journal article·2020-01-15

Efficient PbSe Colloidal Quantum Dot Solar Cells Using SnO2 as a Buffer Layer

Menghua Zhu, Xinxing Liu, Sisi Liu, Chao Chen, Jungang He, Weiwei Liu, Ji Yang, Liang Gao, Guangda Niu, Jiang Tang, Jianbing Zhang

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Abstract

PbSe colloidal quantum dots (CQDs) are widely used in solar cells because of their tunable band gap, solution processability, and efficient multiple exciton generation effect. The most efficient PbSe CQD solar cells use high-temperature-processed ZnO as the electron transport layer (ETL), limiting their applications in flexible photovoltaics. Currently, low-temperature solution-processed SnO2 has been demonstrated as an efficient ETL for high-efficient PbS CQD and perovskite solar cells because of less parasitic light absorption and higher electron mobility. Herein, we introduce low-temperature solution-processed SnO2 as ETL for PbSe CQD solar cells, and fabricate the PbSe CQD absorber layer with a one-step spin-coating method. The champion device with the structure of FTO (SnO2:F)/SnO2/PbSe–PbI2/PbS–EDT (1,2-ethanedithiol)/Au achieves a high open-circuit voltage of 577.1 mV, a short-circuit current density of 24.87 mA cm–2, a fill factor of 67%, and an impressive power conversion efficiency of 9.67%. Our results pave the way for the development of low-temperature flexible PbSe CQD solar cells.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Perovskite Materials and Applications · Chalcogenide Semiconductor Thin Films

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

Affiliations

School of Materials Science and Engineering, Wuhan Institute of Technology, Wuhan 430205, Hubei, P.R. China

Funding

China Postdoctoral Science Foundation · Ministry of Human Resources and Social Security · National Natural Science Foundation of China · Wuhan National Laboratory for Optoelectronics

References (34)

Show source-provided references
1. 10.1021/acs.chemrev.5b0006310.1021/acs.chemrev.5b00063 ↗
2. 10.1021/ar300195810.1021/ar3001958 ↗
3. 10.1021/cr400299t10.1021/cr400299t ↗
4. 10.1038/nnano.2011.4610.1038/nnano.2011.46 ↗
5. 10.1038/nature0485510.1038/nature04855 ↗
6. 10.1039/c3mh00097d10.1039/c3mh00097d ↗
7. 10.1038/nphoton.2011.17110.1038/nphoton.2011.171 ↗
8. 10.1364/oe.14.00327310.1364/oe.14.003273 ↗
9. 10.1002/adma.20130436610.1002/adma.201304366 ↗
10. 10.1038/nmat398410.1038/nmat3984 ↗
11. 10.1038/srep0994510.1038/srep09945 ↗
12. 10.1039/c4ta04272g10.1039/c4ta04272g ↗
13. 10.1007/s12200-012-0285-710.1007/s12200-012-0285-7 ↗
14. 10.1002/adma.20170321410.1002/adma.201703214 ↗
15. 10.1038/nphoton.2011.12310.1038/nphoton.2011.123 ↗
16. 10.1021/acsphotonics.7b0004510.1021/acsphotonics.7b00045 ↗
17. 10.1039/c6cp03790a10.1039/c6cp03790a ↗
18. 10.1515/nanoph-2017-003410.1515/nanoph-2017-0034 ↗
19. 10.1002/adma.20190059310.1002/adma.201900593 ↗
20. 10.1039/c7ta05366e10.1039/c7ta05366e ↗
21. 10.1038/nenergy.2016.17710.1038/nenergy.2016.177 ↗
22. 10.1002/adfm.20170627610.1002/adfm.201706276 ↗
23. 10.1021/jacs.5b0199410.1021/jacs.5b01994 ↗
24. 10.1038/nmat400710.1038/nmat4007 ↗
25. 10.1039/c8tc03599g10.1039/c8tc03599g ↗
26. 10.1016/j.nanoen.2019.10392210.1016/j.nanoen.2019.103922 ↗
27. 10.1021/acsami.8b1566510.1021/acsami.8b15665 ↗
28. 10.1021/nl503085v10.1021/nl503085v ↗
29. 10.1007/s12274-013-0341-710.1007/s12274-013-0341-7 ↗
30. 10.1021/nn405236k10.1021/nn405236k ↗
31. 10.1021/nn900863a10.1021/nn900863a ↗
32. 10.1002/adma.20160575610.1002/adma.201605756 ↗
33. 10.1038/s41565-018-0117-z10.1038/s41565-018-0117-z ↗
34. 10.1021/nl903809r10.1021/nl903809r ↗