Polymer donor with halogenated-aromatic side chain enables efficient ternary organic solar cells

Song-ting Liang , Yun-fan Yang , Dong-xu Li , Jun Yuan , Ying-ping Zou

Journal of Central South University ›› 2025, Vol. 31 ›› Issue (12) : 4319 -4327.

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Journal of Central South University ›› 2025, Vol. 31 ›› Issue (12) : 4319 -4327. DOI: 10.1007/s11771-024-5845-7
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Polymer donor with halogenated-aromatic side chain enables efficient ternary organic solar cells

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Abstract

Ternary strategy has demonstrated great potential in promoting the power conversion efficiency (PCE) of bulk-heterojunction organic solar cells (BHJ OSCs). Two new polymer donors, TPQ-2F-2Cl and TPQ-2F-4F, were synthesized with chlorinated and fluorinated aromatic side chains, respectively, which contributed to distinct noncovalent interactions. Compared with the PM6: L8-BO host system, the TPQ-2F-2Cl based ternary OSCs obtained enhanced exciton dissociation and more balanced carrier mobility. Moreover, benefiting from the favorable miscibility of the PM6: L8-BO: TPQ-2F-2Cl blend, the ternary blending film featured a well-defined fibrillar morphology and improved molecular ordering. Consequently, the optimal PM6: L8-BO:TPQ-2F-2Cl device achieved a more outstanding PCE of 18.2%, a higher open circuit voltage (V oc), and a better fill factor (FF) in comparison with the binary device (PCE=17.7%). In contrast, the addition of TPQ-2F-4F would generate excessive aggregation of blend, thereby reducing the PCE of ternary OSCs (16.0%). This work shows a promising idea for designing efficient third component donor polymers.

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Song-ting Liang, Yun-fan Yang, Dong-xu Li, Jun Yuan, Ying-ping Zou. Polymer donor with halogenated-aromatic side chain enables efficient ternary organic solar cells. Journal of Central South University, 2025, 31(12): 4319-4327 DOI:10.1007/s11771-024-5845-7

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References

[1]

Sun Y-n, Chang M-j, Meng L-x, et al.. Flexible organic photovoltaics based on water-processed silver nanowire electrodes [J]. Nature Electronics, 2019, 2: 513-520.

[2]

Sun C-k, Pan F, Bin H-j, et al.. A low cost and high performance polymer donor material for polymer solar cells [J]. Nature Communications, 2018, 9(1): 743.

[3]

Zheng Z, Yao H-f, Ye L, et al.. PBDB-T and its derivatives: A family of polymer donors enables over 17% efficiency in organic photovoltaics [J]. Materials Today, 2020, 35: 115-130.

[4]

Song W, Fanady B, Peng R-x, et al.. Foldable semitransparent organic solar cells for photovoltaic and photosynthesis [J]. Advanced Energy Materials, 2020, 10(15): 2000136.

[5]

Zhang Y-n, Zheng J-w, Jiang Z-y, et al.. Guided-growth ultrathin metal film enabled efficient semitransparent organic solar cells [J]. Advanced Energy Materials, 2023, 13(7): 2203266.

[6]

Li Y-x, Huang X-j, Sheriff H K M, et al.. Semitransparent organic photovoltaics for building-integrated photovoltaic applications [J]. Nature Reviews Materials, 2023, 8: 186-201.

[7]

Lin Y-z, Wang J-y, Zhang Z-g, et al.. An electron acceptor challenging fullerenes for efficient polymer solar cells [J]. Advanced Materials, 2015, 27(7): 1170-1174.

[8]

Lin Y-z, Zhao F-w, He Q, et al.. Highperformance electron acceptor with thienyl side chains for organic photovoltaics [J]. Journal of the American Chemical Society, 2016, 138(14): 4955-4961.

[9]

Zhao W-c, Li S-s, Yao H-f, et al.. Molecular optimization enables over 13% efficiency in organic solar cells [J]. Journal of the American Chemical Society, 2017, 139(21): 7148-7151.

[10]

Feng L-l, Yuan J, Zhang Z-z, et al.. Thieno [3, 2-b] pyrrolo-fused pentacyclic benzotriazole-based acceptor for efficient organic photovoltaics [J]. ACS Applied Materials & Interfaces, 2017, 9(37): 31985-31992.

[11]

Yuan J, Zhang Y-q, Zhou L-y, et al.. Single-junction organic solar cell with over 15% efficiency using fused-ring acceptor with electron-deficient core [J]. Joule, 2019, 3(4): 1140-1151.

[12]

Jiang K, Wei Q-y, Lai J Y L, et al.. Alkyl chain tuning of small molecule acceptors for efficient organic solar cells [J]. Joule, 2019, 3(12): 3020-3033.

[13]

Zhu C, Yuan J, Cai F-f, et al.. Tuning the electron-deficient core of a non-fullerene acceptor to achieve over 17% efficiency in a single-junction organic solar cell [J]. Energy & Environmental Science, 2020, 13(8): 2459-2466.

[14]

Li C, Zhou J-d, Song J-l, et al.. Non-fullerene acceptors with branched side chains and improved molecular packing to exceed 18% efficiency in organic solar cells [J]. Nature Energy, 2021, 6: 605-613.

[15]

Cui Y, Yao H-f, Zhang J-q, et al.. Single-junction organic photovoltaic cells with approaching 18% efficiency [J]. Advanced Materials, 2020, 32(19): e1908205.

[16]

Wei Q-y, Yuan J, Yi Y-p, et al.. Y6 and its derivatives: Molecular design and physical mechanism [J]. National Science Review, 2021, 8(8): nwab121.

[17]

Cui Y, Xu Y, Yao H-f, et al.. Single-junction organic photovoltaic cell with 19% efficiency [J]. Advanced Materials, 2021, 33(41): 2102420.

[18]

Jiang K, Zhang J, Zhong C, et al.. Suppressed recombination loss in organic photovoltaics adopting a planar-mixed heterojunction architecture [J]. Nature Energy, 2022, 7: 1076-1086.

[19]

Zheng Z, Wang J-q, Bi P-q, et al.. Tandem organic solar cell with 20.2% efficiency [J]. Joule, 2022, 6(1): 171-184.

[20]

Zhang M, Bai Y, Sun C-k, et al.. Perylenediimide derived organic photovoltaic materials [J]. Science China Chemistry, 2022, 65(3): 462-485.

[21]

Wang J-q, Zheng Z, Bi P-q, et al.. Tandem organic solar cells with 20.6% efficiency enabled by reduced voltage losses [J]. National Science Review, 2023, 10(6): nwad085.

[22]

Deng M, Xu X-p, Duan Y-w, et al.. Y-type non-fullerene acceptors with outer branched side chains and inner cyclohexane side chains for 19.36% efficiency polymer solar cells [J]. Advanced Materials, 2023, 35(10): e2210760.

[23]

Han C-y, Wang J-x, Zhang S, et al.. Over 19% efficiency organic solar cells by regulating multidimensional intermolecular interactions [J]. Advanced Materials, 2023, 35(10): e2208986.

[24]

Chen H, Jeong S Y, Tian J-f, et al.. A 19% efficient and stable organic photovoltaic device enabled by a guest nonfullerene acceptor with fibril-like morphology [J]. Energy & Environmental Science, 2023, 16(3): 1062-1070.

[25]

Wang J-q, Bi P-q, Wang Y-f, et al.. Manipulating film formation kinetics enables organic photovoltaic cells with 19.5% efficiency [J]. CCS Chemistry, 2024, 6(1): 218-229.

[26]

Liu T, Ma R-j, Luo Z-h, et al.. Concurrent improvement in JSC and VOC in high-efficiency ternary organic solar cells enabled by a red-absorbing small-molecule acceptor with a high LUMO level [J]. Energy & Environmental Science, 2020, 13(7): 2115-2123.

[27]

Bi P-q, Zhang S-q, Chen Z-h, et al.. Reduced non-radiative charge recombination enables organic photovoltaic cell approaching 19% efficiency [J]. Joule, 2021, 5(9): 2408-2419.

[28]

Bi P-q, Wang J-q, Cui Y, et al.. Enhancing photon utilization efficiency for high-performance organic photovoltaic cells via regulating phase-transition kinetics [J]. Advanced Materials, 2023, 35(16): e2210865.

[29]

Xu X-p, Li Y, Peng Qiang. Recent advances in morphology optimizations towards highly efficient ternary organic solar cells [J]. Nano Select, 2020, 1(1): 30-58.

[30]

Li D-x, Li S-f, Wen C-l, et al.. Quinoxaline-based polymers with asymmetric aromatic side chain enables 16.27% efficiency for organic solar cells [J]. Chinese Journal of Polymer Science, 2023, 41(7): 1002-1010.

[31]

Pang B, Liao C-t, Xu X-p, et al.. B—N-bond-embedded triplet terpolymers with small singlet-triplet energy gaps for suppressing non-radiative recombination and improving blend morphology in organic solar cells [J]. Advanced Materials, 2023, 35(17): e2211871.

[32]

Benten H, Nishida T, Mori D, et al.. High-performance ternary blend all-polymer solar cells with complementary absorption bands from visible to near-infrared wavelengths [J]. Energy & Environmental Science, 2016, 9(1): 135-140.

[33]

Wang L, Zhang L-f, Kim S, et al.. Halogen-free donor polymers based on dicyanobenzotriazole with low energy loss and high efficiency in organic solar cells [J]. Small, 2023, 19(18): e2206607.

[34]

Zhang Y, Yao H-f, Zhang S-q, et al.. Fluorination vs. chlorination: A case study on high performance organic photovoltaic materials [J]. Science China Chemistry, 2018, 61(10): 1328-1337.

[35]

Zhang H, Yao H-f, Hou J-x, et al.. Over 14% efficiency in organic solar cells enabled by chlorinated nonfullerene small-molecule acceptors [J]. Advanced Materials, 2018, 30(28): e1800613.

[36]

Xue L-w, Yang Y-k, Xu J-q, et al.. Side chain engineering on medium bandgap copolymers to suppress triplet formation for high-efficiency polymer solar cells [J]. Advanced Materials, 2017, 29(40): 1703344.

[37]

Arias A C, Granström M, Petritsch K, et al.. Organic photodiodes using polymeric anodes [J]. Synthetic Metals, 1999, 102(1–3): 953-954.

[38]

Yao J, Qiu B-b, Zhang Z-g, et al.. Cathode engineering with perylene-diimide interlayer enabling over 17% efficiency single-junction organic solar cells [J]. Nature Communications, 2020, 11(1): 2726.

[39]

Cowan S, Banerji N, Leong W L, et al.. Charge formation, recombination, and sweep-out dynamics in organic solar cells [J]. Advanced Functional Materials, 2012, 22(6): 1116-1128.

[40]

Riedel I, Parisi J, Dyakonov V, et al.. Effect of temperature and illumination on the electrical characteristics of polymer - fullerene bulk-heterojunction solar cells [J]. Advanced Functional Materials, 2004, 14(1): 38-44.

[41]

Yang R-q, Garcia A, Korystov D, et al.. Control of interchain contacts, solid-state fluorescence quantum yield, and charge transport of cationic conjugated polyelectrolytes by choice of anion [J]. Journal of the American Chemical Society, 2006, 128(51): 16532-16539.

[42]

Jiang K, Zhang G-y, Yang G-f, et al.. Multiple cases of efficient nonfullerene ternary organic solar cells enabled by an effective morphology control method [J]. Advanced Energy Materials, 2018, 8(9): 1701370.

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