<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li S</submitter><funding>Chinese Academy of Sciences</funding><funding>Ningbo Yongjiang Talent Programme</funding><funding>GuangDong Basic and Applied Basic Research Foundation</funding><funding>Strategic Priority Research Program of the Chinese Academy of Sciences</funding><funding>Natural Science Foundation of China</funding><funding>Scientific Research Innovation Project of the Graduate School of South China Normal University</funding><funding>Vacuum Interconnected Nanotech Workstation (Nano-X)</funding><funding>National Natural Science Foundation of China</funding><funding>Energy Revolution S&amp;T Program of Yulin Innovation Institute of Clean Energy</funding><funding>Entrepreneurial and innovative team project of Ningbo Yinzhou District</funding><funding>Science and Technology Major Project of Liaoning Province</funding><pagination>e14577</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12810656</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>38(4)</volume><pubmed_abstract>Rechargeable aqueous zinc-iodine batteries (AZIBs) demonstrate immense potential for large-scale energy storage owing to their high theoretical capacity, resource abundance, and low cost. However, their practical deployment is hampered by the notorious polyiodide shuttle effect and sluggish redox kinetics. Herein, an Al-TCPP(Fe) metal-organic framework (MOF) is designed and synthesized with specific functional sites as an advanced iodine host. The unique microporous structure of this MOF provides significant spatial confinement, which effectively suppresses the dissolution and migration of polyiodide intermediates, thereby mitigating the shuttle effect. Furthermore, precisely engineered Fe-N&lt;sub>4&lt;/sub> catalytic sites embedded within the MOF framework induce a quantum size effect under na</pubmed_abstract><journal>Advanced materials (Deerfield Beach, Fla.)</journal><pubmed_title>Quantum Size Effect Synergizes Space-Limited Domain Action for Advanced Aqueous Zinc-Iodine Batteries.</pubmed_title><pmcid>PMC12810656</pmcid><funding_grant_id>E411130705</funding_grant_id><funding_grant_id>22379047</funding_grant_id><funding_grant_id>2023A395G</funding_grant_id><funding_grant_id>2023B1515120095</funding_grant_id><funding_grant_id>2024JH1/11700013</funding_grant_id><funding_grant_id>XDB0600400</funding_grant_id><funding_grant_id>22309179</funding_grant_id><pubmed_authors>Ma Q</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zhao C</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Jin M</pubmed_authors><pubmed_authors>Feng G</pubmed_authors><pubmed_authors>Li Q</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Nie Y</pubmed_authors><pubmed_authors>Luo D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantum Size Effect Synergizes Space-Limited Domain Action for Advanced Aqueous Zinc-Iodine Batteries.</name><description>Rechargeable aqueous zinc-iodine batteries (AZIBs) demonstrate immense potential for large-scale energy storage owing to their high theoretical capacity, resource abundance, and low cost. However, their practical deployment is hampered by the notorious polyiodide shuttle effect and sluggish redox kinetics. Herein, an Al-TCPP(Fe) metal-organic framework (MOF) is designed and synthesized with specific functional sites as an advanced iodine host. The unique microporous structure of this MOF provides significant spatial confinement, which effectively suppresses the dissolution and migration of polyiodide intermediates, thereby mitigating the shuttle effect. Furthermore, precisely engineered Fe-N&lt;sub>4&lt;/sub> catalytic sites embedded within the MOF framework induce a quantum size effect under na</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T15:41:49.901Z</modification><creation>2026-06-02T03:08:49.709Z</creation></dates><accession>S-EPMC12810656</accession><cross_references><pubmed>41185985</pubmed><doi>10.1002/adma.202514577</doi></cross_references></HashMap>