Distortion modes and ferroelectric properties in hybrid improper ferroelectric Sr3(Sn,Zr)2O7 ceramics

Abstract

In the present work, the distortion modes and ferroelectric properties of Sr3(Sn1− xZr x)2O7 ( x = 0.0, 0.25, 0.5, 0.75, 1.0) ceramics with double-layered Ruddlesden–Popper structures were investigated. The amplitudes of three distortion modes for the ferroelectric phase deviated from the aristotype one were quantified using the symmetry-mode approach adopted in Rietveld refinement against x-ray diffraction patterns. The remanent polarization and the coercive field decreased with increasing the content of Zr4+ cations. The decline of polarization should attribute to the nonpolar secondary phase, while the suppression of a coercive field may connect with the decreased amplitude of the rotation mode. The Curie temperatures increased linearly with increasing x value in Sr3(Sn1− xZr x)2O7 ceramics, inducing from the decline of a tolerance factor. A typical first-order improper ferroelectric phase transition was determined using a differential scanning calorimetry measurement and dielectric characterization. From the present work, a straightforward way to quantify the amplitude of a distortion mode for the ferroelectric phase was given, and the ferroelectric properties could be effectively tuned by substituting the cations at the B site in the Sr-based hybrid improper ferroelectrics.