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Side-Chain Engineering of Nonfullerene Acceptors for Near-Infrared Organic Photodetectors and Photovoltaics AITranslate

University of California; Korea Research Institute of Chemical Technology (KRICT); Pohang University of Science and Technology; University of California; University of California; University of California at Santa Barbara; University of California at Santa Barbara; University of California at Santa Barbara; University of California at Santa Barbara; University of California; Pohang University of Science and Technology; University of California at Santa Barbara; University of California at Santa Barbara
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Publisher: ACS
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Abstract AITranslate

Narrow bandgap n-type molecular semiconductors are relevant as key materials components for the fabrication near-infrared organic solar cells (OSCs) and organic photodetectors (OPDs). We thus designed nearly isostructural nonfullerene electron acceptors, except for the choice of solubilizing units, which absorb from 600 to 1100 nm. Specific molecules include CTIC-4F, CO1-4F, and COTIC-4F, whose optical bandgaps are 1.3, 1.2, and 1.1 eV, respectively. Modulation of intramolecular charge transfer characteristics was achieved by replacing alkoxy groups with alkyl groups on thiophene spacers that connect an electron-rich cyclopentadithiophene core to peripheral electron-poor fragments. OSCs incorporating CTIC-4F and CO1-4F with PTB7-Th achieve power conversion efficiencies of over 10% with short-circuit current densities as high as ∼25 mA·cm–2. The same blends achieve OPD responsivities of 0.52 A·W–1 at ∼920 nm. These findings highlight outstanding opportunities to tune further molecular design so that OPDs may ultimately compete with their silicon counterparts.

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DOI:https://doi.org/10.1021/acsenergylett.9b00721

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Citation Information:

Narrow bandgap n-type molecular semiconductors are relevant as key materials components for the fabrication near-infrared organic solar cells (OSCs) and organic photodetectors (OPDs). We thus designed nearly isostructural nonfullerene electron acceptors, except for the choice of solubilizing units, which absorb from 600 to 1100 nm. Specific molecules include CTIC-4F, CO1-4F, and COTIC-4F, whose optical bandgaps are 1.3, 1.2, and 1.1 eV, respectively. Modulation of intramolecular charge transfer characteristics was achieved by replacing alkoxy groups with alkyl groups on thiophene spacers that connect an electron-rich cyclopentadithiophene core to peripheral electron-poor fragments. OSCs incorporating CTIC-4F and CO1-4F with PTB7-Th achieve power conversion efficiencies of over 10% with short-circuit current densities as high as ∼25 mA·cm–2. The same blends achieve OPD responsivities of 0.52 A·W–1 at ∼920 nm. These findings highlight outstanding opportunities to tune further molecular design so that OPDs may ultimately compete with their silicon counterparts.

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GB/T 7714-2015 [1] Jaewon Lee, SeoJin Ko, Hansol Lee, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.9b00721.
MLA [1] Jaewon Lee, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.9b00721.
APA [1] Jaewon Lee, SeoJin Ko, Hansol Lee, Jianfei Huang, Ziyue Zhu, Martin Seifrid, Joachim Vollbrecht, Viktor V. Brus, Akchheta Karki, Hengbin Wang, Kilwon Cho, ThucQuyen Nguyen, & Guillermo C. Bazan. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.9b00721
IEEE [1] Jaewon Lee, SeoJin Ko, Hansol Lee, Jianfei Huang, Ziyue Zhu, Martin Seifrid, Joachim Vollbrecht, Viktor V. Brus, Akchheta Karki, Hengbin Wang, Kilwon Cho, ThucQuyen Nguyen, and Guillermo C. Bazan, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.9b00721.