Room temperature coexistence of large electric polarization and magnetic order in BiFeO3 single crystals

TL;DR

This study demonstrates that high-quality BiFeO3 single crystals exhibit room temperature ferroelectricity with large polarization and magnetic order, confirmed through various experimental techniques, resolving previous uncertainties about its properties.

Contribution

The paper reports the first clear observation of room temperature ferroelectricity and magnetic order in BiFeO3 single crystals, with detailed synthesis and characterization methods.

Findings

BiFeO3 exhibits ferroelectricity at room temperature.

Large polarization (~60 μC/cm²) comparable to thin films.

Coexistence of magnetic order confirmed by SQUID and Mossbauer spectroscopy.

Abstract

From an experimental point of view, room temperature ferroelectricity in BiFeO3 is raising many questions. Electric measurements made a long time ago on solid-solutions of BiFeO3 with Pb(Ti,Zr)O3 indicate that a spontaneous electric polarization exists in BiFeO3 below the Curie temperature TC=1143K. Yet in most reported works, the synthesised samples are too conductive at room temperature to get a clear polarization loop in the bulk without any effects of extrinsic physical or chemical parameters. Surprisingly, up to now there has been no report of a P(E) (polarization versus electric field) loop at room temperature on single crystals of BiFeO3. We describe here our procedure to synthesize ceramics and to grow good quality sizeable single crystals by a flux method. We demonstrate that BiFeO3 is indeed ferroelectric at room-temperature through evidence by Piezoresponse Force Microscopy and P(E) loops. The polarization is found to be large, around 60 microC/cm2, a value that has only been reached in thin films. Magnetic measurements using a SQUID magnetometer and Mossbauer spectroscopy are also presented. The latter confirms the results of NMR measurements concerning the anisotropy of the hyperfine field attributed to the magnetic cycloidal structure.