<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Khan MA</submitter><funding>U.S. Department of Energy</funding><funding>Camille and Henry Dreyfus Foundation</funding><funding>European Research Council</funding><funding>Higher Education Commission, Pakistan</funding><funding>UK Research and Innovation</funding><funding>European Regional Development Fund</funding><pagination>47036-47043</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12751002</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>147(51)</volume><pubmed_abstract>Electrochemical CO&lt;sub>2&lt;/sub> capture is an emerging technology that promises to be more energy-efficient than traditional thermal or pressure-swing processes. Herein, the first evidence of electrochemical capture of CO&lt;sub>2&lt;/sub> using a covalent organic framework (COF) is presented. We hypothesized that the assembly of anthraquinone units into a well-defined porous framework electrode would lead to enhanced electrochemical CO&lt;sub>2&lt;/sub> capture compared to previous approaches that grafted anthraquinones on carbon supports and suffered from low CO&lt;sub>2&lt;/sub> capacities and stabilities. To test this, an anthraquinone-based COF is employed, and it is found that the quinones are electrochemically accessible for reversible CO&lt;sub>2&lt;/sub> capture in an ionic liquid electrolyte. The system </pubmed_abstract><journal>Journal of the American Chemical Society</journal><pubmed_title>Electrochemical CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; Capture by a Quinone-Based Covalent Organic Framework.</pubmed_title><pmcid>PMC12751002</pmcid><funding_grant_id>MR/T043024/1</funding_grant_id><funding_grant_id>NRPU 15273</funding_grant_id><funding_grant_id>DE-SC0021000</funding_grant_id><funding_grant_id>TC-23-048</funding_grant_id><funding_grant_id>101040394</funding_grant_id><funding_grant_id>2022 FGI 0007</funding_grant_id><pubmed_authors>Amin K</pubmed_authors><pubmed_authors>Ali NZ</pubmed_authors><pubmed_authors>Muzammil M</pubmed_authors><pubmed_authors>Milner PJ</pubmed_authors><pubmed_authors>Lu Y</pubmed_authors><pubmed_authors>Ling J</pubmed_authors><pubmed_authors>Wei Z</pubmed_authors><pubmed_authors>Hartley NA</pubmed_authors><pubmed_authors>Bird S</pubmed_authors><pubmed_authors>Taylor J</pubmed_authors><pubmed_authors>Forse AC</pubmed_authors><pubmed_authors>Munawar M</pubmed_authors><pubmed_authors>Hetze K</pubmed_authors><pubmed_authors>Oschatz M</pubmed_authors><pubmed_authors>Enninful HRNB</pubmed_authors><pubmed_authors>Cao S</pubmed_authors><pubmed_authors>Salam F</pubmed_authors><pubmed_authors>Khan MA</pubmed_authors><pubmed_authors>Xu Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical CO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; Capture by a Quinone-Based Covalent Organic Framework.</name><description>Electrochemical CO&lt;sub>2&lt;/sub> capture is an emerging technology that promises to be more energy-efficient than traditional thermal or pressure-swing processes. Herein, the first evidence of electrochemical capture of CO&lt;sub>2&lt;/sub> using a covalent organic framework (COF) is presented. We hypothesized that the assembly of anthraquinone units into a well-defined porous framework electrode would lead to enhanced electrochemical CO&lt;sub>2&lt;/sub> capture compared to previous approaches that grafted anthraquinones on carbon supports and suffered from low CO&lt;sub>2&lt;/sub> capacities and stabilities. To test this, an anthraquinone-based COF is employed, and it is found that the quinones are electrochemically accessible for reversible CO&lt;sub>2&lt;/sub> capture in an ionic liquid electrolyte. The system </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T07:41:32.66Z</modification><creation>2026-05-27T03:11:59.953Z</creation></dates><accession>S-EPMC12751002</accession><cross_references><pubmed>41363080</pubmed><doi>10.1021/jacs.5c12304</doi></cross_references></HashMap>