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Despite the proliferation of lasing reports in three-dimensional (3D) lead halide perovskites, robust lasing in their single-layer two-dimensional (2D) counterparts, (LA) 2 PbX 4 (LA = spacer cation; X = halide), has remained elusive. Here, we uncover the critical role of metal ns 2 -lone-pair stereochemistry in modulating excitonic properties and enabling lasing in these materials. Using a library of (LA) 2 BI 4 [B = Pb (lead), Sn (tin), or Ge (germanium)], we identify key structural descriptors that link lone pair activity to exciton-phonon coupling and exciton-exciton annihilation. Within a given B-cation series, rigid frameworks with shorter B─I bonds suppress lone pair activity and favor free exciton emission, while enhanced lone pair activity—tuned by the spacer and B-cation—can localize excitons, increase dielectric screening, and suppress exciton-exciton annihilation at high excitation fluences. By balancing these effects through cation selection, we demonstrate lasing in a newly synthesized Pb-based (2FBMZ) 2 PbI 4 (2FBMZ = 5,6-difluoro-1 H -benzimidazole cation) and achieve the most thermally stable lasing in its Sn-based analog. These insights provide design principles for high-brightness 2D perovskite photonic devices.
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Li et al. (2026) studied this question.
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