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Colloidal Synthesis and Photophysics of M3Sb2I9 (M=Cs and Rb) Nanocrystals: Lead‐Free Perovskites

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dc.contributor.author PAL, JAYA en_US
dc.contributor.author MANNA, SUMAN en_US
dc.contributor.author Mondal, Anirban en_US
dc.contributor.author Das, Shyamashis en_US
dc.contributor.author Adarsh, K. V. en_US
dc.contributor.author NAG, ANGSHUMAN en_US
dc.date.accessioned 2019-07-01T05:35:13Z
dc.date.available 2019-07-01T05:35:13Z
dc.date.issued 2017-11 en_US
dc.identifier.citation Angewandte Chemie International Edition, 56(45), 14187-14191. en_US
dc.identifier.issn 1433-7851 en_US
dc.identifier.issn 1521-3773 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3278
dc.identifier.uri https://doi.org/10.1002/anie.201709040 en_US
dc.description.abstract Herein we report the colloidal synthesis of Cs3Sb2I9 and Rb3Sb2I9 perovskite nanocrystals, and explore their potential for optoelectronic applications. Different morphologies, such as nanoplatelets and nanorods of Cs3Sb2I9, and spherical Rb3Sb2I9 nanocrystals were prepared. All these samples show band‐edge emissions in the yellow–red region. Exciton many‐body interactions studied by femtosecond transient absorption spectroscopy of Cs3Sb2I9 nanorods reveals characteristic second‐derivative‐type spectral features, suggesting red‐shifted excitons by as much as 79 meV. A high absorption cross‐section of ca. 10−15 cm2 was estimated. The results suggest that colloidal Cs3Sb2I9 and Rb3Sb2I9 nanocrystals are potential candidates for optical and optoelectronic applications in the visible region, though a better control of defect chemistry is required for efficient applications. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Colloidal Synthesis en_US
dc.subject Photophysics en_US
dc.subject Lead?Free Perovskites en_US
dc.subject Powder X?ray diffraction en_US
dc.subject 2017 en_US
dc.title Colloidal Synthesis and Photophysics of M3Sb2I9 (M=Cs and Rb) Nanocrystals: Lead‐Free Perovskites en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Angewandte Chemie International Edition en_US
dc.publication.originofpublisher Foreign en_US


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