Citation: Shi-Zhe Geng, Wei-Tao Yang, Jian Gao, Shui-Xing Li, Min-Min Shi, Tsz-Ki Lau, Xin-Hui Lu, Chang-Zhi Li, Hong-Zheng Chen. Non-fullerene Acceptors with a Thieno[3,4-c]pyrrole-4,6-dione (TPD) Core for Efficient Organic Solar Cells[J]. Chinese Journal of Polymer Science, ;2019, 37(10): 1005-1014. doi: 10.1007/s10118-019-2309-x shu

Non-fullerene Acceptors with a Thieno[3,4-c]pyrrole-4,6-dione (TPD) Core for Efficient Organic Solar Cells

a.
Key Laboratory of Macromolecular Synthesis and Functionalization (Ministry of Education), State Key Laboratory of Silicon Materials, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China
b.
Department of Physics, The Chinese University of Hong Kong, New Territories, Hong Kong, China

Corresponding author: Min-Min Shi, minminshi@zju.edu.cn Hong-Zheng Chen, hzchen@zju.edu.cn
Received Date: 7 April 2019
Revised Date: 25 May 2019
Available Online: 3 July 2019

To achieve the red-shifted absorptions and appropriate energy levels of A-D-A type non-fullerene acceptors (NFAs), in this work, we design and synthesize two new NFAs, named TPDCIC and TPDCNC, whose electron-donating (D) unit is constructed by a thieno[3,4-c]pyrrole-4,6-dione (TPD) core attached to two cyclopentadithiophene (CPDT) moieties at both sides, and the electron-accepting (A) end-groups are 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile (IC) and 2-(3-oxo-2,3-dihydro-1H-cyclopenta[b]naphthalen-1-ylidene)malononitrile (NC), respectively. Benefiting from TPD core, which easily forms quinoid structure and O···H or O···S intramolecular noncovalent interactions, TPDCIC and TPDCNC show more delocalization of π-electrons and perfect planar molecular geometries, giving the absorption ranges extended to 822 and 852 nm, respectively. Furthermore, the highest occupied molecular orbital (HOMO) levels of TPDCIC and TPDCNC remain relatively low-lying due to the electronegativity of the carbonyl groups on TPD core. Considering that the absorptions and energy levels of the two NFAs match well with those of a widely used polymer donor, PBDB-T, we fabricate two kinds of organic solar cells (OSCs) based on the PBDB-T:TPDCIC and PBDB-T:TPDCNC blended films, respectively. Through a series of optimizations, the TPDCIC-based devices yield an impressing power conversion efficiency (PCE) of 10.12% with a large short-circuit current density (J_SC) of 18.16 mA·cm⁻², and the TPDCNC-based ones exhibit a comparable PCE of 9.80% with a J_SC of 17.40 mA·cm⁻². Our work is the first report of the TPD-core-based A-D-A type NFAs, providing a good reference for the molecular design of high-performance NFAs.
- Non-fullerene acceptors (NFAs),
- Organic solar cells (OSCs),
- Thieno[3,4-c]pyrrole-4,6-dione (TPD),
- Narrow bandgap,
- Energy levels
1. [1]
  Lin, Y.; Zhao, F.; He, Q.; Huo, L.; Wu, Y.; Parker, T. C.; Ma, W.; Sun, Y.; Wang, C.; Zhu, D.; Heeger, A. J.; Marder, S. R.; Zhan, X. High-performance electron acceptor with thienyl side chains for organic photovoltaics. J. Am. Chem. Soc. 2016, 138, 4955-4961. doi: 10.1021/jacs.6b02004
2. [2]
  Li, S.; Liu, W.; Li, C. Z.; Shi, M.; Chen, H. Efficient organic solar cells with non-fullerene acceptors. Small 2017, 13, 1701120. doi: 10.1002/smll.v13.37
3. [3]
  Li, S.; Zhan, L.; Liu, F.; Ren, J.; Shi, M.; Li, C. Z.; Russell, T. P.; Chen, H. An unfused-core-based nonfullerene acceptor enables high-efficiency organic solar cells with excellent morphological stability at high temperatures. Adv. Mater. 2018, 30, 1705208. doi: 10.1002/adma.201705208
4. [4]
  Dai, S.; Zhao, F.; Zhang, Q.; Lau, T. K.; Li, T.; Liu, K.; Ling, Q.; Wang, C.; Lu, X.; You, W.; Zhan, X. Fused nonacyclic electron acceptors for efficient polymer solar cells. J. Am. Chem. Soc. 2017, 139, 1336-1343. doi: 10.1021/jacs.6b12755
5. [5]
  Zhang, K.; Liu, X.; Xu, B.; Cui, Y.; Sun, M.; Hou, J. High-performance fullerene-free polymer solar cells with solution-processed conjugated polymers as anode interfacial layer. Chinese J. Polym. Sci. 2017, 35, 219-229. doi: 10.1007/s10118-017-1888-7
6. [6]
  Wang, S.; Liu, Y.; Yang, J.; Tao, Y.; Guo, Y.; Cao, X.; Zhang, Z.; Li, Y.; Huang, W. Orthogonal solubility in fully conjugated donor-acceptor block copolymers: compatibilizers for polymer/fullerene bulk-heterojunction solar cells. Chinese J. Polym. Sci. 2017, 35, 207-218. doi: 10.1007/s10118-017-1889-6
7. [7]
  Li, S.; Zhang, Z.; Shi, M.; Li, C. Z.; Chen, H. Molecular electron acceptors for efficient fullerene-free organic solar cells. Phys. Chem. Chem. Phys. 2017, 19, 3440-3458. doi: 10.1039/C6CP07465K
8. [8]
  Liu, Y.; Zhang, Z.; Feng, S.; Li, M.; Wu, L.; Hou, R.; Xu, X.; Chen, X.; Bo, Z. Exploiting noncovalently conformational locking as a design strategy for high performance fused-ring electron acceptor used in polymer solar cells. J. Am. Chem. Soc. 2017, 139, 3356-3359. doi: 10.1021/jacs.7b00566
9. [9]
  Li, S.; Ye, L.; Zhao, W.; Zhang, S.; Mukherjee, S.; Ade, H.; Hou, J. Energy-level modulation of small-molecule electron acceptors to achieve over 12% efficiency in polymer solar cells. Adv. Mater. 2016, 28, 9423-9429. doi: 10.1002/adma.201602776
10. [10]
  Lin, Y.; Zhao, F.; Wu, Y.; Chen, K.; Xia, Y.; Li, G.; Prasad, S. K. K.; Zhu, J.; Huo, L.; Bin, H.; Zhang, Z. G.; Guo, X.; Zhang, M.; Sun, Y.; Gao, F.; Wei, Z.; Ma, W.; Wang, C.; Hodgkiss, J.; Bo, Z.; Inganas, O.; Li, Y.; Zhan, X. Mapping polymer donors toward high-efficiency fullerene free organic solar cells. Adv. Mater. 2017, 29, 1604155. doi: 10.1002/adma.v29.3
11. [11]
  Baran, D.; Kirchartz, T.; Wheeler, S.; Dimitrov, S.; Abdelsamie, M.; Gorman, J.; Ashraf, R. S.; Holliday, S.; Wadsworth, A.; Gasparini, N.; Kaienburg, P.; Yan, H.; Amassian, A.; Brabec, C. J.; Durrant, J. R.; McCulloch, I. Reduced voltage losses yield 10% efficient fullerene free organic solar cells with > 1 V open circuit voltages. Energy Environ. Sci. 2016, 9, 3783-3793. doi: 10.1039/C6EE02598F
12. [12]
  Kan, B.; Feng, H.; Wan, X.; Liu, F.; Ke, X.; Wang, Y.; Wang, Y.; Zhang, H.; Li, C.; Hou, J.; Chen, Y. Small-molecule acceptor based on the heptacyclic benzodi(cyclopentadithiophene) unit for highly efficient nonfullerene organic solar cells. J. Am. Chem. Soc. 2017, 139, 4929-4934. doi: 10.1021/jacs.7b01170
13. [13]
  Lin, Y.; Wang, J.; Zhang, Z. G.; Bai, H.; Li, Y.; Zhu, D.; Zhan, X. An electron acceptor challenging fullerenes for efficient polymer solar cells. Adv. Mater. 2015, 27, 1170-1174. doi: 10.1002/adma.201404317
14. [14]
  Yuan, J.; Zhang, Y.; Zhou, L.; Zhang, G.; Yip, H.-L.; Lau, T.-K.; Lu, X.; Zhu, C.; Peng, H.; Johnson, P. A.; Leclerc, M.; Cao, Y.; Ulanski, J.; Li, Y.; Zou, Y. Single-junction organic solar cell with over 15% efficiency using fused-ring acceptor with electron-deficient core. Joule 2019, 3, 1-12. doi: 10.1016/j.joule.2018.12.022
15. [15]
  Chen, H. Electron-deficient core fused-ring based non-fullerene acceptor enables over 15% efficiency in single junction organic solar cells. Sci. China Chem. 2019, DOI: 10.1007/s11426-019-9431-8. doi: 10.1007/s11426-019-9431-8
16. [16]
  Fan, B.; Zhang, D.; Li, M.; Zhong, W.; Zeng, Z.; Ying, L.; Huang, F.; Cao, Y. Achieving over 16% efficiency for single-junction organic solar cells. Sci. China Chem. 2019, DOI: 10.1007/s11426-019-9457-5. doi: 10.1007/s11426-019-9457-5
17. [17]
  Meng, L.; Zhang, Y.; Wan, X.; Li, C.; Zhang, X.; Wang, Y.; Ke, X.; Xiao, Z.; Ding, L.; Xia, R.; Yip, H. L.; Cao, Y.; Chen, Y. Organic and solution-processed tandem solar cells with 17.3% efficiency. Science 2018, 361, 1094-1098. doi: 10.1126/science.aat2612
18. [18]
  Zhu, J.; Ke, Z.; Zhang, Q.; Wang, J.; Dai, S.; Wu, Y.; Xu, Y.; Lin, Y.; Ma, W.; You, W.; Zhan, X. Naphthodithiophene-based nonfullerene acceptor for high-performance organic photovoltaics: Effect of extended conjugation. Adv. Mater. 2018, 30, 1704713. doi: 10.1002/adma.201704713
19. [19]
  Li, W.; Ye, L.; Li, S.; Yao, H.; Ade, H.; Hou, J. A high-efficiency organic solar cell enabled by the strong intramolecular electron push-pull effect of the nonfullerene acceptor. Adv. Mater. 2018, 30, 1707170. doi: 10.1002/adma.201707170
20. [20]
  Li, S.; Zhan, L.; Sun, C.; Zhu, H.; Zhou, G.; Yang, W.; Shi, M.; Li, C. Z.; Hou, J.; Li, Y.; Chen, H. Highly efficient fullerene-free organic solar cells operate at near zero highest occupied molecular orbital offsets. J. Am. Chem. Soc. 2019, 141, 3073-3082. doi: 10.1021/jacs.8b12126
21. [21]
  Yuan, J.; Zhang, Y.; Zhou, L.; Zhang, C.; Lau, T. K.; Zhang, G.; Lu, X.; Yip, H. L.; So, S. K.; Beaupre, S.; Mainville, M.; Johnson, P. A.; Leclerc, M.; Chen, H.; Peng, H.; Li, Y.; Zou, Y. Fused benzothiadiazole: A building block for n-type organic acceptor to achieve high-performance organic solar cells. Adv. Mater. 2019, 1807577. doi: 10.1002/adma.201807577
22. [22]
  Yuan, J.; Huang, T.; Cheng, P.; Zou, Y.; Zhang, H.; Yang, J. L.; Chang, S. Y.; Zhang, Z.; Huang, W.; Wang, R.; Meng, D.; Gao, F.; Yang, Y. Enabling low voltage losses and high photocurrent in fullerene-free organic photovoltaics. Nat. Commun. 2019, 10, 570. doi: 10.1038/s41467-019-08386-9
23. [23]
  Li, S.; Liu, W.; Shi, M..; Mai, J.; Lau, T.-K.; Wan, J.; Lu, X.; Li, C. Z.; Chen, H. A spirobifluorene and diketopyrrolopyrrole moieties based non-fullerene acceptor for efficient and thermally stable polymer solar cells with high open-circuit voltage. Energy Environ. Sci. 2016, 9, 604-610. doi: 10.1039/C5EE03481G
24. [24]
  Chen, C. A.; Yang, P. C.; Wang, S. C.; Tung, S. H.; Su, W. F. Side chain effects on the optoelectronic properties and self-assembly behaviors of terthiophene-thieno[3,4-c] pyrrole-4,6-dione based conjugated polymers. Macromolecules 2018, 51, 7828-7835. doi: 10.1021/acs.macromol.8b01073
25. [25]
  Guo, X.; Zhou, N.; Lou, S. J.; Hennek, J. W.; Ponce Ortiz, R.; Butler, M. R.; Boudreault, P. L.; Strzalka, J.; Morin, P. O.; Leclerc, M.; Lopez Navarrete, J. T.; Ratner, M. A.; Chen, L. X.; Chang, R. P.; Facchetti, A.; Marks, T. J. Bithiopheneimide-dithienosilole/dithienogermole copolymers for efficient solar cells: information from structure-property-device performance correlations and comparison to thieno[3,4-c] pyrrole-4,6-dione analogues. J. Am. Chem. Soc. 2012, 134, 18427-18439. doi: 10.1021/ja3081583
26. [26]
  Guo, X.; Kim, F. S.; Jenekhe, S. A.; Watson, M. D. Phthalimide-based polymers for high performance organic thin-film transistors. J. Am. Chem. Soc. 2009, 131, 7206-7207. doi: 10.1021/ja810050y
27. [27]
  Chu, T. Y.; Lu, J.; Beaupre, S.; Zhang, Y.; Pouliot, J. R.; Zhou, J.; Najari, A.; Leclerc, M.; Tao, Y. Effects of the molecular weight and the side-chain length on the photovoltaic performance of dithienosilole/thienopyrrolodione copolymers. Adv. Funct. Mater. 2012, 22, 2345-2351. doi: 10.1002/adfm.v22.11
28. [28]
  Letizia, J. A.; Salata, M. R.; Tribout, C. M.; Facchetti, A.; Ratner, M. A.; Marks, T. J. N-channel polymers by design: optimizing the interplay of solubilizing substituents, crystal packing, and field-effect transistor characteristics in polymeric bithiophene-imide semiconductors. J. Am. Chem. Soc. 2008, 130, 9679-9694. doi: 10.1021/ja710815a
29. [29]
  Najari, A.; Beaupre, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-Perusse, C.; Leclerc, M. Synthesis and characterization of new thieno[3,4-c] pyrrole-4,6-dione derivatives for photovoltaic applications. Adv. Funct. Mater. 2011, 21, 718-728. doi: 10.1002/adfm.201001771
30. [30]
  Li, Z.; Tsang, S.-W.; Du, X.; Scoles, L.; Robertson, G.; Zhang, Y.; Toll, F.; Tao, Y.; Lu, J.; Ding, J. Alternating copolymers of cyclopenta[2,1-b;3,4-b′] dithiophene and thieno[3,4-c] pyrrole-4,6-dione for high-performance polymer solar cells. Adv. Funct. Mater. 2011, 21, 3331-3336. doi: 10.1002/adfm.201100708
31. [31]
  Li, S.; Ye, L.; Zhao, W.; Liu, X.; Zhu, J.; Ade, H.; Hou, J. Design of a new small-molecule electron acceptor enables efficient polymer solar cells with high fill factor. Adv. Mater. 2017, 29, 1704051. doi: 10.1002/adma.201704051
32. [32]
  Wang, N.; Zhan, L.; Li, S.; Shi, M.; Lau, T. K.; Lu, X.; Shikler, R.; Li, C. Z.; Chen, H. Enhancement of intra- and inter-molecular π-conjugated effects for a non-fullerene acceptor to achieve high-efficiency organic solar cells with an extended photoresponse range and optimized morphology. Mater. Chem. Front. 2018, 2, 2006-2012. doi: 10.1039/C8QM00318A
33. [33]
  Zhao, W.; Qian, D.; Zhang, S.; Li, S.; Inganas, O.; Gao, F.; Hou, J. Fullerene-free polymer solar cells with over 11% efficiency and excellent thermal stability. Adv. Mater. 2016, 28, 4734-4739. doi: 10.1002/adma.v28.23
34. [34]
  Zhao, W.; Li, S.; Zhang, S.; Liu, X.; Hou, J. Ternary polymer solar cells based on two acceptors and one donor for achieving 12.2% efficiency. Adv. Mater. 2017, 29, 1604059. doi: 10.1002/adma.v29.2
35. [35]
  Kang, H.; Kim, G.; Kim, J.; Kwon, S.; Kim, H.; Lee, K. Bulk-heterojunction organic solar cells: five core technologies for their commercialization. Adv. Mater. 2016, 28, 7821-7861. doi: 10.1002/adma.201601197
36. [36]
  Deng, D.; Zhang, Y.; Zhang, J.; Wang, Z.; Zhu, L.; Fang, J.; Xia, B.; Wang, Z.; Lu, K.; Ma, W.; Wei, Z. Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells. Nat. Commun. 2016, 7, 13740. doi: 10.1038/ncomms13740
37. [37]
  Li, S.; Zhan, L.; Zhao, W.; Zhang, S.; Ali, B.; Fu, Z.; Lau, T. K.; Lu, X.; Shi, M.; Li, C. Z.; Hou, J.; Chen, H. Revealing the effects of molecular packing on the performances of polymer solar cells based on A-D-C-D-A type non-fullerene acceptors. J. Mater. Chem. A 2018, 6, 12132-12141. doi: 10.1039/C8TA03753A
38. [38]
  Yuan, L.; Lu, K.; Xia, B.; Zhang, J.; Wang, Z.; Wang, Z.; Deng, D.; Fang, J.; Zhu, L.; Wei, Z. Acceptor end-capped oligomeric conjugated molecules with broadened absorption and enhanced extinction coefficients for high-efficiency organic solar cells. Adv. Mater. 2016, 28, 5980-5985. doi: 10.1002/adma.201600512
39. [39]
  Zhan, L.; Li, S.; Zhang, H.; Gao, F.; Lau, T.-K.; Lu, X.; Sun, D.; Wang, P.; Shi, M.; Li, C. Z.; Chen, H. A near-infrared photoactive morphology modifier leads to significant current improvement and energy loss mitigation for ternary organic solar cells. Adv. Sci. 2018, 5, 1800755. doi: 10.1002/advs.v5.8
40. [40]
  Zheng, Z.; Awartani, O. M.; Gautam, B.; Liu, D.; Qin, Y.; Li, W.; Bataller, A.; Gundogdu, K.; Ade, H.; Hou, J. Efficient charge transfer and fine-tuned energy level alignment in a THF-processed fullerene-free organic solar cell with 11.3% efficiency. Adv. Mater. 2017, 29, 1604241. doi: 10.1002/adma.201604241
41. [41]
  Fan, B.; Zhang, K.; Jiang, X. F.; Ying, L.; Huang, F.; Cao, Y. High-performance nonfullerene polymer solar cells based on imide-functionalized wide-bandgap polymers. Adv. Mater. 2017, 29, 1606396. doi: 10.1002/adma.201606396
42. [42]
  Mai, J.; Xiao, Y.; Zhou, G.; Wang, J.; Zhu, J.; Zhao, N.; Zhan, X.; Lu, X. Hidden structure ordering along backbone of fused-ring electron acceptors enhanced by ternary bulk heterojunction. Adv. Mater. 2018, 30, 1802888. doi: 10.1002/adma.v30.34
43. [43]
  Mai, J.; Lau, T. K.; Li, J.; Peng, S. H.; Hsu, C. S.; Jeng, U. S.; Zeng, J.; Zhao, N.; Xiao, X.; Lu, X. Understanding morphology compatibility for high-performance ternary organic solar cells. Chem. Mater. 2016, 28, 6186-6195. doi: 10.1021/acs.chemmater.6b02264
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