Oxygen vacancies in BaTiO3 based ferroelectrics: electron doping, history dependence of Tc and domain wall pinning

TL;DR

This study investigates how oxygen vacancies affect the elastic and ferroelectric properties of BaTiO3-based materials, revealing their role in Tc shifts, domain wall pinning, and aging effects, with implications for fatigue resistance.

Contribution

It provides a detailed analysis of oxygen vacancy dynamics, their impact on Tc and domain pinning, and differences between materials with varying vacancy behaviors.

Findings

Oxygen vacancies cause peaks in elastic energy loss related to their jumps and reorientations.

Tc shifts are linked to vacancy aggregation and electron doping effects.

BCTZ exhibits higher activation energy, leading to static vacancies and improved fatigue resistance.

Abstract

We measured the complex Young's modulus of BaTiO3-d, BaxSr1-xTi3-d (BST) and Ba0.85Ca0.15Zr0.1Ti0.9O3-d (BCTZ) during heating and cooling runs at various O deficiencies and aging times. The elastic energy loss has peaks due to the jumps of isolated O vacancies (VO) and reorientations of pairs of VO in the paraelectric phase, from which the respective rates and activation energies are measured. These rates control the mechanisms of domain clamping, pinning, fatigue, and anything related to the VO mobility. In the ferroelectric (FE) phase, the drop of the losses due to the domain wall motion upon introduction of VO monitors the degree of pinning. In addition, large shifts of Tc are observed at the same value of d upon varying the permanence time in the FE state, up to DTc = 21K in BST, while no aging effect is found in BCTZ. The phenomenology is explained by considering that Tc is depressed mainly by the mobile electrons doped by VO. Each isolated VO dopes two electrons as itinerant Ti^3+ ions, but, when it forms a stable linear VO-Ti^2+-VO pair, the two electrons of the Ti^2+ are subtracted from the mobile ones, halving doping. The rise of Tc during the initial aging is then explained in terms of the progressive aggregation of the VO. Prolonging aging for years leads to a decrease of Tc, explained assuming that the most stable position of a VO is at 90^o domain walls, whose geometry is incompatible with the pairs. Then, after enough time the initially aggregated VO within the domains dissociate to decorate the 90^o walls, increasing doping and lowering Tc. The absence of such effects in BCTZ is due to larger activation energy for pair reorientation and pair binding energy. Then, at room temperature practically all VO are paired and static over a time scale of hundreds of years, explaining the superior resistance of BCTZ to fatigue.