Drastic Changes in Properties of Donor–Acceptor Polymers Induced by Asymmetric Structural Isomers for Application to Polymer Solar Cells
Source abstract
Abstract
Appropriate design of donor–acceptor (D-A) conjugated polymers is important for enhancing their physical, optical, and electrochemical properties. The rapid development of D-A conjugated polymers based on fullerene and nonfullerene derivatives in the past decade has led to an improvement in the performance of polymer solar cells (PSCs). In this study, we designed and synthesized two donor polymers based on the DTffBT acceptor unit, with matching optical absorption range and energy levels with fullerene (PC71BM) and nonfullerene acceptors (ITIC and IDIC), by introducing asymmetric structural isomers of donor units. We demonstrated that materials design by structural modification dramatically affects the physical, optical, and electrochemical properties as well as the crystallinity and photovoltaic performance of the polymers. The results provide valuable insights into materials design for efficient PSCs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nano and Information Materials (NIMs) Laboratory, Department of Chemistry Engineering, Konkuk University, 120, Neungdong-ro, Gwangjin-gu, Seoul 05029, Republic of Korea
Funding
Korea Institute of Energy Technology Evaluation and Planning · Ministry of Trade, Industry and Energy
References (72)
Show source-provided references
1. 10.1038/nphoton.2009.13010.1038/nphoton.2009.130 ↗
2. 10.1126/science.aad442410.1126/science.aad4424 ↗
3. 10.1021/acs.chemrev.5b0009810.1021/acs.chemrev.5b00098 ↗
4. 10.1039/C5CS00593K10.1039/C5CS00593K ↗
5. 10.1038/nenergy.2015.2710.1038/nenergy.2015.27 ↗
6. 10.1002/adma.20180086810.1002/adma.201800868 ↗
7. 10.1016/j.scib.2018.02.01510.1016/j.scib.2018.02.015 ↗
8. 10.1002/adma.20180061310.1002/adma.201800613 ↗
9. 10.1016/j.scib.2017.11.00310.1016/j.scib.2017.11.003 ↗
10. 10.1016/j.solmat.2018.09.02410.1016/j.solmat.2018.09.024 ↗
11. 10.1016/j.solener.2018.09.00810.1016/j.solener.2018.09.008 ↗
12. 10.1021/acsami.7b1640610.1021/acsami.7b16406 ↗
13. 10.1021/acs.chemrev.6b0017610.1021/acs.chemrev.6b00176 ↗
14. 10.1002/adma.20160543710.1002/adma.201605437 ↗
15. 10.1021/ja312053210.1021/ja3120532 ↗
16. 10.1021/ma200309710.1021/ma2003097 ↗
17. 10.1021/acs.chemmater.6b0085010.1021/acs.chemmater.6b00850 ↗
18. 10.1016/j.orgel.2014.08.02210.1016/j.orgel.2014.08.022 ↗
19. 10.1016/j.polymer.2016.07.08210.1016/j.polymer.2016.07.082 ↗
20. 10.1021/acs.chemmater.7b0072910.1021/acs.chemmater.7b00729 ↗
21. 10.1039/C6TA02298G10.1039/C6TA02298G ↗
22. 10.1002/aenm.20160051510.1002/aenm.201600515 ↗
23. 10.1021/acsami.8b1327410.1021/acsami.8b13274 ↗
24. 10.1039/C3PY00961K10.1039/C3PY00961K ↗
25. 10.1039/C6CC01771A10.1039/C6CC01771A ↗
26. 10.1021/acs.macromol.7b0267610.1021/acs.macromol.7b02676 ↗
27. 10.1039/C7TA10976H10.1039/C7TA10976H ↗
28. 10.1021/ma401298g10.1021/ma401298g ↗
29. 10.1021/ma501894w10.1021/ma501894w ↗
30. 10.1016/j.joule.2017.08.00210.1016/j.joule.2017.08.002 ↗
31. 10.1002/advs.20170015210.1002/advs.201700152 ↗
32. 10.1021/jacs.5b0855610.1021/jacs.5b08556 ↗
33. 10.1016/j.orgel.2016.10.03210.1016/j.orgel.2016.10.032 ↗
34. 10.1002/aenm.20160108110.1002/aenm.201601081 ↗
35. 10.1002/aenm.20160230410.1002/aenm.201602304 ↗
36. 10.1038/ncomms1404710.1038/ncomms14047 ↗
37. 10.1039/C6TA10864D10.1039/C6TA10864D ↗
38. 10.1038/ncomms1309410.1038/ncomms13094 ↗
39. 10.1002/adma.20150595710.1002/adma.201505957 ↗
40. 10.1021/acs.chemmater.6b0536510.1021/acs.chemmater.6b05365 ↗
41. 10.1021/acs.chemmater.5b0294810.1021/acs.chemmater.5b02948 ↗
42. 10.1021/acsenergylett.8b0082510.1021/acsenergylett.8b00825 ↗
43. 10.1039/C6SC01599A10.1039/C6SC01599A ↗
44. 10.1039/C8TA02915F10.1039/C8TA02915F ↗
45. 10.1039/C7PY00924K10.1039/C7PY00924K ↗
46. 10.1039/C7PY00292K10.1039/C7PY00292K ↗
47. 10.1039/C6EE02466A10.1039/C6EE02466A ↗
48. 10.1002/solr.20170023010.1002/solr.201700230 ↗
49. 10.1002/adfm.20150233810.1002/adfm.201502338 ↗
50. 10.1002/aenm.20170189510.1002/aenm.201701895 ↗
51. 10.1021/acsami.6b0019210.1021/acsami.6b00192 ↗
52. 10.1039/C6CC04523E10.1039/C6CC04523E ↗
53. 10.1021/acs.chemmater.5b0093910.1021/acs.chemmater.5b00939 ↗
54. 10.1002/aenm.20140008710.1002/aenm.201400087 ↗
55. 10.1126/sciadv.160007610.1126/sciadv.1600076 ↗
56. 10.1002/adma.20160317810.1002/adma.201603178 ↗
57. 10.1002/cjoc.20180001510.1002/cjoc.201800015 ↗
58. 10.1021/acs.macromol.5b0056410.1021/acs.macromol.5b00564 ↗
59. 10.1002/solr.20180018610.1002/solr.201800186 ↗
60. 10.1039/C7PY00194K10.1039/C7PY00194K ↗
61. 10.1016/j.nanoen.2017.03.01310.1016/j.nanoen.2017.03.013 ↗
62. 10.1016/j.nanoen.2017.05.06010.1016/j.nanoen.2017.05.060 ↗
63. 10.1021/acs.chemmater.7b0133510.1021/acs.chemmater.7b01335 ↗
64. 10.1021/acsami.7b1005910.1021/acsami.7b10059 ↗
65. 10.1002/aenm.20170237710.1002/aenm.201702377 ↗
66. 10.1002/aenm.20170274110.1002/aenm.201702741 ↗
67. 10.1016/j.nanoen.2017.12.00510.1016/j.nanoen.2017.12.005 ↗
68. 10.1021/acs.chemmater.7b0165010.1021/acs.chemmater.7b01650 ↗
69. 10.1002/aenm.20180268610.1002/aenm.201802686 ↗
70. 10.1021/acs.jpclett.8b0324710.1021/acs.jpclett.8b03247 ↗
71. 10.1002/adma.20170717010.1002/adma.201707170 ↗
72. 10.1039/C8EE01546E10.1039/C8EE01546E ↗