Tuning of the Photovoltaic Parameters of Molecular Donors by Covalent Bridging
Source abstract
Abstract
Abstract The synthesis of donor‐acceptor molecules involving triarylamines and dicyanovinyl blocks is described. Optical and electrochemical results show that rigidification of the acceptor part of the molecule by a covalent bridge leads to a ca. 0.20 eV increase of the band gap due to a parallel increase of the lowest unoccupied molecular orbital level. A preliminary evaluation of these compounds as donor materials in organic solar cells shows that although this structural modification reduces the light‐harvesting properties of the donor molecule, it nevertheless induces an increase of the efficiency of the resulting solar cells due to a simultaneous improvement of the open‐circuit voltage and fill factor.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Molecular Junctions and Nanostructures · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (38)
Show source-provided references
1. 10.1021/cr00025a00710.1021/cr00025a007 ↗
2. 10.1021/cm00054a00610.1021/cm00054a006 ↗
3. 10.1002/1439-7641(20020118)3:1<17::AID-CPHC17>3.0.CO;2-N10.1002/1439-7641(20020118)3:1<17::AID-CPHC17>3.0.CO;2-N ↗
4. 10.1002/anie.20110232610.1002/anie.201102326 ↗
5. 10.1039/c2cs15313k10.1039/c2cs15313k ↗
6. 10.1021/cm102189g10.1021/cm102189g ↗
7. 10.1039/c003946b10.1039/c003946b ↗
8. 10.1021/ar900041b10.1021/ar900041b ↗
9. 10.1002/chem.20100115310.1002/chem.201001153 ↗
10. 10.1002/anie.20110513310.1002/anie.201105133 ↗
11. 10.1002/adma.20110316710.1002/adma.201103167 ↗
12. 10.1039/c1cc12139a10.1039/c1cc12139a ↗
13. 10.1039/C2CC16390J10.1039/C2CC16390J ↗
14. 10.1021/ja301872s10.1021/ja301872s ↗
15. 10.1039/c2cc33921h10.1039/c2cc33921h ↗
16. 10.1039/C2RA22818A10.1039/C2RA22818A ↗
17. Jeux V. · RSC Adv. · 2013
18. 10.1039/C3994000176510.1039/C39940001765 ↗
19. 10.1002/adma.1994006110810.1002/adma.19940061108 ↗
20. 10.1021/jo962344710.1021/jo9623447 ↗
21. 10.1002/chem.20050085310.1002/chem.200500853 ↗
22. 10.1021/jo010713f10.1021/jo010713f ↗
23. 10.1021/jo060222110.1021/jo0602221 ↗
24. 10.1021/jp101238k10.1021/jp101238k ↗
25. 10.1016/j.tet.2012.05.05210.1016/j.tet.2012.05.052 ↗
26. 10.1021/jp205451910.1021/jp2054519 ↗
27. 10.3891/acta.chem.scand.20-157710.3891/acta.chem.scand.20-1577 ↗
28. 10.1016/S0040-4020(97)00151-810.1016/S0040-4020(97)00151-8 ↗
29. 10.1021/cm801911n10.1021/cm801911n ↗
30. 10.1021/ja058178e10.1021/ja058178e ↗
31. 10.1021/jp203759e10.1021/jp203759e ↗
32. Lin Y. · J. Mater. Chem. · 2013
33. 10.1021/cr950257t10.1021/cr950257t ↗
34. A.Leliège D.Demeter T.Rousseau P.Blanchard J.Roncali unpublished.
35. 10.1038/nature0194910.1038/nature01949 ↗
36. 10.1002/adfm.20110150810.1002/adfm.201101508 ↗
37. 10.1002/adfm.20100163910.1002/adfm.201001639 ↗
38. 10.1002/aenm.20110006510.1002/aenm.201100065 ↗