Dehydration-Reaction-Based Low-Temperature Synthesis of Amorphous SnOx for High-Performance Perovskite Solar Cells
Source abstract
Abstract
The development of methodologies for synthesizing carrier-transporting materials is critical for optoelectronic device fabrication. Amorphous metal oxides have emerged as potential carrier transport materials for perovskite tandem solar cells and flexible electronics due to their ease of fabrication and excellent electronic properties. However, perovskite solar cells employing amorphous metal oxides as the electron-transporting layers (ETLs) remain inefficient. This research describes a moderate dehydration reaction for the low-temperature synthesis of amorphous SnOx. We investigated this amorphous SnOx as the ETL for perovskite solar cells and demonstrated a maximum power conversion efficiency (PCE) of 20.4%, the greatest efficiency ever attained with an amorphous metal oxide ETL produced below 100 °C. Remarkably, the device maintained 85% of its initial efficiency for more than 4800 h. Furthermore, flexible perovskite solar cells based on this amorphous SnOx have a maximum PCE of 11.7%. Finally, this amorphous SnOx was used to fabricate LEDs and exhibited a maximum external quantum efficiency of over 3%.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Organic Light-Emitting Diodes Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China
School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China
Funding
Ministry of Science and Technology of the People's Republic of China · Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China
References (32)
Show source-provided references
1. 10.1038/nmat459910.1038/nmat4599 ↗
2. 10.1038/nature0309010.1038/nature03090 ↗
3. 10.1016/0022-3093(96)80019-610.1016/0022-3093(96)80019-6 ↗
4. 10.1021/acs.chemrev.8b0053910.1021/acs.chemrev.8b00539 ↗
5. 10.1038/natrevmats.2017.4210.1038/natrevmats.2017.42 ↗
6. 10.1126/science.aaa576010.1126/science.aaa5760 ↗
7. 10.1126/science.aaa272510.1126/science.aaa2725 ↗
8. 10.1007/s11426-019-9448-310.1007/s11426-019-9448-3 ↗
9. 10.1021/ja809598r10.1021/ja809598r ↗
10. 10.1038/s41586-021-03285-w10.1038/s41586-021-03285-w ↗
11. Wang Y. · Sci. China Chem. · 2021 · 64 · s11426
12. Best Research-Cell Efficiencies, NREL. 2021, https://www.nrel.gov/pv/assets/pdfs/best-research-cell-efficiencies-rev210726.pdf2021 (accessed July 2021).
13. 10.1038/s41560-018-0190-410.1038/s41560-018-0190-4 ↗
14. 10.1002/anie.20180978110.1002/anie.201809781 ↗
15. 10.1038/nphoton.2013.34210.1038/nphoton.2013.342 ↗
16. 10.1038/srep1321110.1038/srep13211 ↗
17. 10.1002/aenm.20150189010.1002/aenm.201501890 ↗
18. 10.1021/acsami.6b0765810.1021/acsami.6b07658 ↗
19. 10.1039/C8TA02540A10.1039/C8TA02540A ↗
20. 10.1039/D0TA08554E10.1039/D0TA08554E ↗
21. 10.1021/acsami.7b0511310.1021/acsami.7b05113 ↗
22. 10.1021/acsami.0c0014210.1021/acsami.0c00142 ↗
23. 10.1246/cl.16106010.1246/cl.161060 ↗
24. 10.1016/j.solmat.2018.01.02710.1016/j.solmat.2018.01.027 ↗
25. 10.1002/adfm.20180677910.1002/adfm.201806779 ↗
26. 10.1016/j.solmat.2016.10.00210.1016/j.solmat.2016.10.002 ↗
27. 10.1021/acs.jpclett.6b0029510.1021/acs.jpclett.6b00295 ↗
28. 10.1016/j.nanoen.2016.08.03510.1016/j.nanoen.2016.08.035 ↗
29. 10.1016/j.nanoen.2017.04.03310.1016/j.nanoen.2017.04.033 ↗
30. 10.1117/1.JPE.6.02200210.1117/1.JPE.6.022002 ↗
31. 10.1016/j.jphotochem.2017.11.03110.1016/j.jphotochem.2017.11.031 ↗
32. 10.1038/nnano.2016.11010.1038/nnano.2016.110 ↗