journal article·2016-12-09

Surface Termination, Morphology, and Bright Photoluminescence of Cesium Lead Halide Perovskite Nanocrystals

Stephanie ten Brinck, Ivan Infante

ACS Energy Letters· Volume 1· Issue 6
Publisher page

Abstract

Colloidal cesium lead halide perovskite nanocrystals (CsPbX 3 PNCs, X = Cl, Br, I) exhibit important optoelectronic properties that make them amenable for a plethora of applications. However, the origin of these properties, even for as-synthesized and unpurified PNCs, is largely unknown. Electronic structure calculations are therefore essential to understand with atomistic detail the properties of these nanomaterials; however, finding a model for PNCs that resembles the experiments is a challenging task. Essentially, the main problem is how to correctly terminate a PNC surface that is comprised of a large fraction of the nanocrystal atoms and of ligands employed in the synthesis. Here, we construct nominally trap-free models for PNCs taking into account experimental conditions. With density functional theory we analyze the effect of size, shape, and halide composition on the electronic structure of PNCs. We confirm that the PNC crystalline core exhibits an orthorhombic structure, and we demonstrate that PNCs can be robust light emitters even when a large number of ligands are displaced from the surface.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Perovskite Materials and Applications · Quantum Dots Synthesis And Properties · 2D Materials and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Theoretical Chemistry, Faculty of Sciences, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

References (34)

Show source-provided references
1. 10.1021/nl504877910.1021/nl5048779 ↗
2. 10.1039/C6CC01500J10.1039/C6CC01500J ↗
3. 10.1039/C5TC04116C10.1039/C5TC04116C ↗
4. 10.1021/acsnano.5b0115410.1021/acsnano.5b01154 ↗
5. 10.1039/C5CC08643D10.1039/C5CC08643D ↗
6. 10.1021/acsnano.5b0732810.1021/acsnano.5b07328 ↗
7. 10.1021/acsami.6b0252910.1021/acsami.6b02529 ↗
8. 10.1021/jacs.6b0890010.1021/jacs.6b08900 ↗
9. 10.1126/science.aag270010.1126/science.aag2700 ↗
10. 10.1021/nn506223h10.1021/nn506223h ↗
11. 10.1146/annurev-physchem-040513-10364910.1146/annurev-physchem-040513-103649 ↗
12. 10.1038/nmat353910.1038/nmat3539 ↗
13. 10.1038/nature1456310.1038/nature14563 ↗
14. 10.1002/aenm.20150047710.1002/aenm.201500477 ↗
15. 10.1021/jz501877h10.1021/jz501877h ↗
16. 10.1021/acs.accounts.5b0043110.1021/acs.accounts.5b00431 ↗
17. 10.1021/acs.jpclett.5b0155510.1021/acs.jpclett.5b01555 ↗
18. 10.1039/C5EE03874J10.1039/C5EE03874J ↗
19. 10.1039/C5EE01265A10.1039/C5EE01265A ↗
20. 10.1039/C5EE02925B10.1039/C5EE02925B ↗
21. 10.1038/ncomms849710.1038/ncomms8497 ↗
22. 10.1038/ncomms812410.1038/ncomms8124 ↗
23. 10.1021/acs.jpclett.6b0012210.1021/acs.jpclett.6b00122 ↗
24. 10.1039/C6CP03193E10.1039/C6CP03193E ↗
25. 10.1021/acsnano.5b0629510.1021/acsnano.5b06295 ↗
26. 10.1021/acsnano.6b0386310.1021/acsnano.6b03863 ↗
27. 10.1021/ja408675810.1021/ja4086758 ↗
28. 10.1126/science.125992410.1126/science.1259924 ↗
29. 10.1039/C6CC01088A10.1039/C6CC01088A ↗
30. 10.1039/C5CP00599J10.1039/C5CP00599J ↗
31. 10.1557/mrc.2015.2610.1557/mrc.2015.26 ↗
32. 10.1021/acsnano.5b0576910.1021/acsnano.5b05769 ↗
33. 10.1103/PhysRevLett.78.139610.1103/PhysRevLett.78.1396 ↗
34. 10.1002/wcms.115910.1002/wcms.1159 ↗