Perylene Bisimide as a Promising Zinc Oxide Surface Modifier: Enhanced Interfacial Combination for Highly Efficient Inverted Polymer Solar Cells
Source abstract
Abstract
We report the application of a perylene bisimide (PBI-H) as zinc oxide (ZnO) surface modifier to afford an organic-inorganic co-interlayer for highly efficient inverted organic photovoltaics (i-OPV). By thermal annealing, a N-Zn chemical bond formed between PBI-H and ZnO, inducing close organic-inorganic combination. In addition, this co-interlayer shows decreased work function and increased electron transportation and conductivity, which are benefits for the cathode to enhance charge extraction efficiency and decrease recombination losses. As a result a highly efficient i-OPV was achieved with a power conversion efficiency (PCE) of 9.43% based on this co-interlayer with PTB7:PC71BM as the active layer, which shows over 35% enhancement compared to that of the device without the PBI-H layer. Moreover, this co-interlayer was widely applicable for i-OPVs based on various material systems, such as P3HT:PC61BM and PTB7-Th:PC71BM, resulting in PCE as high as 4.78% and 10.31%, respectively.
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
Institute of Polymer Optoelectronic Materials and Devices, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, People’s Republic of China
Funding
Ministry of Science and Technology of the People's Republic of China · Guangdong Province · National Natural Science Foundation of China · Ministry of Education of the People's Republic of China
References (35)
Show source-provided references
1. 10.1039/b401630k10.1039/b401630k ↗
2. 10.1126/science.293.5532.111910.1126/science.293.5532.1119 ↗
3. 10.1002/adma.20110444710.1002/adma.201104447 ↗
4. 10.1021/ja509261310.1021/ja5092613 ↗
5. 10.1002/adma.20130231510.1002/adma.201302315 ↗
6. 10.1002/adma.20140052510.1002/adma.201400525 ↗
7. 10.1002/aenm.20110071010.1002/aenm.201100710 ↗
8. 10.1039/C5MH00056D10.1039/C5MH00056D ↗
9. 10.1021/am201027j10.1021/am201027j ↗
10. 10.1039/c3cc42529k10.1039/c3cc42529k ↗
11. 10.1039/c4ee00022f10.1039/c4ee00022f ↗
12. 10.1021/jacs.5b0216810.1021/jacs.5b02168 ↗
13. 10.1021/ja000991g10.1021/ja000991g ↗
14. 10.1002/1521-3765(20010518)7:10<2245::AID-CHEM2245>3.0.CO;2-W10.1002/1521-3765(20010518)7:10<2245::AID-CHEM2245>3.0.CO;2-W ↗
15. 10.1063/1.294528110.1063/1.2945281 ↗
16. 10.1002/adma.20130147610.1002/adma.201301476 ↗
17. 10.1039/c3ta11811h10.1039/c3ta11811h ↗
18. 10.1002/aenm.20110015410.1002/aenm.201100154 ↗
19. 10.1002/aenm.20120018410.1002/aenm.201200184 ↗
20. 10.1038/nphoton.2011.31710.1038/nphoton.2011.317 ↗
21. 10.1002/aenm.20140160610.1002/aenm.201401606 ↗
22. 10.1021/ja108259n10.1021/ja108259n ↗
23. 10.1002/adma.20130299110.1002/adma.201302991 ↗
24. 10.1039/c2ee22296e10.1039/c2ee22296e ↗
25. 10.1039/b925382c10.1039/b925382c ↗
26. 10.1063/1.291952410.1063/1.2919524 ↗
27. 10.1021/am100238e10.1021/am100238e ↗
28. 10.1002/adma.20070305010.1002/adma.200703050 ↗
29. 10.1002/aenm.20110052210.1002/aenm.201100522 ↗
30. 10.1021/jp076724f10.1021/jp076724f ↗
31. 10.1002/adma.20130029510.1002/adma.201300295 ↗
32. 10.1002/aenm.20130169210.1002/aenm.201301692 ↗
33. 10.1039/c3mh00159h10.1039/c3mh00159h ↗
34. 10.1002/adma.20100430110.1002/adma.201004301 ↗
35. 10.1021/cg300776y10.1021/cg300776y ↗