Ying Jiang, Yumin Wang, Yumin Wang, Fu Peng, Yi-Xiang Wang, Shangge Zhang, Lin He, Guangyuan Chen, Jianrong Zeng, Fangling Jiang, Lin Zhu, Kai Li, Long Chen, Shuao Wang, Yaxing Wang, Yaxing Wang
ABSTRACT Real‐time monitoring of volatile molecular iodine (I 2 ), a hazardous radioactive byproduct of nuclear processes, is critical for environmental and human safety. Fluorescence quenching offers a promising detection route, but conventional luminophores suffer from thermal instability at operational temperatures. Herein, we report a thermally robust zero‐dimensional antimony halide, [Sr 2 (18‐crown‐6‐ether) 2 (H 2 O) 2 (Cl 2 )]SbCl 5 , as the first luminescent sensor capable of real‐time I 2 detection at elevated temperatures (348 K) in dynamic mode with a limit of detection (LoD) of ∼400 ppb, establishing a benchmark LoD value for high‐temperature iodine sensing via a luminescent technique. This material maintains structural integrity and intense [SbCl 5 ] 2− luminescence at 348 K, which is attributed to hydrogen‐bonding networks that suppress thermal quenching. In addition, the Sb(III) lone pairs serve as electron‐donating sites, capturing I 2 to form polyiodides (i.e., I 3 − and I 5 − ) via electron transfer, which triggers instantaneous luminescence quenching. This work establishes a new paradigm for high‐temperature optical sensors in nuclear safety applications.