Discovery of orbital ordering in Bi2Sr2CaCu2O8+x

Wang, Shuqiu; Kennedy, Niall; Fujita, Kazuhiro; Uchida, Shin-Ichi; Eisaki, Hiroshi; Johnson, Peter D.; Davis, J. C. Séamus; O’Mahony, Shane M.

doi:10.1038/s41563-024-01817-z

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Discovery of orbital ordering in Bi₂Sr₂CaCu₂O_8+x

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Davis, J. C. Séamus
J. C. Séamus Davis, Max Planck Fellow, Max Planck Institute for Chemical Physics of Solids, Max Planck Society;

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Citation

Wang, S., Kennedy, N., Fujita, K., Uchida, S.-I., Eisaki, H., Johnson, P. D., et al. (2024). Discovery of orbital ordering in Bi₂Sr₂CaCu₂O_8+x. Nature Materials, 1-20. doi:10.1038/s41563-024-01817-z.

Cite as: https://hdl.handle.net/21.11116/0000-000F-1A3E-0

Abstract

The primordial ingredient of cuprate superconductivity is the CuO2 unit cell. Theories usually concentrate on the intra-atom Coulombic interactions dominating the 3d9 and 3d10 configurations of each copper ion. However, if Coulombic interactions also occur between electrons of the 2p6 orbitals of each planar oxygen atom, spontaneous orbital ordering may split their energy levels. This long-predicted intra-unit-cell symmetry breaking should generate an orbitally ordered phase, for which the charge transfer energy ε separating the 2p6 and 3d10 orbitals is distinct for the two oxygen atoms. Here we introduce sublattice-resolved ε(r) imaging to CuO2 studies and discover intra-unit-cell rotational symmetry breaking of ε(r). Spatially, this state is arranged in disordered Ising domains of orthogonally oriented orbital order bounded by dopant ions, and within whose domain walls low-energy electronic quadrupolar two-level systems occur. Overall, these data reveal a Q = 0 orbitally ordered state that splits the oxygen energy levels by ~50 meV, in underdoped CuO2. © The Author(s) 2024.