Yixie Chen, Xingrong Quan, DongYun Li, Ye Yang, Jianwu Wei, Yihua Yang, Xiaohua Lan, Xinguo Zhang, Qi Pang, Chunyan Zhou, Liya Zhou, Peican Chen
Intrinsically chiral active optical materials are currently a subject of intense research. While chiral ligand modification is an effective strategy for imparting chirality to perovskite quantum dots (PQDs), it faces challenges related to a limited luminescence dissymmetry factor and stability. Herein, this work reports a one-pot synthesis of R-/S-CsPbBr 3 @SiO 2 PQDs. The chiral characteristics of R-/S-CsPbBr 3 @SiO 2 PQDs originate from the surface anchoring of R-/S-2-phenylglycinol (R-/S-Phe), which triggers chiral lattice distortion of the [PbBr 6 ] 4– octahedra and strong electronic coupling. Notably, the silica shell acts not just as a protective barrier but as a spatial confinement matrix that facilitates a higher density of chiral ligand loading, thereby amplifying the dissymmetry factor ( g lum = −1.14 × 10 –2 ) by nearly an order of magnitude compared to bare counterparts. The encapsulated PQDs simultaneously achieve a high photoluminescence quantum yield of 84 ± 1%, exceptional water stability, and intense circularly polarized luminescence. This work offers a strategy for enhancing the chiroptical signals in multifunctional chiral metal halides.