BaTiO3-based ferroelectric ceramics show interesting properties such as high dielectric constant, low losses, high hydrostatic piezoelectric coefficient and PTCR effect. For these reasons, barium titanate is widely used in the electronic industry for manufacturing miniaturised multilayer ceramic capacitors, underwater transducers and self-regulating thermistors. BaZrxTi1-xO3 (BZT) solid solution possesses the perovskite structure and shows a series of phase transitions and a progressive evolution of ferroelectric order, from long-range order typical of classic ferroelectrics (x = 0-0.15), via a diffuse transition behaviour (x = 0.15-0.25), to short-range order typical of relaxors (x >= 0.25) and finally paraelectric non polar state for neat BaZrO3. The trivalent europium ion (Eu3+) is well known for its strong luminescence in the red spectral region. Even very small variations in the coordination sphere of europium ions induce major changes in the emission spectrum. Thanks to these features, Eu3+ is a unique and powerful local structural probe. In this framework, we have investigated the photoluminescence (PL) emission of dense BZT ceramics doped with Eu3+ at the Ba site with composition EuyBa1-yZrxTi1-x-y/4O3 (y = 0.01, x = 0, 0.05, 0.15, 0.30, 0.50, 0.70, 1) in the temperature range -100 to 140 °C. The ceramics were prepared by the classical solid-state route and sintered at 1450-1550 °C. The dielectric permittivity of the samples was measured from -150 to 150 °C at 10e2-10e6 Hz to determine reference values of the phase transition temperatures and the type of polar order. The PL bands revealed significant shape and intensity variations which can be correlated with the existence and nature (long-range or short-range) of polar order rather than the phase transitions. The spectral features observed for compositions with long-range ferroelectric order (x = 0-0.15) support the off-centre displacement of the Eu3+ ion with respect to the lattice position occupied by barium.
Photoluminescence and evolution of polar order in Eu:BaZrxTi1-xO3 ceramics
Bottaro G;Canu G;Buscaglia MT;Costa C;Buscaglia V
2018
Abstract
BaTiO3-based ferroelectric ceramics show interesting properties such as high dielectric constant, low losses, high hydrostatic piezoelectric coefficient and PTCR effect. For these reasons, barium titanate is widely used in the electronic industry for manufacturing miniaturised multilayer ceramic capacitors, underwater transducers and self-regulating thermistors. BaZrxTi1-xO3 (BZT) solid solution possesses the perovskite structure and shows a series of phase transitions and a progressive evolution of ferroelectric order, from long-range order typical of classic ferroelectrics (x = 0-0.15), via a diffuse transition behaviour (x = 0.15-0.25), to short-range order typical of relaxors (x >= 0.25) and finally paraelectric non polar state for neat BaZrO3. The trivalent europium ion (Eu3+) is well known for its strong luminescence in the red spectral region. Even very small variations in the coordination sphere of europium ions induce major changes in the emission spectrum. Thanks to these features, Eu3+ is a unique and powerful local structural probe. In this framework, we have investigated the photoluminescence (PL) emission of dense BZT ceramics doped with Eu3+ at the Ba site with composition EuyBa1-yZrxTi1-x-y/4O3 (y = 0.01, x = 0, 0.05, 0.15, 0.30, 0.50, 0.70, 1) in the temperature range -100 to 140 °C. The ceramics were prepared by the classical solid-state route and sintered at 1450-1550 °C. The dielectric permittivity of the samples was measured from -150 to 150 °C at 10e2-10e6 Hz to determine reference values of the phase transition temperatures and the type of polar order. The PL bands revealed significant shape and intensity variations which can be correlated with the existence and nature (long-range or short-range) of polar order rather than the phase transitions. The spectral features observed for compositions with long-range ferroelectric order (x = 0-0.15) support the off-centre displacement of the Eu3+ ion with respect to the lattice position occupied by barium.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
