Enhanced Photocurrent Spectral Response in Low‐Bandgap Polyfluorene and C70‐Derivative‐Based Solar Cells
Source abstract
Abstract
Abstract Plastic solar cells have been fabricated using a low‐bandgap alternating copolymer of fluorene and a donor–acceptor–donor moiety (APFO‐Green1), blended with 3′‐(3,5‐bis‐trifluoromethylphenyl)‐1′‐(4‐nitrophenyl)pyrazolino[70]fullerene (BTPF70) as electron acceptor. The polymer shows optical absorption in two wavelength ranges, λ < 500 nm and 600 < λ < 1000 nm. The BTPF70 absorbs light at λ < 700 nm. A broad photocurrent spectral response in the wavelength range 300 < λ < 1000 nm is obtained in solar cells. A photocurrent density of 3.4 mA cm–2, open‐circuit voltage of 0.58 V, and power‐conversion efficiency of 0.7 % are achieved under illumination of AM1.5 (1000 W m–2) from a solar simulator. Synthesis of BTPF70 is presented. Photoluminescence quenching and electrochemical studies are used to discuss photoinduced charge transfer.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Fullerene Chemistry and Applications · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (30)
Show source-provided references
1. 10.1002/1616-3028(200102)11:1<15::AID-ADFM15>3.0.CO;2-A10.1002/1616-3028(200102)11:1<15::AID-ADFM15>3.0.CO;2-A ↗
2. 10.1002/adfm.20039001110.1002/adfm.200390011 ↗
3. 10.1063/1.144698810.1063/1.1446988 ↗
4. 10.1016/S0040-6090(01)01584-X10.1016/S0040-6090(01)01584-X ↗
5. 10.1016/S0379-6779(00)01501-010.1016/S0379-6779(00)01501-0 ↗
6. 10.1016/S0379-6779(02)01168-210.1016/S0379-6779(02)01168-2 ↗
7. 10.1016/j.tsf.2003.10.08510.1016/j.tsf.2003.10.085 ↗
8. 10.1039/b306630d10.1039/b306630d ↗
9. 10.1021/jo001755r10.1021/jo001755r ↗
10. 10.1002/1616-3028(200108)11:4<255::AID-ADFM255>3.0.CO;2-I10.1002/1616-3028(200108)11:4<255::AID-ADFM255>3.0.CO;2-I ↗
11. 10.1063/1.182507010.1063/1.1825070 ↗
12. 10.1063/1.173706410.1063/1.1737064 ↗
13. 10.1016/j.synthmet.2004.08.00210.1016/j.synthmet.2004.08.002 ↗
14. 10.1002/1616-3028(200110)11:5<374::AID-ADFM374>3.0.CO;2-W10.1002/1616-3028(200110)11:5<374::AID-ADFM374>3.0.CO;2-W ↗
15. 10.1063/1.165087810.1063/1.1650878 ↗
16. 10.1007/s00339-003-2498-510.1007/s00339-003-2498-5 ↗
17. 10.1038/3143510.1038/31435 ↗
18. 10.1016/S0379-6779(97)81154-X10.1016/S0379-6779(97)81154-X ↗
19. 10.1103/PhysRevB.51.717910.1103/PhysRevB.51.7179 ↗
20. 10.1103/PhysRevB.49.1674610.1103/PhysRevB.49.16746 ↗
21. 10.1002/anie.20035164710.1002/anie.200351647 ↗
22. 10.1021/jo961070k10.1021/jo961070k ↗
23. 10.1021/ja00095a00510.1021/ja00095a005 ↗
24. 10.1016/S0040-4020(02)00552-510.1016/S0040-4020(02)00552-5 ↗
25. J. Chlistunoff D. Cliffel A. J. Bard inHandbook of Organic Conductive Molecules and Polymers: Charge‐Transfer Salts Fullerenes and Photoconductors Vol. 1 (Ed: H. S. Nalwa) Wiley and Sons New York1997 Ch. 7.
26. 10.1103/PhysRevB.52.R1166510.1103/PhysRevB.52.R11665 ↗
27. 10.1002/1616-3028(200112)11:6<420::AID-ADFM420>3.0.CO;2-K10.1002/1616-3028(200112)11:6<420::AID-ADFM420>3.0.CO;2-K ↗
28. 10.1021/cm047811c10.1021/cm047811c ↗
29. 10.1016/S1566-1199(02)00051-410.1016/S1566-1199(02)00051-4 ↗
30. 10.1021/ja00360a00410.1021/ja00360a004 ↗