<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Benin BM</submitter><funding>European Research Council</funding><funding>H2020 Marie Skłodowska-Curie Actions</funding><pagination>11329-11333</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6175341</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>57(35)</volume><pubmed_abstract>The spatial localization of charge carriers to promote the formation of bound excitons and concomitantly enhance radiative recombination has long been a goal for luminescent semiconductors. Zero-dimensional materials structurally impose carrier localization and result in the formation of localized Frenkel excitons. Now the fully inorganic, perovskite-derived zero-dimensional Sn&lt;sup>II&lt;/sup> material Cs&lt;sub>4&lt;/sub> SnBr&lt;sub>6&lt;/sub> is presented that exhibits room-temperature broad-band photoluminescence centered at 540 nm with a quantum yield (QY) of 15±5 %. A series of analogous compositions following the general formula Cs&lt;sub>4-x&lt;/sub> A&lt;sub>x&lt;/sub> Sn(Br&lt;sub>1-y&lt;/sub> I&lt;sub>y&lt;/sub> )&lt;sub>6&lt;/sub> (A=Rb, K; x≤1, y≤1) can be prepared. The emission of these materials ranges from 500 nm to 620 nm with the possibility to compositionally tune the Stokes shift and the self-trapped exciton emission bands.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>Highly Emissive Self-Trapped Excitons in Fully Inorganic Zero-Dimensional Tin Halides.</pubmed_title><pmcid>PMC6175341</pmcid><funding_grant_id>642656</funding_grant_id><funding_grant_id>306733</funding_grant_id><funding_grant_id>H2020-MSCA-ITN-642656</funding_grant_id><pubmed_authors>Worle M</pubmed_authors><pubmed_authors>Raino G</pubmed_authors><pubmed_authors>Infante I</pubmed_authors><pubmed_authors>Kovalenko MV</pubmed_authors><pubmed_authors>Morad V</pubmed_authors><pubmed_authors>Nazarenko O</pubmed_authors><pubmed_authors>Dirin DN</pubmed_authors><pubmed_authors>Fischer M</pubmed_authors><pubmed_authors>Benin BM</pubmed_authors><pubmed_authors>Yakunin S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Highly Emissive Self-Trapped Excitons in Fully Inorganic Zero-Dimensional Tin Halides.</name><description>The spatial localization of charge carriers to promote the formation of bound excitons and concomitantly enhance radiative recombination has long been a goal for luminescent semiconductors. Zero-dimensional materials structurally impose carrier localization and result in the formation of localized Frenkel excitons. Now the fully inorganic, perovskite-derived zero-dimensional Sn&lt;sup>II&lt;/sup> material Cs&lt;sub>4&lt;/sub> SnBr&lt;sub>6&lt;/sub> is presented that exhibits room-temperature broad-band photoluminescence centered at 540 nm with a quantum yield (QY) of 15±5 %. A series of analogous compositions following the general formula Cs&lt;sub>4-x&lt;/sub> A&lt;sub>x&lt;/sub> Sn(Br&lt;sub>1-y&lt;/sub> I&lt;sub>y&lt;/sub> )&lt;sub>6&lt;/sub> (A=Rb, K; x≤1, y≤1) can be prepared. The emission of these materials ranges from 500 nm to 620 nm with the possibility to compositionally tune the Stokes shift and the self-trapped exciton emission bands.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2024-11-13T16:45:21.27Z</modification><creation>2019-03-27T00:03:01Z</creation></dates><accession>S-EPMC6175341</accession><cross_references><pubmed>29999575</pubmed><doi>10.1002/anie.201806452</doi></cross_references></HashMap>