journal article·2017-11-01

Structurally Simple and Easily Accessible Perylenes for Dye-Sensitized Solar Cells Applicable to Both 1 Sun and Dim-Light Environments

Hsien-Hsin Chou, Yu-Chieh Liu, Guanjie Fang, Qiao-Kai Cao, Tzu-Chien Wei, Chen-Yu Yeh

Publisher page

Abstract

The need for low-cost and highly efficient dyes for dye-sensitized solar cells under both the sunlight and dim light environments is growing. We have devised GJ -series push–pull organic dyes which require only four synthesis steps. These dyes feature a linear molecular structure of donor–perylene–ethynylene–arylcarboxylic acid, where donor represents N, N -diarylamino group and arylcarboxylic groups represent benzoic, thienocarboxylic, 2-cyano-3-phenylacrylic, 2-cyano-3-thienoacrylic, and 4-benzo[ c ][1,2,5]thiadiazol-4-yl-benzoic groups. In this study, we demonstrated that a dye without tedious and time-consuming synthesis efforts can perform efficiently. Under the illumination of AM1.5G simulated sunlight, the benzothiadiazole-benzoic-containing GJ-BP dye shows the best power conversion efficiency (PCE) of 6.16% with V OC of 0.70 V and J SC of 11.88 mA cm –2 using liquid iodide-based electrolyte. It also shows high performance in converting light of 6000 lx light intensity, that is, incident power of ca. 1.75 mW cm –2, to power output of 0.28 mW cm –2 which equals a PCE of 15.79%. Interestingly, the benzoic-containing dye GJ-P with a simple molecular structure has comparable performance in generating power output of 0.26 mW cm –2 (PCE of 15.01%) under the same condition and is potentially viable toward future application.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Transition Metal Oxide Nanomaterials

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

Affiliations

Department of Chemistry and Research Center for Sustainable Energy & Nanotechnology, National Chung Hsing University, Taichung 402, Taiwan

Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300, Taiwan

Funding

Ministry of Science and Technology, Taiwan

References (70)

Show source-provided references
1. 10.1021/cr900356p10.1021/cr900356p ↗
2. 10.1021/ar980112j10.1021/ar980112j ↗
3. 10.1039/C4EE01724B10.1039/C4EE01724B ↗
4. 10.1002/aenm.20170003210.1002/aenm.201700032 ↗
5. 10.1039/C6TA04097G10.1039/C6TA04097G ↗
6. 10.1021/acs.jpcc.5b0810110.1021/acs.jpcc.5b08101 ↗
7. 10.1002/adfm.20150344810.1002/adfm.201503448 ↗
8. 10.1038/nphoton.2017.6010.1038/nphoton.2017.60 ↗
9. 10.1016/j.ccr.2010.11.00610.1016/j.ccr.2010.11.006 ↗
10. 10.1038/353737a010.1038/353737a0 ↗
11. 10.1039/c2jm34289h10.1039/c2jm34289h ↗
12. 10.1002/anie.20151150610.1002/anie.201511506 ↗
13. 10.1039/C4DT02756F10.1039/C4DT02756F ↗
14. 10.1021/cr500196410.1021/cr5001964 ↗
15. 10.1021/ar900034t10.1021/ar900034t ↗
16. 10.1016/j.ccr.2004.01.00710.1016/j.ccr.2004.01.007 ↗
17. 10.1039/C2CS35257E10.1039/C2CS35257E ↗
18. 10.1039/c2jm30362k10.1039/c2jm30362k ↗
19. 10.1039/C4RA16493H10.1039/C4RA16493H ↗
20. 10.1039/C2CS35346F10.1039/C2CS35346F ↗
21. 10.1039/c3cs35372a10.1039/c3cs35372a ↗
22. 10.1021/ol902327p10.1021/ol902327p ↗
23. 10.1021/jacs.5b0153710.1021/jacs.5b01537 ↗
24. 10.1002/anie.20150119510.1002/anie.201501195 ↗
25. 10.1039/C4EE03934C10.1039/C4EE03934C ↗
26. 10.1039/C5EE02822A10.1039/C5EE02822A ↗
27. 10.1021/acs.jpclett.6b0114910.1021/acs.jpclett.6b01149 ↗
28. 10.1002/anie.20090253210.1002/anie.200902532 ↗
29. 10.1039/C3TC32315C10.1039/C3TC32315C ↗
30. 10.1002/chem.20120119610.1002/chem.201201196 ↗
31. 10.1002/asia.20100089510.1002/asia.201000895 ↗
32. 10.1039/c1jm10993f10.1039/c1jm10993f ↗
33. 10.1021/jp906409q10.1021/jp906409q ↗
34. 10.1021/ol070556s10.1021/ol070556s ↗
35. 10.1021/jp970683d10.1021/jp970683d ↗
36. 10.1021/ol201303h10.1021/ol201303h ↗
37. 10.1002/jccs.20100016310.1002/jccs.201000163 ↗
38. 10.1021/ja409291g10.1021/ja409291g ↗
39. 10.1021/jp511687e10.1021/jp511687e ↗
40. 10.1021/am507261j10.1021/am507261j ↗
41. 10.1021/ph500134610.1021/ph5001346 ↗
42. 10.1002/aenm.20140024410.1002/aenm.201400244 ↗
43. 10.1039/C5TA09136E10.1039/C5TA09136E ↗
44. 10.1039/C6TA10506H10.1039/C6TA10506H ↗
45. 10.1021/acsami.6b0207510.1021/acsami.6b02075 ↗
46. 10.1039/C5EE03309H10.1039/C5EE03309H ↗
47. 10.1021/jo801262210.1021/jo8012622 ↗
48. 10.1021/ja027355y10.1021/ja027355y ↗
49. 10.1021/cr400675m10.1021/cr400675m ↗
50. 10.1126/science.120968810.1126/science.1209688 ↗
51. 10.1002/anie.20130934310.1002/anie.201309343 ↗
52. 10.1038/nchem.186110.1038/nchem.1861 ↗
53. 10.1021/ja207367t10.1021/ja207367t ↗
54. 10.1039/c3cc44555k10.1039/c3cc44555k ↗
55. 10.1002/anie.20130007010.1002/anie.201300070 ↗
56. 10.1039/C4RA07304E10.1039/C4RA07304E ↗
57. 10.1002/chem.20160218810.1002/chem.201602188 ↗
58. 10.1021/ja960830610.1021/ja9608306 ↗
59. 10.1021/ja960937t10.1021/ja960937t ↗
60. 10.1016/S0040-4039(00)91094-310.1016/S0040-4039(00)91094-3 ↗
61. Smith, M. B.; March, J.March’s Advanced Organic Chemistry Reactions, Mechanisms, and Structure,6th ed.John Wiley & Sons, Inc.:Hoboken, NJ, 2007; p2374.10.1002/0470084960 ↗
62. 10.1021/acs.jpcc.6b0855310.1021/acs.jpcc.6b08553 ↗
63. 10.1002/advs.20170009910.1002/advs.201700099 ↗
64. 10.1021/jp808275z10.1021/jp808275z ↗
65. 10.1002/adma.20120137210.1002/adma.201201372 ↗
66. Bisquert J. · 2010 · 457
67. 10.1021/ja076525+10.1021/ja076525+ ↗
68. 10.1021/ma501894w10.1021/ma501894w ↗
69. 10.1016/j.cap.2009.11.06410.1016/j.cap.2009.11.064 ↗
70. 10.1063/1.218606910.1063/1.2186069 ↗