发光
材料科学
卤化物
手性(物理)
光致发光
量子产额
光电子学
金属
锰
金属卤化物
光化学
氢键
卤化氢
圆极化
超分子手性
纳米技术
结晶学
量子点
量子效率
作者
Fei Ge,Haihua Zhang,Hongbing Fu,Junbo Gong
摘要
ABSTRACT Chiral metal halides have emerged as promising candidates for circularly polarized luminescence (CPL) due to their structural versatility and exceptional optoelectronic properties. However, achieving both a high luminescence dissymmetry factor ( g lum ) and photoluminescence quantum yield (PLQY) remains a critical challenge due to the inherent trade‐off between inducing chirality and minimizing non‐radiative losses driven by polyhedral distortion. Here, we present a ligand‐engineering approach to design a pair of chiral metal halide co‐crystals, achieving near‐unity PLQY (98%) and a | g lum | of 7.4 × 10 −3 . By leveraging Coulomb interactions instead of conventional hydrogen bonding between ligands and inorganic halide units, we effectively circumvent polyhedral distortions and substantially reduce electron–phonon coupling. This structural innovation reduces the non‐radiative decay rate by nearly three orders of magnitude, from 2.20 × 10 4 to 51.9 s −1 , thereby substantially enhancing luminescence efficiency. Consequently, the resulting figure‐of‐merit (FOM = PLQY × | g lum |) reaches an impressive 7.25 × 10 −3 , surpassing conventional hydrogen‐bonded counterparts by more than an order of magnitude (6.7 × 10 −4 ). This co‐crystal strategy paves the way for developing advanced CPL emitters with superior performance.
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