journal article·2019-10

Two Well‐Compatible Acceptors with Efficient Energy Transfer Enable Ternary Organic Photovoltaics Exhibiting a 13.36% Efficiency

Jianxiao Wang, Xiaoling Ma, Jian Wang, Ruijie Ming, Qiaoshi An, Jian Zhang, Chuluo Yang, Fujun Zhang

Small· Volume 15· Issue 41
Publisher page

Abstract

Abstract Organic photovoltaics (OPVs) are fabricated with PM6 as donor and T6Me, IT‐2F, or their mixture as acceptor. A 13.36% power conversion efficiency (PCE) is achieved from the optimized ternary OPVs with 50 wt% IT‐2F in acceptors, which is attributed to the enhanced photon harvesting of ternary active layers and improved exciton utilization efficiency through energy transfer from IT‐2F to T6Me. The efficient energy transfer from IT‐2F to T6Me can be confirmed from the photoluminescence spectra of neat and blend films, which may provide additional channels to enhance exciton utilization efficiency for achieving short‐circuit current density (JSC) improvement of ternary OPVs. It should be highlighted that the fill factor (FF) of ternary OPVs can be monotonously increased along with the incorporation of IT‐2F, indicating the gradually optimized phase separation degree of ternary active layers. The third component IT‐2F plays a key role in optimizing phase separation as a morphology regulator. Over 8% PCE improvement is achieved in the optimized ternary OPVs compared with the over 12% PCEs of the corresponding binary OPVs, respectively. This work indicates that the performance of ternary OPVs can be well optimized by carefully picking materials with good compatibility and complementary absorption spectra, as well as the appropriate energy levels.
Source: crossref · 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 Luminescence and Optical Information Ministry of Education Beijing Jiaotong University 100044 Beijing P. R. China

College of Physics and Electronic Engineering Taishan University 271021 Taian Shandong Province P. R. China

Department of Chemistry and Hubei Key Lab on Organic and Polymeric Optoelectronic Materials Wuhan University 430072 Wuhan P. R. China

Department of Material Science and Technology Guangxi Key Laboratory of Information Materials Guilin University of Electronic Technology 1 Jinji Road 541004 Guilin P. R. China

Key Laboratory of Polymer Science and Technology College of Materials Science and Engineering, Shenzhen University 518060 Shenzhen P. R. China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Beijing Municipality

References (51)

Show source-provided references
1. 10.1038/natrevmats.2018.310.1038/natrevmats.2018.3 ↗
2. 10.1039/C7CS00892A10.1039/C7CS00892A ↗
3. 10.1002/adma.20180086810.1002/adma.201800868 ↗
4. 10.1016/j.scib.2019.03.02410.1016/j.scib.2019.03.024 ↗
5. 10.1126/science.aat261210.1126/science.aat2612 ↗
6. 10.1007/s11426-019-9457-510.1007/s11426-019-9457-5 ↗
7. 10.1002/adma.20180441610.1002/adma.201804416 ↗
8. 10.1002/aenm.20140089110.1002/aenm.201400891 ↗
9. 10.1038/nphoton.2015.12810.1038/nphoton.2015.128 ↗
10. 10.1002/anie.20180629110.1002/anie.201806291 ↗
11. 10.1021/acs.chemmater.6b0226410.1021/acs.chemmater.6b02264 ↗
12. 10.1002/aenm.20160250910.1002/aenm.201602509 ↗
13. 10.1002/adma.20160424110.1002/adma.201604241 ↗
14. 10.1002/adma.20170300510.1002/adma.201703005 ↗
15. 10.1039/C8TC06089D10.1039/C8TC06089D ↗
16. 10.1021/acsenergylett.8b0010010.1021/acsenergylett.8b00100 ↗
17. 10.1039/C7TA00211D10.1039/C7TA00211D ↗
18. 10.1039/C8EE01700J10.1039/C8EE01700J ↗
19. 10.1039/C8TA03453B10.1039/C8TA03453B ↗
20. 10.1039/C8EE00215K10.1039/C8EE00215K ↗
21. 10.1002/adfm.20180700610.1002/adfm.201807006 ↗
22. 10.1002/aenm.20180042410.1002/aenm.201800424 ↗
23. 10.1039/C9TA01497G10.1039/C9TA01497G ↗
24. 10.1038/nmat479710.1038/nmat4797 ↗
25. 10.1016/j.nanoen.2016.02.03210.1016/j.nanoen.2016.02.032 ↗
26. 10.1016/j.nanoen.2017.05.06010.1016/j.nanoen.2017.05.060 ↗
27. 10.1038/s41560-018-0234-910.1038/s41560-018-0234-9 ↗
28. 10.1002/aenm.20170285410.1002/aenm.201702854 ↗
29. 10.1021/acsami.7b1815210.1021/acsami.7b18152 ↗
30. 10.1016/j.nanoen.2017.12.05010.1016/j.nanoen.2017.12.050 ↗
31. 10.1016/j.joule.2018.10.01610.1016/j.joule.2018.10.016 ↗
32. 10.1038/nphoton.2015.12610.1038/nphoton.2015.126 ↗
33. 10.1002/adma.20170229110.1002/adma.201702291 ↗
34. 10.1007/s11426-016-0461-110.1007/s11426-016-0461-1 ↗
35. 10.1039/C8EE01107A10.1039/C8EE01107A ↗
36. 10.1016/j.solener.2016.09.04910.1016/j.solener.2016.09.049 ↗
37. 10.1016/j.nanoen.2018.11.01010.1016/j.nanoen.2018.11.010 ↗
38. 10.1021/am507581w10.1021/am507581w ↗
39. 10.1002/aenm.20180196810.1002/aenm.201801968 ↗
40. 10.1016/j.nanoen.2019.04.01810.1016/j.nanoen.2019.04.018 ↗
41. 10.1002/adma.20180180110.1002/adma.201801801 ↗
42. 10.1002/solr.20170004410.1002/solr.201700044 ↗
43. 10.1039/C7TA10763C10.1039/C7TA10763C ↗
44. 10.1002/adfm.20180161110.1002/adfm.201801611 ↗
45. 10.1039/C8NR01421C10.1039/C8NR01421C ↗
46. 10.1016/j.mtener.2019.04.00510.1016/j.mtener.2019.04.005 ↗
47. 10.1002/adfm.20160356410.1002/adfm.201603564 ↗
48. 10.1021/acs.nanolett.6b0541810.1021/acs.nanolett.6b05418 ↗
49. 10.1002/smtd.20170022910.1002/smtd.201700229 ↗
50. 10.1002/lpor.20180020410.1002/lpor.201800204 ↗
51. 10.1002/smll.20180427110.1002/smll.201804271 ↗