1,8-Naphthalimide-Based Planar Small Molecular Acceptor for Organic Solar Cells
Source abstract
Abstract
Four small molecular acceptors (SM1-4) comprising a central benzene core, two thiophene bridges and two 1,8-naphthalimide (NI) terminal groups were designed and synthesized by direct C-H activation. SM1 has a planar chemical structure and forms H-aggregation as films. By attachment of different substituents on the central benzene ring, the dihedral angles between the two NI end groups of SM1-4 gradually increased, leading to a gradual decrease of planarity. SM1-4 all possess a high-lying LUMO level, matching with wide band gap (WBG) polymer donors which usually have a high-lying LUMO level. When used in OSCs, devices based on SM1 and WBG donor PCDTBT-C12 gave higher electron mobility, superior film morphology and better photovoltaic performance. After optimization, a PCE of 2.78% with a V(oc) of 1.04 V was achieved for SM1 based devices, which is among the highest PCEs with a V(oc) higher than 1 V. Our results have demonstrated that NI based planar small molecules are potential acceptors for WBG polymer based OSCs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Semiconductor materials and interfaces
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing Key Laboratory of Energy Conversion and Storage Materials, College of Chemistry, Beijing Normal University, Beijing 100875, China
College of Materials Science and Optoelectronic Technology University of Chinese Academy of Sciences, No.19A Yuquan Road, Beijing, 100049, China
Funding
Ministry of Education of the People's Republic of China · Natural Science Foundation of Beijing Municipality · National Natural Science Foundation of China
References (31)
Show source-provided references
1. 10.1038/nmat210210.1038/nmat2102 ↗
2. 10.1007/s10118-013-1275-y10.1007/s10118-013-1275-y ↗
3. 10.1039/c0ee00668h10.1039/c0ee00668h ↗
4. 10.1039/C4MH00042K10.1039/C4MH00042K ↗
5. 10.1039/C5TA04310G10.1039/C5TA04310G ↗
6. 10.1038/ncomms924210.1038/ncomms9242 ↗
7. 10.1002/aenm.20140092910.1002/aenm.201400929 ↗
8. 10.1021/ja508814z10.1021/ja508814z ↗
9. 10.1021/acsami.5b0201210.1021/acsami.5b02012 ↗
10. 10.1002/adma.20140542910.1002/adma.201405429 ↗
11. 10.1021/ja511060210.1021/ja5110602 ↗
12. 10.1002/adma.20100140210.1002/adma.201001402 ↗
13. 10.1021/ja513189710.1021/ja5131897 ↗
14. 10.1002/adma.20140199210.1002/adma.201401992 ↗
15. 10.1002/adfm.20100236710.1002/adfm.201002367 ↗
16. 10.1039/c3ee41096j10.1039/c3ee41096j ↗
17. 10.1007/s11426-014-5278-510.1007/s11426-014-5278-5 ↗
18. 10.1021/la00018a05210.1021/la00018a052 ↗
19. 10.1039/C5TC01148E10.1039/C5TC01148E ↗
20. 10.1021/ja111259510.1021/ja1112595 ↗
21. 10.1002/adma.20130442710.1002/adma.201304427 ↗
22. 10.1002/adfm.20090083210.1002/adfm.200900832 ↗
23. 10.1039/b912824g10.1039/b912824g ↗
24. 10.1016/j.solmat.2008.06.00110.1016/j.solmat.2008.06.001 ↗
25. 10.1039/C4TC00994K10.1039/C4TC00994K ↗
26. 10.1063/1.165087810.1063/1.1650878 ↗
27. 10.1002/adfm.20040055910.1002/adfm.200400559 ↗
28. 10.1021/cm500633910.1021/cm5006339 ↗
29. 10.1002/adma.20140548510.1002/adma.201405485 ↗
30. 10.1021/jm100025u10.1021/jm100025u ↗
31. 10.1021/am508068m10.1021/am508068m ↗