Wide-Angle X-ray Diffraction Evidence of Structural Coherence in CsPbBr3 Nanocrystal Superlattices
Source abstract
Abstract
Films made of colloidal CsPbBr3 nanocrystals packed in isolated or densely-packed superlattices display a remarkably high degree of structural coherence. The structural coherence is revealed by the presence of satellite peaks accompanying Bragg reflections in wide-angle X-ray diffraction experiments in parallel-beam reflection geometry. The satellite peaks, also called "superlattice reflections", arise from the interference of X-rays diffracted by the atomic planes of the orthorhombic perovskite lattice. The interference is due to the precise spatial periodicity of the nanocrystals separated by organic ligands in the superlattice. The presence of satellite peaks is a fingerprint of the high crystallinity and long-range order of nanocrystals, comparable to those of multilayer superlattices prepared by physical methods. The angular separation between satellite peaks is highly sensitive to changes in the superlattice periodicity. These characteristics of the satellite peaks are exploited to track the superlattice compression under vacuum, as well as to observe the superlattice growth in situ from colloidal solutions by slow solvent evaporation.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Perovskite Materials and Applications · Solid-state spectroscopy and crystallography · Crystal Structures and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nanochemistry Department, Istituto Italiano di Tecnologia, Via Morego 30, 16163 Genova, Italy
Istituto di Cristallografia - Consiglio Nazionale delle Ricerche (IC-CNR), via Amendola 122/O, I-70126 Bari, Italy
Funding
H2020 Marie Sklodowska-Curie Actions · FP7 Ideas: European Research Council
References (29)
Show source-provided references
1. 10.1021/nl504877910.1021/nl5048779 ↗
2. 10.1126/science.aam709310.1126/science.aam7093 ↗
3. 10.1038/s41563-018-0018-410.1038/s41563-018-0018-4 ↗
4. 10.1021/acs.chemrev.8b0064410.1021/acs.chemrev.8b00644 ↗
5. 10.1021/acs.nanolett.7b0214710.1021/acs.nanolett.7b02147 ↗
6. 10.1038/s41586-018-0683-010.1038/s41586-018-0683-0 ↗
7. 10.1002/adma.20180111710.1002/adma.201801117 ↗
8. 10.1021/acs.jpclett.9b0017810.1021/acs.jpclett.9b00178 ↗
9. 10.1107/S002188987701267910.1107/S0021889877012679 ↗
10. 10.1103/PhysRevLett.44.159710.1103/PhysRevLett.44.1597 ↗
11. 10.1149/1.209593010.1149/1.2095930 ↗
12. 10.1126/science.270.5240.133510.1126/science.270.5240.1335 ↗
13. Holý V. C. · 1999
14. 10.1021/acsnano.7b0001710.1021/acsnano.7b00017 ↗
15. 10.1021/acs.nanolett.7b0125310.1021/acs.nanolett.7b01253 ↗
16. 10.1021/acs.chemmater.7b0089510.1021/acs.chemmater.7b00895 ↗
17. 10.1021/acsnano.7b0835710.1021/acsnano.7b08357 ↗
18. 10.1021/acsenergylett.7b0122610.1021/acsenergylett.7b01226 ↗
19. 10.1021/acs.nanolett.8b0359810.1021/acs.nanolett.8b03598 ↗
20. 10.1107/S002188987500950810.1107/S0021889875009508 ↗
21. 10.1039/C8CP04724C10.1039/C8CP04724C ↗
22. 10.1103/PhysRevB.97.23530410.1103/PhysRevB.97.235304 ↗
23. 10.1039/C6CC01088A10.1039/C6CC01088A ↗
24. 10.1023/A:102283680082010.1023/A:1022836800820 ↗
25. Bowen D. K. · 199810.1201/b12575 ↗
26. Dhez P. · 198810.1007/978-1-4757-0091-6 ↗
27. Schmidt O. · 2007
28. 10.1063/1.170019610.1063/1.1700196 ↗
29. 10.1038/ncomms1013610.1038/ncomms10136 ↗