First-principles calculations of spin-split bands in chiral hybrid organic-inorganic perovskites (/-PEA)PbI and (/-NEA)PbI
arXiv:2607.00933
Abstract
Chiral hybrid organic-inorganic perovskites provide a promising platform for investigating the physics of chirality-driven spin-split bands because they combine robust molecular chirality with strong spin-orbit coupling from heavy inorganic ions. First-principles calculations including spin-orbit coupling are performed for the one-dimensional chiral perovskites (/-PEA)PbI and (/-NEA)PbI to compare their spin-split band structures and to identify the factors controlling their differences. In (/-PEA)PbI, the lowest conduction bands predominantly consist of Pb orbitals, whereas in (/-NEA)PbI, they are formed by hybridization between Pb orbitals and the lowest unoccupied molecular orbital of NEA. Both compounds exhibit pronounced spin splitting near the valence-band maximum and conduction-band minimum. The effective spin splitting of the edges of the valence bands is stronger in (/-NEA)PbI, despite similar linear-in- splitting coefficients near the relevant high-symmetry points. This enhancement originates from larger gaps induced by spin-orbit coupling at high-symmetry points and band (anti)crossings in the multiband structure. For a given molecular handedness, the PEA- and NEA-based compounds exhibit opposite spin textures, consistent with the opposite chiral distortions of the [PbI] octahedra and with the previously observed opposite signs of circular dichroism. Group-theoretical analysis for the nonsymmorphic space group further accounts for band sticking, symmetry-enforced degeneracies, and the disappearance of spin polarization at specific Brillouin-zone-boundary points. These results provide a solid foundation for future studies of chirality-dependent electromagnetic responses, including circular dichroism, in chiral hybrid organic-inorganic perovskites.
11 pages, 9 figures