First-principles calculations reveal spin-momentum locking in low-dimensional perovskites, suggesting new engineering avenues.
Chiral hybrid organic-inorganic pyramidal perovskites provide a fertile platform for spin-orbit-driven functionalities. Using first-principles calculations, we show that chiral cation substitution in quasi-one-dimensional Pb-Br pyramidal chains induces sizable spin splitting (up to ∼170 meV) and an emergent one-dimensional (1D) spin-momentum locking near the band edges. Although the nonsymmorphic chiral space group permits independent linear spin-orbit coupling channels along all three spatial directions, the electronic structure self-selects a single dominant channel due to a symmetry-dimensionality mismatch between the three-dimensional (3D) chiral lattice and the quasi-one-dimensional electronic manifold. This mechanism is not symmetry-enforced but emergent, and establishes a transferable physical principle for engineering spin textures in low-dimensional chiral solids.
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Naidel A. M. S. Caturello (2026) studied this question.
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