulations ranging from 1 to 5 mum in period was grown along a KLTN sample with period dispersion lower than 2%. (C) 2004 Elsevier B.V. All rights reserved.
Resistance degradation in potassium lithium tantalate niobate (KLTN) doped with iron and titanium was measured in a single sample containing various concentrations of interstitial hydrogen. In this crystal the degradation arose from the migration of interstitial hydrogen and not oxygen vacancies, as reported in previous research. Interstitial hydrogen and oxygen vacancy defects both arise to compensate the valence shortfall of the substitutional iron impurities and the thermodynamic balance between the two compensation mechanisms can be controlled using reaction chemistry techniques. Through appropriate annealing treatments a single crystal of KLTN was prepared in three states: hydrogen-rich oxidized, hydrogen-poor reduced, and hydrogen-rich reduced. The characteristic degradation times for the three cases were 29, 2710, and 26 min, respectively. The degradation rate is correlated with hydrogen concentration and not oxidation state of the crystal. Infrared absorption from near the two electrodes of the hydrogen-rich reduced crystal after degradation confirmed polarization of the hydrogen concentration. Electrocoloration was also found to correlate with hydrogen-it was observed in both hydrogen-rich states, but was absent from the hydrogen-poor crystal. (C) 2004 American Institute of Physics.