Lead titanate

Abstract: Understanding the suppression of ferroelectricity in perovskite thin films is a fundamental issue that has remained unresolved for decades. We report a synchrotron x-ray study of lead titanate as a function of temperature and film thickness for films as thin as a single unit cell. At room temperature, the ferroelectric phase is stable for thicknesses down to 3 unit cells (1.2 nanometers). Our results imply that no thickness limit is imposed on practical devices by an intrinsic ferroelectric size effect.

Abstract: The paper will trace the evolution of understanding related to the modification of sharp ferroelectric phase transition behavior that occurs in composition systems which exhibit diffuse and relaxor ferroelectric properties. The focus will be primarily upon the perovskite structure families where cations of different valence occupying similar crystallographic sites in the structure appear to play an important role. Limited ordering in the Pb(B1B2)O3 systems will be discussed and possible mechanisms for self limiting to nanometer scales in some systems explored. New studies of the break up of the simple ferroelectric behavior in lanthanum modified lead zirconate titanate (PLZT) and in lead titanate (PLT) systems will be discussed and the relevance to the general problem of relaxor behavior examined. Evidence for enhanced polarization fluctuations and super paraelectric behavior at high temperatures will be discussed and random field and spin glass models for the lower temperature state considered. ...

Abstract: A piezoelectric material is one that generates a voltage in response to a mechanical strain (and vice versa). The most useful piezoelectric materials display a transition region in their composition phase diagrams, known as a morphotropic phase boundary, where the crystal structure changes abruptly and the electromechanical properties are maximal. As a result, modern piezoelectric materials for technological applications are usually complex, engineered, solid solutions, which complicates their manufacture as well as introducing complexity in the study of the microscopic origins of their properties. Here we show that even a pure compound, in this case lead titanate, can display a morphotropic phase boundary under pressure. The results are consistent with first-principles theoretical predictions, but show a richer phase diagram than anticipated; moreover, the predicted electromechanical coupling at the transition is larger than any known. Our results show that the high electromechanical coupling in solid solutions with lead titanate is due to tuning of the high-pressure morphotropic phase boundary in pure lead titanate to ambient pressure. We also find that complex microstructures or compositions are not necessary to obtain strong piezoelectricity. This opens the door to the possible discovery of high-performance, pure-compound electromechanical materials, which could greatly decrease costs and expand the utility of piezoelectric materials.