journal article·2018-06-25

Tuning the Photovoltaic Performance of DSSCs by Appending Various Donor Groups on trans-Dimesityl Porphyrin Backbone

Ravi Kumar, Vediappan Sudhakar, Kamal Prakash, Kothandam Krishnamoorthy, Muniappan Sankar

ACS Applied Energy Materials· Volume 1· Issue 6
Publisher page

Abstract

Five cost-effective porphyrin based sensitizers with various donor groups (bisthiophene, N,N-dimethylaminophenyl, triphenylamine, carbazole and phenothiazine) and meso-dimesityl as auxiliary groups have been synthesized through the shortest possible synthetic route for the practical commercialization of these dyes. trans-A2BC porphyrin dyes show power conversion efficiencies (η) ranging from 5.3% to 7.11% under 1 sun illumination and highly depend on donor strength of appended moiety. Our molecular design incorporates trans-10,20-dimesityl groups, which prevents the π–π aggregation between the porphyrin units onto the TiO2 surface. The porphyrin dye (RA-200-Zn) bearing phenothiazine as donor unveils the highest photon-to-current conversion efficiency (PCE) of 7.1% and showed butterfly conformation, which can restrict the intermolecular aggregation. Further, this dye shows a broader absorption on TiO2 surface and significantly increased IPCE values in visible region as compared to the other dyes, which assured better light harvesting ability with high short-circuit current density (Jsc) of 14.2 mA cm–2.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Porphyrin and Phthalocyanine Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Indian Institute of Technology (IIT) Roorkee, Roorkee 247667, India

Polymers and Advanced Materials (PAM) Laboratory, CSIR-NCL, Pune 411008, India

Funding

Science and Engineering Research Board · Board of Research in Nuclear Sciences · Ministry of Human Resource Development

References (84)

Show source-provided references
1. 10.1038/353737a010.1038/353737a0 ↗
2. 10.1021/cr900356p10.1021/cr900356p ↗
3. 10.1021/ar900141y10.1021/ar900141y ↗
4. 10.1038/ncomms165510.1038/ncomms1655 ↗
5. 10.1002/aenm.20160211710.1002/aenm.201602117 ↗
6. 10.1021/ja052467l10.1021/ja052467l ↗
7. 10.1021/ja801942j10.1021/ja801942j ↗
8. 10.1021/nn900756s10.1021/nn900756s ↗
9. 10.1021/nn101384e10.1021/nn101384e ↗
10. 10.1039/c2ee03418b10.1039/c2ee03418b ↗
11. 10.1021/cm903698810.1021/cm9036988 ↗
12. 10.1021/acsami.5b0617010.1021/acsami.5b06170 ↗
13. 10.1002/ange.20080471910.1002/ange.200804719 ↗
14. 10.1039/c0jm03811c10.1039/c0jm03811c ↗
15. 10.1039/c2jm15928g10.1039/c2jm15928g ↗
16. 10.1002/chem.20140201010.1002/chem.201402010 ↗
17. 10.1021/ja048827710.1021/ja0488277 ↗
18. 10.1039/c3ta11242j10.1039/c3ta11242j ↗
19. 10.1002/ejoc.20120147910.1002/ejoc.201201479 ↗
20. 10.1039/c3tc32165g10.1039/c3tc32165g ↗
21. 10.1039/b905831a10.1039/b905831a ↗
22. 10.1021/jp503455m10.1021/jp503455m ↗
23. 10.1021/la404780810.1021/la4047808 ↗
24. 10.1021/ol500663b10.1021/ol500663b ↗
25. 10.1039/c1ee01141c10.1039/c1ee01141c ↗
26. 10.1039/b906596b10.1039/b906596b ↗
27. 10.1021/am405610b10.1021/am405610b ↗
28. 10.1021/am502239610.1021/am5022396 ↗
29. 10.1021/jp051855710.1021/jp0518557 ↗
30. 10.1002/adma.20060102010.1002/adma.200601020 ↗
31. 10.1016/j.dyepig.2012.02.01510.1016/j.dyepig.2012.02.015 ↗
32. 10.1021/ja803534u10.1021/ja803534u ↗
33. 10.1016/j.dyepig.2014.10.02610.1016/j.dyepig.2014.10.026 ↗
34. 10.1039/b918282a10.1039/b918282a ↗
35. 10.1002/chem.20130489710.1002/chem.201304897 ↗
36. 10.1039/C4CC07963A10.1039/C4CC07963A ↗
37. 10.1021/cm400800h10.1021/cm400800h ↗
38. 10.1038/srep0403310.1038/srep04033 ↗
39. 10.1021/ja203708k10.1021/ja203708k ↗
40. 10.1039/c2ee22108j10.1039/c2ee22108j ↗
41. 10.1039/C7CP00612H10.1039/C7CP00612H ↗
42. 10.1039/C4RA03088E10.1039/C4RA03088E ↗
43. 10.1016/j.dyepig.2015.11.00810.1016/j.dyepig.2015.11.008 ↗
44. 10.1039/C2CS35257E10.1039/C2CS35257E ↗
45. 10.1039/C4TA03435J10.1039/C4TA03435J ↗
46. 10.1016/j.dyepig.2017.07.05310.1016/j.dyepig.2017.07.053 ↗
47. 10.1039/C4DT02756F10.1039/C4DT02756F ↗
48. 10.1021/cr500196410.1021/cr5001964 ↗
49. 10.1021/ar900034t10.1021/ar900034t ↗
50. 10.1039/c2jm16804a10.1039/c2jm16804a ↗
51. 10.1039/c0cc02213f10.1039/c0cc02213f ↗
52. 10.1039/c3ee44168g10.1039/c3ee44168g ↗
53. 10.1126/science.120968810.1126/science.1209688 ↗
54. 10.1002/anie.20130934310.1002/anie.201309343 ↗
55. 10.1039/b926726c10.1039/b926726c ↗
56. 10.1038/nchem.186110.1038/nchem.1861 ↗
57. 10.1039/C3CC47985D10.1039/C3CC47985D ↗
58. 10.1021/am507503d10.1021/am507503d ↗
59. 10.1039/C5NJ02610E10.1039/C5NJ02610E ↗
60. 10.1039/c2cc33337f10.1039/c2cc33337f ↗
61. 10.1039/c0cc00257g10.1039/c0cc00257g ↗
62. 10.1039/c1cc12764k10.1039/c1cc12764k ↗
63. 10.1039/c2ee03308a10.1039/c2ee03308a ↗
64. 10.1039/c2cc31111a10.1039/c2cc31111a ↗
65. 10.1021/acsami.6b0380610.1021/acsami.6b03806 ↗
66. 10.1021/acsami.5b1062410.1021/acsami.5b10624 ↗
67. 10.1021/am301440710.1021/am3014407 ↗
68. 10.1039/C5RA26754D10.1039/C5RA26754D ↗
69. 10.1021/ol202351710.1021/ol2023517 ↗
70. 10.1021/jo982452o10.1021/jo982452o ↗
71. 10.1016/j.dyepig.2011.12.00610.1016/j.dyepig.2011.12.006 ↗
72. 10.1039/b809376h10.1039/b809376h ↗
73. 10.1021/bi00312a02310.1021/bi00312a023 ↗
74. 10.1021/ja800066y10.1021/ja800066y ↗
75. 10.1016/j.dyepig.2015.09.00110.1016/j.dyepig.2015.09.001 ↗
76. 10.1039/C5TC04418A10.1039/C5TC04418A ↗
77. 10.1039/C7TC03406G10.1039/C7TC03406G ↗
78. 10.1155/2014/83426910.1155/2014/834269 ↗
79. Barsoukov E. · 200510.1002/0471716243 ↗
80. 10.1063/1.169049510.1063/1.1690495 ↗
81. 10.1021/am500575s10.1021/am500575s ↗
82. 10.1039/c1jm12181b10.1039/c1jm12181b ↗
83. 10.1021/acsami.5b0769010.1021/acsami.5b07690 ↗
84. 10.1039/C6TC01269H10.1039/C6TC01269H ↗