Non ergodic aging in potassium niobo-tantalate crystals

Abstract.

Slow dynamics has been studied in various potassium niobo-tantalate crystals (KTN) by recording the complex dielectric constant after several thermal histories: isothermal evolution following controlled cooling or rapid quenching, positive or negative temperature cycles. The results reveal most of the behaviours of aging already found in lithium-potassium tantalate (KLT): effective ergodicity breaking (the asymptotic value of the dielectric constant varies as the logarithm of the cooling rate R), quasi-independence of the isothermal evolution with respect to a sojourn at lower temperature. But some differences between KTN and KLT are noticeable: coefficients of log |R| with opposite signs, role of the quenching temperature on the subsequent evolution, no overshot after a temperature jump. In order to explain the results we propose to extend the model initially developped for KLT taking into account the different nature of the low temperature phase, paraelectric for KLT and ferroelectric for KTN. In this model the variations of the dielectric constant are attributed to the slow movements of polarization domain walls hindered by static random fields. By measuring the dielectric constant during cooling and immediate heating at the same rate, an illustrative comparison is provided, showing that the evolution of the domain size is reversible in KLT and not in KTN.