journal article·2019-02-06

Easily Accessible Low Band Gap Polymer for Efficient Nonfullerene Polymer Solar Cells with a Low Eloss of 0.55 eV

Minwoo Park, Jae Woong Jung

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Abstract

Polymer solar cells (PSCs) have been attracting attention as a promising photovoltaic technology, and power conversion efficiencies (PCEs) of over 14% have been demonstrated. However, the state-of-the-art conjugated polymers for PSCs are based on the complex molecular structure that requires several steps for synthesis and purification, which impedes low materials cost for the PSCs. Thus, it is a key challenge to develop high-performance conjugated polymers with easily accessible building blocks for applications in practical PSCs. Here, a novel low band gap polymer (PFBTBOX) which comprises readily available building blocks was designed and synthesized to be used as an electron donor for PSCs. Affirmative optoelectronic properties of PFBTBOX for photovoltaic applications resulted in high PCEs up to 10.20 and 8.11% with nonfullerene and fullerene acceptors, respectively. Moreover, PFBTBOX exhibited minimal energy loss as low as 0.55 eV with a nonfullerene acceptor, indicating that PFBTBOX is a promising electron donor polymer for practical PSCs with high efficiency exceeding 10%.
Source: openalex_inverted_index · 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

Department of Chemical and Biological Engineering, Sookmyung Women’s University, Seoul 04310, Republic of Korea

Department of Advanced Materials Engineering for Information & Electronics, Kyung Hee University, 1732 Deogyeong-daero, Giheung-gu, Yongin-si, Gyeonggi-do 446-701, Republic of Korea

Funding

National Research Foundation of Korea · Korea Electric Power Corporation

References (33)

Show source-provided references
1. 10.1126/science.270.5243.178910.1126/science.270.5243.1789 ↗
2. 10.1021/acs.chemrev.5b0009810.1021/acs.chemrev.5b00098 ↗
3. 10.1038/natrevmats.2018.310.1038/natrevmats.2018.3 ↗
4. 10.1038/ncomms241110.1038/ncomms2411 ↗
5. 10.1039/c5ee02145f10.1039/c5ee02145f ↗
6. 10.1021/ja401434x10.1021/ja401434x ↗
7. 10.1021/jacs.6b0852310.1021/jacs.6b08523 ↗
8. 10.1007/s11426-017-9199-110.1007/s11426-017-9199-1 ↗
9. 10.1038/s41560-018-0234-910.1038/s41560-018-0234-9 ↗
10. 10.1002/adma.20180086810.1002/adma.201800868 ↗
11. 10.1039/c5py00358j10.1039/c5py00358j ↗
12. 10.1002/aenm.20150006510.1002/aenm.201500065 ↗
13. 10.1021/acsami.5b0344610.1021/acsami.5b03446 ↗
14. 10.1002/adma.20150390210.1002/adma.201503902 ↗
15. 10.1021/ja206610u10.1021/ja206610u ↗
16. 10.1016/j.nanoen.2017.06.05110.1016/j.nanoen.2017.06.051 ↗
17. 10.1002/cssc.20150085010.1002/cssc.201500850 ↗
18. 10.1039/c2ee21149a10.1039/c2ee21149a ↗
19. 10.1039/c5ee00855g10.1039/c5ee00855g ↗
20. 10.1002/adma.20150121410.1002/adma.201501214 ↗
21. 10.1021/ma201848z10.1021/ma201848z ↗
22. 10.1002/pola.2814510.1002/pola.28145 ↗
23. 10.1038/ncomms629310.1038/ncomms6293 ↗
24. 10.1016/j.nanoen.2017.12.00510.1016/j.nanoen.2017.12.005 ↗
25. 10.1039/c1cc12040a10.1039/c1cc12040a ↗
26. 10.1039/c6ta08591a10.1039/c6ta08591a ↗
27. 10.1039/c5ee02871j10.1039/c5ee02871j ↗
28. 10.1016/j.joule.2017.09.02010.1016/j.joule.2017.09.020 ↗
29. 10.1021/acsami.5b0344610.1021/acsami.5b03446 ↗
30. 10.1063/1.182977710.1063/1.1829777 ↗
31. 10.1021/acs.chemmater.5b0179910.1021/acs.chemmater.5b01799 ↗
32. 10.1021/acs.chemmater.5b0248010.1021/acs.chemmater.5b02480 ↗
33. 10.1039/c3ee40689j10.1039/c3ee40689j ↗