journal article·2020-06-23

Roles of Acceptor Guests in Tuning the Organic Solar Cell Property Based on an Efficient Binary Material System with a Nearly Zero Hole-Transfer Driving Force

Xiaofang Li, Ming-Ao Pan, Tsz-Ki Lau, Wanru Liu, Kun Li, Nannan Yao, Fugang Shen, Shuying Huo, Fengling Zhang, Yishi Wu, Xuemei Li, Xinhui Lu, He Yan, Chuanlang Zhan

Chemistry of Materials· Volume 32· Issue 12
Publisher page

Abstract

Sub-picosecond hole transfer has been recently observed in several narrow band gap nonfullerene small-molecule acceptor (NFA)-based binary blended organic solar cell (OSC) systems operating with negligible energetic driving forces. As the driving forces are near zero, how the added acceptor/donor guests tune the barrier-free hole-transfer dynamics of these systems remains very unclear. In this study, we report a new NFA (BTCT-2Cl) that conducts a sub-picosecond hole transfer (2 ps) for efficient photocurrent generation when pairing with PM6 though the energetic offset is only 0.02 eV. We observe that the added nonfullerene and PCBM components differently tune the charge generation and recombination when selectively exciting BTCT-2Cl. After adding PC71BM, the hole transfer from the host BTCT-2Cl to the host donor is greatly accelerated, with the rate significantly reduced to 0.29 ps and the charge generation becomes more efficient; on the contrary, recombination is prolonged and a larger fill factor is obtained after adding an NFA guest, here, IT-4F. The different tuning on the host binary hole-transfer dynamics is likely related with the phase crystallinity and the domain size changed after adding different acceptor guests. Over 16% efficiency is obtained on the PC71BM-based ternary device that outperforms the host binary and the IT-4F-based ternary solar cells (both showing over 15% efficiencies). The results clearly demonstrate that adding PCBM or NFA guests enables a very effective and different tuning on the hole-transfer rates and the recombination rates between the barrier-free host binary components, hence leading to efficient tuning on the short-circuit current density and fill factor, which outlines new strategies toward designing high-efficiency ternary blended OSC systems. © 2020 American Chemical Society.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Conducting polymers and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Key Laboratory of Excitonic Materials Chemistry and Devices (EMC&D), College of Chemistry and Environmental Science, Inner Mongolia Normal University, Huhhot 010022, China

College of Chemistry and Environmental Science, Hebei University, Baoding 071002, China

Department of Chemistry and Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration & Reconstruction, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong HKG, China

Department of Physics, Chinese University of Hong Kong, New Territories, Kowloon, Hong Kong HKG, China

Beijing Key Laboratory for Optical Materials and Photonic Devices, Department of Chemistry, Capital Normal University, Beijing 100048, China

Biomolecular and Organic Electronics, Department of Physics, Chemistry and Biology, Linköing University, 58183 Linköing, Sweden

School of Chemistry & Chemical Engineering, Linyi University, Linyi 276000, China

Funding

Natural Science Foundation of Hebei Province · Research Grants Council, University Grants Committee · Shandong Province · Knut och Alice Wallenbergs Stiftelse · China Scholarship Council · National Natural Science Foundation of China · Swedish Government Research Area in Materials Science on Functional Materials at Linko?ping University

References (60)

Show source-provided references
1. 10.1038/nmat506310.1038/nmat5063 ↗
2. 10.1038/s41566-018-0104-910.1038/s41566-018-0104-9 ↗
3. 10.1039/c7cs00892a10.1039/c7cs00892a ↗
4. 10.1002/aenm.20190099910.1002/aenm.201900999 ↗
5. 10.1021/acs.chemmater.8b0504710.1021/acs.chemmater.8b05047 ↗
6. 10.1021/acsenergylett.8b0062710.1021/acsenergylett.8b00627 ↗
7. 10.1021/acs.chemmater.8b0108910.1021/acs.chemmater.8b01089 ↗
8. 10.1021/acs.chemmater.9b0124210.1021/acs.chemmater.9b01242 ↗
9. 10.1021/acs.chemmater.8b0227610.1021/acs.chemmater.8b02276 ↗
10. 10.1021/jacs.8b1365310.1021/jacs.8b13653 ↗
11. 10.1021/acs.chemmater.9b0195710.1021/acs.chemmater.9b01957 ↗
12. 10.1021/acs.chemmater.9b0491110.1021/acs.chemmater.9b04911 ↗
13. 10.1021/acs.chemmater.9b0369410.1021/acs.chemmater.9b03694 ↗
14. 10.1002/aenm.20180301210.1002/aenm.201803012 ↗
15. 10.1002/adma.20180784210.1002/adma.201807842 ↗
16. 10.1021/jacs.8b1298210.1021/jacs.8b12982 ↗
17. 10.1038/s41467-018-04502-310.1038/s41467-018-04502-3 ↗
18. 10.1021/jacs.7b0999810.1021/jacs.7b09998 ↗
19. 10.1002/adma.20180421510.1002/adma.201804215 ↗
20. 10.1038/ncomms1365110.1038/ncomms13651 ↗
21. 10.1002/aenm.20170232410.1002/aenm.201702324 ↗
22. 10.1021/jacs.6b0174410.1021/jacs.6b01744 ↗
23. 10.1039/c6ta07672f10.1039/c6ta07672f ↗
24. 10.1039/c7ta01554b10.1039/c7ta01554b ↗
25. 10.1038/nenergy.2016.8910.1038/nenergy.2016.89 ↗
26. 10.1021/jacs.8b1212610.1021/jacs.8b12126 ↗
27. 10.1038/s41467-020-14549-w10.1038/s41467-020-14549-w ↗
28. 10.1126/science.121774510.1126/science.1217745 ↗
29. 10.1126/science.124624910.1126/science.1246249 ↗
30. 10.1038/nmat442410.1038/nmat4424 ↗
31. Yao H. · J. Am. Chem. Soc. · 2019 · 141 · 774310.1021/jacs.8b12937 ↗
32. Yuan J. · Joule · 2019 · 3 · 110.1016/j.joule.2018.12.022 ↗
33. Fan B. · Sci. China: Chem. · 2019 · 62 · 74610.1007/s11426-019-9457-5 ↗
34. Xu X. · Adv. Mater. · 2019 · 31 · 190187210.1002/adma.201901872 ↗
35. Wu Y. · Sci. China: Chem. · 2019 · 63 · 26510.1007/s11426-019-9599-1 ↗
36. Lin Y. · Adv. Mater. · 2019 · 31 · 190296510.1002/adma.201902965 ↗
37. Sun H. · Energy Environ. Sci. · 2019 · 12 · 332810.1039/C9EE01890E ↗
38. Xiong J. · Sci. Bull. · 2019 · 64 · 157310.1016/j.scib.2019.10.002 ↗
39. 10.1002/adma.20190386810.1002/adma.201903868 ↗
40. 10.1016/j.joule.2019.09.01010.1016/j.joule.2019.09.010 ↗
41. 10.1002/adma.20190344110.1002/adma.201903441 ↗
42. 10.1002/adma.20190632410.1002/adma.201906324 ↗
43. 10.1021/jacs.9b0993910.1021/jacs.9b09939 ↗
44. 10.1021/acs.chemmater.9b0294310.1021/acs.chemmater.9b02943 ↗
45. Song J. · Adv. Mater. · 2019 · 31 · 190564510.1002/adma.201905645 ↗
46. An Q. · Sci. Bull. · 2020 · 65 · 53810.1016/j.scib.2020.01.012 ↗
47. 10.1039/c9ee03710a10.1039/c9ee03710a ↗
48. 10.1039/c9ta06929a10.1039/c9ta06929a ↗
49. 10.1002/adma.20190230210.1002/adma.201902302 ↗
50. 10.1038/s41566-019-0573-510.1038/s41566-019-0573-5 ↗
51. 10.1021/acsenergylett.9b0144710.1021/acsenergylett.9b01447 ↗
52. 10.1016/j.cclet.2017.11.01810.1016/j.cclet.2017.11.018 ↗
53. 10.1002/aenm.20190004110.1002/aenm.201900041 ↗
54. 10.1002/aenm.20190172810.1002/aenm.201901728 ↗
55. 10.1002/aenm.20190329810.1002/aenm.201903298 ↗
56. 10.1021/acs.jpclett.0c0040510.1021/acs.jpclett.0c00405 ↗
57. 10.1038/srep4426910.1038/srep44269 ↗
58. 10.1021/cm500633910.1021/cm5006339 ↗
59. 10.1039/c3ee24312e10.1039/c3ee24312e ↗
60. 10.1002/polb.2342610.1002/polb.23426 ↗