<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zheng GS</submitter><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>2365</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10943204</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>It remains a challenge to obtain biocompatible afterglow materials with long emission wavelengths, durable lifetimes, and good water solubility. Herein we develop a photooxidation strategy to construct near-infrared afterglow carbon nanodots with an extra-long lifetime of up to 5.9 h, comparable to that of the well-known rare-earth or organic long-persistent luminescent materials. Intriguingly, size-dependent afterglow lifetime evolution from 3.4 to 5.9 h has been observed from the carbon nanodots systems in aqueous solution. With structural/ultrafast dynamics analysis and density functional theory simulations, we reveal that the persistent luminescence in carbon nanodots is activated by a photooxidation-induced dioxetane intermediate, which can slowly release and convert energy into lumin</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Photooxidation triggered ultralong afterglow in carbon nanodots.</pubmed_title><pmcid>PMC10943204</pmcid><funding_grant_id>12261141661</funding_grant_id><pubmed_authors>Lou Q</pubmed_authors><pubmed_authors>Liu KK</pubmed_authors><pubmed_authors>Li PF</pubmed_authors><pubmed_authors>Dong L</pubmed_authors><pubmed_authors>Zang JH</pubmed_authors><pubmed_authors>Niu CY</pubmed_authors><pubmed_authors>Cheng Z</pubmed_authors><pubmed_authors>Shi XJ</pubmed_authors><pubmed_authors>Zheng GS</pubmed_authors><pubmed_authors>Shen CL</pubmed_authors><pubmed_authors>Shan CX</pubmed_authors><pubmed_authors>Jiang TC</pubmed_authors><pubmed_authors>Song RW</pubmed_authors><pubmed_authors>Lv CF</pubmed_authors><pubmed_authors>Deng Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Photooxidation triggered ultralong afterglow in carbon nanodots.</name><description>It remains a challenge to obtain biocompatible afterglow materials with long emission wavelengths, durable lifetimes, and good water solubility. Herein we develop a photooxidation strategy to construct near-infrared afterglow carbon nanodots with an extra-long lifetime of up to 5.9 h, comparable to that of the well-known rare-earth or organic long-persistent luminescent materials. Intriguingly, size-dependent afterglow lifetime evolution from 3.4 to 5.9 h has been observed from the carbon nanodots systems in aqueous solution. With structural/ultrafast dynamics analysis and density functional theory simulations, we reveal that the persistent luminescence in carbon nanodots is activated by a photooxidation-induced dioxetane intermediate, which can slowly release and convert energy into lumin</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-26T22:56:50.649Z</modification><creation>2025-04-06T17:26:33.175Z</creation></dates><accession>S-EPMC10943204</accession><cross_references><pubmed>38491012</pubmed><doi>10.1038/s41467-024-46668-z</doi></cross_references></HashMap>