Spectroscopic study demonstrates emergent circularly polarized luminescence in self-assembled chiral CsPbBr3 nanocube superlattices, indicating that ordered assembly enhances weak chiroptical...
Chiral surface ligands can impart optical activity to all-inorganic perovskite nanocrystals, but how this affects chiroptical properties of their assemblies remains unclear. Here we show that self-assembly of CsPbBr3 nanocubes synthesized with a small amount of added chiral ligand N-benzylcinchonidinium bromide (BCD-Br) results in measurable circularly polarized luminescence (CPL). BCD-Br-treated nanocrystals show weak circular dichroism but no detectable CPL in colloidal dispersion. Upon assembly into CsPbBr3 and mixed halide superlattices, they exhibit CPL with a luminescence dissymmetry factor, glum, of (5 ± 2) × 10–3, whereas untreated controls remain near the noise level. Polarization-resolved transient absorption (TA) reveals an extended spin lifetime of hundreds of picoseconds in BCD-Br-treated nanocrystals, while linear-response time-dependent density functional theory (LR-TDDFT) calculations suggest that inter-nanocrystal coupling can enhance the chiroptical response. These results support the idea that ordered nanocrystal assembly can convert weak ligand-induced chirality into an emergent chiroptical response in perovskite nanocrystal solids.
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Mandal et al. (2026) studied this question.
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