<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jiang Z</submitter><funding>N/A</funding><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>827</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9929054</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Distinctive upconversion or downshifting of lanthanide nanocrystals holds promise for biomedical and photonic applications. However, either process requires high-energy lasers at discrete wavelengths for excitation. Here we demonstrate that co-sensitization can break this limitation with ultrawide excitation bands. We achieve co-sensitization by employing Nd&lt;sup>3+&lt;/sup> and Ho&lt;sup>3+&lt;/sup> as the co-sensitizers with complementary absorptions from the ultraviolet to infrared region. Symmetric penta-layer core-shell nanostructure enables tunable fluorescence in the visible and the second near-infrared window when incorporating different activators (Er&lt;sup>3+&lt;/sup>, Ho&lt;sup>3+&lt;/sup>, Pr&lt;sup>3+&lt;/sup>, and Tm&lt;sup>3+&lt;/sup>). Transient spectra confirm the directional energy transfer from sensitiz</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Ultra-wideband-responsive photon conversion through co-sensitization in lanthanide nanocrystals.</pubmed_title><pmcid>PMC9929054</pmcid><funding_grant_id>81971704</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Qiu H</pubmed_authors><pubmed_authors>He L</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Yu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultra-wideband-responsive photon conversion through co-sensitization in lanthanide nanocrystals.</name><description>Distinctive upconversion or downshifting of lanthanide nanocrystals holds promise for biomedical and photonic applications. However, either process requires high-energy lasers at discrete wavelengths for excitation. Here we demonstrate that co-sensitization can break this limitation with ultrawide excitation bands. We achieve co-sensitization by employing Nd&lt;sup>3+&lt;/sup> and Ho&lt;sup>3+&lt;/sup> as the co-sensitizers with complementary absorptions from the ultraviolet to infrared region. Symmetric penta-layer core-shell nanostructure enables tunable fluorescence in the visible and the second near-infrared window when incorporating different activators (Er&lt;sup>3+&lt;/sup>, Ho&lt;sup>3+&lt;/sup>, Pr&lt;sup>3+&lt;/sup>, and Tm&lt;sup>3+&lt;/sup>). Transient spectra confirm the directional energy transfer from sensitiz</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-18T13:37:51.783Z</modification><creation>2025-04-04T11:16:32.92Z</creation></dates><accession>S-EPMC9929054</accession><cross_references><pubmed>36788239</pubmed><doi>10.1038/s41467-023-36510-3</doi></cross_references></HashMap>