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4 pages; International audience; We report the direct measurement of antiferromagnetic spin polarization at the oxygen sites in the multiferroic TbMn2O5, through resonant soft x-ray magnetic scattering. This supports recent theoretical models suggesting that the oxygen spin polarization is key to the magnetoelectric coupling mechanism. The spin polarization is observed through a resonantly enhanced diffraction signal at the oxygen K edge at the commensurate antiferromagnetic wave vector. Using the FDMNES code we have accurately reproduced the experimental data. We have established that the resonance arises through the spin polarization on the oxygen sites hybridized with the square based pyramid Mn3þ ions. Furthermore we have discovered that the position of the Mn3þ ion directly influences the oxygen spin polarization.

Bond valence sum calculations have previously suggested that iron oxyborate exhibits charge order of the Fe ions with integer 2+/3+ valence states. Meanwhile transition metal oxides typically show much smaller, fractional charge disproportionations. Using resonant x-ray diffraction at the iron K edge, we find resonant features which are much larger than those ordinarily observed in charge ordered oxides. Simulations were subsequently performed using a cluster-based, monoelectronic code. The nanoscale domain structure prevents precise fitting; nevertheless the simulations confirm the diagonal charge order symmetry, as well as the unusually large charge disproportionation. We have demonstrated the conversion of linearly to nonlinearly polarized light and vice versa through full polarization analysis. Simulations show that this effect principally results from interference between the isotropic and anisotropic scattering terms. This mechanism is likely to account for similar observations in alternative systems.

We have investigated orbital ordering in the bilayer manganite, Pr (Sr0.1 Ca0.9) 2 Mn2 O7, using synchrotron x-ray diffraction techniques, in particular resonant soft x-ray diffraction. Diffraction signals are observed at (0, 1 2, 0) above 300 K and (1 2, 0,0) below 300 K, corresponding to orbital stripes along the a and b axes, respectively. The previously observed transition at 300 K is evidence of a rotation of the orientation of the 3d orbital stripes. Large resonances of the orbital signals are observed at the MnL edges, with a complex dependence on incident photon energy indicative of a weakly Jahn-Teller distorted system. A structural transition observed at 92 K is found not to involve a further change in the orbital order. © 2009 The American Physical Society.