Structural phase transitions of robust insulating Bi1-xLa xFe1-yTiyO3 multiferroics

Abstract

In contrast to leaky BiFeO3, of which two structural phase transitions of cycloidal modulated antiferromagnetic-paramagnetic and ferroelectric-paraelectric are observed below 850°C, chemical co-substitution to form Bi1-xLaxFe1-yTi yO3 ternary solid solution makes these multiferroic ceramics become robust insulating low dielectric loss and exhibit rich structural phase transitions. Differential thermal analysis and temperature-dependent X-ray diffraction measurements probe four first-order structural phase transitions, e.g., TH=305°C, T N=365°C, TC=810°C, and TS=830°C observed in the Bi0.98La0.02Fe0.99Ti 0.01O3 system, which are reasonably attributed to Brazovskii-type cycloidal modulated antiferromagnetic-helimagnetic (at T H) and helimagnetic-paramagnetic (at TN) magnetic phase transitions, ferroelectric-paraelectric (at TC) and rhombohedral-cubic (at TS) structural phase transitions, respectively. Magnetic phase transition temperatures change a little but ferroelectric and lattice structural phase transition temperatures decrease gradually with increasing co-substitution up to composition-induced rhombohedral-(pseudo-)cubic structural phase boundary. The first-order nature of magnetic phase transition and emergence of helimagnetic phase were attributed to Ti3+ d1 magnetic disorder distribution in the Fe 3+ d5-O-Fe3+ d5 chains, while the first-order nature becomes weak with increasing co-substitution, owing to decreased ferroelectric rhombohedral lattice distortion. An intermediate rhombohedral paraelectric phase is discovered intervening between ferroelectric rhombohedral and paraelectric cubic phase, of which the temperature range defined by difference between TC and TS increases with increasing co-substitution. It was found that TC and TS are able to be predicted quantitatively by reduced mass of unit cell. These findings enrich our understanding of ferroic phase transitions and advance designing novel high temperature multiferroic compounds. © 2014 AIP Publishing LLC.