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Ionic Conduction (ionic + conduction)
Selected AbstractsStructure, Ionic Conduction and Dielectric Relaxation in a Novel Fast Ion Conductor, Na2Cd(SO4)2.CHEMINFORM, Issue 18 2007Diptikanta Swain Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Ionic Conduction and Dielectric Properties in the Telluric Sulfate K2(SO4)×Te(OH)6.CHEMINFORM, Issue 44 2003C. Boudaya Abstract For Abstract see ChemInform Abstract in Full Text. [source] Investigation of the Role of Ionic Liquids in Imparting Electrocatalytic Behavior to Carbon Paste ElectrodeELECTROANALYSIS, Issue 21 2007Norouz Maleki Abstract In this paper, a survey has been undertaken to clarify the possible reasons for the electrocatalytic activity obtained by the presence of ionic liquid in carbon paste electrode (CPE). For this purpose, the effect of the addition of traces of ionic liquid to conventional CPE was investigated. Fe(CN)63,/4, was used as a probe and two ionic liquids, namely n -octylpyridinum hexafluorophosphate and 1-octyl-3-methylimidazolium hexaflourophosphate were tested for their electrocatalytic activity. The reasons for this electrocatalytic behavior were evaluated and it was found that different factors such as increase in the ionic conduction of the binder, decrease in the resistance of the modified electrode, increase in ion exchange properties of the electrode and the inherent catalytic activity of ionic liquids are responsible for the considerable improved electrochemical response obtained in the presence of traces of ionic liquid. [source] Low-Temperature Superionic Conductivity in Strained Yttria-Stabilized ZirconiaADVANCED FUNCTIONAL MATERIALS, Issue 13 2010Michael Sillassen Abstract Very high lateral ionic conductivities in epitaxial cubic yttria-stabilized zirconia (YSZ) synthesized on single-crystal SrTiO3 and MgO substrates by reactive direct current magnetron sputtering are reported. Superionic conductivities (i.e., ionic conductivities of the order ,1 ,,1cm,1) are observed at 500,°C for 58-nm-thick films on MgO. The results indicate a superposition of two parallel contributions , one due to bulk conductivity and one attributable to conduction along the film,substrate interface. Interfacial effects dominate the conductivity at low temperatures (<350,°C), showing more than three orders of magnitude enhancement compared to bulk YSZ. At higher temperatures, a more bulk-like conductivity is observed. The films have a negligible grain-boundary network, thus ruling out grain boundaries as a pathway for ionic conduction. The observed enhancement in lateral ionic conductivity is caused by a combination of misfit dislocation density and elastic strain in the interface. These very high ionic conductivities in the temperature range 150,500,°C are of great fundamental importance but may also be technologically relevant for low-temperature applications. [source] Sintering Behavior and Conductivity Study of Yttrium-Doped BaCeO3,BaZrO3 Solid Solutions Using ZnO AdditivesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2009He Wang The effect of ZnO on the crystal structure, sintering behavior, and electrical conductivity of yttrium-doped BaCeO3,BaZrO3 was investigated by unfixing or fixing the yttrium content noted as BaCe0.5Zr0.3Y0.2,xZnxO2.9,0.5x and BaCe0.5Zr0.3Y0.2O2.9+yZnO, respectively. Studies on the two series revealed that BaO·ZnO eutectic, rather than ZnO, was responsible for the sintering densification. For BaCe0.5Zr0.3Y0.2,xZnxO2.9,0.5x, the evaporation of ZnO·BaO eutectic was observed after sintering at 1300°C for 10 h, and few impurities were detected by XRD with x<0.20. For BaCe0.5Zr0.3Y0.2O2.9+yZnO, the concomitant loss of BaO with ZnO caused A-site deficiency and led to impurities of Y2O3 for y=0.08 and 0.14, and Y2BaZnO5 for y=0.20 during the sintering. For both series, ZnO enhanced the relative density, which was above 97% with x or y varying from 0.02 to 0.08. Energy-dispersive X-ray spectroscopy analysis revealed that ZnO hardly entered the perovskite phase. The conductivity study also suggested that ZnO did not serve as a dopant and that yttrium content was essential for sustaining a high ionic conduction. Excessive ZnO was especially detrimental to the grain boundary conduction and thus lowered the total electrical conduction. The optimized composition of BaCe0.5Zr0.3Y0.2O2.9+0.04ZnO has been obtained, with both a high relative density (,98.5%) and a high electrical conductivity (1.35 × 10,2 S/cm at 600°C). [source] Influences of ZnO on the Properties of SrZr0.9Y0.1O2.95 Protonic ConductorJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 5 2008Zhenzhen Peng The effects of ZnO additive on the microstructure, phase formation, and electrical conduction of yttrium-doped strontium zirconate were investigated. The sintering temperature of SrZr0.9Y0.1O2.95 can be lowered to 1350°C by addition of ZnO. The electrical conduction is found to be strongly correlated with the ZnO contents. When the ZnO content is <5 mol%, the electrical conductivity increased with an increase in the ZnO contents. Electromotive force measurements under fuel cell conditions indicated a pure ionic conduction over this range of ZnO contents. However, it had a detrimental effect on the electrical conduction when the ZnO content was more than 6 mol%. The main reason for this is discussed according to the defect chemistry and microstructure. [source] Solid-State Ionics: Roots, Status, and Future ProspectsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2002Philippe Knauth This review represents the authors' view of the evolution of solid-state ionics over approximately the past 100 years. A brief history, introducing milestones of the development of this discipline, is followed by a short summary of the theory of ionic conduction in the bulk and the more recently developed theory of ionic conduction at interfaces. The central part of the article gives examples of ionic-conducting materials systems with structures ranging from one- to three-dimensional disorder. Important experimental techniques for analyzing ionic conduction, including alternating-current impedance spectroscopy, direct-current coulometry, and direct-current current-voltage measurements with blocking electrodes, are also summarized. The main technological applications, that is, batteries, solid-oxide fuel cells, electrochemical sensors, electrochromic windows, and oxygen-separation membranes, are reviewed. Finally, new concepts in solid-state ionics are presented, including the investigation of new materials (such as nanostructured phases), the study of boundaries (for example, using microelectrodes), the development of computational techniques, and the connections with other classes of materials (notably magnetic and semiconducting materials). [source] Structural analysis of lithium lanthanum titanate with perovskite structurePHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue 5 2009Koji Ohara Abstract Neutron and high-energy X-ray diffraction analysis of polycrystalline La4/3-xLi3xTi2O6 have been performed to clarify the extent of disorder of the distribution of La and Li ions and to understand the relation of these distributions to ionic conduction. The distributions of the La and Li ions in a 10 × 10 × 20 cubic box (i.e., 10 × 10 × 10 unit cell) super-structure, in which Ti and O atoms are fixed onto their regular sites, were obtained by the reverse Monte Carlo (RMC) structural modelling of both diffraction data sets. When the occupancy of La ions in the planes perpendicular to the c-axis is analysed, one can find a La-rich and La-poor layers alternating, which is consistent with the results of earlier Rietveld analysis (Stramare et al., Chem. Mater. 15, 3974 (2003) [1]). Of particular interest, the Li ions are found mainly on the interstitial sites between the O-3 triangle plane of the TiO6 octahedron and a La ion, which is different from the earlier work (Yashima et al., J. Am. Chem. Soc. 127, 3491 (2005) [2]). (© 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Planar aqueous electrode technique for polymer impedance spectroscopyPOLYMER ENGINEERING & SCIENCE, Issue 3 2009T. Bai In this article, we develop an aqueous electrode technique that can adapt to complex sample geometries while maintaining perfect contact between the electrodes and the measured sample. In contrast to surface deposited electrodes, the aqueous electrode technique measures the ionic conduction of the polymer sample instead of the inherent dielectric properties of the polymer. Polymer ionic conduction is often related to the polymer thermodynamic state, which itself is closely linked to many other polymer properties. As such, the aqueous electrode method provides an approach to conduct in situ monitoring of polymer samples subjected to degradation; changes in the impedance provide an indication of polymer sample degradation. This article presents the aqueous electrode setup and discusses experimental results obtained using it. Changes in the impedance response of PVC and polyimide films due to moisture absorption, ionic conduction, pinholes, chemical degradation, and temperature are presented. POLYM. ENG. SCI., 2009. © 2008 Society of Plastics Engineers [source] Preparation, characterization and application of zwitterionic polymers and membranes: current developments and perspectivePOLYMER INTERNATIONAL, Issue 12 2009Fengqin Xuan Abstract Because of their unique pendant-side chain structures and excellent properties, zwitterionic polymers and membranes, especially zwitterionic hybrids, have attracted increasing interest in recent years. Presently, they can be potentially applied in such fields as nonlinear optical systems, ionic conduction, biomedical processing and chemical separation. In view of their significance to academia and industrial processes, this review gives a brief summary of current developments in the preparation, characterization and potential application of zwitterionic polymers and membranes. Novel approaches to prepare zwitterionic hybrids are highlighted. The present state and future perspective are also discussed. Hopefully, this review can promote the understanding of zwitterionic hybrid polymers and membranes. Copyright © 2009 Society of Chemical Industry [source] Crystallinity, thermal properties, morphology and conductivity of quaternary plasticized PEO-based polymer electrolytesPOLYMER INTERNATIONAL, Issue 3 2007Yan-Jie Wang Abstract Quaternary plasticized solid polymer electrolyte (SPE) films composed of poly(ethylene oxide), LiClO4, Li1.3Al0.3Ti1.7(PO4)3, and either ethylene carbonate or propylene carbonate as plasticizer (over a range of 10,40 wt%) were prepared by a solution-cast technique. X-ray diffraction (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS) indicated that components such as LiClO4 and Li1.3Al0.3Ti1.7(PO4)3 and the plasticizers exerted important effects on the plasticized quaternary SPE systems. XRD analysis revealed the influence from each component on the crystalline phase. DSC results demonstrated the greater flexibility of the polymer chains, which favored ionic conduction. SEM examination revealed the smooth and homogeneous surface morphology of the plasticized polymer electrolyte films. EIS suggested that the temperature dependence of the films' ionic conductivity obeyed the Vogel,Tamman,Fulcher (VTF) relation, and that the segmental movement of the polymer chains was closely related to ionic conduction with increasing temperature. The pre-exponential factor and pseudo activation energy both increased with increasing plasticizer content and were maximized at 40 wt% plasticizer content. The charge transport in all polymer electrolyte films was predominantly reliant on lithium ions. All transference numbers were less than 0.5. Copyright © 2006 Society of Chemical Industry [source] | |||||||||||||