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dc.contributor.authorJayakrishnan, A. R.por
dc.contributor.authorAlex, Kevin V.por
dc.contributor.authorThomas, Athulpor
dc.contributor.authorSilva, J. P. B.por
dc.contributor.authorKamakshi, K.por
dc.contributor.authorDabra, Navneetpor
dc.contributor.authorSekhar, K. C.por
dc.contributor.authorAgostinho Moreira, J.por
dc.contributor.authorGomes, M. J. M.por
dc.date.accessioned2018-12-18T19:01:21Z-
dc.date.issued2019-
dc.identifier.citationA.R. Jayakrishnan, Kevin V . Alex, Athul Thomas, J.P .B. Silva, K. Kamakshi, Navneet Dabra, K.C. Sekhar, J. Agostinho Moreira and M.J.M. Gomes, Composition-dependent xBa(Zr0.2Ti0.8)O3-(1-x) (Ba0.7Ca0.3)TiO3 bulk ceramics for high energy storage applications, Ceramics International, https://doi.org/10.1016/j.ceramint.2018.11.250por
dc.identifier.issn0272-8842por
dc.identifier.urihttps://hdl.handle.net/1822/57395-
dc.description.abstractThis work reports the composition dependent microstructure, dielectric, ferroelectric and energy storage properties, and the phase transitions sequence of lead free xBa(Zr0.2Ti0.8)O3-(1-x)(Ba0.7Ca0.3)TiO3 [xBZT-(1-x)BCT] ceramics, with x = 0.4, 0.5 and 0.6, prepared by solid state reaction method. The XRD and Raman scattering results confirm the coexistence of rhombohedral and tetragonal phases at room temperature (RT). The temperature dependence of Raman scattering spectra, dielectric permittivity and polarization points a first phase transition from ferroelectric rhombohedral phase to ferroelectric tetragonal phase at a temperature (TR-T) of 40 0C and a second phase transition from ferroelectric tetragonal phase - paraelectric pseudocubic phase at a temperature (TT-C) of 110 0C. The dielectric analysis suggests that the phase transition at TT-C is of diffusive type and the BZT-BCT ceramics are a relaxor type ferroelectric materials. The composition induced variation in the temperature dependence of dielectric losses was correlated with full width half maxima (FWHM) of A1, E(LO) Raman mode. The saturation polarization (Ps) ≈ 8.3 μC/cm2 and coercive fields ≈ 2.9 kV/cm were found to be optimum at composition x = 0.6 and is attributed to grain size effect. It is also shown that BZT-BCT ceramics exhibit a fatigue free response up to 105 cycles. The effect of a.c. electric field amplitude and temperature on energy storage density and storage efficiency is also discussed. The presence of high TT-C (110 0C), a high dielectric constant (εr ≈ 12285) with low dielectric loss (0.03), good polarization (Ps) ≈ 8.3 μC/cm2) and large recoverable energy density (W = 121 mJ/cm3) with an energy storage efficiency (η) of 70 % at an electric field of 25 kV/cm in 0.6BZT 0.4BCT ceramics make them suitable candidates for energy storage capacitor applications.por
dc.description.sponsorshipThis work was supported by (i) DST-SERB, Govt. of India through grant ECR/2017/000068 and (ii) UGC through Grant Nos. F.4-5(59-FRP/ 2014(BSR)). The authors AR Jayakrishnan acknowledges Central University of Tamil Nadu, India for his Ph.D fellowship. K.V.A. acknowledges the DST for the Inspire fellowship IF170601. J.P.B.S. is grateful for the financial support through the FCT Grant SFRH/BPD/92896/2013.The authors thank to Vivek Sudarsanan from the Central University of Kerala for XRD measurements.por
dc.language.isoengpor
dc.publisherElsevierpor
dc.relationECR/2017/000068por
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F92896%2F2013/PTpor
dc.rightsopenAccesspor
dc.subjectDielectric constantpor
dc.subjectEnergy storage capacitorspor
dc.subjectFatiguepor
dc.subjectLead free ceramicspor
dc.subjectRaman spectroscopypor
dc.subjectSpontaneous polarizationpor
dc.titleComposition-dependent xBa(Zr0.2Ti0.8)O3-(1-x)(Ba0.7Ca0.3)TiO3 bulk ceramics for high energy storage applicationspor
dc.typearticlepor
dc.peerreviewedyespor
oaire.citationStartPage5808por
oaire.citationEndPage5818por
oaire.citationIssue5por
oaire.citationVolume45por
dc.identifier.doi10.1016/j.ceramint.2018.11.250por
dc.subject.fosCiências Naturais::Ciências Físicaspor
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersionpor
dc.subject.wosScience & Technologypor
sdum.journalCeramics Internationalpor
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