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光谱响应达1.5微米的灵敏短波红外有机光电探测器

Sensitive SWIR Organic Photodetectors with Spectral Response Reaching 1.5 µm.

作者信息

Zhang Yi, Chen Jingwen, Yang Jie, Fu Muyi, Cao Yunhao, Dong Minghao, Yu Jiangkai, Dong Sheng, Yang Xiye, Shao Lin, Hu Zhengwei, Cai Houji, Liu Chunchen, Huang Fei

机构信息

State Key Laboratory of Luminescent Materials and Devices, Guangdong Basic Research Center of Excellence for Energy & Information Polymer Materials, Institute of Polymer Optoelectronic Materials and Devices, School of Materials Science and Engineering, South China University of Technology, Guangzhou, 510640, P. R. China.

Lumidar Technology Co., Ltd., Guangzhou, 510530, P. R. China.

出版信息

Adv Mater. 2024 Oct;36(41):e2406950. doi: 10.1002/adma.202406950. Epub 2024 Aug 17.

Abstract

The performance of organic photodetectors (OPDs) sensitive to the short-wavelength infrared (SWIR) light lags behind commercial indium gallium arsenide (InGaAs) photodetectors primarily due to the scarcity of organic semiconductors with efficient photoelectric responses exceeding 1.3 µm. Limited by the Energy-gap law, ultralow-bandgap organic semiconductors usually suffer from severe non-radiative transitions, resulting in low external quantum efficiency (EQE). Herein, a difluoro-substituted quinoid terminal group (QC-2F) with exceptionally strong electron-negativity is developed for constructing a new non-fullerene acceptor (NFA), Y-QC4F with an ultralow bandgap of 0.83 eV. This subtle structural modification significantly enhances intermolecular packing order and density, enabling an absorption onset up to 1.5 µm while suppressing non-radiation recombination in Y-QC4F films. SWIR OPDs based on Y-QC4F achieve an impressive detectivity (D*) over 10 Jones from 0.4 to 1.5 µm under 0 V bias, with a maximum of 1.68 × 10 Jones at 1.16 µm. Furthermore, the resulting OPDs demonstrate competitive performance with commercial photodetectors for high-quality SWIR imaging even under 1.4 µm irradiation.

摘要

对短波长红外(SWIR)光敏感的有机光电探测器(OPD)的性能落后于商用铟镓砷(InGaAs)光电探测器,这主要是由于缺乏具有超过1.3μm高效光电响应的有机半导体。受能隙定律限制,超低带隙有机半导体通常存在严重的非辐射跃迁,导致外部量子效率(EQE)较低。在此,开发了一种具有极强电负性的二氟取代醌型端基(QC-2F),用于构建一种新的非富勒烯受体(NFA),即带隙为0.83 eV的超低带隙Y-QC4F。这种细微的结构修饰显著增强了分子间堆积顺序和密度,使吸收起始波长达到1.5μm,同时抑制了Y-QC4F薄膜中的非辐射复合。基于Y-QC4F的SWIR OPD在0 V偏压下,在0.4至1.5μm范围内实现了超过10 Jones的令人印象深刻的探测率(D*),在1.16μm处最大为1.68×10 Jones。此外,即使在1.4μm辐照下,所得的OPD在高质量SWIR成像方面也表现出与商用光电探测器相竞争的性能。

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