材料科学
三苯胺
响应度
工作职能
暗电流
光电探测器
单层
两性离子
光电子学
密度泛函理论
自组装单层膜
电子迁移率
噪音(视频)
化学物理
电流密度
光化学
光电二极管
含时密度泛函理论
电子
有机半导体
萃取(化学)
菁
电子传输链
比探测率
纳米技术
工作(物理)
作者
Jiyoung Shin,Gyeong Min Lee,Juyeon Shin,Jaewoong Kim,Tae Hyuk Kim,Do Yeon Kim,Myeong In Kim,Kyeounghak Kim,Jae Won Shim,In Hwan Jung
标识
DOI:10.1002/adfm.202524099
摘要
ABSTRACT Phosphonic acid (PA)‐based self‐assembled monolayer (SAM) materials have emerged as promising hole transport materials (HTMs) for photodiodes such as organic/perovskite solar cells and photodetectors. In this study, we reveal for the first time that triphenylamine (TPA)‐based PA‐type SAMs spontaneously form zwitterionic structures, which are key in strengthening the binding strength of the anchoring group on the ITO surface and enhancing interfacial adhesion. The electrostatic interaction of the zwitterion induced a strong interfacial dipole, dramatically increasing the work function (WF) to 5.33 eV (0.28 eV higher than the control). Notably, TPA does not function merely as an electron‐donating group, but rather as a strong Brønsted base. DFT calculations confirmed that zwitterion formation is energetically favorable and crucial for WF modulation. Thus, zwitterionic SAMs in near‐infrared organic photodetectors effectively improve hole extraction and suppress dark current density through their dual functionality of hole transporting and electron blocking. The optimized devices achieved remarkably low dark current density (1.41 × 10 −9 A/cm 2 ) and noise current (2.8 × 10 −14 A), combined with high responsivity (0.496 A/W) and specific detectivity (3.78 × 10 12 Jones) at −0.1 V. This study highlights the potential of zwitterionic structures as HTMs and offers a powerful molecular design strategy for SAM‐type HTMs.
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