Sn Perovskite Solar Cells via 2D/3D Bilayer Formation through a Sequential Vapor Process
Source abstract
Abstract
Sn-based perovskite solar cells are attracting great attention because of their potential for efficiency enhancement and their relative eco-friendliness compared with Pb-based perovskite solar cells. The main challenges lie in improving the oxidation stability and ensuring a uniform morphology of the Sn-based perovskite films. Here, we introduce a bilayer structure of 2D PEA2SnI4 and 3D MASnI3 perovskite (PEA = phenethylammonium; MA = methylammonium) formed by a sequential vapor process that combines vacuum deposition and vapor reaction. The vapor process ensures that the perovskite thin films are uniform and enables the fabrication of an upper layer with fine thickness control without damaging the lower layer. With the introduction of the 2D layer, Sn oxidation is suppressed and the crystallinity of the 3D layer is enhanced. A planar-type solar cell fabricated using the optimized 2D/3D structure exhibits an average efficiency of 9.2 ± 0.2%.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Dankook University, Cheonan 31116, Korea
Department of Physics, Dankook University, Cheonan 31116, Korea
Funding
National Research Foundation of Korea
References (33)
Show source-provided references
1. NREL. Best Research-Cell Efficiency Chart. https://www.nrel.gov/pv/cell-efficiency.html (accessed 2020-09-25).
2. 10.1002/adma.20130517210.1002/adma.201305172 ↗
3. 10.1039/C4EE01076K10.1039/C4EE01076K ↗
4. 10.1021/jacs.6b0833710.1021/jacs.6b08337 ↗
5. 10.1002/adma.20160474410.1002/adma.201604744 ↗
6. 10.1002/aenm.20180313510.1002/aenm.201803135 ↗
7. 10.1021/acsenergylett.7b0097610.1021/acsenergylett.7b00976 ↗
8. 10.1021/acs.jpclett.8b0319410.1021/acs.jpclett.8b03194 ↗
9. 10.1002/adma.20180483510.1002/adma.201804835 ↗
10. 10.1002/anie.20190241810.1002/anie.201902418 ↗
11. 10.1002/adma.20170380010.1002/adma.201703800 ↗
12. 10.1039/C8TA05916K10.1039/C8TA05916K ↗
13. 10.1002/adfm.20180805910.1002/adfm.201808059 ↗
14. 10.1021/acs.jpclett.9b0202410.1021/acs.jpclett.9b02024 ↗
15. 10.1021/jacs.7b0181510.1021/jacs.7b01815 ↗
16. 10.1021/acsenergylett.8b0008510.1021/acsenergylett.8b00085 ↗
17. 10.1002/adfm.20170692310.1002/adfm.201706923 ↗
18. 10.1002/adfm.20180769610.1002/adfm.201807696 ↗
19. 10.1021/jacs.5b0379610.1021/jacs.5b03796 ↗
20. 10.1021/acs.chemmater.6b0084710.1021/acs.chemmater.6b00847 ↗
21. 10.1002/anie.20160369410.1002/anie.201603694 ↗
22. 10.1016/j.solener.2018.11.06110.1016/j.solener.2018.11.061 ↗
23. 10.1007/s13391-018-0095-110.1007/s13391-018-0095-1 ↗
24. 10.1002/aenm.20170201910.1002/aenm.201702019 ↗
25. 10.1002/1521-3951(200202)229:3<1349::AID-PSSB1349>3.0.CO;2-R10.1002/1521-3951(200202)229:3<1349::AID-PSSB1349>3.0.CO;2-R ↗
26. 10.1021/acsenergylett.7b0063610.1021/acsenergylett.7b00636 ↗
27. 10.1021/acsenergylett.0c0117410.1021/acsenergylett.0c01174 ↗
28. 10.1021/acsenergylett.6b0051310.1021/acsenergylett.6b00513 ↗
29. 10.1021/acs.nanolett.7b0121110.1021/acs.nanolett.7b01211 ↗
30. 10.1016/j.nanoen.2019.04.04010.1016/j.nanoen.2019.04.040 ↗
31. 10.1002/adma.20140537210.1002/adma.201405372 ↗
32. 10.1063/1.282136810.1063/1.2821368 ↗
33. 10.1021/acs.jpclett.6b0011810.1021/acs.jpclett.6b00118 ↗