Enhanced molecular planarity for high-performance photodetectors: Effect of backbone conformation via alkyl substitution position control in dithienoquinoxaline-based conjugated polymers
•Two novel isomerized CPs, PBQx-i-4F and PBQx-o-4F, were design and synthesized.•The relationship between molecule structure and OPD performance was systematically revealed.•PBQx-i-4FT based OPD device exhibited excellent performance with R of 410 mA W−1 and D* of 2.59 × 1013 Jones.•Our findings pro...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2024-05, Vol.488, p.150566, Article 150566 |
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Zusammenfassung: | •Two novel isomerized CPs, PBQx-i-4F and PBQx-o-4F, were design and synthesized.•The relationship between molecule structure and OPD performance was systematically revealed.•PBQx-i-4FT based OPD device exhibited excellent performance with R of 410 mA W−1 and D* of 2.59 × 1013 Jones.•Our findings provide further insights into design new CPs for high-performance organic semiconductors.
Conjugated polymers (CPs) with donor and acceptor units exhibit a flexible conformation due to the rotation of the single bond of the bridge groups which greatly hinders a precise study of their photodetection properties. Moreover, the modulation mechanism related to complex factors of CPs molecular conformation on photodetection performance is not clear, causing CP-based organic photodiodes (OPDs) to generally suffer from high dark current and low specific detectivity. In this work, we synthesized two novel PBQx-i-4F and PBQx-o-4F CPs by combining fluorinated BDT with DTQx units using i- and o-alkylated side chain-based thiophene linkages, respectively. Quantum simulation and photo-physics study revealed that PBQx-i-4F displayed a dominant trans conformation, a more planar molecule structure, and high utilization efficiency of photoinduced excitons. The OPDs based on PBQx-i-4F exhibited higher on–off ratios by over two orders of magnitude and higher detectivity (Dsh*) by nearly one order of magnitude compared with those based on PBQx-o-4F. PBQx-i-4F with the i-alkyl substitution on the thiophene linkage displayed enhanced planarity, resulting in more ordered packing and larger population of face-on orientation in film, where decreased trap density and trap-assisted recombination led to reduced dark current and improved charge transport. In summary, our work provides an insight into the relationship between the fine-tuning of the molecular conformation, planarity, and packing of CPs and their photodetection properties in OPDs. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2024.150566 |