This research demonstrates optimized non‐fullerene acceptor enhances performance of SWIR photodetectors, indicating improved detectivity and lower dark current.
Short‐wavelength infrared organic photodetectors (SWIR OPDs) hold significant application potential due to their strong penetration depth and high resolution. However, the SWIR OPDs suffer from low SWIR sensitivity or large dark current under bias. In this study, an A‐D‐A′‐D‐A‐type non‐fullerene acceptor (NFA) with thiadiazoloquinoxaline as core unit, namely BTQ‐Ph, was obtained through C‐H activated direct arylation coupling and modular synthesis. The BTQ‐Ph possessed an ultra‐narrow optical bandgap of 0.95 eV with a maximum absorption peak at 1097 nm, indicating noticeable SWIR responsiveness. The SWIR OPD based on BTQ‐Ph exhibited a broad spectral response from 500 to 1300 nm. The D sh * value of BTQ‐Ph‐based OPD obtains 1.4 × 10 13 Jones at 1110 nm and remains a high detectivity of 5.06 × 10 12 Jones at 1200 nm under self‐powered mode. Importantly, a low dark current of 2.2 × 10 −7 A cm −2 can be achieved under a working bias of −1.0 V, leading to a significant detectivity level exceeding 10 11 Jones. This work demonstrates that deeply engaging in the optimization of A‐D‐A′‐D‐A‐type molecular framework is a highly effective approach for high‐performing SWIR OPDs.
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Chen et al. (2025) studied this question.
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