Effects of Bis(imidazolium) Molten Salts with Different Substituents of Imidazolium Cations on the Performance of Efficient Dye-Sensitized Solar Cells
Source abstract
Abstract
Bis(imidazolium) iodides (bis-Im(+)I(-)s) are synthesized with different substituents and used as electrolytes in dye-sensitized solar cells (DSSCs). Three kinds of low-volatility electrolytes are prepared by using 1,1'-methylene bis(3-imidazolium) diiodide (MIDI), 1,1'-methylene bis(3-n-methylimidazolium) diiodide (MMIDI), and 1,1'-methylene-bis(3-n-ethylimidazolium) diiodide (MEIDI) as the iodide sources. The effects of these substituents on the photovoltaic performance of the cells are investigated. It is found that the device shows a lower short-circuit photocurrent (Jsc), higher open-voltage (Voc) and fill factor (FF) with the increased cation size in electrolyte. These results are explained by electrostatic interactions between the solvated Im(+) and the negatively charged species. Meanwhile, the explanation is supported by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), open circuit voltage decay (OCVD), and dark current measurements.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Conducting polymers and applications · TiO2 Photocatalysis and Solar Cells · Analytical Chemistry and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physics and Technology, Key Laboratory of Artificial Micro/Nano Structures of Ministry of Education, Wuhan University, Wuhan, 430072, China
References (37)
Show source-provided references
1. Schlapbach L. · Nature · 2001 · 414 · 35310.1038/35104634 ↗
2. Grätzel M. · Inorg. Chem. · 2005 · 44 · 684110.1021/ic0508371 ↗
3. Huang X. · Chem. Soc. Rev. · 2013 · 42 · 17310.1039/C2CS35288E ↗
4. Chung I. · Nature · 2012 · 485 · 48610.1038/nature11067 ↗
5. Chae J. · J. Power Sources · 2011 · 196 · 414310.1016/j.jpowsour.2010.12.109 ↗
6. Zhang X. · J. Phys. Chem. C · 2011 · 115 · 1266510.1021/jp201853c ↗
7. Sauvage F. · J. Am. Chem. Soc. · 2011 · 133 · 930410.1021/ja110541t ↗
8. Weiqing L. · Prog. Chem. · 2012 · 24 · 722
9. Cheon J. Y. · Chem. Commun. · 2012 · 48 · 805710.1039/c2cc30923h ↗
10. Zhang C. · J. Phys. Chem. C · 2011 · 115 · 865310.1021/jp111585s ↗
11. Zhang Q. · Small · 2012 · 8 · 371110.1002/smll.201201759 ↗
12. Roh D. K. · Nanoscale · 2011 · 3 · 416210.1039/c1nr10525f ↗
13. Chang Y. H. · Polymer · 2012 · 53 · 200810.1016/j.polymer.2012.03.020 ↗
14. Boschloo G. · Acc. Chem. Res. · 2009 · 42 · 181910.1021/ar900138m ↗
15. Chen C. · J. Phys. Chem. C · 2009 · 113 · 6290
16. Quintana M. · J. Photochem. Photobiol., A. · 2009 · 202 · 15910.1016/j.jphotochem.2008.11.024 ↗
17. Daeneke T. · Nat. Chem. · 2011 · 3 · 21310.1038/nchem.966 ↗
18. Cheng M. · Energy Environ. Sci. · 2012 · 5 · 629010.1039/C1EE02540F ↗
19. Yanagida S. · Acc. Chem. Res. · 2009 · 42 · 182710.1021/ar900069p ↗
20. Kuang D. · Small · 2007 · 3 · 209410.1002/smll.200700211 ↗
21. Cao Y. · J. Phys. Chem. C · 2008 · 112 · 1377510.1021/jp805027v ↗
22. Wang P. · J. Am. Chem. Soc. · 2003 · 125 · 116610.1021/ja029294+ ↗
23. Ogihara W. · Polym. J. · 2006 · 38 · 11710.1295/polymj.38.117 ↗
24. Kanzaki T. · Photochem. Photobiol. Sci. · 2006 · 5 · 38910.1039/b517588g ↗
25. Quezada C. · J. Org. Chem. · 2003 · 671 · 18310.1016/S0022-328X(03)00100-1 ↗
26. Tai Q. · ACS Nano · 2011 · 5 · 379510.1021/nn200133g ↗
27. Imoto K. · Sol. Energy Mater. Sol. Cells · 2003 · 79 · 45910.1016/S0927-0248(03)00021-7 ↗
28. Roy-Mayhew J. · ACS Nano · 2011 · 5 · 16510.1021/nn102353h ↗
29. Lee W. J. · ACS Appl. Mater. Inter. · 2009 · 1 · 114510.1021/am800249k ↗
30. Joshi P. · ACS Appl. Mater. Inter. · 2010 · 2 · 357210.1021/am100742s ↗
31. Mei X. · Nanotechnology · 2010 · 21 · 39520210.1088/0957-4484/21/39/395202 ↗
32. Li G. · Angew. Chem., Int. Ed. · 2010 · 49 · 365310.1002/anie.201000659 ↗
33. Adachi M. · J. Phys. Chem. B · 2006 · 110 · 1387210.1021/jp061693u ↗
34. Bisquert J. · J. Am. Chem. Soc. · 2004 · 126 · 1355010.1021/ja047311k ↗
35. Liu Y. · Nanoscale · 2012 · 4 · 686310.1039/c2nr31954c ↗
36. Zaban A. · ChemPhysChem · 2003 · 4 · 85910.1002/cphc.200200615 ↗
37. Kuang D. · Adv. Mater. · 2007 · 19 · 113310.1002/adma.200602172 ↗