共轭体系
场效应晶体管
扩展(谓词逻辑)
有机半导体
半导体
晶体管
材料科学
有机场效应晶体管
领域(数学)
光电子学
聚合物
物理
数学
计算机科学
量子力学
纯数学
电压
复合材料
程序设计语言
作者
Zhou Yang,Chuanqi Miao,Zhenhuang Su,Xingyu Gao,Haoyu Wei,Kai‐Kai Liu,Haichang Zhang
标识
DOI:10.1021/acsmaterialslett.4c01654
摘要
In the current state of organic semiconductor development, n-type semiconductors are significantly less advanced than their p-type counterparts, particularly in the realm of high-electron-mobility materials, which are crucial for high-grade organic field-effect transistors (OFETs) in commercial electronics. Over the past few years, the incorporation of B←N coordination units has emerged as a promising approach to enhancing n-type properties. However, the exploration of polymers with π-conjugated extensions in different directions has been largely overlooked. This study introduces two novel B←N coordinated BDP-based polymers, P1 and P2, synthesized with distinct π-conjugated extension directions: along the backbone and perpendicular to it, respectively. P1, with its advantages in energy levels, planarity, crystallinity, and backbone transport, demonstrates an electron mobility of 1.81 cm2 V–1 s–1, which is more than twice the performance of P2. This achievement sets a new benchmark for B←N coordinated n-type OFETs, marking one of the highest reported electron mobilities to date.
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