ترغب بنشر مسار تعليمي؟ اضغط هنا

Dynamic behavior of polar nanoregions in re-entrant relaxor 0.6Bi(Mg1/2Ti1/2)O3-0.4PbTiO3

173   0   0.0 ( 0 )
 نشر من قبل Laijun Liu
 تاريخ النشر 2020
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

The existence of polar nanoregions is the most important characteristic of ferroelectric relaxors, however, the size determination and dynamic of PNRs remains uncertain. We reveal a re-entrant relaxor behavior and ferroelectric-paraelectric transition coexists in complex perovskite oxide 0.6Bi(Mg1/2Ti1/2)O3-0.4PbTiO3. Two dielectric anomalies (i) the low-temperature re-entrant relaxor transition and (ii) the high-temperature diffuse phase transition (DPT) were described by the phenomenological statistical model. The sizes of the two kinds of polar nanoregions (PNRs) corresponding to two ferroelectric states were obtained. The dynamic of PNRs were analyzed using isothermal electrical modulus, which shows three critical temperatures associated with the diffuse phase transition, the formation and freezing of PNRs, respectively. The temperature evolution of the PNRs evolution depends on the stoichiometry of bismuth. The results provide new insights into the dynamic behavior of PNRs and the modification way of re-entrant relaxor behavior.



قيم البحث

اقرأ أيضاً

207 - Wei Peng 2009
We present electric and magnetic properties of 0.8Pb(Fe1/2Nb1/2)O3-0.2Pb(Mg1/2W1/2)O3 films epitaxially grown on (001) SrTiO3 substrates using pulsed laser deposition. A narrow deposition window around 710 oC and 0.2 mbar has been identified to achie ve epitaxial single-phase thin films. A typical Vogel-Fulcher relaxor-like dielectric and magnetic susceptibility dispersion is observed, suggesting magnetoelectric relaxor behavior in these films similar to the bulk. We determine a magnetic cluster freezing temperature of 36 K, while observing weak ferromagnetism via magnetic hysteresis loops up to 300 K.
Local inhomogeneities known as polar nanoregions (PNR) play a key role in governing the dielectric properties of relaxor ferroelectrics - a special class of material that exhibits an enormous electromechanical response and is easily polarized with an external field. Using neutron inelastic scattering methods, we show that the PNR can also significantly affect the structural properties of the relaxor ferroelectric Pb(Zn1/3Nb2/3)O3-4.5%PbTiO3 (PZN-4.5%PT). A strong interaction is found between the PNR and the propagation of sound waves, i.e. acoustic phonons, the visibility of which can be enhanced with an external electric field. A comparison between acoustic phonons propagating along different directions reveals a large asymmetry in the lattice dynamics that is induced by the PNR. We suggest that a phase instability induced by this PNR-phonon interaction may contribute to the ultrahigh piezoelectric response of this and related relaxor ferroelectric materials. Our results also naturally explain the emergence of the various observed monoclinic phases in these systems.
A new class of superparamagnetism was found in relaxor ferroelectric 2/3BiFeO$_{3}$-1/3BaTiO$_{3}$. The size of the magnetic particle, estimated from the superparamagnetic magnetization curve, coincides with the size of the polar nanoregion (PNR), wh ich governs the relaxor ferroelectric property. This suggests that the magnetic domain is identical to the PNR. The temperature variations in the sizes of the magnetic domains and PNRs estimated by our neutron diffraction measurements support this picture. Since the same domain provides both electric and magnetic properties, strong coupling between the two properties through the domain size is expected.
Single crystals of Pb(In1/2Nb1/2)O3-Pb(Mg1/3Nb2/3)O3-PbTiO3 (PIN-PMN-PT) poled along [001] were investigated by dielectric, x-ray, and polarized light (PLM) and piezo-force microscopy (PFM) methods. PLM revealed {100} macro-domain plates that formed after poling, whose size increased on heating between room temperature and a rhombohedral rightarrow tetragonal phase transition, above which point a break-up of the macro-domain plates was observed. Corresponding PFM studies demonstrated that poling reduced the size of stripe-like domains that were internal to the macro-domain plates, whose size also increased on heating to TR-T. The temperature dependence of both the size of the macro-domain plates and internal sub-domains followed the Arrhenius relation with the activation energy of 0.4-0.5eV. The coercive field displays an abnormal increase on heating below TR-T, different than that for PMN-PT. The anomalously increased coercive field can be ascribed to the Arrhenius-type domain growth, indicating a simple thermally activated process and an important role of hierarchial domains in the improved performance of PIN-PMN-PT.
We have characterized the dynamics of the polar nanoregions in Pb(Mg$_{1/3}$Nb$_{2/3}$)O$_{3}$ (PMN) through high-resolution neutron backscattering and spin-echo measurements of the diffuse scattering cross section. We find that the diffuse scatterin g intensity consists of emph{both} static and dynamic components. The static component first appears at the Curie temperature $Theta sim 400$ K, while the dynamic component freezes completely at the temperature T$_{f} sim 200$ K; together, these components account for all of the observed spectral weight contributing to the diffuse scattering cross section. The integrated intensity of the dynamic component peaks near the temperature at which the frequency-dependent dielectric constant reaches a maximum (T$_{max}$) when measured at 1 GHz, i. e. on a timescale of $sim 1$ ns. Our neutron scattering results can thus be directly related to dielectric and infra-red measurements of the polar nanoregions. Finally, the global temperature dependence of the diffuse scattering can be understood in terms of just two temperature scales, which is consistent with random field models.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا