High Entropy Oxide Relaxor Ferroelectrics

TL;DR

This paper introduces a new class of high entropy relaxor ferroelectrics created through entropy-assisted synthesis, demonstrating their unique phase transition behaviors and potential for advanced electromechanical applications.

Contribution

It presents the synthesis and characterization of a novel high entropy relaxor ferroelectric material with multiple phase transitions and high Curie temperature, expanding the design space for functional ferroelectrics.

Findings

High entropy Ba(5B)O films exhibit multiple phase transitions.

The material has a high Curie temperature of 570 K.

First principles calculations support the feasibility of highly disordered perovskites.

Abstract

Relaxor ferrolectrics are important in technological applications due to a strong electromechanical response, energy storage capacity, electrocaloric effect, and pyroelectric energy conversion properties. Current efforts to discover and design new materials in this class generally rely on substitutional doping of known ferroelectrics, as slight changes to local compositional order can significantly affect the Curie temperature, morphotropic phase boundary, and electromechanical responses. In this work, we demonstrate that moving to the strong limit of compositional complexity in an ABO3 perovskite allows stabilization of novel relaxor responses that do not rely on a single narrow phase transition region. Entropy-assisted synthesis approaches are used to create single crystal Ba(Ti0.2Sn0.2Zr0.2Hf0.2Nb0.2)O3 [Ba(5B)O] films. The high levels of configurational disorder present in this system is found to influence dielectric relaxation, phase transitions, nano-polar domain formation, and Curie temperature. Temperature-dependent dielectric, Raman spectroscopy and second-harmonic generation measurements reveal multiple phase transitions, a high Curie temperature of 570 K, and the relaxor ferroelectric nature of Ba(5B)O films. The first principles theory calculations are used to predict possible combinations of cations to quantify the relative feasibility of formation of highly disordered single-phase perovskite systems. The ability to stabilize single-phase perovskites with such a large number of different cations on the B-sites offers new possibilities for designing high-performance materials for piezoelectric, pyroelectric and tunable dielectric applications.