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On the structure, synthesis, and characterization of ultrafast blue-emitting CsPbBr.sub.3./sub. nanoplatelets
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SYSNO ASEP 0520348 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title On the structure, synthesis, and characterization of ultrafast blue-emitting CsPbBr3 nanoplatelets Author(s) Tomanová, K. (CZ)
Čuba, V. (CZ)
Brik, M.G. (CN)
Mihóková, Eva (FZU-D) RID, ORCID, SAI
Turtos, R.M. (CH)
Lecoq, P. (CH)
Auffray, E. (CH)
Nikl, Martin (FZU-D) RID, ORCID, SAINumber of authors 8 Article number 011104 Source Title APL Materials - ISSN 2166-532X
Roč. 7, č. 1 (2019), s. 1-12Number of pages 12 s. Language eng - English Country US - United States Keywords nanoplatelets ; TOF PET ; photoluminescence ; scintillators ; nanocomposite ; crystal-structure ; perovskites ; CsPbBr3 Subject RIV CF - Physical ; Theoretical Chemistry OECD category Physical chemistry R&D Projects GA17-06479S GA ČR - Czech Science Foundation (CSF) EF16_027/0008215 GA MŠMT - Ministry of Education, Youth and Sports (MEYS) Method of publishing Open access Institutional support FZU-D - RVO:68378271 UT WOS 000457407500005 EID SCOPUS 85060452038 DOI 10.1063/1.5079300 Annotation We synthesize colloidal CsPbBr3 nanoplatelets emitting blue light with fast sub-nanosecond decay. We also prepare a nanocomposite material by embedding the nanoplatelets in the polystyrene matrix. We show that blue emission is preserved provided the composite is not exposed to UV/vis light and/or elevated temperatures. Motivated by conflicting information from the literature about the room temperature structure of colloidal CsPbX3 (X = Cl, Br, I) particles, that results being orthorhombic, rather than cubic, we perform ab initio electronic structure calculations of bulk crystals with an orthorhombic structure. We calculate optical properties, as well as exciton diameters and binding energies and compare them to those previously obtained for cubic CsPbX3 crystals.
Workplace Institute of Physics Contact Kristina Potocká, potocka@fzu.cz, Tel.: 220 318 579 Year of Publishing 2020 Electronic address http://hdl.handle.net/11104/0305030
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