Nuclei position-control and crystal growth-guidance on frozen substrates for high-performance perovskite solar cells
Source abstract
Abstract
Nucleation and crystal growth are key stages for high-quality perovskite films that dominate the performance of perovskite solar cells. However, the position of nuclei in the films and the orientation of the crystal growth have not yet been intendedly controlled during their fabrication. In this study, we developed a method of spin-coating perovskite films on frozen substrates to control the position of the nuclei and the direction of the crystal growth at the same time. In this way, the position of the crystal nuclei and the growth orientation of the perovskite crystals in the perovskite films can be simultaneously controlled. A high-quality perovskite film with grains spanning vertically the entire film thickness has been obtained using this new method. And an efficient inverted planar solar cell (ITO/PEDOT:PSS/CH3NH3PbI3/PC61BM/BCP/Ag) with the highest power conversion efficiency of 17.14% and open-circuit voltage of 1.14 V has been achieved by using this technique.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Clean Energy and Advanced Materials
School of Materials and Energy
Southwest University
Chongqing 400715
P. R. China
College of Physics and Electronics Engineering
Chongqing Normal University
Chongqing 401331
Chongqing Key Laboratory for Advanced Materials and Technologies of Clean Energy
Funding
National Natural Science Foundation of China · Fundamental Research Funds for the Central Universities
References (31)
Show source-provided references
1. Stranks · Science · 2013 · 342 · 34110.1126/science.1243982 ↗
2. Shi · Materials · 2018 · 11 · 72910.3390/ma11050729 ↗
3. Dong · Science · 2015 · 347 · 96710.1126/science.aaa5760 ↗
4. Wang · Adv. Funct. Mater. · 2019 · 29 · 190041710.1002/adfm.201900417 ↗
5. Xiao · Angew. Chem., Int. Ed. · 2014 · 53 · 989810.1002/anie.201405334 ↗
6. Jeon · Nat. Mater. · 2014 · 13 · 89710.1038/nmat4014 ↗
7. Ma · ACS Appl. Mater. Interfaces · 2017 · 9 · 3392510.1021/acsami.7b10022 ↗
8. Xiao · Adv. Mater. · 2014 · 26 · 650310.1002/adma.201401685 ↗
9. Wang · RSC Adv. · 2016 · 6 · 4329910.1039/C6RA05893K ↗
10. Li · Science · 2016 · 353 · 5810.1126/science.aaf8060 ↗
11. Nie · Science · 2015 · 347 · 52210.1126/science.aaa0472 ↗
12. Zhang · J. Mater. Chem. A · 2019 · 7 · 280410.1039/C8TA10170A ↗
13. Ren · J. Mater. Chem. A · 2017 · 5 · 2032710.1039/C7TA06334B ↗
14. Liu · ACS Appl. Mater. Interfaces · 2017 · 9 · 1238210.1021/acsami.6b16541 ↗
15. Zhu · ACS Appl. Mater. Interfaces · 2017 · 9 · 610410.1021/acsami.6b15563 ↗
16. Yu · Nanoscale · 2017 · 9 · 256910.1039/C6NR08741H ↗
17. Ma · Nanoscale · 2016 · 8 · 1830910.1039/C6NR04741F ↗
18. Chen · RSC Adv. · 2018 · 8 · 1596110.1039/C8RA01633J ↗
19. Yao · Org. Electron. · 2018 · 59 · 26010.1016/j.orgel.2018.05.017 ↗
20. Bai · Nano Energy · 2017 · 34 · 5810.1016/j.nanoen.2017.02.019 ↗
21. Wang · Sol. RRL · 2018 · 2 · 180002710.1002/solr.201800027 ↗
22. Ma · Nanoscale · 2018 · 11 · 170
23. Miyano · Acc. Chem. Res. · 2016 · 49 · 30310.1021/acs.accounts.5b00436 ↗
24. Suarez · J. Phys. Chem. Lett. · 2014 · 5 · 162810.1021/jz5006797 ↗
25. Gonzalez-Pedro · Nano Lett. · 2014 · 14 · 88810.1021/nl404252e ↗
26. Wu · Org. Electron. · 2015 · 26 · 26510.1016/j.orgel.2015.07.057 ↗
27. Wu · Nanoscale · 2014 · 6 · 1050510.1039/C4NR03181D ↗
28. Yaug · ACS Appl. Mater. Interfaces · 2017 · 9 · 2314110.1021/acsami.7b03941 ↗
29. Hu · ACS Appl. Mater. Interfaces · 2017 · 9 · 4390210.1021/acsami.7b14592 ↗
30. Liu · J. Mater. Chem. A · 2017 · 5 · 570110.1039/C6TA10212C ↗
31. Huang · Nat. Rev. Mater. · 2017 · 2 · 1704210.1038/natrevmats.2017.42 ↗