Phase Regulation of CsPb2Br5/CsPbBr3 Perovskite Nanocrystals by Doping with Divalent Cations: Implications for Optoelectronic Devices with Enhanced Stability and Reduced Toxicity
Source abstract
Abstract
Inorganic metal halide perovskites are generally considered as highly attractive materials for optoelectronic application devices. Unfortunately, Pb-based perovskite nanocrystals (NCs) are unstable because of their sensitivity to water, oxygen, light, and thermal treatment, which seriously limits their practical application. Herein, the dual-phase CsPb2Br5/CsPbBr3 NCs were synthesized first, and then the dual-phase M2+-doped CsPb2Br5/CsPbBr3 NCs (M = Ca2+, Sr2+, and Ba2+) with low toxicity were simply and rapidly prepared at room temperature based on the CsPb2Br5/CsPbBr3 NCs. The Sr2+-doped samples show outstanding stability and photoluminescence quantum yield due to the elimination of structural distortion and lattice contraction caused by the almost equal radii of Sr2+ (1.18 Å) and Pb2+ (1.19 Å). Interestingly, with the increase in M2+ concentration, the dual-phase quasi-2D tetragonal CsPb2Br5/CsPbBr3 NCs gradually transformed into single-phase 3D cubic Cs(Pb/M)Br3. These high-performance perovskite luminescent materials are expected to be used in light-emitting devices and other optoelectronic devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · 2D Materials and Applications · Solid-state spectroscopy and crystallography
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China
Chongqing Key Laboratory of Soft-Matter Material Chemistry and Function Manufacturing, Chongqing 400715, China
Funding
Natural Science Foundation of Chongqing · Program for Innovation Team Building at Institutions of Higher Education in Chongqing · National Natural Science Foundation of China
References (31)
Show source-provided references
1. 10.1021/acsanm.1c0040710.1021/acsanm.1c00407 ↗
2. 10.1021/acsanm.9b0118710.1021/acsanm.9b01187 ↗
3. 10.1021/acs.chemmater.9b0044210.1021/acs.chemmater.9b00442 ↗
4. 10.1021/acsnano.9b0931510.1021/acsnano.9b09315 ↗
5. 10.1021/acsanm.0c0232310.1021/acsanm.0c02323 ↗
6. 10.1002/anie.20170389810.1002/anie.201703898 ↗
7. 10.1021/acs.chemrev.8b0064410.1021/acs.chemrev.8b00644 ↗
8. 10.1002/adfm.20190748110.1002/adfm.201907481 ↗
9. 10.1021/acs.inorgchem.9b0001010.1021/acs.inorgchem.9b00010 ↗
10. 10.1021/acsnano.6b0874710.1021/acsnano.6b08747 ↗
11. 10.1021/jacs.8b0476310.1021/jacs.8b04763 ↗
12. 10.1039/C8NR10110H10.1039/C8NR10110H ↗
13. 10.1016/j.matdes.2019.10824610.1016/j.matdes.2019.108246 ↗
14. 10.1021/acs.chemmater.0c0409710.1021/acs.chemmater.0c04097 ↗
15. 10.1016/j.ceramint.2019.07.30410.1016/j.ceramint.2019.07.304 ↗
16. 10.1039/C8NR06879H10.1039/C8NR06879H ↗
17. 10.1021/acs.jpcc.8b1020010.1021/acs.jpcc.8b10200 ↗
18. 10.1002/cssc.20170113110.1002/cssc.201701131 ↗
19. 10.1103/PhysRevB.96.15544210.1103/PhysRevB.96.155442 ↗
20. 10.1016/j.optmat.2019.10952810.1016/j.optmat.2019.109528 ↗
21. 10.1088/1361-6528/aa892e10.1088/1361-6528/aa892e ↗
22. 10.3389/fphy.2017.0006910.3389/fphy.2017.00069 ↗
23. 10.1007/s40820-021-00596-510.1007/s40820-021-00596-5 ↗
24. 10.1021/acs.jpclett.6b0140610.1021/acs.jpclett.6b01406 ↗
25. 10.1039/C8TC05741A10.1039/C8TC05741A ↗
26. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
27. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
28. 10.1103/PhysRevB.47.55810.1103/PhysRevB.47.558 ↗
29. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
30. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
31. 10.1063/1.47293310.1063/1.472933 ↗