Miscibility Matching and Bimolecular Crystallization Affording High-Performance Ternary Nonfullerene Solar Cells
Source abstract
Abstract
How the interaction between a third component and a donor/acceptor affects the crystallization and phase separation of the active layer remains to be explored from the perspective of miscibility. To demonstrate the miscibility matching in nonfullerene-based ternary organic solar cells, the poly[(4,4′-bis(2-butyloctoxycarbonyl-[2,2′-bithiophene]-5,5-diyl)-alt-(2,2′-bithiophene-5,5′-diyl)] (PDCBT) and poly(3-hexylthiophene) (P3HT), showing similar chemical structures despite their dissimilar side chains, were selected as third components to incorporate into the poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b′]dithiophene))-alt-(5,5-(1′,3′-di-2-thienyl-5′,7′-bis(2-ethylhexyl)benzo[1′,2′-c:4′,5′-c′]dithiophene-4,8-dione))]:3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone)-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene (PBDB-T:ITIC) system. On the basis of the melting point depression method, the Flory–Huggins interaction parameters for PDCBT:PBDB-T(1:9) and P3HT:PBDB-T(1:9) blends were calculated to be −0.08 and −0.07, respectively, whereas the values are 0.99, 0.66, and 0.41 for PDCBT:ITIC, PBDB-T:ITIC, and P3HT:ITIC blends, respectively. PDCBT and P3HT tend to form bimolecular crystals with PBDB-T, as revealed by grazing incidence wide-angle X-ray scattering (GIWAXS). The more evident phase separation induced by poor miscibility between PDCBT and ITIC in addition to bimolecular crystallization between PDCBT and PBDB-T contributes to the obvious enhancement in power conversion efficiency (PCE) from 9.40% to 10.97%. Unfortunately, the miscibility mismatch and the change in charge transport upon the incorporation of P3HT into PBDB-T:ITIC results in the nonuniform P3HT distribution and energy level alignment, leading to a serious reduction in the PCE value. Miscibility matching in the selection of an appropriate third component should be a reasonable way to guide the fabrication of high-performance ternary organic solar cells.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Polymer crystallization and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Jialuo Road, Shanghai 201204, China
Institute of Advanced Scientific Research (IASR), Jiangxi Normal University, 99 Ziyang Avenue, Nanchang 330022, China
Funding
National Natural Science Foundation of China
References (54)
Show source-provided references
1. 10.1016/j.scib.2019.03.02410.1016/j.scib.2019.03.024 ↗
2. 10.1021/acs.chemrev.7b0053510.1021/acs.chemrev.7b00535 ↗
3. 10.1002/aenm.20170305810.1002/aenm.201703058 ↗
4. 10.1063/1.172362110.1063/1.1723621 ↗
5. 10.1016/S0032-3861(99)00713-210.1016/S0032-3861(99)00713-2 ↗
6. 10.1126/science.251.4996.89810.1126/science.251.4996.898 ↗
7. 10.1002/polb.1993.09031080110.1002/polb.1993.090310801 ↗
8. 10.1002/adma.20170711410.1002/adma.201707114 ↗
9. 10.1021/jacs.5b0722810.1021/jacs.5b07228 ↗
10. 10.1002/aenm.20180229310.1002/aenm.201802293 ↗
11. Rubinstein M. · 200310.1093/oso/9780198520597.001.0001 ↗
12. Liu F. · 1995
13. 10.1002/pol.1962.120571650710.1002/pol.1962.1205716507 ↗
14. 10.1021/ja305875u10.1021/ja305875u ↗
15. 10.1021/ma200855r10.1021/ma200855r ↗
16. 10.1021/ma502122710.1021/ma5021227 ↗
17. 10.1021/ma070712a10.1021/ma070712a ↗
18. 10.1021/ja405493j10.1021/ja405493j ↗
19. 10.1038/s41563-017-0005-110.1038/s41563-017-0005-1 ↗
20. 10.1002/adfm.20130009910.1002/adfm.201300099 ↗
21. 10.1021/ja208556410.1021/ja2085564 ↗
22. 10.1039/C5EE02641E10.1039/C5EE02641E ↗
23. 10.1002/advs.20190056510.1002/advs.201900565 ↗
24. 10.1039/C7TC03565A10.1039/C7TC03565A ↗
25. 10.1021/acs.macromol.9b0041110.1021/acs.macromol.9b00411 ↗
26. 10.1002/adma.20160460310.1002/adma.201604603 ↗
27. 10.1002/adma.20120430610.1002/adma.201204306 ↗
28. 10.1002/adfm.20040034510.1002/adfm.200400345 ↗
29. 10.1063/1.357490710.1063/1.3574907 ↗
30. 10.1088/1742-6596/247/1/01200710.1088/1742-6596/247/1/012007 ↗
31. 10.1021/jp902956210.1021/jp9029562 ↗
32. 10.1021/ma60048a04010.1021/ma60048a040 ↗
33. 10.1002/adma.20160180310.1002/adma.201601803 ↗
34. Hu W. · 2013
35. 10.1002/smtd.20170022910.1002/smtd.201700229 ↗
36. 10.1038/ncomms1365110.1038/ncomms13651 ↗
37. 10.1002/aenm.20170216610.1002/aenm.201702166 ↗
38. 10.1002/aenm.20180354110.1002/aenm.201803541 ↗
39. 10.1002/adma.20170025410.1002/adma.201700254 ↗
40. 10.1002/adfm.20080168410.1002/adfm.200801684 ↗
41. 10.1002/aenm.20120039210.1002/aenm.201200392 ↗
42. 10.1021/acs.chemmater.7b0006710.1021/acs.chemmater.7b00067 ↗
43. 10.1002/adma.20170524310.1002/adma.201705243 ↗
44. 10.1021/am502122a10.1021/am502122a ↗
45. 10.1016/j.solmat.2011.08.00510.1016/j.solmat.2011.08.005 ↗
46. 10.1021/jz400723u10.1021/jz400723u ↗
47. 10.1002/adfm.20090147310.1002/adfm.200901473 ↗
48. 10.1016/j.jlumin.2006.01.27210.1016/j.jlumin.2006.01.272 ↗
49. 10.1016/j.solmat.2013.07.05010.1016/j.solmat.2013.07.050 ↗
50. 10.1039/b918362k10.1039/b918362k ↗
51. 10.1002/aenm.20120107610.1002/aenm.201201076 ↗
52. 10.1002/adma.20110277510.1002/adma.201102775 ↗
53. 10.1021/cm302861s10.1021/cm302861s ↗
54. 10.1002/adma.20110279010.1002/adma.201102790 ↗