<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Xu J</submitter><pubmed_abstract>In this work, we show that the spin dynamics of excitons can be dramatically altered by Maxwell magnetic field coupling, together with an ion-enhanced, low-internal-splitting-energy organic semiconducting emitter. By employing a unique, alternating current (AC)-driven organic electroluminescent (OEL) device architecture that optimizes this magnetic field coupling, almost complete control over the singlet-to-triplet ratio (from fluorescent to phosphorescent emission in a single device) is realized. We attribute this spin population control to magnetically sensitive polaron-spin pair intersystem crossings (ISCs) that can be directly manipulated through external driving conditions. As an illustration of the utility of this approach to spin-tailoring, we demonstrate a simple hybrid (double-layer) fluorescence-phosphorescence (F-P) device using a polyfluorene-based emitter with a strong external Zeeman effect and ion-induced long carrier diffusion. Remarkable control over de-excitation pathways is achieved by controlling the device-driving frequency, resulting in complete emission blue-red color tunability. Picosecond photoluminescence (PL) spectroscopy directly confirms that this color control derives from the magnetic manipulation of the singlet-to-triplet ratios. These results may pave the way to far more exotic organic devices with magnetic-field-coupled organic systems that are poised to usher in an era of dynamic spintronics at room temperature.</pubmed_abstract><journal>Light, science &amp; applications</journal><pagination>46</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6107016</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tailoring spin mixtures by ion-enhanced Maxwell magnetic coupling in color-tunable organic electroluminescent devices.</pubmed_title><pmcid>PMC6107016</pmcid><pubmed_authors>Dun C</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Cui Y</pubmed_authors><pubmed_authors>Shao L</pubmed_authors><pubmed_authors>Carroll DL</pubmed_authors><pubmed_authors>Li P</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Smith GM</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Xu J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tailoring spin mixtures by ion-enhanced Maxwell magnetic coupling in color-tunable organic electroluminescent devices.</name><description>In this work, we show that the spin dynamics of excitons can be dramatically altered by Maxwell magnetic field coupling, together with an ion-enhanced, low-internal-splitting-energy organic semiconducting emitter. By employing a unique, alternating current (AC)-driven organic electroluminescent (OEL) device architecture that optimizes this magnetic field coupling, almost complete control over the singlet-to-triplet ratio (from fluorescent to phosphorescent emission in a single device) is realized. We attribute this spin population control to magnetically sensitive polaron-spin pair intersystem crossings (ISCs) that can be directly manipulated through external driving conditions. As an illustration of the utility of this approach to spin-tailoring, we demonstrate a simple hybrid (double-layer) fluorescence-phosphorescence (F-P) device using a polyfluorene-based emitter with a strong external Zeeman effect and ion-induced long carrier diffusion. Remarkable control over de-excitation pathways is achieved by controlling the device-driving frequency, resulting in complete emission blue-red color tunability. Picosecond photoluminescence (PL) spectroscopy directly confirms that this color control derives from the magnetic manipulation of the singlet-to-triplet ratios. These results may pave the way to far more exotic organic devices with magnetic-field-coupled organic systems that are poised to usher in an era of dynamic spintronics at room temperature.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2021-02-20T18:22:41Z</modification><creation>2019-03-26T23:53:36Z</creation></dates><accession>S-EPMC6107016</accession><cross_references><pubmed>30839638</pubmed><doi>10.1038/s41377-018-0046-5</doi></cross_references></HashMap>