Correlations between tetragonality, polarization, and ionic displacement in PbTiO3-derived ferroelectric perovskite solid solutions

We use first-principles density-functional theory calculations to investigate the dependence of tetragonality on local structure in a variety of ferroelectric solid solutions. We demonstrate that tetragonality is strongly coupled to the B-cation displacement and weakly coupled to the A-cation displacement. Examination of various BiMO3 additives to PbTiO3 for different M 3+ ionic sizes reveals that substitution of either small B cations or low doping of large B cations gives rise to large spontaneous polarization and tetragonality. Understanding how the phase transition temperature Tc and tetragonality are affected by Pband Bi-based perovskite additives provides a rational path for designing new high-temperature piezoelectric materials.