Effect of Different Numbers of −CH2– Units on the Performance of Isoquinolinium Dyes
Source abstract
Abstract
Three new dyes have been synthesized to investigate the influence of the distance between the electron acceptor and TiO2 surface on the performance of dye-sensitized solar cells (DSSCs). In these dyes, the isoquinolinium acceptor, with a -(CH2)nCOOH anchoring group, and a functionalized triphenylamine donor are separated by an oligothiophene bridge. The physical and electrochemical properties of the dyes were investigated systematically. The results prove that different numbers of -CH2- units between the isoquinolinium acceptor and the carboxyl anchoring group have a less pronounced effect on the physical and electrochemical properties of these dyes. However, when applied in DSSCs, a sharp decrease in the short-circuit current (Jsc) was observed with increasing numbers of -CH2- units. For example, the device containing the organic dye bearing three -CH2- units produced the lowest Jsc of 7.94 mA·cm(-2). In contrast, the device containing the dye bearing only one -CH2- unit exhibited the highest Jsc of 13.88 mA·cm(-2). The higher photocurrent obtained with the device incorporating the dye with one -CH2- unit resulted in a higher power conversion efficiency of 6.8%.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Photochemistry and Electron Transfer Studies · Nonlinear Optical Materials Studies · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Fine Chemicals, DUT−KTH Joint Education and Research Centre on Molecular Devices, Dalian University of Technology (DUT), 2 Linggong Road, 116024 Dalian, China
Ångström Laboratory, Center of Molecular Devices, Department of Chemistry, Uppsala University, Box 523, 75120 Uppsala, Sweden
School of Chemical Science and Engineering, Centre of Molecular Devices, Department of Chemistry, KTH Royal Institute of Technology, Teknikringen 30, 10044 Stockholm, Sweden
References (38)
Show source-provided references
1. Cai S. · J. Mater. Chem. A · 2013 · 1 · 1129510.1039/c3ta11748k ↗
2. Zhang M. · Energy Environ. Sci. · 2013 · 6 · 294410.1039/c3ee42331j ↗
3. Ning Z. · J. Phys. Chem. C · 2009 · 113 · 1030710.1021/jp902408z ↗
4. Paek S. · J. Phys. Chem. C · 2012 · 116 · 2320510.1021/jp305989g ↗
5. Zhou J. · J. Am. Chem. Soc. · 2013 · 135 · 848410.1021/ja403318y ↗
6. Zeng W. · Chem. Mater. · 2010 · 22 · 191510.1021/cm9036988 ↗
7. Tian H. · J. Phys. Chem. C · 2008 · 112 · 1102310.1021/jp800953s ↗
8. Hagberg D. P. · Chem. Commun. · 2006 · 21 · 224510.1039/b603002e ↗
9. Kitamura T. · Chem. Mater. · 2004 · 16 · 180610.1021/cm0349708 ↗
10. Karlsson K. M. · Chem.—Eur. J. · 2011 · 17 · 641510.1002/chem.201003730 ↗
11. Horiuchi T. · J. Am. Chem. Soc. · 2004 · 126 · 1221810.1021/ja0488277 ↗
12. Ito S. · Adv. Mater. · 2006 · 18 · 120210.1002/adma.200502540 ↗
13. He J. · Chem.—Eur. J. · 2012 · 18 · 790310.1002/chem.201103702 ↗
14. Liu B. · J. Mater. Chem. · 2012 · 22 · 1537910.1039/c2jm32333h ↗
15. Chang D. W. · Org. Lett. · 2011 · 13 · 388010.1021/ol2012378 ↗
16. Do K. · Org. Lett. · 2012 · 14 · 22210.1021/ol203012s ↗
17. Tian H. · J. Mater. Chem. · 2011 · 21 · 1246210.1039/c1jm12071a ↗
18. Tian H. · J. Phys. Chem. C · 2008 · 112 · 1102310.1021/jp800953s ↗
19. Zhang J. · Energy Environ. Sci. · 2013 · 6 · 160410.1039/c3ee40375k ↗
20. Tsao H. N. · ChemSusChem · 2011 · 4 · 59110.1002/cssc.201100120 ↗
21. Tian H. · Chem. Commun. · 2009 · 45 · 628810.1039/b912746a ↗
22. Zhao J. · J. Mater. Chem. A · 2013 · 1 · 244110.1039/c2ta00905f ↗
23. Teng C. · J. Phys. Chem. C · 2010 · 114 · 910110.1021/jp101238k ↗
24. Ziolek M. · Phys. Chem. Chem. Phys. · 2010 · 12 · 809810.1039/c002338h ↗
25. Yang C. J. · J. Mater. Chem. · 2012 · 22 · 404010.1039/c2jm13961h ↗
26. Kim S. · Tetrahedron · 2007 · 63 · 920610.1016/j.tet.2007.06.061 ↗
27. Sayama K. · Chem. Commun. · 2000 · 13 · 117310.1039/b001517m ↗
28. Hara K. · Adv. Funct. Mater. · 2005 · 15 · 24610.1002/adfm.200400272 ↗
29. Boschloo G. · J. Phys. Chem. B · 2005 · 109 · 1209310.1021/jp0513770 ↗
30. Morandeira A. · J. Am. Chem. Soc. · 2007 · 129 · 925010.1021/ja0722980 ↗
31. Kroeze J. E. · J. Am. Chem. Soc. · 2006 · 128 · 1637610.1021/ja065653f ↗
32. Wang Z. · Chem. Mater. · 2008 · 20 · 399310.1021/cm8003276 ↗
33. Pei K. · Chem.—Eur. J. · 2012 · 18 · 819010.1002/chem.201103542 ↗
34. Bandi Z. Z. · Appl. Phys. Lett. · 1998 · 73 · 327610.1063/1.122743 ↗
35. Kuang D. · J. Am. Chem. Soc. · 2006 · 128 · 414610.1021/ja058540p ↗
36. Haque S. A. · J. Phys. Chem. B · 2000 · 104 · 53810.1021/jp991085x ↗
37. Ardo S. · Chem. Soc. Rev. · 2009 · 38 · 11510.1039/B804321N ↗
38. Pastore M. · Phys. Chem. Chem. Phys. · 2012 · 14 · 92010.1039/C1CP22663K ↗