Organic Photosensitizers Incorporating Rigid Benzo[1,2-b:6,5-b′]dithiophene Segment for High-Performance Dye-Sensitized Solar Cells
Source abstract
Abstract
Benzo[1,2- b:6,5- b ′]dithiophene ( BDT ) entity with rigid skeleton is introduced into the conjugated spacer of organic dyes, with triphenylamine as the electron donor and 2-cyanoacrylic acid as the acceptor, have been prepared for dye-sensitized solar cells. Inserting an aromatic entity between BDT and the anchor extends the absorption wavelength of the dyes and improves the dark current suppression efficiency, and consequently leads to better cell performance. Addition of chenodeoxycholic acid coadsorbent alleviates dye aggregation and results in better cell efficiency. The dye inserted with 4 H -cyclopenta[2,1- b:3,4- b ′]dithiophene entity achieves the best efficiency (9.11%) when I – /I 3 – was used as the electrolyte. When Co(phen) 3 2+/3+ was used as the electrolyte, the efficiency further boosts to 9.88%.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Advanced Nanomaterials in Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Chemistry, Academia Sinica, No. 128, Section 2, Academia Road, Nankang District, Taipei 11529, Taiwan
Department of Chemistry, National Taiwan Normal University, 117 Taipei, Taiwan
Funding
Academia Sinica · Ministry of Science and Technology, Taiwan
References (50)
Show source-provided references
1. 10.1038/353737a010.1038/353737a0 ↗
2. 10.1021/cr900356p10.1021/cr900356p ↗
3. 10.1039/c2jm30362k10.1039/c2jm30362k ↗
4. 10.1002/cphc.20120021810.1002/cphc.201200218 ↗
5. 10.1002/tcr.20150000710.1002/tcr.201500007 ↗
6. 10.1038/nphoton.2017.6010.1038/nphoton.2017.60 ↗
7. 10.1002/aenm.20170003210.1002/aenm.201700032 ↗
8. 10.1021/nn900756s10.1021/nn900756s ↗
9. 10.1038/nchem.186110.1038/nchem.1861 ↗
10. 10.1039/C5EE02822A10.1039/C5EE02822A ↗
11. 10.1039/C5CC06759F10.1039/C5CC06759F ↗
12. 10.1039/C5TC02356D10.1039/C5TC02356D ↗
13. 10.1021/am506714510.1021/am5067145 ↗
14. 10.1002/cssc.20150019310.1002/cssc.201500193 ↗
15. 10.1039/C5CC07105D10.1039/C5CC07105D ↗
16. 10.1039/C6TA02275H10.1039/C6TA02275H ↗
17. 10.1039/C6RA00651E10.1039/C6RA00651E ↗
18. 10.1016/j.nanoen.2017.07.04710.1016/j.nanoen.2017.07.047 ↗
19. 10.1002/solr.20170002010.1002/solr.201700020 ↗
20. 10.1039/C6TC00353B10.1039/C6TC00353B ↗
21. 10.1039/C5PY00305A10.1039/C5PY00305A ↗
22. 10.1039/C6CP05173A10.1039/C6CP05173A ↗
23. 10.1021/ol301730c10.1021/ol301730c ↗
24. 10.1021/ol302704v10.1021/ol302704v ↗
25. 10.1021/am406050j10.1021/am406050j ↗
26. 10.1039/C4TA05807K10.1039/C4TA05807K ↗
27. 10.1002/ejoc.20120142410.1002/ejoc.201201424 ↗
28. 10.1039/c2jm30427a10.1039/c2jm30427a ↗
29. 10.1039/C6SC03938C10.1039/C6SC03938C ↗
30. 10.1021/acsami.6b1115210.1021/acsami.6b11152 ↗
31. 10.1039/C6TA05588E10.1039/C6TA05588E ↗
32. 10.1021/cm504594610.1021/cm5045946 ↗
33. 10.1021/acs.chemmater.5b0200610.1021/acs.chemmater.5b02006 ↗
34. 10.1038/nchem.96610.1038/nchem.966 ↗
35. 10.1039/C3TA12901B10.1039/C3TA12901B ↗
36. 10.1021/acssuschemeng.6b0070610.1021/acssuschemeng.6b00706 ↗
37. 10.1039/C7TA05632J10.1039/C7TA05632J ↗
38. 10.1039/c3ta14392a10.1039/c3ta14392a ↗
39. 10.1002/cssc.20140241410.1002/cssc.201402414 ↗
40. 10.1021/cm702631r10.1021/cm702631r ↗
41. 10.1002/asia.20120064810.1002/asia.201200648 ↗
42. 10.1021/jp026963x10.1021/jp026963x ↗
43. 10.1039/C3SC51844B10.1039/C3SC51844B ↗
44. 10.1039/C4TA02777A10.1039/C4TA02777A ↗
45. 10.1002/cssc.20140321110.1002/cssc.201403211 ↗
46. 10.1080/0144235X.2012.73353910.1080/0144235X.2012.733539 ↗
47. 10.1039/c2ee23081j10.1039/c2ee23081j ↗
48. 10.1021/ar500337g10.1021/ar500337g ↗
49. 10.1039/C6TA11091F10.1039/C6TA11091F ↗
50. 10.1039/C2CS35257E10.1039/C2CS35257E ↗