期刊
NPJ QUANTUM MATERIALS
卷 4, 期 -, 页码 -出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/s41535-019-0155-2
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资金
- Australian Institute of Nuclear Science and Engineering Ltd (AINSE)
- Australian Research Council (ARC) [DP160100545]
- Australian Research Council Centre of Excellence in Future Low-Energy Electronics Technologies [CE170100039]
- Australian Government
- ARC Discovery Program
- Alexander von Humboldt Foundation
- Transregional Collaborative Research Center (SFB/TRR) SPIN+X
- Department of Energy, Office of Basic Energy Sciences [ER-46612]
- DARPA [HR0011727183-D18AP00010]
- Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions
Understanding and manipulating complex spin texture in multiferroics can offer new perspectives for electric field-controlled spin manipulation. In BiFeO3, a well-known room temperature multiferroic, the competition between various exchange interactions manifests itself as non-collinear spin order, i.e., an incommensurate spin cycloid with period 64 nm. We report on the stability and systematic expansion of the length of the spin cycloid in (110)-oriented epitaxial Co-doped BiFeO3 thin films. Neutron diffraction shows (i) this cycloid, despite its partly out-of-plane canted propagation vector, can be stabilized in thinnest films; (ii) the cycloid length expands significantly with decreasing film thickness; (iii) theory confirms a unique [11 (2) over bar] cycloid propagation direction; and (iv) in the temperature dependence the cycloid length expands significantly close to T-N. These observations are supported by Monte Carlo simulations based on a first-principles effective Hamiltonian method. Our results therefore offer new opportunities for nanoscale magnonic devices based on complex spin textures.
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