Abstract

As an effort to develop new multiferroic materials at room temperature, we have interstitially doped (x mol %) low dimensional CuO with strong superexchange interactions into lead-free ferroelectric Sr2Bi4Ti5O18 (SBT) ceramics. Upon increase of CuO doping concentration (x = 0, 0.25, 0.5, 0.75 & 1) in SBT + x mol % compound a small and noticeable, but not appreciable, SrTiO3 secondary phase segregates in the SBT. Thus, CuO doping induces SrTiO3 phase and induced volume increase with “x”. The undoped SBT shows weak magnetization (μemu/g) at room temperature and magnetization enhances three-fold (memu/g) with CuO doping in SBT. The thermomagnetic studies of all the samples under zero field cooled, and field cooled modes show typical paramagnetic nature below room temperature and no spin glass-like phases. The Curie–Weiss law analysis suggest that antiferromagnetic interactions are predominant at low temperature in all the CuO doped samples except x = 0.75, which show ferromagnetic interactions. In the direct test for magnetoelectric properties, all the samples show similar magnetoelectric coupling coefficient (α). Among all, the x = 1 sample shows relatively low “α” indicating the magnetoelectric coupling weakens at high CuO concentration. Further, in an indirect test (magnetocapacitance) for magnetoelectric coupling shows similar to magnetoelectric behavior. As reported, the magnetocapacitance may originate from magnetoresistance (MR) and Maxwell–Wagner polarization effect. Our low field MR study on all samples suggests that large magnetocapacitance in x = 1 sample is not due to the extrinsic phenomenon. However further studies are essential to confirm our present inference.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.