journal article·2018-12-05

Nonhalogenated Solvent-Processed All-Polymer Solar Cells over 7.4% Efficiency from Quinoxaline-Based Polymers

Liuyang Zhou, Xuan He, Tsz-Ki Lau, Beibei Qiu, Tao Wang, Xinhui Lu, Beata Luszczynska, Jacek Ulanski, Shutao Xu, Guohui Chen, Jun Yuan, Zhi-Guo Zhang, Yongfang Li, Yingping Zou

ACS Applied Materials & Interfaces· Volume 10· Issue 48
Publisher page

Abstract

Two conjugated polymers, with different side chains of alkoxy-substituted difluorobenzene and alkyl-substituted difluorobenzene based on quinoxaline (Qx) as the electron acceptor unit and benzodithiophene as the electron donor unit, named HFQx-T and HFAQx-T, were used as electron donor polymers to fabricate all-polymer solar cells (all-PSCs) with a naphthalenediimide–bithiophene n-type semiconducting polymer (N2200). Usually, halogenated solvents are harmful to natural environment and human beings, and solvent additives were disadvantageous in the process of roll-to-roll technology. The Qx-based polymers are successfully used to fabricate high-performance all-PSCs, which processed with the nonhalogenated solvent tetrahydrofuran (THF) at room temperature. With THF as the processing solvent, the active layer showed a higher absorption coefficient, better phase separation, exciton dissociation, and charge carrier mobilities than that processed with CHCl3. Moreover, the photovoltaic properties have been dramatically improved with THF. The optimized device of HFAQx-T:N2200 processed with THF delivered an efficient power conversion efficiency (PCE) of 7.45%, which is the highest PCE for all-PSCs from Qx-based polymers processed by a nonhalogenated solvent.
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

College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China

Institute of Inorganic and Analytical Chemistry, University of Münster, Corrensstraße 28/30, 48149 Münster, Germany

Department of Physics, The Chinese University of Hong Kong, New Territories, Kowloon 999077, Hong Kong, P. R. China

Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China

State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082, China

Department of Molecular Physics, Lodz University of Technology, Zeromskiego 116, 90-924 Lodz, Poland

Funding

Ministry of Science and Technology of the People's Republic of China · Natural Science Foundation of?Hunan Province · National Natural Science Foundation of China

References (56)

Show source-provided references
1. 10.1039/c6cc01771a10.1039/c6cc01771a ↗
2. 10.1039/c7ta10262c10.1039/c7ta10262c ↗
3. 10.1021/acs.chemmater.7b0253610.1021/acs.chemmater.7b02536 ↗
4. 10.1021/acs.chemmater.7b0392810.1021/acs.chemmater.7b03928 ↗
5. 10.1039/c8ta00581h10.1039/c8ta00581h ↗
6. 10.1038/ncomms629310.1038/ncomms6293 ↗
7. 10.1002/solr.20180003810.1002/solr.201800038 ↗
8. 10.1039/c7ta02486j10.1039/c7ta02486j ↗
9. 10.1021/jacs.8b0269510.1021/jacs.8b02695 ↗
10. 10.1039/c8ta00479j10.1039/c8ta00479j ↗
11. 10.1039/c8ta01765d10.1039/c8ta01765d ↗
12. 10.1002/aenm.20180002910.1002/aenm.201800029 ↗
13. 10.1002/anie.20100540810.1002/anie.201005408 ↗
14. 10.1002/anie.20170767810.1002/anie.201707678 ↗
15. 10.1002/aenm.20160050410.1002/aenm.201600504 ↗
16. 10.1039/c3ee43041c10.1039/c3ee43041c ↗
17. 10.1016/j.nanoen.2018.01.01210.1016/j.nanoen.2018.01.012 ↗
18. 10.1039/c4ee01326c10.1039/c4ee01326c ↗
19. 10.1039/c0cs00194e10.1039/c0cs00194e ↗
20. 10.1039/c7ee01858d10.1039/c7ee01858d ↗
21. 10.1002/adma.20170390610.1002/adma.201703906 ↗
22. 10.1021/jacs.6b0482210.1021/jacs.6b04822 ↗
23. 10.1002/adfm.20170201610.1002/adfm.201702016 ↗
24. 10.1002/adma.20170397310.1002/adma.201703973 ↗
25. 10.1002/adfm.20170651710.1002/adfm.201706517 ↗
26. 10.1039/c8ta00368h10.1039/c8ta00368h ↗
27. 10.1039/c7ee00619e10.1039/c7ee00619e ↗
28. 10.1002/adma.20170483710.1002/adma.201704837 ↗
29. 10.1002/adma.20180249910.1002/adma.201802499 ↗
30. 10.1002/adma.20160042610.1002/adma.201600426 ↗
31. 10.1021/acs.jpcc.5b0173310.1021/acs.jpcc.5b01733 ↗
32. 10.1016/j.orgel.2015.12.02410.1016/j.orgel.2015.12.024 ↗
33. 10.1021/jp510996w10.1021/jp510996w ↗
34. 10.1002/adma.20150462910.1002/adma.201504629 ↗
35. 10.1002/adma.20150321810.1002/adma.201503218 ↗
36. 10.1016/j.orgel.2016.07.00710.1016/j.orgel.2016.07.007 ↗
37. 10.1016/j.orgel.2017.02.02910.1016/j.orgel.2017.02.029 ↗
38. 10.1016/j.nanoen.2016.10.00810.1016/j.nanoen.2016.10.008 ↗
39. 10.1021/acs.macromol.5b0056410.1021/acs.macromol.5b00564 ↗
40. 10.1021/acsami.5b0706610.1021/acsami.5b07066 ↗
41. 10.1021/acsami.7b1099510.1021/acsami.7b10995 ↗
42. 10.1016/j.orgel.2017.07.00510.1016/j.orgel.2017.07.005 ↗
43. 10.1039/c6tc05381e10.1039/c6tc05381e ↗
44. 10.1038/s41467-018-03207-x10.1038/s41467-018-03207-x ↗
45. 10.1021/acs.macromol.8b0032610.1021/acs.macromol.8b00326 ↗
46. 10.1021/acsami.7b0394710.1021/acsami.7b03947 ↗
47. 10.1038/nature0772710.1038/nature07727 ↗
48. 10.1002/adma.20140247310.1002/adma.201402473 ↗
49. 10.1002/adfm.20170718510.1002/adfm.201707185 ↗
50. 10.1021/jacs.5b1073510.1021/jacs.5b10735 ↗
51. 10.1038/ncomms1365110.1038/ncomms13651 ↗
52. 10.1039/c4ee00022f10.1039/c4ee00022f ↗
53. 10.1002/adma.20170612410.1002/adma.201706124 ↗
54. 10.1039/c8ta01692e10.1039/c8ta01692e ↗
55. 10.1002/adma.20180288810.1002/adma.201802888 ↗
56. 10.1021/acs.chemmater.6b0226410.1021/acs.chemmater.6b02264 ↗