Synthesis of heteroleptic Ru(II) complexes ligated with 1,3-dihydro-1,1,3,3-tetramethyl-7,8-diazacyclopenta[1]phenanthren-2-one and application in dye-sensitized solar cells
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Abstract
Abstract Four heteroleptic ruthenium(II) complexes, HJ1–HJ4 [Ru(L)(DTDP)(NCS)2][TBA], (where DTDP = 1,3-dihydro-1,1,3,3-tetramethyl-7,8-diazacyclopenta[1]phenanthren-2-one, L = 4,4′-dicarboxy-2,2′-bipyridine (dcbpy, HJ1), 4,4′-bis(E-carboxyvinyl)-2,2′-bipyridine (dcvbpy, HJ2), 4,7-dicarboxy-1,10-phenanthroline (dcphen, HJ3), or 4,7-bis(E-carboxyvinyl)-1,10-phenanthroline (dcvphen, HJ4)), were synthesized from one-pot reaction of [RuCl2(p-cymene)]2 and DTDP ligand followed by addition of the second ligand (L = dcbpy, dcvbpy, dcphen, or dcvphen). Final products were obtained as tetrabutylammonium salt form of ruthenium(II) complexes with reasonable yields. We demonstrated that a dye-sensitized solar cell (DSSC) fabricated with HJ1 dye exhibited a conversion efficiency (η) of 2.8%, which is close to that of standard N719 dye, while other cells fabricated with HJ2–HJ4 dye had conversion efficiencies (η) of between 1.2 and 2.0%.
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OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Polyoxometalates: Synthesis and Applications
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References (27)
Show source-provided references
1. Chopra · Prog. Photovoltaics: Res. Appl. · 2004 · 12 · 6910.1002/pip.541 ↗
2. Polo · Coord. Chem. Rev. · 2004 · 248 · 134310.1016/j.ccr.2004.04.013 ↗
3. Hagfeldt · Chem. Rev. · 2010 · 110 · 659510.1021/cr900356p ↗
4. Guo · Dyes Pigm. · 2012 · 92 · 106210.1016/j.dyepig.2011.07.007 ↗
5. Balzani · Chem. Rev. · 1996 · 96 · 75910.1021/cr941154y ↗
6. Williams · Chem. Soc. Rev. · 2009 · 38 · 178310.1039/b804434c ↗
7. Vougioukalakis · Coord. Chem. Rev. · 2011 · 255 · 260210.1016/j.ccr.2010.11.006 ↗
8. O’Regan · Nature · 1991 · 353 · 73710.1038/353737a0 ↗
9. Nazeeruddin · J. Am. Chem. Soc. · 1993 · 115 · 638210.1021/ja00067a063 ↗
10. Nazeeruddin · Inorg. Chem. · 1999 · 38 · 629810.1021/ic990916a ↗
11. Wang · J. Am. Chem. Soc. · 2005 · 127 · 80810.1021/ja0436190 ↗
12. Ocakoglu · Dyes Pigm. · 2007 · 75 · 38510.1016/j.dyepig.2006.06.016 ↗
13. Wang · Nat. Mater. · 2003 · 2 · 40210.1038/nmat904 ↗
14. Mishra · Adv. Funct. Mater. · 2011 · 21 · 96310.1002/adfm.201001863 ↗
15. Han · Inorg. Chem. · 2011 · 50 · 327110.1021/ic101909e ↗
16. Hussain · Phys. Chem. Chem. Phys. · 2013 · 15 · 840110.1039/c3cp51260f ↗
17. Huang · J. Phys. Chem. C · 2013 · 117 · 205910.1021/jp3118693 ↗
18. Ocakoglu · Synth. Met. · 2013 · 174 · 2410.1016/j.synthmet.2013.04.016 ↗
19. Tak · Monatsh. Chem. · 2014 · 145 · 110110.1007/s00706-014-1175-z ↗
20. Kim · Talanta · 2004 · 62 · 59510.1016/j.talanta.2003.09.001 ↗
21. Lee · J. Organomet. Chem. · 2005 · 690 · 200210.1016/j.jorganchem.2004.11.048 ↗
22. Lee · Bull. Korean Chem. Soc. · 2006 · 27 · 9910.5012/bkcs.2006.27.1.099 ↗
23. Garelli · J. Organic Chem. · 1992 · 57 · 304610.1021/jo00037a019 ↗
24. Yanagida · J. Chem. Soc., Dalton Trans. · 2000 · 281710.1039/b002391o ↗
25. Bellusci · Inorg. Chem. · 2005 · 44 · 181810.1021/ic048951r ↗
26. Klein · Inorg. Chem. · 2005 · 44 · 17810.1021/ic048810p ↗
27. Bernhard · Synthesis · 1996 · 1996 · 19210.1055/s-1996-4183 ↗