Efficient Copper Mediators Based on Bulky Asymmetric Phenanthrolines for DSSCs
Source abstract
Abstract
In the context of the development of new electron mediators for dye-sensitized solar cells that could efficiently substitute the more common I3(-)/I(-) redox couple, we have prepared a series of Cu(I)- phenanthroline complexes through an easy synthetic route. The novel [Cu(2-mesityl-4,7-dimethyl-1,10-phenanthroline)2]PF6 (3) is of particular interest because the presence of the bulky mesityl groups protects as a kiss lock the Cu center, leading to superior dye regeneration kinetics with respect to simpler phenanthroline-based Cu(I) complexes and to a lower dark current with respect the I3(-)/I(-). The exploitation of a dual-component electrolyte constituted by (3) and a Fe(II) comediator, in combination with the [Ru(4,4'-dicarboxy-2,2'-bipyridine)2(4,4'-dinonyl-2,2'-bipyridine)](PF6)2 sensitizer, allowed us to increase the performance of the cell, reaching Jsc values of 4.0 mA cm(-2), comparable to that recorded with I3(-)/I(-) (3.8 mA cm(-2)).
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Polyoxometalates: Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Dipartimento di Chimica, Università degli Studi di Milano, UdR dell’INSTM, Via Golgi 19, Milano 20133 Italy
Dipartimento di Scienze Chimiche e Farmaceutiche, Università degli Studi di Ferrara, Via Fossato di Mortara 17, Ferrara 44121, Italy
Funding
Ministero dell'Istruzione, dell'Università e della Ricerca
References (47)
Show source-provided references
1. O’Regan B. · Nature · 1991 · 353 · 73710.1038/353737a0 ↗
2. Graetzel M. · Nature · 2001 · 414 · 33810.1038/35104607 ↗
3. Bredas J.-L. · Acc. Chem. Res. · 2009 · 42 · 168910.1021/ar900238j ↗
4. Nozik A. J. · Chem. Rev. · 2010 · 110 · 644310.1021/cr1003419 ↗
5. Wong W. Y. · Acc. Chem. Res. · 2010 · 43 · 124610.1021/ar1000378 ↗
6. Hagfeldt A. · Chem. Rev. · 2010 · 110 · 659510.1021/cr900356p ↗
7. Snaith H. J. · Adv. Funct. Mater. · 2010 · 20 · 1310.1002/adfm.200901476 ↗
8. Nazeeruddin M. K. · Sol. Energy · 2011 · 85 · 117210.1016/j.solener.2011.01.018 ↗
9. Bignozzi C. A. · Coord. Chem. Rev. · 2013 · 257 · 147210.1016/j.ccr.2012.09.008 ↗
10. Yella A. · Science · 2011 · 334 · 62910.1126/science.1209688 ↗
11. Colombo A. · Inorg. Chim. Acta · 2013 · 407 · 20410.1016/j.ica.2013.07.028 ↗
12. Bozic-Weber B. · Dalton Trans. · 2012 · 41 · 1415710.1039/c2dt31159c ↗
13. Bozic-Weber B. · Phys. Chem. Chem. Phys. · 2013 · 15 · 450010.1039/c3cp50562f ↗
14. Hewat T. E. · Dalton Trans. · 2014 · 43 · 412710.1039/C3DT53334D ↗
15. Bozic-Weber B. · Dalton Trans. · 2013 · 42 · 1229310.1039/c3dt51416a ↗
16. Hattori S. · J. Am. Chem. Soc. · 2005 · 127 · 964810.1021/ja0506814 ↗
17. Bai Y. · Chem. Commun. · 2011 · 47 · 437610.1039/c1cc10454c ↗
18. Gray, H. B.; Solomon, E. I.Copper Proteins;Spiro, T. G., Ed.Wiley:New York, 1981; pp1–39;
19. Sykes A. G. · Adv. Inorg. Chem. · 1991 · 36 · 37710.1016/S0898-8838(08)60044-6 ↗
20. Adman E. T. · Adv. Protein Chem. · 1991 · 42 · 14510.1016/S0065-3233(08)60536-7 ↗
21. Gross E. L. · Photosynth. Res. · 1993 · 37 · 10310.1007/BF02187469 ↗
22. Rorabacher D. B. · Chem. Rev. · 2004 · 104 · 65110.1021/cr020630e ↗
23. Ruthkosky M. · Inorg. Chem. · 1996 · 35 · 640610.1021/ic960503z ↗
24. Wang P. · Nat. Mater. · 2003 · 2 · 40210.1038/nmat904 ↗
25. Gritzner G. · Pure Appl. Chem. · 1984 · 56 · 46110.1351/pac198456040461 ↗
26. Mba M. · J. Phys. Chem. C · 2013 · 117 · 1988510.1021/jp4067586 ↗
27. Kubas G. J. · Inorg. Synth. · 1979 · 19 · 9010.1002/9780470132500.ch18 ↗
28. Jakobsen S. · Tetrahedron Lett. · 2011 · 52 · 307210.1016/j.tetlet.2011.04.006 ↗
29. 2000
30. Altomare A. · J. Appl. Crystallogr. · 1999 · 32 · 11510.1107/S0021889898007717 ↗
31. Sheldrick G. M. · Acta Crystallogr., Sect. A · 2008 · 64 · 11210.1107/S0108767307043930 ↗
32. Ferrugia L. J. · J. Appl. Crystallogr. · 1999 · 32 · 83710.1107/S0021889899006020 ↗
33. Nazeeruddin M. K. · J. Am. Chem. Soc. · 1993 · 115 · 638210.1021/ja00067a063 ↗
34. Bard A. J. · 2001
35. 10.1016/j.electacta.2014.07.08610.1016/j.electacta.2014.07.086 ↗
36. Everly R. M. · J. Phys. Chem. · 1991 · 95 · 907110.1021/j100176a011 ↗
37. Koumura N. · J. Am. Chem. Soc. · 2006 · 128 · 1425610.1021/ja0645640 ↗
38. Boaretto, R.; Busatto, E.; Carli, S.; Fracasso, S.; Caramori, S.; Bignozzi, C. A.Process for the Synthesis of Precursor Complexes of Titanium Dioxide Sensitization Dyes Based on Ruthenium Polypyridine Complexes. PCT Intl. Appl. WO 2012073268 A1, 2012.
39. Cazzanti S. · J. Am. Chem. Soc. · 2006 · 128 · 999610.1021/ja062087f ↗
40. Martineau D. · Inorg. Chem. · 2007 · 46 · 227210.1021/ic062042f ↗
41. Grabulosa A. · Inorg. Chem. · 2009 · 48 · 803010.1021/ic9009256 ↗
42. Caramori S. · Chem.—Eur. J. · 2010 · 16 · 261110.1002/chem.200902761 ↗
43. Boschloo G. · J. Phys. Chem. B · 2006 · 110 · 1314410.1021/jp0619641 ↗
44. Kusama H. · Sol. Energy Mater. Sol. Cells · 2003 · 80 · 16710.1016/j.solmat.2003.08.001 ↗
45. Abbotto A. · Dalton Trans. · 2012 · 41 · 1173110.1039/c2dt31551c ↗
46. Dragonetti C. · Inorg. Chim. Acta · 2013 · 405 · 9810.1016/j.ica.2013.05.006 ↗
47. Dragonetti C. · Inorg. Chem. · 2013 · 52 · 1072310.1021/ic401794g ↗