Trans‐spatial Structure Additive Passivated Sn(II) for High‐efficiency CsSnI3 Perovskite Solar Cells Fabricated in Humid Air
Source abstract
Abstract
Abstract Black crystalline γ‐CsSnI3 is an ideal light absorption material to replace lead‐based perovskite due to its low biotoxicity and excellent photoelectric properties. However, CsSnI3 is usually prepared in a low humidity inert atmosphere because of its oxidation in air. The severe preparation environment, on the other hand, will surely raise the economic cost of mass production. Therefore, a kind of additive engineering is proposed to introduce (1R, 2R)‐(−)‐1,2‐diaminocyclohexane (transDACH), a small nitrogen‐containing ligand with trans‐spatial structure, into the perovskite layer, which can stabilize Sn2+ in the preparation process, allowing for the preparation of efficient and stable perovskite solar cells under high humidity conditions. The forward scan maximum power conversion efficiency (PCE) of the CsSnI3‐transDACH device reaches 5.49%, the highest for hole‐free carbon‐based CsSnI3 PSCs prepared in humid air conditions. Furthermore, the transDACH‐modified devices retain 73.7% of their original PCEs after 160 hours of storage in ambient air conditions.
Source: crossref · 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 School of Chemistry and Chemical Engineering Guangxi Key Laboratory of Electrochemical Energy Materials Guangxi University Nanning 530004 P. R. China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Guangxi Province
References (43)
Show source-provided references
1.
2. 10.1021/ja809598r10.1021/ja809598r ↗
3. N. R. E. Laboratory “Best Research-Cell Efficiency Chart.” can be found under https://www.nrel.gov/pv/cell-efficiency.html (accessed June 2022)
4.
5. 10.1126/science.aam632310.1126/science.aam6323 ↗
6. 10.1038/nmat457210.1038/nmat4572 ↗
7.
8. 10.1002/adma.20140199110.1002/adma.201401991 ↗
9. 10.1063/1.344251110.1063/1.3442511 ↗
10. 10.1021/ic401215x10.1021/ic401215x ↗
11. Wu B. · Adv. Funct. Mater. · 2017 · 27 · 1
12. 10.1002/adma.20160141810.1002/adma.201601418 ↗
13. 10.1063/1.173603410.1063/1.1736034 ↗
14. Chen Z. · Appl. Phys. Lett. · 2012 · 101 · 4
15.
16. 10.1021/ja301539s10.1021/ja301539s ↗
17. 10.1016/j.jssc.2013.07.00810.1016/j.jssc.2013.07.008 ↗
18. 10.1039/c0dt01601b10.1039/c0dt01601b ↗
19. 10.1039/C9EE01479A10.1039/C9EE01479A ↗
20.
21. 10.1021/jacs.6b1073410.1021/jacs.6b10734 ↗
22. 10.1002/anie.20181153910.1002/anie.201811539 ↗
23. 10.1002/ange.20181153910.1002/ange.201811539 ↗
24.
25. 10.1007/s00706-017-1933-910.1007/s00706-017-1933-9 ↗
26. 10.1039/C7TA00929A10.1039/C7TA00929A ↗
27. 10.1002/adfm.20190519710.1002/adfm.201905197 ↗
28. 10.1021/acsaem.8b0086610.1021/acsaem.8b00866 ↗
29. 10.1021/jacs.0c1306910.1021/jacs.0c13069 ↗
30. 10.1021/acsenergylett.1c0034210.1021/acsenergylett.1c00342 ↗
31. 10.1002/adma.20210441410.1002/adma.202104414 ↗
32. 10.1002/anie.20191542210.1002/anie.201915422 ↗
33. 10.1002/ange.20191542210.1002/ange.201915422 ↗
34. Xu Y. · Nano Energy · 2022 · 95 · 10
35.
36. 10.1038/nenergy.2016.17810.1038/nenergy.2016.178 ↗
37. 10.1039/C8TA10901J10.1039/C8TA10901J ↗
38. 10.1038/s41467-020-16726-310.1038/s41467-020-16726-3 ↗
39. 10.1021/jacs.6b1073410.1021/jacs.6b10734 ↗
40. 10.1038/srep2104210.1038/srep21042 ↗
41. 10.1016/j.poly.2015.10.02910.1016/j.poly.2015.10.029 ↗
42. Zuo L. J. · Sci. Adv. · 2017 · 3 · 1
43. 10.1126/science.aba089310.1126/science.aba0893 ↗