Enabling Fast Photoresponse in Near‐Infrared Organic Phototransistors by Manipulating Minority Charge Trapping and Recombination

俘获 材料科学 光电子学 载流子 接受者 激子 有机太阳能电池 电荷(物理) 离解(化学) 聚合物 物理 复合材料 化学 物理化学 生物 量子力学 凝聚态物理 生态学
作者
Yu Tang,Huaijie Fu,Ning Li,Yuanhong Hu,Lixiang Chen,Weiyao Jia,Qiaoming Zhang,Yanlian Lei
出处
期刊:Advanced Optical Materials [Wiley]
卷期号:11 (4) 被引量:11
标识
DOI:10.1002/adom.202202008
摘要

Abstract The organic phototransistors (OPTs) featuring built‐in amplification afford ultrahigh photoresponse. However, the response speed is usually slow in disordered OPTs, limited by the charge trapping/recombination process caused by inherent trap sites. This work studies the relationship between the photoinduced charge carrier dynamics and photoresponse characteristics in a near‐infrared (NIR) light‐sensitive OPT. It is found that the introduction of a small amount of electron acceptor into a p‐type polymer, forming a donor:acceptor bulk‐heterojunction (BHJ), in the OPT channel can dramatically improve the overall response speed of the detector. This is because the exciton dissociation and charge separation at the donor/acceptor interface not only improves the photoresponse but also reduces the minority charge trapping. Less charge trapping/recombination is essential to achieve a fast response in OPTs. As a result, the rise and fall time are improved from 1.3 and 3.5 s for the polymer‐only‐based NIR OPTs to 16 and 119 ms for the organic BHJ‐based NIR OPTs, making it suitable for use in medically relevant photoplethysmography applications.

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