Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10077
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dc.contributor.authorMONDAL, BARNALIen_US
dc.contributor.authorMehta, Sakshien_US
dc.contributor.authorMondal, Abhishakeen_US
dc.contributor.authorNAG, ANGSHUMANen_US
dc.date.accessioned2025-05-22T05:11:40Z
dc.date.available2025-05-22T05:11:40Z
dc.date.issued2025-05en_US
dc.identifier.citationJournal of Physical Chemistry Letters, 16(20), 4937–4943.en_US
dc.identifier.issn1948-7185en_US
dc.identifier.urihttps://doi.org/10.1021/acs.jpclett.5c00822en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10077
dc.description.abstract0D perovskite derivatives such as Cs2WCl6 and Cs2WOxCl6–x have been recently shown to emit near-infrared (NIR) radiation. The d–d electronic transition of W4+/W5+ yields an NIR emission. However, the close proximity of those ions can quench the photoluminescence via concentration quenching. To address this issue, here we dilute the emission centers by doping a small amount of W into the Cs2SnCl6 0D perovskite. The results suggest that the dopant centers are [WOCl5]2– replacing [SnCl6]2– octahedra in the host lattice. The optimal 3.3% W-doped Cs2SnCl6 exhibits NIR (965 nm) emission with over 52 times higher intensity compared to that of Cs2WOxCl6–x. The suppression of concentration quenching in W-doped Cs2SnCl6 also significantly alters its temperature-dependent (7–300 K) photoluminescence compared to that of Cs2WOxCl6–x. Finally, we demonstrated NIR phosphor-converted light-emitting diodes of W-doped Cs2SnCl6 showing an output power of 10.3 mW at 400 mA. This is the first report of W doping in 0D perovskites showing its potential as an NIR phosphor.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectDopingen_US
dc.subjectImpuritiesen_US
dc.subjectPerovskitesen_US
dc.subjectPoweren_US
dc.subjectQuenchingen_US
dc.subject2025-MAY-WEEK3en_US
dc.subjectTOC-MAY-2025en_US
dc.subject2025en_US
dc.titleW-Doped Cs2SnCl6 for Near-Infrared Emissionen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleJournal of Physical Chemistry Lettersen_US
dc.publication.originofpublisherForeignen_US
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