Perovskite/TiO2 Interface Passivation Using Poly(vinylcarbazole) and Fullerene for the Photovoltaic Conversion Efficiency of 21%
Source abstract
Abstract
Poly(vinylcarbazole) (PVCz) dispersed the typical fullerene derivative, PCBM, well in its solution, which was then coated onto a mesoporous titanium oxide (TiO2) layer. PVCz served as a scaffold to fix PCBM homogeneously and to prevent its elution out upon the following perovskite layer formation. A series of perovskite cells were fabricated upon the PVCz/PCBM-modified TiO2 layer. Many of the cells were characterized by a photovoltaic conversion efficiency of >20%, and the top cells had an efficiency of 21.1% (with an average of 21.0%). Fluorescence decay from the perovskite layer of the cell was unchanged with the PVCz/PCBM modification, suggesting an efficient charge transport to the electron-transporting layers. On the other hand, the PVCz/PCBM modification or passivation significantly reduced electroluminescence intensity under an inverse bias application, supporting an efficient suppression of carrier recombination at the TiO2 and perovskite interface.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Applied Chemistry and Research Institute for Science and Engineering, Waseda University, Tokyo 169-8555, Japan
Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo 153-8904, Japan
Funding
New Energy and Industrial Technology Development Organization
References (41)
Show source-provided references
1. 10.1021/ja809598r10.1021/ja809598r ↗
2. 10.1002/smll.20170417710.1002/smll.201704177 ↗
3. 10.1002/anie.20170322610.1002/anie.201703226 ↗
4. 10.1021/acsenergylett.7b0051710.1021/acsenergylett.7b00517 ↗
5. 10.1021/jacs.7b1043010.1021/jacs.7b10430 ↗
6. 10.1002/aenm.20180024910.1002/aenm.201800249 ↗
7. 10.1016/j.orgel.2018.10.02810.1016/j.orgel.2018.10.028 ↗
8. 10.1002/adfm.20170628710.1002/adfm.201706287 ↗
9. 10.1002/aenm.20170339210.1002/aenm.201703392 ↗
10. 10.1002/adma.20170523010.1002/adma.201705230 ↗
11. 10.1021/acsenergylett.8b0054810.1021/acsenergylett.8b00548 ↗
12. 10.1038/s41598-017-12436-x10.1038/s41598-017-12436-x ↗
13. 10.1021/acsami.8b0799910.1021/acsami.8b07999 ↗
14. 10.1002/ente.20170030810.1002/ente.201700308 ↗
15. 10.1038/ncomms1230510.1038/ncomms12305 ↗
16. 10.1039/C6EE03182J10.1039/C6EE03182J ↗
17. 10.1039/C5NR01364J10.1039/C5NR01364J ↗
18. 10.1021/acs.jpclett.6b0161710.1021/acs.jpclett.6b01617 ↗
19. 10.1039/C5TC03109E10.1039/C5TC03109E ↗
20. 10.1002/admi.20180032610.1002/admi.201800326 ↗
21. 10.1002/adfm.20140165810.1002/adfm.201401658 ↗
22. 10.1038/ncomms1037910.1038/ncomms10379 ↗
23. 10.1002/aenm.20150247210.1002/aenm.201502472 ↗
24. 10.1039/C7EE01096F10.1039/C7EE01096F ↗
25. 10.1126/science.270.5243.178910.1126/science.270.5243.1789 ↗
26. 10.1021/acsnano.7b0775410.1021/acsnano.7b07754 ↗
27. 10.1039/C6TA00253F10.1039/C6TA00253F ↗
28. 10.1126/science.aap928210.1126/science.aap9282 ↗
29. 10.1002/smll.20170400710.1002/smll.201704007 ↗
30. 10.1016/j.nanoen.2018.04.06810.1016/j.nanoen.2018.04.068 ↗
31. 10.1557/mrc.2017.13510.1557/mrc.2017.135 ↗
32. 10.1002/pi.554510.1002/pi.5545 ↗
33. 10.1038/s41428-018-0116-910.1038/s41428-018-0116-9 ↗
34. 10.1080/1558372080223172610.1080/15583720802231726 ↗
35. 10.1039/C6TA09314K10.1039/C6TA09314K ↗
36. 10.1126/science.aah555710.1126/science.aah5557 ↗
37. 10.1039/C5EE03874J10.1039/C5EE03874J ↗
38. 10.1038/s41467-018-04029-710.1038/s41467-018-04029-7 ↗
39. 10.1126/science.aan230110.1126/science.aan2301 ↗
40. 10.1016/j.solmat.2016.12.04310.1016/j.solmat.2016.12.043 ↗
41. 10.1021/acs.nanolett.8b0070110.1021/acs.nanolett.8b00701 ↗