Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10927
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dc.contributor.authorSAIKIA, SAJIDen_US
dc.contributor.authorGHOSH, ANIMESHen_US
dc.contributor.authorNAG, ANGSHUMANen_US
dc.date.accessioned2026-04-29T08:28:39Z
dc.date.available2026-04-29T08:28:39Z
dc.date.issued2026-04en_US
dc.identifier.citationACS Energy Letters, 11(04), 3024–3037.en_US
dc.identifier.issn2380-8195en_US
dc.identifier.urihttps://doi.org/10.1021/acsenergylett.6c00105en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/10927
dc.description.abstractTransition-metal-doped oxide-based phosphors led to near-infrared (NIR) light-emitting diodes and lasers. Mostly, the first transition series (3d) metal ions, like Cr3+, are doped. Interestingly, heavier transition-metal ions, like Mo3+, Re4+, and Os4+, in their low oxidation states, can be doped in halide perovskites, unlike the oxide hosts that stabilize the higher oxidation state. Consequently, doping heavier transition metal ions in halide hosts opens up new avenues to tailor NIR-I/II emissions for both narrow and broad-band d–d transitions. Furthermore, characteristics such as (i) tunability of crystal field parameters by halide ions, (ii) host emissions, and (iii) colloidal nanocrystal synthesis add new NIR functionalities to transition-metal-doped halide perovskites compared to oxides. Here we provide insights on recent progresses on the NIR emitting transition-metal-doped halides, connecting synthetic materials chemistry, spectroscopy and device fabrication. The present challenges and future opportunities are discussed.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectInfrared lighten_US
dc.subjectLuminescenceen_US
dc.subjectNanocrystalsen_US
dc.subjectPerovskitesen_US
dc.subjectPhosphorsen_US
dc.subject2026-APR-WEEK4en_US
dc.subjectTOC-APR-2026en_US
dc.subject2026en_US
dc.titleTransition-Metal-Doped Halide Perovskites for Near-Infrared Emissions: Beyond Oxidesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleACS Energy Lettersen_US
dc.publication.originofpublisherForeignen_US
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