Imidazole-Extended Non-Fullerene Acceptors With Tunable Crystallinity for Ultrasensitive, Ultrafast Near-Infrared Organic Photodetectors

Chengwei Shan , Zihao Li , Han Gao , Yuang Fu , Zhaojin Wang , Xinhui Lu , Xianyong Zhou , Bin-Bin Yu , Philip C. Y. Chow , Aung Ko Ko Kyaw , Chang Liu , Tianshuo Zhao , Hanjian Lai

Aggregate ›› 2026, Vol. 7 ›› Issue (8) : e70417

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Aggregate ›› 2026, Vol. 7 ›› Issue (8) :e70417 DOI: 10.1002/agt2.70417
RESEARCH ARTICLE
Imidazole-Extended Non-Fullerene Acceptors With Tunable Crystallinity for Ultrasensitive, Ultrafast Near-Infrared Organic Photodetectors
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Abstract

Emerging optoelectronic tasks such as night-vision imaging and wearable health monitoring call for near-infrared (NIR) photodetectors that operate without external bias, exhibit minimal dark current, and respond within nanoseconds. Organic photodetectors (OPDs) have yet to meet these benchmarks, hindered by the scarcity of NIR-absorbing molecules and poor control over active-layer crystallinity. Here we report a unified approach that couples molecular engineering, morphology tuning, and trap-state suppression to accelerate charge dynamics in OPDs. Three non-fullerene acceptors-CA1, CA2, and CA3 were constructed by extending the π-backbone of an imidazole-centered core. DFT calculations and single-crystal analyses show that each additional fused ring systematically modulates backbone planarity and intermolecular packing, which in turn governs charge mobility and defect density. CA2 strikes an optimal balance: its moderate rigidity and favorable surface energy match the donor polymer, producing a bicontinuous fibrillar network with low energetic disorder. Conversely, the highly crystalline CA1 readily self-aggregates, introducing grain boundaries that act as recombination centers. Consequently, the PM6:CA2 blends deliver outstanding OPD performance, with a record-low dark current of 2.54 × 10−12 A cm−2 at zero bias. They also feature a total noise current of 8.51 × 10−15 A·Hz−1/2, yielding a detectivity peak of 1.08 × 1013 Jones (specific detectivity from real noise) at 840 nm. In addition, the devices exhibit a wide linear dynamic range of 167.8 dB and fast transient responses of 307 ns (rise) and 319 ns (fall). The detector enables cuff-free deep-tissue photoplethysmography and a 10 Mbps optical data link, underscoring the potential of imidazole-extended acceptors for sensitive, ultrafast NIR OPDs.

Keywords

fused-ring extension / imidazole acceptors / organic photodetectors / single crystal

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Chengwei Shan, Zihao Li, Han Gao, Yuang Fu, Zhaojin Wang, Xinhui Lu, Xianyong Zhou, Bin-Bin Yu, Philip C. Y. Chow, Aung Ko Ko Kyaw, Chang Liu, Tianshuo Zhao, Hanjian Lai. Imidazole-Extended Non-Fullerene Acceptors With Tunable Crystallinity for Ultrasensitive, Ultrafast Near-Infrared Organic Photodetectors. Aggregate, 2026, 7 (8) : e70417 DOI:10.1002/agt2.70417

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References

[1]

F. P. G. de Arquer, A. Armin, P. Meredith, and E. H. Sargent, “Solution-Processed Semiconductors for Next-Generation Photodetectors,” Nature Reviews Materials 2 (2017): 16100.

[2]

P. C. Y. Chow and T. Someya, “Organic Photodetectors for Next-Generation Wearable Electronics,” Advanced Materials 32 (2020): 1902045.

[3]

C. Wang, X. T. Zhang, and W. P. Hu, “Organic Photodiodes and Phototransistors Toward Infrared Detection: Materials, Devices, and Applications,” Chemical Society Reviews 49 (2020): 653–670.

[4]

B. Y. Yin, X. Zhou, Y. Y. Li, et al., “Sensitive Organic Photodetectors With Spectral Response up to 1.3 µm Using a Quinoidal Molecular Semiconductor,” Advanced Materials 36 (2024): 2310811.

[5]

Z. L. Che, C. C. Yan, X. D. Wang, and L. S. Liao, “Organic Near-Infrared Optoelectronic Materials and Devices: An Overview,” Advanced Photonics 6 (2024): 014001.

[6]

C. Fuentes-Hernandez, W. F. Chou, T. M. Khan, et al., “Large-Area Low-Noise Flexible Organic Photodiodes for Detecting Faint Visible Light,” Science 370 (2020): 698–701.

[7]

X. F. Xu, X. B. Zhou, K. Zhou, Y. X. Xia, W. Ma, and O. Inganäs, “Large-Area, Semitransparent, and Flexible All-Polymer Photodetectors,” Advanced Functional Materials 28 (2018): 1805570.

[8]

K. Cho, J. W. Ha, M. Nam, et al., “Crystallization-Driven Optimization of Morphology and Performance in Near-Infrared Organic Photodetectors via Alkyl Side Chain Tuning of Narrow Bandgap Non-Fullerene Acceptors,” Advanced Functional Materials 34 (2024): 2400676.

[9]

J. Kublitski, A. Hofacker, B. K. Boroujeni, et al., “Reverse Dark Current in Organic Photodetectors and the Major Role of Traps as Source of Noise,” Nature Communications 12 (2021): 551.

[10]

Y. Zhang, J. W. Chen, J. Yang, et al., “Sensitive SWIR Organic Photodetectors With Spectral Response Reaching 1.5 µm,” Advanced Materials 36 (2024): 2406950.

[11]

M. Y. Liu, W. R. Li, Z. X. Peng, X. X. Shao, J. Liu, and L. X. Wang, “Electron Acceptors Based on Resonant N—B←N Unit With Improved Exciton Dissociation for High-Performance Short-Wavelength Infrared Organic Photodetectors,” Angewandte Chemie International Edition 64 (2025): e202407007.

[12]

J. E. Zhu, R. Zeng, E. J. Zhou, et al., “A Refined Bulk P-I-N Structure in All-Polymer Solar Cells To Achieve 20.1% Efficiency and Improved Stability,” Journal of the American Chemical Society 147 (2025): 24491–24501.

[13]

H. Lu, D. W. Li, W. L. Liu, et al., “Designing A-D-A Type Fused-Ring Electron Acceptors with a Bulky 3D Substituent at the Central Donor Core to Minimize Non-Radiative Losses and Enhance Organic Solar Cell Efficiency,” Angewandte Chemie International Edition 63 (2024): e202407007.

[14]

C. Li, J. L. Song, H. J. Lai, et al., “Non-Fullerene Acceptors With High Crystallinity and Photoluminescence Quantum Yield Enable >20% Efficiency Organic Solar Cells,” Nature Materials 24 (2025): 433–443.

[15]

H. Y. Chen, Y. T. Huang, R. Zhang, et al., “Organic Solar Cells With 20.82% Efficiency and High Tolerance of Active Layer Thickness Through Crystallization Sequence Manipulation,” Nature Materials 24 (2025): 444–453.

[16]

Y. W. Lang, H. J. Lai, Y. Fu, et al., “Balanced Miscibility and Crystallinity by 2D Acceptors Enabled Halogen-Free Solvent-Processed Organic Solar Cells to Achieve 19.28% Efficiency,” Advanced Materials 37 (2025): 2413270.

[17]

K. An, W. K. Zhong, F. Peng, et al., “Mastering Morphology of Non-Fullerene Acceptors Towards Long-Term Stable Organic Solar Cells,” Nature Communications 14 (2023): 2688.

[18]

L. L. Zhan, S. X. Li, Y. K. Li, et al., “Desired Open-Circuit Voltage Increase Enables Efficiencies Approaching 19% in Symmetric-Asymmetric Molecule Ternary Organic Photovoltaics,” Joule 6 (2022): 662–675.

[19]

W. X. Liu, W. J. Guo, L. L. Fu, et al., “Terminal Fluorination Modulates Crystallinity and Aggregation of Fully Non-Fused Ring Electron Acceptors for High-Performance and Durable Near-Infrared Organic Photodetectors,” Angewandte Chemie International Edition 64 (2025): e202416751.

[20]

C. W. Shan, T. Liu, J. L. Zhou, et al., “High-Performance Organic Solar Cell and Self-Power Photodetector With Chemically Robust, Near-Infrared Acceptor Enabled by Strengthening Interfacial Contact and Compositional Modulation,” Chemical Engineering Journal 471 (2023): 144451.

[21]

C. W. Shan, D. Luo, J. Zeng, et al., “High-Detectivity Photomultiplication-Type Organic Photodetectors With Non-Fused Ring Electron Acceptor Enabled by solid Additive-Induced Efficient Hole Tunneling Injection,” Chemical Engineering Journal 505 (2025): 159658.

[22]

J. F. Huang, J. Lee, J. Vollbrecht, et al., “A High-Performance Solution-Processed Organic Photodetector for Near-Infrared Sensing,” Advanced Materials 32 (2020): 1906027.

[23]

J. Yuan, Y. Q. Zhang, L. Y. Zhou, et al., “Single-Junction Organic Solar Cell With Over 15% Efficiency Using Fused-Ring Acceptor With Electron-Deficient Core,” Joule 3 (2019): 1140–1151.

[24]

H. J. Lai and F. He, “Crystal Engineering in Organic Photovoltaic Acceptors: A 3D Network Approach,” Advanced Energy Materials 10 (2020): 2002678.

[25]

J. W. Qiao, F. Z. Cui, W. Q. Zhang, et al., “Enhanced Exciton Delocalization in Organic Near-Infrared Photodetectors via Solid Additive-Mediated J-Aggregation,” Advanced Materials 37 (2025): 2418844.

[26]

C. W. Shan, Y. Wang, D. Luo, et al., “High Detectivity in Photomultiplication-Type Organic Photodetectors: A Study on EQE and Dark Current Balance via Processing Methods,” Advanced Materials Technologies 10 (2025): 2401574.

[27]

Q. Wang, F. Z. Cui, M. Z. Sha, et al., “Efficient All-Polymer Photomultiplication-Type Organic Photodetectors with Prolonged Crystallization Process,” Advanced Functional Materials 33 (2023): 2304169.

[28]

Y. N. Xu, Y. Zhao, J. D. Zhang, et al., “Tuning of Molecular Aggregation and Photoresponse of Narrow-Band Organic Photodetectors,” ACS Applied Electronic Materials 5 (2023): 2375–2385.

[29]

H. L. Quan, Z. M. Zhong, T. Y. Hao, et al., “High-Performance Organic Photodetectors Enabled by a Refined Fibrillar Multiphase Morphology,” Chemical Engineering Journal 452 (2023): 139295.

[30]

M. S. Kim, D. Luo, W. Jang, et al., “High-Sensitivity Organic Photodetector Based on Surface-Concentrated Nonfused Ring Electron Acceptor,” Advanced Optical Materials 11 (2023): 2202525.

[31]

J. Wang, J. W. Zhu, C. X. Li, et al., “High-Efficiency Organic Solar Cells Enabled by Non-Fullerene Acceptors with Benzimidazole as the Central Core,” Advanced Functional Materials 33 (2023): 2304449.

[32]

H. H. Zhang, Y. Q. Chai, J. P. Zhao, et al., “Asymmetric Acceptor Featuring Fused-Imidazole Central Core Enabling Organic Solar Cells with 19.4% Efficiency,” Advanced Energy Materials 15 (2025): 2500332.

[33]

H. J. Lai, X. Lai, Z. Y. Chen, et al., “Crystallography, Packing Mode, and Aggregation State of Chlorinated Isomers for Efficient Organic Solar Cells,” CCS Chemistry 5 (2023): 1118–1129.

[34]

M. Q. Yang, B. Y. Yin, G. J. Hu, et al., “Sensitive Short-Wavelength Infrared Photodetection With a Quinoidal Ultralow Band-Gap N-Type Organic Semiconductor,” Chem 10 (2024): 1425–1444.

[35]

Y. J. Chen, Y. Q. Zheng, Y. Y. Jiang, H. J. Fan, and X. Z. Zhu, “Carbon-Bridged 1,2-Bis(2-thienyl)ethylene: An Extremely Electron Rich Dithiophene Building Block Enabling Electron Acceptors With Absorption Above 1000 nm for Highly Sensitive NIR Photodetectors,” Journal of the American Chemical Society 143 (2021): 4281–4289.

[36]

B. M. Xie, R. H. Xie, K. Zhang, et al., “Self-Filtering Narrowband High Performance Organic Photodetectors Enabled by Manipulating Localized Frenkel Exciton Dissociation,” Nature Communications 11 (2020): 2871.

[37]

D. S. Qiu, C. W. Shan, Y. W. Lang, et al., “Anthra 2,1-b:3,4-b' Dithiophene-7,12-Dione-Based Polymer Donors: Boosting Responsivity and Thermal Stability for Organic Photodetectors,” Advanced Functional Materials 35 (2025), 2507494.

[38]

S. X. Li, L. L. Zhan, N. N. Yao, et al., “Unveiling Structure-Performance Relationships From Multi-Scales in Non-Fullerene Organic Photovoltaics,” Nature Communications 12 (2021): 4627.

[39]

C. J. Zhang, S. Mahadevan, J. Yuan, et al., “Unraveling Urbach Tail Effects in High-Performance Organic Photovoltaics: Dynamic vs Static Disorder,” ACS Energy Letters 7 (2022): 1971–1979.

[40]

M. Kang, S. Yoon, J. Cho, J. Kim, and D. S. Chung, “Reactive Dedoping of Polymer Semiconductors to Boost Self-Powered Schottky Diode Performances,” ACS Applied Materials & Interfaces 11 (2019): 8365–8373.

[41]

Y. Y. Wang, M. Q. Yang, Y. Y. Li, et al., “Silicon-Rivalling Large-Area Flexible Broadband Organic Photodetectors,” Advanced Materials 38 (2025): e16087.

[42]

S. S. Li, L. Ye, W. C. Zhao, et al., “A Wide Band Gap Polymer With a Deep Highest Occupied Molecular Orbital Level Enables 14.2% Efficiency in Polymer Solar Cells,” Journal of the American Chemical Society 140 (2018): 7159–7167.

[43]

T. Liu, L. J. Huo, S. Chandrabose, et al., “Optimized Fibril Network Morphology by Precise Side-Chain Engineering to Achieve High-Performance Bulk-Heterojunction Organic Solar Cells,” Advanced Materials 30 (2018): 1707353.

[44]

X. X. Xia, T. K. Lau, X. Y. Guo, et al., “Uncovering the Out-of-plane Nanomorphology of Organic Photovoltaic Bulk Heterojunction by GTSAXS,” Nature Communications 12 (2021): 6226.

[45]

J. Q. Mai, T. K. Lau, J. Li, et al., “Understanding Morphology Compatibility for High-Performance Ternary Organic Solar Cells,” Chemistry of Materials 28 (2016): 6186–6195.

[46]

D. P. Qian, Z. L. Zheng, H. F. Yao, et al., “Design Rules for Minimizing Voltage Losses in High-Efficiency Organic Solar Cells,” Nature Materials 17 (2018): 703–709.

[47]

Z. Chen, X. Chen, Z. Y. Jia, et al., “Triplet Exciton Formation for Non-Radiative Voltage Loss in High-Efficiency Nonfullerene Organic Solar Cells,” Joule 5 (2021): 1832–1844.

[48]

T. Y. Chen, S. X. Li, Y. K. Li, et al., “Compromising Charge Generation and Recombination of Organic Photovoltaics with Mixed Diluent Strategy for Certified 19.4% Efficiency,” Advanced Materials 35 (2023): 2300400.

[49]

Y. Y. Jiang, S. M. Sun, R. J. Xu, et al., “Non-Fullerene Acceptor With Asymmetric Structure and Phenyl-Substituted Alkyl Side Chain for 20.2% Efficiency Organic Solar Cells,” Nature Energy 9 (2024): 975–986.

[50]

C. Li, J. Zhou, J. Song, et al., “Non-Fullerene Acceptors With Branched Side Chains and Improved Molecular Packing to Exceed 18% Efficiency in Organic Solar Cells,” Nature Energy 6 (2021): 605–613.

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