TiO2-Assisted Photoisomerization of Azo Dyes Using Self-Assembled Monolayers: Case Study on para-Methyl Red Towards Solar-Cell Applications
Source abstract
Abstract
The optical and electronic properties of a TiO2 nanoparticle-assisted photo-isomerizable surface, prepared by an azo dye/TiO2 nanocomposite film, are examined experimentally and computationally. The azo dye, para-methyl red, undergoes photoisomerization at room temperature, catalyzed by the TiO2 nanoparticle supports, while it exhibits negligible photoisomerization in solvents under otherwise identical conditions. Density functional theory and time-dependent density functional theory are employed to explain the origin of this photoisomerization in these dye···TiO2 nanoparticle self-assembled monolayers (SAMs). The device performance of these SAMs when embedded into dye-sensitized solar cells is used to further elucidate the nature of this azo dye photoisomerization and relate it to the ensuing optoelectronic properties.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Quantum Dots Synthesis And Properties · Photochromic and Fluorescence Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Cavendish Laboratory, University of Cambridge, J. J. Thomson Avenue, Cambridge, CB3 0HE, United Kingdom
Argonne National Laboratory, 9700 S Cass Avenue, Argonne, Illinois 60439, United States
References (44)
Show source-provided references
1. Klajn R. · Chem. Soc. Rev. · 2010 · 39 · 220310.1039/b920377j ↗
2. Han M. · Chem. Commun. · 2010 · 46 · 359810.1039/b921801g ↗
3. Kubitschke J. · Eur. J. Org. Chem. · 2010 · 2010 · 504110.1002/ejoc.201000650 ↗
4. Natansohn A. · Chem. Rev. · 2002 · 102 · 413910.1021/cr970155y ↗
5. Browne W. R. · Annu. Rev. Phys. Chem. · 2009 · 60 · 40710.1146/annurev.physchem.040808.090423 ↗
6. Bandara H. M. D. · Chem. Soc. Rev. · 2012 · 41 · 180910.1039/C1CS15179G ↗
7. Zhang J. · Chem. Mater. · 2001 · 13 · 232310.1021/cm000752s ↗
8. Comstock M. · Phys. Rev. Lett. · 2007 · 99 · 03830110.1103/PhysRevLett.99.038301 ↗
9. Jung U. · Langmuir · 2011 · 27 · 589910.1021/la104654p ↗
10. Morgenstern K. · Acc. Chem. Res. · 2009 · 42 · 21310.1021/ar800021q ↗
11. Saha S. · Chem. Soc. Rev. · 2007 · 36 · 7710.1039/B607187B ↗
12. Zhang H. · Erviron. Sci. Technol. · 2010 · 44 · 110710.1021/es9029123 ↗
13. O’Regan B. · Nature · 1991 · 353 · 73710.1038/353737a0 ↗
14. Hardin B. E. · Nat. Photonics · 2012 · 6 · 16210.1038/nphoton.2012.22 ↗
15. Grätzel M. · Nature · 2001 · 414 · 33810.1038/35104607 ↗
16. Kim S. · J. Am. Chem. Soc. · 2006 · 128 · 1670110.1021/ja066376f ↗
17. Nazeeruddin M. K. · J. Am. Chem. Soc. · 2005 · 127 · 1683510.1021/ja052467l ↗
18. Zhang L. · ACS Sustain. Chem. Eng. · 2013 · 1 · 144010.1021/sc400183t ↗
19. El-Zohry A. · J. Phys. Chem. C · 2012 · 116 · 2614410.1021/jp306636w ↗
20. Galoppini E. · Coord. Chem. Rev. · 2004 · 248 · 128310.1016/j.ccr.2004.03.016 ↗
21. Brewster T. P. · Inorg. Chem. · 2013 · 52 · 675210.1021/ic4010856 ↗
22. Ooyama Y. · Angew. Chem. Int. Ed. · 2011 · 123 · 756710.1002/ange.201102552 ↗
23. Mao J. · Angew. Chem., Int. Ed. · 2012 · 51 · 987310.1002/anie.201204948 ↗
24. Long B. · J. Am. Chem. Soc. · 2003 · 125 · 1549010.1021/ja037592g ↗
25. Yabe A. · Thin Solid Films · 1988 · 160 · 3310.1016/0040-6090(88)90044-2 ↗
26. Niino H. · Chem. Lett. · 1988 · 122710.1246/cl.1988.1227 ↗
27. Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G. A.; Nakatsuji, H.; Caricato, M.; Li, X.; Hratchian, H. P.; Izmaylov, A. F.; Bloino, J.; Zheng, G.; Sonnenb, D. J.Gaussian 09, Revision B 01 2009.
28. Becke A. D. · J. Chem. Phys. · 1993 · 7 · 564810.1063/1.464913 ↗
29. Gordon M. S. · J. Am. Chem. Soc. · 1982 · 104 · 279710.1021/ja00374a017 ↗
30. Rassolov V. A. · J. Comput. Chem. · 2001 · 22 · 97610.1002/jcc.1058 ↗
31. Sánchez-de-Armas R. · Phys. Chem. Chem. Phys. · 2012 · 14 · 22510.1039/C1CP22058F ↗
32. Sánchez-de-Armas R. · J. Chem. Theory Comput. · 2010 · 6 · 285610.1021/ct100289t ↗
33. Hagfeldt A. · Chem. Rev. · 2010 · 110 · 659510.1021/cr900356p ↗
34. Dennington, R.; Keith, T.; Millam, J.GaussView;Gaussian:Wallingford, CT, 2009.
35. Tiago M. L. · J. Chem. Phys. · 2005 · 122 · 09431110.1063/1.1861873 ↗
36. Ida A. · Phys. Chem. Chem. Phys. · 2011 · 13 · 2031810.1039/c1cp22095k ↗
37. Wen J. · J. Phys. Chem. C · 2013 · 117 · 1993410.1021/jp404434r ↗
38. Miertuš S. · Chem. Phys. · 1981 · 55 · 11710.1016/0301-0104(81)85090-2 ↗
39. Tao T. · Dyes Pigm. · 2012 · 92 · 91610.1016/j.dyepig.2011.09.008 ↗
40. Clifford J. N. · J. Am. Chem. Soc. · 2004 · 126 · 522510.1021/ja039924n ↗
41. Wu Y. · Energy Environ. Sci. · 2012 · 5 · 826110.1039/c2ee22108j ↗
42. Kalyanasundaram, K.Dye-Sensitized Solar Cells;EPFL Press:Lausanne, Switzerland, 2010; p19.10.1201/b16409 ↗
43. Hara K. · Adv. Funct. Mater. · 2005 · 15 · 24610.1002/adfm.200400272 ↗
44. Lin Y.-D. · J. Mater. Chem. · 2011 · 21 · 1490710.1039/c1jm11623a ↗