<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ma Y</submitter><funding>Hainan Province Science and Technology Special Fund</funding><funding>Innovation Fund for Scientific and Technological Personnel of Hainan Province</funding><funding>National Natural Science Foundation of China</funding><funding>Specific research fund of the Innovation Platform for Academicians of Hainan Province</funding><funding>National Key Research and Development Program of China</funding><pagination>e00697</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12376611</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(30)</volume><pubmed_abstract>The leakage of nuclear pollution highlights the critical importance of effectively separating radioactive pollutants. Radioactive iodine, a high-yield fission product of nuclear reactions, poses serious environmental and health risks. However, the lack of efficient adsorbents makes the management of aqueous radioactive iodine pollution a significant challenge. N-doped materials are among the most recognized adsorbents for iodine removal, but their weak binding affinity and limited number of iodine-binding N-sites hinder their practical application. Herein, a covalent organic framework (COFs) named phen-TPA is synthesized, featuring an increased number and optimized local chemical environment of iodine-binding N-sites. This material demonstrates record-breaking iodine removal kinetics, with</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Local Charge Density Enhancement Strategy in Nitrogen-rich Covalent Organic Framework for Boosted Iodine Removal From Water.</pubmed_title><pmcid>PMC12376611</pmcid><funding_grant_id>U2167220</funding_grant_id><funding_grant_id>22327807</funding_grant_id><funding_grant_id>22366013</funding_grant_id><funding_grant_id>22365012</funding_grant_id><funding_grant_id>KJRC2023B01</funding_grant_id><funding_grant_id>YSPTZX202316</funding_grant_id><funding_grant_id>2023YFC2809000</funding_grant_id><funding_grant_id>ZDYF2024SHFZ066</funding_grant_id><funding_grant_id>U23A20104</funding_grant_id><pubmed_authors>Wang N</pubmed_authors><pubmed_authors>Pan J</pubmed_authors><pubmed_authors>Rong H</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Cao X</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Liu T</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Local Charge Density Enhancement Strategy in Nitrogen-rich Covalent Organic Framework for Boosted Iodine Removal From Water.</name><description>The leakage of nuclear pollution highlights the critical importance of effectively separating radioactive pollutants. Radioactive iodine, a high-yield fission product of nuclear reactions, poses serious environmental and health risks. However, the lack of efficient adsorbents makes the management of aqueous radioactive iodine pollution a significant challenge. N-doped materials are among the most recognized adsorbents for iodine removal, but their weak binding affinity and limited number of iodine-binding N-sites hinder their practical application. Herein, a covalent organic framework (COFs) named phen-TPA is synthesized, featuring an increased number and optimized local chemical environment of iodine-binding N-sites. This material demonstrates record-breaking iodine removal kinetics, with</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-09T17:51:31.892Z</modification><creation>2026-04-08T01:07:02.968Z</creation></dates><accession>S-EPMC12376611</accession><cross_references><pubmed>40391680</pubmed><doi>10.1002/advs.202500697</doi></cross_references></HashMap>