Pith. sign in

REVIEW

Large geometric polarization and magnetic behavior in the multiferroic quasi-2D SrNiF₄ fluoride

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2406.03610 v1 pith:4DQMMYBX submitted 2024-06-05 cond-mat.mtrl-sci

Large geometric polarization and magnetic behavior in the multiferroic quasi-2D SrNiF₄ fluoride

classification cond-mat.mtrl-sci
keywords polarizationferroelectricfluorideantiferromagneticbehaviorcompoundgammageometric
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
read the original abstract

In the last decades, multifunctional single-crystals that show, for example, multiferroic and magnetoelectric responses have attracted considerable attention due to the potential applications and physical phenomena involved in the entanglement of the ferroic orders. This paper investigates the structural, ferroelectric, and magnetic properties of the unexplored layered SrNiF$_4$ fluoride compound. We show that, in terms of the vibrational phonon modes, this fluoride compound shows a tangible ferroelectric behavior with a spontaneous polarization as large as $P_s$ = 14.8 $\mu$C$\cdot$cm$^{-2}$ standing as one of the largest among its family. Besides, based on our findings such ferroelectric polarization presents a geometric origin that is strongly entangled with the octahedral rotations within the $\Gamma_2^-$ phonon mode and enhanced by the structure's $\Gamma_1^+$ mode. We also observed that the spontaneous polarization is coupled to the noncollinear $G$-type antiferromagnetic ordering in the structure allowing a switching of the weak antiferromagnetic component when the polarization is reversed.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.