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SpectrallySwitchable Photodetection with Near-Infrared-AbsorbingCovalent Organic Frameworks

机译:光谱地具有近红外吸收能力的可切换光电检测共价有机框架

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摘要

Most covalent organic frameworks (COFs) to date are made from relatively small aromatic subunits, which can only absorb the high-energy part of the visible spectrum. We have developed near-infrared-absorbing low bandgap COFs by incorporating donor–acceptor-type isoindigo- and thienoisoindigo-based building blocks. The new materials are intensely colored solids with a high degree of long-range order and a pseudo-quadratic pore geometry. Growing the COF as a vertically oriented thin film allows for the construction of an ordered interdigitated heterojunction through infiltration with a complementary semiconductor. Applying a thienoisoindigo-COF:fullerene heterojunction as the photoactive component, we realized the first COF-based UV- to NIR-responsive photodetector. We found that the spectral response of the device is reversibly switchable between blue- and red-sensitive, and green- and NIR-responsive. To the best of our knowledge, this is the first time that such nearly complete inversion of spectral sensitivity of a photodetector has been achieved. This effect could lead to potentialapplications in information technology or spectral imaging.
机译:迄今为止,大多数共价有机骨架(COF)由相对较小的芳族亚基制成,它们只能吸收可见光谱的高能部分。通过结合基于供体-受体型异靛蓝和硫代异靛蓝的构建基,我们已经开发了吸收近红外的低带隙COF。新材料是具有强烈的长程有序和拟二次孔隙几何形状的深色固体。将COF生长为垂直取向的薄膜允许通过用互补半导体的渗透来构造有序的叉指异质结。以硫代异靛蓝-COF:富勒烯异质结作为光敏组分,我们实现了首个基于COF的对NIR响应的UV-紫外线探测器。我们发现该设备的光谱响应可在蓝和红敏感,绿和近红外响应之间可逆切换。据我们所知,这是第一次实现光电探测器光谱灵敏度的几乎完全反转。这种影响可能导致潜在的在信息技术或光谱成像中的应用。

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