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Park, SoHyun; Hartl, Anna ORCID logoORCID: https://orcid.org/0000-0002-8615-2755; Sheptyakov, Denis ORCID logoORCID: https://orcid.org/0000-0002-3001-6586; Hoelzel, Markus und Arauzo, Ana ORCID logoORCID: https://orcid.org/0000-0002-5999-341X (13. September 2021): Structural Investigation into Magnetic Spin Orders of a Manganese Phosphatic Oxyhydroxide, Mn5(PO4)2(PO3(OH))2(HOH)4. In: Symmetry, Bd. 13, Nr. 9: S. 1-18 [PDF, 51MB]

Abstract

The ferri- and antiferromagnetic structures of a hureaulite-type synthetic compound, Mn2+5(PO4)2(PO3(OH))2(HOH)4, were elucidated by high-resolution neutron powder diffraction in combination with magnetic susceptibility and heat capacity measurements. At 6.17 K, the paramagnetic phase (space group: C2/c) transforms to inherit a ferrimagnetic order (magnetic space group: C2'/c'), followed at 1.86 K by an incommensurately modulated antiferromagnetic order (magnetic superspace group: P21/c.1'(α0γ)00s with the propagation vector k(0.523(2), 0, 0.055(1)). In the ferrimagnetic state, antiferromagnetic interactions are dominant for both intra and inter pentamers of Mn2+(O, HOH)6 octahedra. Differently aligned spin-canting sublattices seen in the ferrimagnetic models at 3.4, 4.5, and 6.1 K explain a weak ferromagnetism in the title compound. The observation of magnetic moments vigorously changing in a small temperature range of 6.1-1.5 K adumbrates a high complexity of interplaying structural and magnetic orders in this manganese phosphatic oxyhydroxide.

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