Congratulations to Tao Song for publishing on Angew. Chem. Int. Ed. https://doi.org/10.1002/anie.202400769

Generating circularly polarized luminescence (CPL) with simultaneous high photoluminescence quantum yield (PLQY) and dissymmetry factor (g_lum) is difficult due to usually unmatched electric transition dipole moment (μ) and magnetic transition dipole moment (m) of materials. Herein we tackle this issue by playing a “cascade cationic insertion” trick to achieve strong CPL (with PLQY of ~ 100%) in lead-free metal halides with high g_lum values reaching -2.3×10^-2 without using any chiral inducers. Achiral solvents of hydrochloric acid (HCl) and N, N-dimethylformamide (DMF) infiltrate the crystal lattice via asymmetric hydrogen bonding, distorting the perovskite structure to induce the “intrinsic” chirality. Surprisingly, additional insertion of Cs⁺ cation to substitute partial (CH₃)₂NH²⁺ transforms the chiral space group to achiral but the crystal maintains chiroptical activity. Further doping of Sb³⁺ stimulates strong photoluminescence as a result of self-trapped excitons (STEs) formation without disturbing the crystal framework. The chiral perovskites of indium-antimony chlorides embedded on LEDs chips demonstrate promising potential as CPL emitters. Our work presents rare cases of chiroptical activity of highly luminescent perovskites from only achiral building blocks via spontaneous resolution as a result of symmetry breaking.