Effective End Group Modification of Poly(3-hexylthiophene) with Functional Electron-Deficient Moieties for Performance Improvement in Polymer Solar Cell
Source abstract
Abstract
A series of end-functionalized poly(3-hexylthiophene)s (P3HTs) were synthesized by end-capping with electron-deficient moieties (EDMs, oxadiazole (OXD) and triazole (TAZ)) to prevent the negative influence of bromine chain ends in the common uncapped P3HT in polymer solar cell (PSC) applications. On the basis of the electron-withdrawing capability of the planar OXD end groups, P3HT-end-OXD relative to the uncapped P3HT exhibits a raised absorption coefficient, extended exciton lifetime, and increased crystalline order in the blend with PCBM, leading to an effectual improvement in photovoltaic parameters. However, P3HT-end-TAZ has an opposite result even worse than that of the uncapped P3HT, arising from bulky TAZ end groups. As a consequence, P3HT-end-OXD gives a power conversion efficiency (PCE) of 4.24%, which is higher than those of the uncapped P3HT (3.28%) and P3HT-end-TAZ (0.50%). The result demonstrates that the EDM modification is a valuable method to tailor the structural defect of polymer chain ends. However, the efficacy is dependent on the structure of EDM.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Organic Light-Emitting Diodes Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering and Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing-Hua University, Hsinchu 30013, Taiwan, Republic of China
Funding
Ministry of Science and Technology, Taiwan
References (50)
Show source-provided references
1. 10.1021/cm102419z10.1021/cm102419z ↗
2. 10.1021/cr900150b10.1021/cr900150b ↗
3. 10.1038/nnano.2011.110.1038/nnano.2011.1 ↗
4. 10.1038/4435910.1038/44359 ↗
5. 10.1002/adfm.20050021110.1002/adfm.200500211 ↗
6. 10.1021/ja303813s10.1021/ja303813s ↗
7. 10.1021/jo00056a02410.1021/jo00056a024 ↗
8. 10.1021/ja00106a02710.1021/ja00106a027 ↗
9. 10.1021/ma001677+10.1021/ma001677+ ↗
10. 10.1021/ar800130s10.1021/ar800130s ↗
11. 10.1021/ja048918410.1021/ja0489184 ↗
12. 10.1103/PhysRevB.74.11531810.1103/PhysRevB.74.115318 ↗
13. 10.1021/jp072306z10.1021/jp072306z ↗
14. 10.1002/adma.20090280310.1002/adma.200902803 ↗
15. 10.1039/b923752f10.1039/b923752f ↗
16. 10.1002/adma.20100462910.1002/adma.201004629 ↗
17. 10.1038/nphoton.2012.1110.1038/nphoton.2012.11 ↗
18. 10.1021/ma061873210.1021/ma0618732 ↗
19. 10.1021/cr050149z10.1021/cr050149z ↗
20. 10.1002/anie.20070250610.1002/anie.200702506 ↗
21. 10.1002/adma.20050129710.1002/adma.200501297 ↗
22. 10.1002/aenm.20140177010.1002/aenm.201401770 ↗
23. 10.1016/j.synthmet.2006.06.00710.1016/j.synthmet.2006.06.007 ↗
24. 10.1021/jp044079w10.1021/jp044079w ↗
25. 10.1021/ja054777+10.1021/ja054777+ ↗
26. 10.1039/c3ra46725b10.1039/c3ra46725b ↗
27. Iqbal R. · J. Chem. Soc. Pak. · 2006 · 28 · 165
28. 10.1016/j.synthmet.2009.03.02910.1016/j.synthmet.2009.03.029 ↗
29. 10.1002/adma.20040013710.1002/adma.200400137 ↗
30. Frisch M. J. · 2009
31. 10.1063/1.233537710.1063/1.2335377 ↗
32. 10.1038/nmat157410.1038/nmat1574 ↗
33. 10.1021/ja806493n10.1021/ja806493n ↗
34. 10.1002/adfm.20080014510.1002/adfm.200800145 ↗
35. 10.1103/PhysRevB.67.06420310.1103/PhysRevB.67.064203 ↗
36. 10.1063/1.156852610.1063/1.1568526 ↗
37. 10.1103/PhysRevB.75.16520410.1103/PhysRevB.75.165204 ↗
38. 10.1016/S0169-4332(02)00756-010.1016/S0169-4332(02)00756-0 ↗
39. 10.1021/ma00043a01910.1021/ma00043a019 ↗
40. 10.1039/c1cc13477a10.1039/c1cc13477a ↗
41. 10.1039/C3PY01231J10.1039/C3PY01231J ↗
42. 10.1021/nl048120i10.1021/nl048120i ↗
43. 10.1038/ncomms418010.1038/ncomms4180 ↗
44. 10.1002/adfm.20070145910.1002/adfm.200701459 ↗
45. 10.1002/macp.20100037910.1002/macp.201000379 ↗
46. 10.1166/jnn.2014.843610.1166/jnn.2014.8436 ↗
47. 10.1002/mame.20130016810.1002/mame.201300168 ↗
48. 10.1002/adfm.20060062410.1002/adfm.200600624 ↗
49. 10.1039/c4tc00003j10.1039/c4tc00003j ↗
50. 10.1039/c3cp51383a10.1039/c3cp51383a ↗