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Oxygen-nonstoichiometry-driven phase transition in Sr1−xNdxCoO3−δ (x = 0.1, 0.2, 0.3) perovskites

Abstract

We report a systematic study of the interplay between oxygen nonstoichiometry, crystal structure, and magnetic/electrotransport properties in Sr1−xNdxCoO3−δ (x = 0.1, 0.2, 0.3). High-resolution neutron powder diffraction combined with synchrotron x-ray powder diffraction reveals that increasing the oxygen content induces a structural transition from a layered I4/mmm (2ap × 2ap × 4ap) to an oxygen-deficient orthorhombic Pmmm (ap × ap × 2ap) phases with preferential oxygen-vacancy occupation. This transition is accompanied by a crossover from G-type antiferromagnetic with a weak ferromagnetic component to a ferromagnetic state, and a drastic decay in resistivity. The evolution of the magnetic and transport properties is discussed in terms of changes in the Co spin state, enhanced Co 3d - O 2p orbital overlap upon oxygen uptake, and a magnetically inhomogeneous ferromagnetic state associated with residual oxygen vacancies and mixed Co3+/Co4+ valence. Our findings experimentally confirm that the stabilization of the layered "314" structure is driven by the presence and ordering of oxygen vacancies rather than A-site cation ordering, whereas the oxygen-deficient oxidized compounds represent an intermediate orthorhombic state preceding fully stoichiometric phases.

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BibTeX
@misc{tereshko2026oxygennonstoichiometrydriven,
  title = {{Oxygen-nonstoichiometry-driven phase transition in $\mathrmSr_1-x\mathrmNd_x\mathrmCoO_3-δ$ ($x = 0.1, 0.2, 0.3$) perovskites}},
  author = {Nina Tereshko and Roman Lanovsky and Olivier Toulemonde and Maxim Bushinsky and Stanislav Savvin and Vadim Sikolenko and Lingyan Xu and Aleksandr Nikitin},
  howpublished = {arXiv},
  year = {2026},
  month = nov,
  doi = {10.48550/arxiv.2607.10346},
  eprint = {2607.10346},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2607.10346},
}
RIS
TY  - UNPB
TI  - Oxygen-nonstoichiometry-driven phase transition in Sr_1−xNd_xCoO_3−δ (x = 0.1, 0.2, 0.3) perovskites
AU  - Nina Tereshko
AU  - Roman Lanovsky
AU  - Olivier Toulemonde
AU  - Maxim Bushinsky
AU  - Stanislav Savvin
AU  - Vadim Sikolenko
AU  - Lingyan Xu
AU  - Aleksandr Nikitin
PY  - 2026
DA  - 2026/11/04
PB  - arXiv
DO  - 10.48550/arxiv.2607.10346
UR  - https://arxiv.org/abs/2607.10346
AB  - We report a systematic study of the interplay between oxygen nonstoichiometry, crystal structure, and magnetic/electrotransport properties in Sr_1−xNd_xCoO_3−δ (x = 0.1, 0.2, 0.3). High-resolution neutron powder diffraction combined with synchrotron x-ray powder diffraction reveals that increasing the oxygen content induces a structural transition from a layered I4/mmm (2a_p × 2a_p × 4a_p) to an oxygen-deficient orthorhombic Pmmm (a_p × a_p × 2a_p) phases with preferential oxygen-vacancy occupation. This transition is accompanied by a crossover from G-type antiferromagnetic with a weak ferromagnetic component to a ferromagnetic state, and a drastic decay in resistivity. The evolution of the magnetic and transport properties is discussed in terms of changes in the Co spin state, enhanced Co 3d - O 2p orbital overlap upon oxygen uptake, and a magnetically inhomogeneous ferromagnetic state associated with residual oxygen vacancies and mixed Co^3+/Co^4+ valence. Our findings experimentally confirm that the stabilization of the layered "314" structure is driven by the presence and ordering of oxygen vacancies rather than A-site cation ordering, whereas the oxygen-deficient oxidized compounds represent an intermediate orthorhombic state preceding fully stoichiometric phases.
ER  -