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AC Conductivity and dielectric properties of lepidocrocite-type alkali titanate tunable by interlayer cation and intralayer metal

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dc.contributor.author Charoonsuk T.
dc.contributor.author Sriphan S.
dc.contributor.author Pulphol P.
dc.contributor.author Vittayakorn W.
dc.contributor.author Vittayakorn N.
dc.contributor.author Maluangnont T.
dc.date.accessioned 2021-04-05T03:05:10Z
dc.date.available 2021-04-05T03:05:10Z
dc.date.issued 2020
dc.identifier.issn 201669
dc.identifier.other 2-s2.0-85094983748
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/12710
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-85094983748&doi=10.1021%2facs.inorgchem.0c02264&partnerID=40&md5=449e043695bc705ffcf576e6a55881c6
dc.description.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. ©
dc.rights Srinakharinwirot University
dc.subject Activation energy
dc.subject Dielectric losses
dc.subject Permittivity
dc.subject Positive ions
dc.subject Sintering
dc.subject Zinc compounds
dc.subject Charge compensation
dc.subject Chemical compositions
dc.subject Composition dependence
dc.subject Compositional variation
dc.subject Dielectric permittivities
dc.subject Electrostatic attractions
dc.subject Interlayer distance
dc.subject Sheet charge density
dc.subject Titanium compounds
dc.title AC Conductivity and dielectric properties of lepidocrocite-type alkali titanate tunable by interlayer cation and intralayer metal
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Inorganic Chemistry. Vol 59, No.21 (2020), p.15813-15823
dc.identifier.doi 10.1021/acs.inorgchem.0c02264


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