Abstract
A small-molecule acceptor, S-Cb, substituted with a cyclobutyl group that introduces high ring strain, was designed and synthesized. Thanks to the rigid and planar structure of cyclobutyl, S-Cb can form interchain supramolecular interactions through hydrogen bonding with L8-BO at the external side chains. This clamping effect not only effectively suppresses the electron-phonon coupling but also promotes the formation of high-quality acceptor alloy phases in the ternary active layer, thereby optimizing carrier behaviors and reducing non-radiative energy loss. The clamping effect reaches its maximum when S-Cb and L8-BO are in equal proportion, where organic solar cells (OSCs) based on D18:S-Cb:L8-BO achieved an impressive efficiency of 20.93%, with a certified efficiency of 20.74%. In summary, the cyclobutyl-mediated interchain supramolecular interactions suppress the electron-phonon coupling and optimize the acceptor alloy phase for efficient ternary OSCs.
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Data availability
All data supporting the findings of this study are available within the main text and the Supplementary Information file. Additional data are available from the corresponding author upon request. The X-ray crystallographic coordinates for the structures reported in this study have been deposited at the Cambridge Crystallographic Data Centre (CCDC) under deposition number 2423862 (S-Cb). The crystallographic data can also be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
References
Panidi, J. et al. Advances in Organic and Perovskite Photovoltaics Enabling a Greener Internet of Things. Adv. Funct. Mater. 32, 2200694 (2022).
Kini, G. P. et al. Latest Progress on Photoabsorbent Materials for Multifunctional Semitransparent Organic Solar Cells. Adv. Funct. Mater. 31, 2007931 (2021).
Li, Y. et al. Flexible and Semitransparent Organic Solar Cells. Adv. Energy Mater. 8, 1701791 (2018).
Yi, J. et al. Advantages, challenges and molecular design of different material types used in organic solar cells. Nat. Rev. Mater. 9, 46–62 (2024).
Ma, R. et al. Organic solar cells: beyond 20%. Sci. China Mater. 68, 1689–1701 (2025).
Li, C. et al. Organic solar cells with 21% efficiency enabled by a hybrid interfacial layer with dual-component synergy. Nat. Mater. 24, 1626–1634 (2025).
Li, C. et al. Non-fullerene acceptors with high crystallinity and photoluminescence quantum yield enable >20% efficiency organic solar cells. Nat. Mater. 24, 433–443 (2025).
Deng, J. et al. Acceptor Crystallinity Engineering Enables >20% Efficiency Binary Organic Solar Cells with 83.0% Fill Factor. Adv. Mater. 37, 2501243 (2025).
Wang, L. et al. Diluted Ternary Heterojunctions to Suppress Charge Recombination for Organic Solar Cells with 21% Efficiency. Adv. Mater. 37, 2419923 (2025).
Wang, G. et al. 27.09%-efficiency silicon heterojunction back contact solar cell and going beyond. Nat. Commun. 15, 8931 (2024).
Shen, Y. et al. Strain regulation retards natural operation decay of perovskite solar cells. Nature 635, 882–889 (2024).
You, S. et al. C60-based ionic salt electron shuttle for high-performance inverted perovskite solar modules. Science 388, 964–968 (2025).
Graziosi, P. et al. Electron-phonon coupling and mobility modeling in organic semiconductors: Method and application to two tetracene polymorphs. Phys. Rev. Mater. 9, 024603 (2025).
Ge, Z. et al. Regulating electron-phonon coupling by solid additive for efficient organic solar cells. Angew. Chem. Int. Ed. 64, e202413309 (2025).
Handa, T. et al. Long-lived hot carriers in a polymeric semiconductor. Nat. Mater. 24, 1333–1334 (2025).
Benduhn, J. et al. Intrinsic non-radiative voltage losses in fullerene-based organic solar cells. Nat. Energy 2, 17053 (2017).
Chen, X. et al. Assessing the nature of the charge-transfer electronic states in organic solar cells. Nat. Commun. 9, 5295 (2018).
Vukmirović, N. Electron-phonon coupling in crystalline organic semiconductors: microscopic evidence for nonpolaronic charge carriers. Phys. Rev. Lett. 109, 126407 (2012).
Zhang, K. et al. Dredging photocarrier trapping pathways via “charge bridge” driven exciton–phonon decoupling enables efficient and photothermal stable quaternary organic solar cells. Energy Environ. Sci. 16, 3350–3362 (2023).
Fu, Z. et al. π–π stacking modulation via polymer adsorption for elongated exciton diffusion in high-efficiency thick-film organic solar cells. Adv. Mater. 36, 2313532 (2024).
Jiang, Y. et al. Suppressing electron-phonon coupling in organic photovoltaics for high-efficiency power conversion. Nat. Commun. 14, 5079 (2023).
Dai, T. et al. Optimizing molecular crystallinity and suppressing electron-phonon coupling in completely non-fused ring electron acceptors for organic solar cells. Angew. Chem. Int. Ed. 63, e202403051 (2024).
Zhang, K. et al. Reducing limitations of aggregation-induced photocarrier trapping for photovoltaic stability via tailoring intermolecular electron-phonon coupling in highly efffcient quaternary polymer solar cells. Adv. Energy Mater. 12, 2103371 (2022).
Yang, F. et al. Oligomerized electron acceptors with alkynyl linkages to suppress electron-phonon coupling for low-energy-loss organic solar cells. Angew. Chem. Int. Ed. 64, e202501302 (2025).
Qiu, W. et al. Breaking 20% efficiency of all-polymer solar cells via Benzo[1,2-d:4,5-d′]Bisthiazole-Based Terpolymer donor strategy for fine morphology optimization. Adv. Funct. Mater. 35, 2503009 (2025).
Fu, J. et al. Rational molecular and device design enables organic solar cells approaching 20% efficiency. Nat. Commun. 15, 1830 (2024).
Chen, C. et al. Molecular interaction induced dual fibrils towards organic solar cells with certified efficiency over 20%. Nat. Commun. 15, 6865 (2024).
Song, J. et al. Non-halogenated solvent-processed organic solar cells with approaching 20 % efficiency and improved photostability. Angew. Chem. Int. Ed. 63, e202404297 (2024).
Sun, Y. et al. π-extended nonfullerene acceptor for compressed molecular packing in organic solar cells to achieve over 20% efficiency. J. Am. Chem. Soc. 146, 12011–12019 (2024).
Luo, Z. et al. Approaching 20% efficiency in ortho-xylene processed organic solar cells by a Benzo[a]phenazine-Core-Based 3D network acceptor with large electronic coupling and long exciton diffusion length. Adv. Mater. 36, 2407517 (2024).
Chen, H. et al. Organic solar cells with 20.82% efficiency and high tolerance of active layer thickness through crystallization sequence manipulation. Nat. Mater. 24, 444–453 (2025).
Jiang, Y. et al. Non-fullerene acceptor with asymmetric structure and phenyl-substituted alkyl side chain for 20.2% efficiency organic solar cells. Nat. Energy 9, 975–986 (2024).
Zhu, L. et al. Achieving 20.8% organic solar cells via additive-assisted layer-by-layer fabrication with bulk p-i-n structure and improved optical management. Joule 8, 3153–3168 (2024).
Ma, R. et al. Triplet state suppression for energy loss reduction in 20% nonhalogenated solvent processed binary organic solar cells. Adv. Mater. 37, 2500861 (2025).
Wei, N. et al. Constructing multiscale fibrous morphology to achieve 20% efficiency organic solar cells by mixing high and low molecular weight D18. Adv. Mater. 36, 2408934 (2024).
Wang, Y. et al. A novel upside-down thermal annealing method toward high-quality active layers enables organic solar cells with efficiency approaching 20%. Adv. Mater. 36, 2411957 (2024).
Xu, S. et al. High-performance indoor organic photovoltaics based on vertical acenaphthylene derivatives with halogen substitution: Suppressing energetic disorder and optimizing charge dynamics. Mater. Sci. Eng. R. 166, 101066 (2025).
Dong, J. et al. Dielectric constant engineering of nonfullerene acceptors enables a record fill factor of 83.58% and a high efficiency of 20.80% in organic solar cells. Energy Environ. Sci. 18, 4982–4995 (2025).
Wang, J. et al. Tandem organic solar cells with 21.5% efficiency. Adv. Mater. 37, e10378 (2025).
Gao, W. et al. Achieving 19% power conversion efficiency in planar-mixed heterojunction organic solar cells using a pseudosymmetric electron acceptor. Adv. Mater. 34, 2202089 (2022).
Yuan, J. et al. Single-junction organic solar cell with over 15% efficiency using fused-ring acceptor with electron-deficient core. Joule 3, 1140–1151 (2019).
Liu, K. et al. 19.7% efficiency binary organic solar cells achieved by selective core fluorination of nonfullerene electron acceptors. Joule 8, 835–851 (2024).
Wang, J. et al. Isomerism Effect of 3D dimeric acceptors for non-halogenated solvent-processed organic solar cells with 20 % efficiency. Angew. Chem. Int. Ed. 64, e202423562 (2025).
Shi, W. et al. A large conjugated rigid dimer acceptor enables 20.19% efficiency in organic solar cells. Energy Environ. Sci. 18, 5356–5364 (2025).
Li, L. et al. Side-chain cyclization enhancing molecular rigidity and π-π stacking yields as-cast binary organic solar cells with 19.1% efficiency. Sci. China Chem. 68, 2500–2512 (2025).
Root, S. et al. Measuring the glass transition temperature of conjugated polymer films with ultraviolet-visible spectroscopy. Chem. Mater. 29, 2646–2654 (2017).
Wang, R. et al. Central core-twisted conformation acceptors achieving 20.60% efficiency via suppression of nonradiative losses without sacrificing current and fill factor in binary organic solar cells. J. Am. Chem. Soc. 147, 43629–43639 (2025).
Xiong, X. et al. Melamine-doped cathode interlayer enables high-efficiency organic solar cells. ACS Energy Lett. 6, 3582–3589 (2021).
Hou, J. et al. Organic solar cells based on non-fullerene acceptors. Nat. Mater. 17, 119–128 (2018).
Qian, D. et al. Design rules for minimizing voltage losses in high-efficiency organic solar cells. Nat. Mater. 17, 703–709 (2018).
Alkauskas, A. et al. First-principles calculations of luminescence spectrum line shapes for defects in semiconductors: the example of GaN and ZnO. Phys. Rev. lett. 109, 267401 (2012).
Ghosh, P. et al. Decoupling excitons from high-frequency vibrations in organic molecules. Nature 629, 355–362 (2024).
Chen, X. K. et al. A unified description of non-radiative voltage losses in organic solar cells. Nat. Energy 6, 799–806 (2021).
Guha, S. et al. Temperature-dependent photoluminescence of organic semiconductors with varying backbone conformation. Phys. Rev. B 67, 125204 (2003).
Cui, F. et al. Vertical-phase-locking effect in efficient and stable all-polymer-hosted solar cells. ACS Energy Lett. 7, 3709–3717 (2022).
Ding, P. et al. Stability of organic solar cells: toward commercial applications. Chem. Soc. Rev. 53, 2350–2387 (2024).
Acknowledgements
This work was supported by the National Natural Science Foundation of China under Grant Nos. U23A20371 (W.G.) and U21A2078 (Z.W.). Z.W. acknowledges the support from FuXiaQuan Self-created Zone Collaborative Project (3502ZCQXT2023006). W.G. acknowledges the support from the Scientific Research Funds of Huaqiao University (605-50Y23024) and the Xiamen Outstanding Young Talents Program (605-52424047). G.L. acknowledges the support from Research Grants Council of Hong Kong (Project Nos. 15221320, 15307922, and C4005-22Y), RGC Senior Research Fellowship Scheme (SRFS2223-5S01), the Hong Kong Polytechnic University: SirSze-yuen Chung Endowed Professorship Fund (8-8480), RISE (Q-CDC6), PRI (Q-CD7X, CDAJ), and Guangdong-Hong Kong-Macao Joint Laboratory for Photonic-Thermal-Electrical Energy Materials and Devices (GDSTC No. 2019B121205001). R.M. thanks the PolyU Distinguished Postdoctoral Fellowship (1-YW4C).
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W.G., H.X., R.M., Z.W., and G.L. conceived the idea. W.G. designed and synthesized S-Cb, and performed TGA, DSC, single-crystal growth and analysis, temperature-dependent NMR, and GIWAXS measurements. Y.H. and J.W. conducted the theoretical simulations. J.Z. carried out the UV-vis absorption, PL, CV, and SCLC measurements. R.M. and H.X. fabricated and characterized the device, including J-V, EQE, Eloss, certified efficiency, PiFM, and prepared samples for morphology testing. T.A.D.P. and J.W. performed the fs-TAS measurements and analyzed the data. W.G., H.X., R.M., Z.W., and G.L. contributed to the preparation of this manuscript, with C.D. and J.-X.T. providing constructive suggestions during the writing and revision of the first draft.
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Gao, W., Hai, Y., Zeng, J. et al. Interchain supramolecular interactions drive nearly 21% efficiency organic solar cells. Nat Commun (2026). https://doi.org/10.1038/s41467-026-71199-0
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DOI: https://doi.org/10.1038/s41467-026-71199-0


