Magneto-orbital ordering in the divalent <i>A</i>-site quadruple perovskite manganites <i>A</i>Mn<sub>7</sub>O<sub>12</sub> (<i>A</i> = Sr, Cd, and Pb)
ORAL
Abstract
Through analysis of variable temperature neutron powder diffraction data, we present solutions for the magnetic structures of SrMn7O12, CdMn7O12, and PbMn7O12 in all long-range ordered phases. The three compounds were found to have magnetic structures analogous to that reported for CaMn7O12. They all feature a higher temperature lock-in phase with commensurate magneto-orbital coupling, and a delocked, multi-k magnetic ground state where incommensurate magneto-orbital coupling gives rise to a constant-moment magnetic helix with modulated spin helicity. CdMn7O12 represents a special case in which the orbital modulation is commensurate with the crystal lattice and involves stacking of fully and partially polarized orbital states. Our results provide a robust confirmation of the phenomenological model for magneto-orbital coupling previously presented for CaMn7O12. Furthermore, we show that the model is universal to the A2+ quadruple perovskite manganites synthesised to date, and that it is tunable by selection of the A-site ionic radius.
*RDJ acknowledges support from a Royal Society University Research Fellowship. We acknowledge support from the JSPS (Japan), grant numbers 15H05433, 15K14133 and 16H04501, and from the EPSRC (UK), grant number EP/M020517/1.
–
Presenters
-
Roger Johnson
- Clarendon Laboratory, University of Oxford
- Clarendon Laboratory, Department of Physics, University of Oxford
- Physics, University of Oxford