材料科学
外延
有机半导体
电子迁移率
光电子学
检出限
溶剂
烷基
表征(材料科学)
工作(物理)
溶解过程
半导体
选择性
有机溶剂
极限(数学)
灵敏度(控制系统)
化合物半导体
纳米技术
过程(计算)
过程开发
化学
催化作用
载流子
聚合物
降级(电信)
作者
Y Li,Yiwen Ren,Wenbin Shi,Z Q Chen,Xi Zhang,Fangxu Yang,Liqiang Li,W HU,Lingjie Sun
出处
期刊:SmartMat
[Wiley]
日期:2026-05-13
卷期号:7 (3)
摘要
ABSTRACT The fundamental trade‐off between high intrinsic carrier mobility and solution processability severely limits the development of organic single crystals (OSCs). For instance, while 2,6‐diphenylanthracene (DPA) is a benchmark candidate for direct X‐ray detection, its intrinsic insolubility hinders solution processing, and conventional solubilizing alkyl modifications inevitably degrade transport efficiency. Here, we report a facile surfactant‐assisted near‐room‐temperature solution epitaxy method to overcome this bottleneck, fabricating centimeter‐scale ultrathin DPA two‐dimensional (2D) OSCs utilizing a common solvent at 35°C. Electrical characterization reveals that the as‐fabricated DPA 2DOSCs exhibit a maximum mobility of 5.55 cm 2 /(V ∙ s), an order of magnitude higher than that of the alkylated C 6 ‐DPA counterpart. This superior charge transport efficiency directly translates into exceptional X‐ray detection performance, achieving a high sensitivity of 7.02 × 10 3 μC/(Gy∙cm 2 ) and a low detection limit of 24.05 nGy/s. This work not only provides a facile low‐energy route to process intrinsically insoluble organic semiconductors but also establishes high‐mobility DPA 2DOSCs as a premier platform for next‐generation large‐area organic direct X‐ray detectors.
科研通智能强力驱动
Strongly Powered by AbleSci AI