<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Meng Y</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>933</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12830983</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(1)</volume><pubmed_abstract>The non-radiative metallic core (MC) centered lowest excited states of most ligand-stabilized metallic clusters commonly quench radiative but high-lying ligand-centered excited states, e.g. intra-ligand charge transfer (LCT), which is one of the key issues limiting efficiencies of electroluminescent (EL) clusters. Herein, we realize the desired excited state reversal in a cubic [PXZDBFDP]&lt;sub>2&lt;/sub>Cu&lt;sub>4&lt;/sub>I&lt;sub>4&lt;/sub> (PXZDBFDP = 10-(4,6-bis(diphenylphosphino)dibenzo[b,d]furan-2-yl)-10H-phenoxazine) modified with strongly electron-donating phenoxazine (PXZ) to strengthen donor-acceptor (D-A) interactions and enhance LCT. Consequently, its thoroughly LCT-featured first singlet (S&lt;sub>1&lt;/sub>) and triplet (T&lt;sub>1&lt;/sub>) excited states are energetically lower than its Cu&lt;sub>4&lt;/sub></pubmed_abstract><journal>Nature communications</journal><pubmed_title>Excited state reversal in copper iodide clusters enables 100% exciton radiation.</pubmed_title><pmcid>PMC12830983</pmcid><funding_grant_id>22325502, 92461304, W2412073, 22305073 and 52273173</funding_grant_id><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Duan C</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Han C</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Meng Y</pubmed_authors><pubmed_authors>Fei J</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Excited state reversal in copper iodide clusters enables 100% exciton radiation.</name><description>The non-radiative metallic core (MC) centered lowest excited states of most ligand-stabilized metallic clusters commonly quench radiative but high-lying ligand-centered excited states, e.g. intra-ligand charge transfer (LCT), which is one of the key issues limiting efficiencies of electroluminescent (EL) clusters. Herein, we realize the desired excited state reversal in a cubic [PXZDBFDP]&lt;sub>2&lt;/sub>Cu&lt;sub>4&lt;/sub>I&lt;sub>4&lt;/sub> (PXZDBFDP = 10-(4,6-bis(diphenylphosphino)dibenzo[b,d]furan-2-yl)-10H-phenoxazine) modified with strongly electron-donating phenoxazine (PXZ) to strengthen donor-acceptor (D-A) interactions and enhance LCT. Consequently, its thoroughly LCT-featured first singlet (S&lt;sub>1&lt;/sub>) and triplet (T&lt;sub>1&lt;/sub>) excited states are energetically lower than its Cu&lt;sub>4&lt;/sub></description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T20:15:09.455Z</modification><creation>2026-06-04T03:14:10.58Z</creation></dates><accession>S-EPMC12830983</accession><cross_references><pubmed>41402303</pubmed><doi>10.1038/s41467-025-67664-x</doi></cross_references></HashMap>