材料科学
共聚物
电化学
晶体管
方位(导航)
聚合物
光电子学
纳米技术
高分子化学
场效应晶体管
化学
电压
物理化学
计算机科学
电气工程
电极
复合材料
人工智能
工程类
作者
Jong‐Ho Kim,Xinglong Ren,Youcheng Zhang,Daniele Fazzi,Suraj Manikandan,Jens Wenzel Andreasen,Xiuming Sun,Sarah Ursel,Hio‐Ieng Un,Sébastien Peralta,Mingfei Xiao,James S. Town,Arkadios Marathianos,Stefan Roesner,Thanh‐Tuân Bui,Sabine Ludwigs,Henning Sirringhaus,Suhao Wang
出处
期刊:Advanced Science
[Wiley]
日期:2023-08-07
卷期号:10 (29): e2303837-e2303837
被引量:21
标识
DOI:10.1002/advs.202303837
摘要
Abstract n‐Type organic electrochemical transistors (OECTs) and organic field‐effect transistors (OFETs) are less developed than their p‐type counterparts. Herein, polynaphthalenediimide (PNDI)‐based copolymers bearing novel fluorinated selenophene‐vinylene‐selenophene (FSVS) units as efficient materials for both n‐type OECTs and n‐type OFETs are reported. The PNDI polymers with oligo(ethylene glycol) (EG7) side chains P(NDIEG7‐FSVS), affords a high µC* of > 0.2 F cm −1 V −1 s −1 , outperforming the benchmark n‐type Pg4NDI‐T2 and Pg4NDI‐gT2 by two orders of magnitude. The deep‐lying LUMO of −4.63 eV endows P(NDIEG7‐FSVS) with an ultra‐low threshold voltage of 0.16 V. Moreover, the conjugated polymer with octyldodecyl (OD) side chains P(NDIOD‐FSVS) exhibits a surprisingly low energetic disorder with an Urbach energy of 36 meV and an ultra‐low activation energy of 39 meV, resulting in high electron mobility of up to 0.32 cm 2 V −1 s −1 in n‐type OFETs. These results demonstrate the great potential for simultaneously achieving a lower LUMO and a tighter intermolecular packing for the next‐generation efficient n‐type organic electronics.
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