卤化物
无定形固体
探测器
材料科学
金属
X射线探测器
X射线
光电子学
纳米技术
化学
无机化学
光学
物理
结晶学
冶金
作者
Oluwadara Joshua Olasupo,Abiodun M. Adewolu,Mohammad Khizr,Tarannuma Ferdous Manny,He Liu,Tunde Blessed Shonde,Md. Shariful Islam,Sahel Moslemi,E. K. Kim,J. S. Raaj Vellore Winfred,Thilina N. D. D. Gamaralalage,Yan‐Yan Hu,Ranjan Das,Biwu Ma
标识
DOI:10.1002/ange.202509589
摘要
Zero‐dimensional (0D) organic metal halide hybrids (OMHHs) are emerging materials with significant potential for optoelectronic applications, including direct X‐ray detectors. While 0D OMHH single crystals exhibit excellent X‐ray detection properties, their scalability remains a significant challenge due to the time‐intensive growth process and difficulty in producing large single crystals exceeding a few centimeters. This limitation hinders their practicality for large‐area detector applications. Here, we report for the first time the development of amorphous 0D OMHH films via solution processing for efficient direct X‐ray detection. By reacting a non‐crystalline organic halide, triphenyl(9‐phenyl‐9H‐carbazol‐3‐yl)phosphonium bromide (TPPCarzBr), with zinc bromide (ZnBr2), we have successfully produced amorphous 0D (TPPCarz)2ZnBr4 films with controlled thickness via facile solution processing. The organic cations (TPPCarz+) feature a lower bandgap than the ZnBr42‐ anions, enabling efficient molecular sensitization, where ZnBr42‐ anions serve as X‐ray absorbers and TPPCarz+ cations as charge transporters. Direct X‐ray detectors based on 0D (TPPCarz)2ZnBr4 films demonstrate outstanding performance, achieving a stable X‐ray detection sensitivity of 2,165 μC Gyair−1cm−2 at 20 V.mm−1 and a detection limit of 6.01 nGyair s−1. The amorphous nature of these films enhances their processability, allowing for fabrication in various sizes and shapes, and making them highly adaptable for scalable detector applications.
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