Dielectric relaxation and polar phonon softening in relaxor ferroelectric PbMg_(1/3)Ta_(2/3)O_3

Physics – Condensed Matter – Materials Science

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subm. to J. Appl. Phys

Scientific paper

10.1063/1.2784972

Relaxor ferroelectric PbMg_1/3Ta_2/3O_3 ceramics and thin films were investigated by means of broad-band dielectric, time-domain terahertz (THz) and Fourier-transform infrared (IR) spectroscopy in the frequency range 100 Hz - 90 THz at temperatures 100 - 490 K, the THz and IR spectra were studied from 20 to 900K. Diffused and strongly temperature dependent peak in the complex permittivity is caused by a dielectric relaxation due to the dynamics of polar clusters. The relaxation appears below Burns temperature T_d in the THz range, slows down on cooling through the microwave and MHz range and anomalously broadens. The shortest and longest relaxation times of the distribution of relaxation times follow Arrhenius and Vogel-Fulcher law, respectively. The degree of B-site order has only a small influence on the parameters of the dielectric relaxation and almost no influence on the phonon parameters. Below T_m ~ 180K, the distribution of relaxation frequencies becomes broader than our experimental spectral range and frequency independent dielectric losses develop below 100 GHz in the spectra. Although the macroscopic crystal structure is cubic, IR spectra give evidence about the lower local symmetry which can be assigned to the presence of polar clusters below T_d. Infrared spectra above T_d still reveal more modes than predicted by selection rules in the paraelectric phase of the Fm-3m space group so that we suggest selection rules which take into account chemical inhomogeneity in the beta''-perovskite sublattice.

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