journal article·2021-01-25

Molecular Engineering of Indoline Dyes and Their Application in Dye-Sensitized Solar Cells: Effect of Planarity and Side Chain on Interfacial Charge-Transfer Processes

Lu Tian, Yajun Wang, Yushuang Zhang, Xiaoyan Li, Wenjun Wu, Bo Liu

ACS Applied Energy Materials· Volume 4· Issue 1
Publisher page

Abstract

Interfacial charge-transfer is the critical process during the operation of dye-sensitized solar cells, determining the photovoltaic performance of the cell. Interfacial charge-transfer processes are affected by many factors, such as the energy level and side chain. According to our previous work, the planarization of the carbazole segment can significantly improve the interfacial charge-transfer performance. However, whether the planarization strategy is universally effective in various dye systems is still uncertain. Moreover, the planarization of the molecule also leads to unfavorable π-aggregation. Thus, herein, the planarization strategy is further applied on indoline dyes while the alkyl chain is also introduced to investigate the effect of the above two factors on interfacial charge-transfer processes. With the improvement of the planarity and the introduction of an alkyl chain, interfacial charge-transfer processes, including charge injection, dye regeneration, and charge recombination, are efficiently optimized, suggesting a certain universality of our planarization strategy. It is noteworthy that the overlong alkyl chain still negatively affects these processes. Accordingly, the improvement of donor planarity as well as the introduction of a suitable alkyl chain can finely optimize interfacial charge-transfer processes, providing a promising strategy for the development of an efficient organic sensitizer.
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Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Advanced Photocatalysis Techniques · Quantum Dots Synthesis And Properties

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

Affiliations

Hebei Key Laboratory of Organic Functional Molecules, College of Chemistry and Material Science, Hebei Normal University, No. 20, East Road of Nan Er Huan, Shijiazhuang 050023, P. R. China

Key Laboratory for Advanced Materials and Institute of Fine Chemicals, Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, P. R. China

Funding

Natural Science Foundation of Hebei Province · National Natural Science Foundation of China · Key Foundation of Science and Technology for Colleges and Universities in Hebei Province · Scientific Committee of Shanghai · Hebei Province

References (30)

Show source-provided references
1. 10.1021/acsami.5b0247510.1021/acsami.5b02475 ↗
2. 10.1021/acsaem.0c0021610.1021/acsaem.0c00216 ↗
3. 10.1039/C9EE04200H10.1039/C9EE04200H ↗
4. 10.1039/C8TA02281J10.1039/C8TA02281J ↗
5. 10.1021/acsami.5b0640410.1021/acsami.5b06404 ↗
6. 10.1016/j.dyepig.2017.06.06810.1016/j.dyepig.2017.06.068 ↗
7. 10.1021/acsenergylett.7b0043810.1021/acsenergylett.7b00438 ↗
8. 10.1021/acsomega.0c0125510.1021/acsomega.0c01255 ↗
9. 10.1002/aenm.20180240510.1002/aenm.201802405 ↗
10. 10.1021/jacs.9b0330210.1021/jacs.9b03302 ↗
11. 10.1016/j.cclet.2019.12.03810.1016/j.cclet.2019.12.038 ↗
12. 10.1021/jacs.7b1234810.1021/jacs.7b12348 ↗
13. 10.1016/j.dyepig.2018.08.03510.1016/j.dyepig.2018.08.035 ↗
14. 10.1038/s41560-020-0624-710.1038/s41560-020-0624-7 ↗
15. 10.1002/anie.20120494810.1002/anie.201204948 ↗
16. 10.1021/acsaem.7b0024410.1021/acsaem.7b00244 ↗
17. 10.1021/acsaem.0c0046410.1021/acsaem.0c00464 ↗
18. 10.3390/ma1309206510.3390/ma13092065 ↗
19. 10.1021/acs.jpcc.9b0398610.1021/acs.jpcc.9b03986 ↗
20. 10.1016/j.jphotochem.2019.03.04310.1016/j.jphotochem.2019.03.043 ↗
21. 10.1021/acsami.7b1206610.1021/acsami.7b12066 ↗
22. 10.1039/C9SC01577A10.1039/C9SC01577A ↗
23. 10.1002/anie.20170630810.1002/anie.201706308 ↗
24. 10.1002/adfm.20100180110.1002/adfm.201001801 ↗
25. 10.1021/am500575s10.1021/am500575s ↗
26. 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.; Sonnenberg, J. L.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Montgomery, J. A., Jr.; Peralta, J. J. E.; Ogliaro, F.; Bearpark, M.; Heyd, J. J.; Brothers, E.; Kudin, K. N.; Staroverov, V. N.; Kobayashi, R.; Normand, J.; Raghavachari, K.; Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Rega, N.; Millam, J. M.; Klene, M.; Knox, J. E.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Zakrzewski, V. G.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Dapprich, S.; Daniels, A. D.; Farkas, O.; Foresman, J. B.; Ortiz, J. V.; Cioslowski, J.; Fox, D. J. Gaussian 09, Revision B.01. Gaussian, Inc.: Wallingford CT, 2010.
27. 10.1016/j.jphotochem.2008.12.00610.1016/j.jphotochem.2008.12.006 ↗
28. 10.1021/jz200290c10.1021/jz200290c ↗
29. 10.1038/nchem.186110.1038/nchem.1861 ↗
30. 10.1021/acsami.6b1115210.1021/acsami.6b11152 ↗