<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Junisu BA</submitter><funding>Institute for Information Industry, Ministry of Science and Technology, Taiwan</funding><pagination>33245-33255</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12713784</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(49)</volume><pubmed_abstract>Block copolymer micelles mediate PbBr&lt;sub>2&lt;/sub> complexation through two distinct pathways: an architecture-dependent interfacial process under static conditions and a shear-dominated mechanism under dynamic mixing. This study reveals how the polystyrene-&lt;i>block&lt;/i>-poly(2-vinylpyridine) (PS-&lt;i>b&lt;/i>-P2VP) asymmetry governs the chain adsorption conformations (&lt;i>trains&lt;/i>, &lt;i>loops&lt;/i>, and &lt;i>tails&lt;/i>) on PbBr&lt;sub>2&lt;/sub> surfaces and its complexation outcome. Under static conditions, the process is kinetically limited by micellar diffusion. Upon reaching the PbBr&lt;sub>2&lt;/sub> surface, the strong pyridine-Pb&lt;sup>2+&lt;/sup> coordination induces a restructuring of the micelle core. For asymmetric PS-&lt;i>b&lt;/i>-P2VP with long P2VP blocks, a thin PS shell allows the P2VP core to deform and sp</pubmed_abstract><journal>Langmuir : the ACS journal of surfaces and colloids</journal><pubmed_title>Micelle-Mediated PbBr&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; Complexation: Influence of Block Copolymer Architecture and Mixing Conditions.</pubmed_title><pmcid>PMC12713784</pmcid><funding_grant_id>NSTC 112-2811-E-006 -042 -MY2</funding_grant_id><funding_grant_id>NSTC 111-2221-E-006-232-MY3</funding_grant_id><pubmed_authors>Junisu BA</pubmed_authors><pubmed_authors>Sun YS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Micelle-Mediated PbBr&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; Complexation: Influence of Block Copolymer Architecture and Mixing Conditions.</name><description>Block copolymer micelles mediate PbBr&lt;sub>2&lt;/sub> complexation through two distinct pathways: an architecture-dependent interfacial process under static conditions and a shear-dominated mechanism under dynamic mixing. This study reveals how the polystyrene-&lt;i>block&lt;/i>-poly(2-vinylpyridine) (PS-&lt;i>b&lt;/i>-P2VP) asymmetry governs the chain adsorption conformations (&lt;i>trains&lt;/i>, &lt;i>loops&lt;/i>, and &lt;i>tails&lt;/i>) on PbBr&lt;sub>2&lt;/sub> surfaces and its complexation outcome. Under static conditions, the process is kinetically limited by micellar diffusion. Upon reaching the PbBr&lt;sub>2&lt;/sub> surface, the strong pyridine-Pb&lt;sup>2+&lt;/sup> coordination induces a restructuring of the micelle core. For asymmetric PS-&lt;i>b&lt;/i>-P2VP with long P2VP blocks, a thin PS shell allows the P2VP core to deform and sp</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T05:45:53.735Z</modification><creation>2026-05-26T03:12:14.536Z</creation></dates><accession>S-EPMC12713784</accession><cross_references><pubmed>41339310</pubmed><doi>10.1021/acs.langmuir.5c04107</doi></cross_references></HashMap>