Improved Phase Stability of Formamidinium Lead Triiodide Perovskite by Strain Relaxation
Source abstract
Abstract
Though formamidinium lead triiodide (FAPbI 3 ) possesses a suitable band gap and good thermal stability, the phase transition from the pure black perovskite phase (α-phase) to the undesirable yellow nonperovskite polymorph (δ-phase) at room temperature, especially under humid air, hinders its practical application. Here, we investigate the intrinsic instability mechanism of the α-phase at ambient temperature and demonstrate the existence of an anisotropic strained lattice in the (111) plane that drives phase transformation into the δ-phase. Methylammonium bromide (MABr) alloying (or FAPbI 3 -MABr) was found to cause lattice contraction, thereby balancing the lattice strain. This led to dramatic improvement in the stability of α-FAPbI 3 . Solar cells fabricated using FAPbI 3 -MABr demonstrated significantly enhanced stability under the humid air.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Solid-state spectroscopy and crystallography · Chalcogenide Semiconductor Thin Films
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Energy Harvesting Materials and System, Virginia Tech, Blacksburg, Virginia 24061, United States
Chemistry and Nanoscience Center, National Renewable Energy Laboratory, Golden, Colorado 80401, United States
Funding
Office of Naval Research · U.S. Department of Energy · Solar Energy Technologies Program · Institute for Critical Technology and Applied Science, Virginia Polytechnic Institute and State University
References (29)
Show source-provided references
1. 10.1002/adma.20150009910.1002/adma.201500099 ↗
2. 10.1126/science.aaa272510.1126/science.aaa2725 ↗
3. 10.1021/acsenergylett.6b0021510.1021/acsenergylett.6b00215 ↗
4. 10.1002/aenm.20150047710.1002/aenm.201500477 ↗
5. 10.1021/jz501210910.1021/jz5012109 ↗
6. 10.1039/c3ta10518k10.1039/c3ta10518k ↗
7. 10.1002/adma.20150259710.1002/adma.201502597 ↗
8. 10.1039/C6NJ00188B10.1039/C6NJ00188B ↗
9. 10.1039/C6RA19582B10.1039/C6RA19582B ↗
10. 10.1039/c3ee43822h10.1039/c3ee43822h ↗
11. 10.1021/cm404006p10.1021/cm404006p ↗
12. 10.1021/nl501299210.1021/nl5012992 ↗
13. 10.1021/acsenergylett.6b0000210.1021/acsenergylett.6b00002 ↗
14. 10.1021/acs.chemmater.5b0410710.1021/acs.chemmater.5b04107 ↗
15. 10.1021/acs.jpclett.5b0143210.1021/acs.jpclett.5b01432 ↗
16. 10.1038/nature1413310.1038/nature14133 ↗
17. 10.1126/science.aaa927210.1126/science.aaa9272 ↗
18. 10.1002/aenm.20150131010.1002/aenm.201501310 ↗
19. 10.1021/acs.jpclett.5b0038010.1021/acs.jpclett.5b00380 ↗
20. 10.1039/C3TA13606J10.1039/C3TA13606J ↗
21. 10.1016/0001-6160(53)90006-610.1016/0001-6160(53)90006-6 ↗
22. 10.1107/S002188980803176210.1107/S0021889808031762 ↗
23. 10.1107/S002188989709895610.1107/S0021889897098956 ↗
24. 10.1039/C4SC02211D10.1039/C4SC02211D ↗
25. 10.1103/PhysRevB.75.21430710.1103/PhysRevB.75.214307 ↗
26. 10.1016/j.nanoen.2016.02.03110.1016/j.nanoen.2016.02.031 ↗
27. 10.1038/nmat401410.1038/nmat4014 ↗
28. 10.1016/j.nanoen.2015.08.02310.1016/j.nanoen.2015.08.023 ↗
29. 10.1021/ja504539w10.1021/ja504539w ↗