Computational modeling reveals how structural symmetry tunes Rashba splitting and exciton binding in metal halide perovskites, indicating spin-orbit coupling acts primarily via band edges.
We used DFT-1/2+SOC band structures mapped to Wannier tight-binding Hamiltonians and solved with the Bethe−Salpeter equation to examine how confinement, polymorphism, and metal off-centering tune excitons in Pb- and Sn-iodide perovskites in 3D (MA(Pb or Sn)I₃), quasi-2D (BA₂(PborSn)I₄), and model quasi-1D (BA₃(PborSn)I₅). The 3D polymorphs show a clear trend: as symmetry increases from orthorhombic to tetragonal to pseudocubic, Eb decreases. At fixed dimensionality, restoring local metal-centered symmetry suppresses Rashba splitting. It reduces or preserves Eb, indicating that SOC affects excitons mainly through band-edge structure rather than direct strengthening of the electron−hole Coulomb kernel. Low-dimensional compounds retain much larger Eb than 3D analogs, although quasi-1D is not monotonic with quasi-2D. Photoluminescence spectra place the lowest excitons at the optical gap, consistent with bright ground-state excitons.
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Queiroz et al. (2026) studied this question.
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