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High Performance Photovoltaic Applications Using Solution-Processed Small Molecules
Abstract
Energy remains a critical issue for the survival and prosperity of humancivilization. Many experts believe that the eventual solution for sustainable energy is the use of direct solar energy as the main energy source. Among the options for renewable energy, photovoltaic technologies that harness solar energy offer a way to harness an unlimited resource and minimum environment impact in contrast with other alternatives such as water, nuclear, and wind energy. Currently, almost all commercial photovoltaic technologies use Si-based technology, which has a number of disadvantages including high cost, lack of flexibility, and the serious environmental impact of the Si industry. Other technologies, such as organic photovoltaic (OPV) cells, can overcome some of these issues. Today, polymer-based OPV (P-OPV) devices have achieved power conversion efficiencies (PCEs) that exceed 9%. Compared with P-OPV, small molecules based OPV (SM-OPV) offers further advantages, including a defined structure for more reproducible performance, higher mobility and open circuit voltage, and easier synthetic control that leads to more diversified structures. Therefore, while largely undeveloped, SM-OPV is an important emerging technology with performance comparable to P-OPV. In this Account, we summarize our recent results on solution-processed SM-OPV. We believe that solution processing is essential for taking full advantage of OPV technologies. Our work started with the synthesis of oligothiophene derivatives with an acceptor-donor-acceptor (A-D-A) structure. Both the backbone conjugation length and electron withdrawing terminal groups play an important role in the light absorption, energy levels and performance of the devices. Among those molecules, devices using a 7-thiophene-unit backbone and a 3-ethylrhodanine (RD) terminal unit produced a 6.1% PCE. With the optimized conjugation length and terminal unit, we borrowed from the results with P-OPV devices to optimize the backbone. Thus we selected BDT (benzo[1,2-b:4,5-b']dithiophene) and DTS (dithienosilole) to replace the central thiophene unit, leading to a PCE of 8.12%. In addition to our molecules, Bazan and co-workers have developed another excellent system using DTS as the core unit that has also achieved a PCE greater than 8%.
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Citations
Cites
Small molecule semiconductors for high-efficiency organic photovoltaics
Lin, Y., Li, Y., & Zhan, X. (2012) · Chemical Society Reviews · doi:10.1039/c2cs15313k · Cited by 1,751
Cited by
Ye, L., Zhang, S., Huo, L., Zhang, M., & Hou, J. (2014) · Accounts of Chemical Research · doi:10.1021/ar5000743 · Cited by 699
Oligomer Molecules for Efficient Organic Photovoltaics
Lin, Y., & Zhan, X. (2016) · Accounts of Chemical Research · doi:10.1021/acs.accounts.5b00363 · Cited by 601
Kan, B., Feng, H., Wan, X., Liu, F., Ke, X., Wang, Y., Wang, Y., Zhang, H., Li, C., Hou, J., et al. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b01170 · Cited by 474
Self-citationSmall is Powerful: Recent Progress in Solution‐Processed Small Molecule Solar Cells
Collins, S. D., Ran, N. A., Heiber, M. C., & Nguyen, T. (2017) · Advanced Energy Materials · doi:10.1002/aenm.201602242 · Cited by 414
Porphyrin‐Based Bulk Heterojunction Organic Photovoltaics: The Rise of the Colors of Life
Kesters, J., Verstappen, P., Kelchtermans, M., Lutsen, L., Vanderzande, D., & Maes, W. (2015) · Advanced Energy Materials · doi:10.1002/aenm.201500218 · Cited by 193
Metadata
- Authors
- Chen, Y., Wan, X., & Long, G.
- Venue
- Accounts of Chemical Research
- Publisher
- American Chemical Society (ACS)
- Published
- 2013-07-31
- Volume
- 46
- Issue
- 11
- Pages
- 2645-2655
- ISSN
- 0001-4842 (ISSN-L)
- 1520-4898
- OpenAlex
- W2335025690
- Cited by
- 667
- References
- 1
- FWCI
- 58.51
- Type
- journal article
- Language
- en
- Open access
- closed
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