Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12710
Title: AC Conductivity and dielectric properties of lepidocrocite-type alkali titanate tunable by interlayer cation and intralayer metal
Authors: Charoonsuk T.
Sriphan S.
Pulphol P.
Vittayakorn W.
Vittayakorn N.
Maluangnont T.
Keywords: Activation energy
Dielectric losses
Permittivity
Positive ions
Sintering
Zinc compounds
Charge compensation
Chemical compositions
Composition dependence
Compositional variation
Dielectric permittivities
Electrostatic attractions
Interlayer distance
Sheet charge density
Titanium compounds
Issue Date: 2020
Abstract: The lepidocrocite-type layered alkali titanate AxMyTi2-yO4 has diverse chemical compositions with variation in charge per formula unit x, the interlayer cation A+, and the intralayer metal M. Despite this multivariable nature, the composition dependence of physical properties is not well explored. We report herein the AC conductivity and the complementary dielectric properties of Cs0.7M0.35Ti1.65O4, K0.8M0.4Ti1.6O4 (M = Zn, Ni), and the mixed-interlayer ion Cs0.6K0.1Zn0.35Ti1.65O4. For Cs0.7Zn0.35Ti1.65O4, the total AC conductivity is ~7 × 10-8 to 2 × 10-6 S·cm-1 at 200-350 °C, associating with an activation energy Ea ∼865 meV. Meanwhile, the conductivity of K0.8Zn0.4Ti1.6O4 is higher by 1 order of magnitude at much lower temperature (25-150 °C) and a smaller Ea ∼250 meV. This difference originates from the compositional robustness of the cesium-containing samples, contrasting with the sintering-induced changes in the potassium analogues. For the latter, the loss of the interlayer K+ ion results in (i) generation of carriers due to charge compensation, (ii) reduction of sheet charge density and weakening of electrostatic attraction, and (iii) widening of the interlayer distance, all contributing to a lower Ea in K0.8M0.4Ti1.6O4. The angular frequency dependence of conductivity, dielectric permittivity (up to a colossal value of 109), and dielectric loss follows the universal power law. Our work demonstrates the potential of simple compositional variation for electrical properties tuning, prompting a more in-depth investigation covering a wider range of possible candidates of x, A+, and M in lepidocrocite titanate. ©
URI: https://ir.swu.ac.th/jspui/handle/123456789/12710
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85094983748&doi=10.1021%2facs.inorgchem.0c02264&partnerID=40&md5=449e043695bc705ffcf576e6a55881c6
ISSN: 201669
Appears in Collections:Scopus 1983-2021

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