Research output: Contribution to journal › Article › peer-review
Circularly Polarized Luminescence in Chiral Antimony(III) Chloride [Sb2Cl10]4– Dimers Induced by Asymmetric Hydrogen Bonding. / Luo, Qiulian; Li, Jing; Wei, Jianwu; Luo, Binbin; Zhou, Liya; Chen, Peican; Tian, Jie; Pan, Jiahong; Emeline, Alexei V.; Pang, Qi.
In: Inorganic Chemistry, Vol. 64, No. 26, 2025, p. 13134-13144.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Circularly Polarized Luminescence in Chiral Antimony(III) Chloride [Sb2Cl10]4– Dimers Induced by Asymmetric Hydrogen Bonding
AU - Luo, Qiulian
AU - Li, Jing
AU - Wei, Jianwu
AU - Luo, Binbin
AU - Zhou, Liya
AU - Chen, Peican
AU - Tian, Jie
AU - Pan, Jiahong
AU - Emeline, Alexei V.
AU - Pang, Qi
N1 - PMID: 40545641
PY - 2025
Y1 - 2025
N2 - Metal halide species with multimeric anionic frameworks exhibit outstanding coordination chiralities and intriguing photophysical properties, making them highly promising for emerging photonic applications. However, their chiroptical activities remain largely unexplored to date. Herein, lead-free chiral hybrid 0D materials composed of edge-sharing [Sb2Cl10]4– dimers were synthesized via a natural cooling crystallization. The 0D chiral crystals R/S-1 [(R/S-MBA)4Sb2Cl10] show broad yellow photoluminescence stemming from self-trapped exciton states with a PL peak at 596 nm. R/S-1 exhibits strong circular dichroism (|gCD| ≈ 7 × 10–3) and efficient circularly polarized luminescence (|glum| ≈ 5 × 10–3). This is attributed to the chiral organic cations inducing inorganic sublattice chirality through asymmetric hydrogen-bonding interactions, while the inorganic lattice components adopt a helical arrangement following a 21 symmetry operation. Density functional theory calculations verify a Rashba-type band splitting for R/S-1, confirming the noncentrosymmetric structural distortion and substantial spin–orbit interaction induced by chiral organic cations. Furthermore, we applied chiral scintillators R/S-1 to achieve X-ray-driven asymmetric photopolymerization using circularly polarized emission. This study offers a pathway for the exploration and development of novel lead-free chiral metal halides.
AB - Metal halide species with multimeric anionic frameworks exhibit outstanding coordination chiralities and intriguing photophysical properties, making them highly promising for emerging photonic applications. However, their chiroptical activities remain largely unexplored to date. Herein, lead-free chiral hybrid 0D materials composed of edge-sharing [Sb2Cl10]4– dimers were synthesized via a natural cooling crystallization. The 0D chiral crystals R/S-1 [(R/S-MBA)4Sb2Cl10] show broad yellow photoluminescence stemming from self-trapped exciton states with a PL peak at 596 nm. R/S-1 exhibits strong circular dichroism (|gCD| ≈ 7 × 10–3) and efficient circularly polarized luminescence (|glum| ≈ 5 × 10–3). This is attributed to the chiral organic cations inducing inorganic sublattice chirality through asymmetric hydrogen-bonding interactions, while the inorganic lattice components adopt a helical arrangement following a 21 symmetry operation. Density functional theory calculations verify a Rashba-type band splitting for R/S-1, confirming the noncentrosymmetric structural distortion and substantial spin–orbit interaction induced by chiral organic cations. Furthermore, we applied chiral scintillators R/S-1 to achieve X-ray-driven asymmetric photopolymerization using circularly polarized emission. This study offers a pathway for the exploration and development of novel lead-free chiral metal halides.
M3 - Article
VL - 64
SP - 13134
EP - 13144
JO - Inorganic Chemistry
JF - Inorganic Chemistry
SN - 0020-1669
IS - 26
ER -
ID: 140870613