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Complex magnetic order in nickelate slabs

MPS-Authors
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Zhong,  Z.
Former Research Groups, Max Planck Institute for Solid State Research, Max Planck Society;
Department Nanoscale Science (Klaus Kern), Max Planck Institute for Solid State Research, Max Planck Society;

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Cristiani,  G.
Scientific Facility Thin Film Technology (Gennady Logvenov), Max Planck Institute for Solid State Research, Max Planck Society;

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Logvenov,  G.
Scientific Facility Thin Film Technology (Gennady Logvenov), Max Planck Institute for Solid State Research, Max Planck Society;

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Wang,  Y.
Department Nanoscale Science (Klaus Kern), Max Planck Institute for Solid State Research, Max Planck Society;

van Aken,  P. A:
Max Planck Society;

Hansmann,  P.
Max Planck Society;

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Le Tacon,  M.
Solid State Spectroscopy, Max Planck Institute for Solid State Research, Max Planck Society;

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Keimer,  B.
Department Solid State Spectroscopy (Bernhard Keimer), Max Planck Institute for Solid State Research, Max Planck Society;

Benckiser,  E.
Max Planck Society;

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Citation

Hepting, M., Green, R., Zhong, Z., Bluschke, M., Suyolcu, Y., Macke, S., et al. (2018). Complex magnetic order in nickelate slabs. Nature Physics, 14(11), 1097-1102.


Cite as: https://hdl.handle.net/21.11116/0000-000E-D9EA-6
Abstract
Magnetic ordering phenomena have a profound influence on the macroscopic properties of correlated-electron materials, but their realistic prediction remains a formidable challenge. An archetypical example is the ternary nickel oxide system RNiO3 (R = rare earth), where the period-four magnetic order with proposals of collinear and non-collinear structures and the amplitude of magnetic moments on different Ni sublattices have been subjects of debate for decades(1-6). Here we introduce an elementary model system-NdNiO3 slabs embedded in a non-magnetic NdGaO3 matrix-and use polarized resonant X-ray scattering (RXS) to show that both collinear and non-collinear magnetic structures can be realized, depending on the slab thickness. The crossover between both spin structures is correctly predicted by density functional theory and can be qualitatively understood in a low-energy spin model. We further demonstrate that the amplitude ratio of magnetic moments in neighbouring NiO6 octahedra can be accurately determined by RXS in combination with a correlated double cluster model. Targeted synthesis of model systems with controlled thickness and synergistic application of polarized RXS and ab initio theory thus provide new perspectives for research on complex magnetism, in analogy to two-dimensional materials created by exfoliation(7).