成核
材料科学
印刷电子产品
有机电子学
纳米技术
数码产品
拓扑(电路)
分子
晶体管
苯并噻吩
墨水池
化学
物理
有机化学
电气工程
噻吩
电压
复合材料
物理化学
工程类
量子力学
作者
Xiaobin Ren,Fengquan Qiu,Wei Deng,Xiaochen Fang,Y. H. Wu,Shengyu Yu,Xinyue Liu,Souren Grigorian,Jialin Shi,Jiansheng Jie,Xiaohong Zhang,Xiujuan Zhang,Xiujuan Zhang,Xiujuan Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-12-06
卷期号:17 (24): 25175-25184
被引量:16
标识
DOI:10.1021/acsnano.3c08135
摘要
Printable organic semiconducting single crystals (OSSCs) offer tantalizing opportunities for next-generation wearable electronics, but their development has been plagued by a long-standing yet inherent problem─spatially uncontrolled and stochastic nucleation events─which usually causes the formation of polycrystalline films and hence limited performance. Here, we report a convenient approach to precisely manipulate the elusive molecule nucleation process for high-throughput inkjet printing of OSSCs with record-high mobility. By engineering curvature of the contact line with a teardrop-shaped micropattern, molecule nucleation is elegantly anchored at the vertex of the topological structure, enabling formation of a single nucleus for the subsequent growth of OSSCs. Using this approach, we achieve patterned growth of 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene single crystals, yielding a breakthrough for an organic field-effect transistor array with a high average mobility of 12.5 cm2 V-1 s-1. These findings not only provide keen insights into controlling molecule nucleation kinetics but also offer opportunities for high-performance printed electronics.
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