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Temperature- and frequency-dependent hysteresis scaling behaviour and phase transitions in a [001]c 0.73Pb(Mg1/3Nb2/3)O3-0.27PbTiO3 single crystal
Affiliation:1. Functional Materials Research Laboratory, Tongji University, Siping Road, Shanghai 200092, China;2. University of Macau, Macau, China;1. Université François Rabelais de Tours, CNRS, CEA, INSA CVL, GREMAN UMR 7347, IUT de BLOIS 15 rue de la chocolaterie, CS 32903, 41029 Blois Cedex, France;2. Laboratoire des Sciences des Procédés et des Matériaux, CNRS, LSPM–UPR 3407, Université Paris 13, Sorbonne Paris Cité, 99 Avenue J.B. Clément, 93430 Villetaneuse, France;3. Université de Montpellier, IES, CNRS, UMR 5214, F-34000 Montpellier, France;1. State Key Laboratory of Powder Metallurgy, Central South University, Changsha, Hunan, 410083, PR China;2. Institute of Electro Ceramics & Devices, School of Materials Science and Engineering, Hefei University of Technology, Hefei, 230009, PR China
Abstract:The dielectric properties and bipolar polarization-electric field (P-E) and strain-electric field (S-E) dynamic hysteresis of a relaxor 001]c 0.73Pb(Mg1/3Nb2/3)O3-0.27PbTiO3 (PMN-0.27PT) single crystal were investigated to reveal more details of the temperature-induced phase transitions. Different linear scaling relations for ferroelectric hysteresis area <A>, coercive field Ec, saturation polarization Ps and remnant polarization Pr versus temperature τ were measured in different temperature regions. For each measurement frequency f, all hysteresis parameters were found to decrease linearly with temperature in the temperature range of the single rhombohedral (R) phase or tetragonal (T) phase, and the rate of decrease in the T phase was observed to be much larger than the corresponding rate in the R phase. In the temperature range near the R-T phase transition, the exponent α in the power law <A>∝f α for the R phase was found to be smaller than that for the T phase, and the magnitude of α depended strongly on temperature when the crystal was in the R-T coexisting phase state. Our experimental and theoretical results indicate that the difference in the activation energy and dipole moment in the R and T phases may lead to the observed discrepancy for the P-E and S-E hysteresis behaviour in different temperature regions.
Keywords:Temperature-induced phase transition  PMN-PT  Dynamic hysteresis  Scaling behaviour
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