Molecular Engineering of Simple Carbazole‐Triphenylamine Hole Transporting Materials by Replacing Benzene with Pyridine Unit for Perovskite Solar Cells
Source abstract
Abstract
Four carbazole‐triphenylamine hole transporting materials (HTMs) with a pyridine or benzene on the N of carbazole have been designed and developed. The molecular structures on their photophysical, electrochemical, thermal, as well as photovoltaic properties in perovskite solar cells (PSCs) are comprehensively analyzed. It is noted that the pyridine‐contained compounds show bathochromic spectra response, slightly lower HOMO level, and higher thermal stability than their benzene‐contained counterparts. Photoluminescence study indicates that the molecule with a pyridine unit possess better hole extraction properties on the perovskite/HTM interface. When used in PSCs, pyridine‐contained HTMs exhibit higher efficiency and better stability than benzene‐contained HTMs. Moreover, the PSCs based on the pyridine‐contained HTM exhibit a promising power conversion efficiency of 18.45% with good light‐soaking and long‐term stability, which is even better than that of conventional spiro‐OMeTAD under the same conditions. Therefore, the results provide a promising strategy to design and develop novel HTM molecules for efficient and stable PSCs.
Source: crossref · Quality: baseline
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
Beijing Key Laboratory of Novel Thin‐Film Solar Cells, School of Renewable Energy North China Electric Power University Beijing 102206 P. R. China
National Institute of Biological Science Beijing 102206 P. R. China
Funding
National Natural Science Foundation of China
References (40)
Show source-provided references
1. 10.1021/ja809598r10.1021/ja809598r ↗
2. 10.1126/science.124398210.1126/science.1243982 ↗
3. 10.1126/science.124316710.1126/science.1243167 ↗
4. 10.1038/srep0059110.1038/srep00591 ↗
5. 10.1038/nature1413310.1038/nature14133 ↗
6. 10.1016/j.mtener.2018.07.00310.1016/j.mtener.2018.07.003 ↗
7. 10.1126/science.aan230110.1126/science.aan2301 ↗
8. 10.1038/s41560-018-0200-610.1038/s41560-018-0200-6 ↗
9. NREL Research Cell Record Efficiency Chart https://www.nrel.gov/pv/assets/images/efficiency-chart-20180716.jpg.
10. 10.1038/2693610.1038/26936 ↗
11. 10.1002/ange.20131087710.1002/ange.201310877 ↗
12. 10.1016/B978-0-12-813731-4.00009-610.1016/B978-0-12-813731-4.00009-6 ↗
13. 10.1039/C8TC04191A10.1039/C8TC04191A ↗
14. 10.1002/anie.20160175710.1002/anie.201601757 ↗
15. 10.1038/nenergy.2015.1710.1038/nenergy.2015.17 ↗
16. 10.1002/aenm.20160047410.1002/aenm.201600474 ↗
17. 10.1002/adma.20140241510.1002/adma.201402415 ↗
18. 10.1016/j.nanoen.2017.01.01510.1016/j.nanoen.2017.01.015 ↗
19. 10.1002/anie.20150466610.1002/anie.201504666 ↗
20. 10.1016/j.nanoen.2017.08.01610.1016/j.nanoen.2017.08.016 ↗
21. 10.1021/acsnano.6b0244210.1021/acsnano.6b02442 ↗
22. 10.1021/acs.jpcc.8b0816810.1021/acs.jpcc.8b08168 ↗
23. 10.1002/anie.20151187710.1002/anie.201511877 ↗
24. 10.1002/adfm.20170435110.1002/adfm.201704351 ↗
25. 10.1039/C7TA04762B10.1039/C7TA04762B ↗
26. 10.1002/chem.20160518710.1002/chem.201605187 ↗
27. 10.1002/ente.20170030410.1002/ente.201700304 ↗
28. 10.1039/C5TA03046C10.1039/C5TA03046C ↗
29. 10.1039/C5EE02608C10.1039/C5EE02608C ↗
30. 10.1016/j.dyepig.2016.12.02210.1016/j.dyepig.2016.12.022 ↗
31. 10.1039/C5TA03865K10.1039/C5TA03865K ↗
32. 10.1002/cssc.20160168310.1002/cssc.201601683 ↗
33. 10.1021/jacs.5b1107610.1021/jacs.5b11076 ↗
34. 10.1002/adma.20160404810.1002/adma.201604048 ↗
35. 10.1038/ncomms678410.1038/ncomms6784 ↗
36. 10.1021/acs.jpcc.7b0084710.1021/acs.jpcc.7b00847 ↗
37. 10.1002/aenm.20150153410.1002/aenm.201501534 ↗
38. 10.1039/C7CC03444J10.1039/C7CC03444J ↗
39. 10.1002/cssc.20170097310.1002/cssc.201700973 ↗
40. 10.1002/aenm.20170068310.1002/aenm.201700683 ↗