<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Seo H</submitter><funding>DOE | SC | Basic Energy Sciences (BES)</funding><pagination>313</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9852473</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Direct air capture of carbon dioxide is a viable option for the mitigation of CO&lt;sub>2&lt;/sub> emissions and their impact on global climate change. Conventional processes for carbon capture from ambient air require 230 to 800 kJ thermal per mole of CO&lt;sub>2&lt;/sub>, which accounts for most of the total cost of capture. Here, we demonstrate electrochemical direct air capture using neutral red as a redox-active material in an aqueous solution enabled by the inclusion of nicotinamide as a hydrotropic solubilizing agent. The electrochemical system demonstrates a high electron utilization of 0.71 in a continuous flow cell with an estimated minimum work of 35 kJ&lt;sub>e&lt;/sub> per mole of CO&lt;sub>2&lt;/sub> from 15% CO&lt;sub>2&lt;/sub>. Further exploration using ambient air (410 ppm CO&lt;sub>2&lt;/sub> in the presence of 20% oxygen) as a feed gas shows electron utilization of 0.38 in a continuous flow cell to provide an estimated minimum work of 65 kJ&lt;sub>e&lt;/sub> per mole of CO&lt;sub>2&lt;/sub>.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Electrochemical direct air capture of CO&lt;sub>2&lt;/sub> using neutral red as reversible redox-active material.</pubmed_title><pmcid>PMC9852473</pmcid><funding_grant_id>FWP 76830</funding_grant_id><pubmed_authors>Hatton TA</pubmed_authors><pubmed_authors>Seo H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical direct air capture of CO&lt;sub>2&lt;/sub> using neutral red as reversible redox-active material.</name><description>Direct air capture of carbon dioxide is a viable option for the mitigation of CO&lt;sub>2&lt;/sub> emissions and their impact on global climate change. Conventional processes for carbon capture from ambient air require 230 to 800 kJ thermal per mole of CO&lt;sub>2&lt;/sub>, which accounts for most of the total cost of capture. Here, we demonstrate electrochemical direct air capture using neutral red as a redox-active material in an aqueous solution enabled by the inclusion of nicotinamide as a hydrotropic solubilizing agent. The electrochemical system demonstrates a high electron utilization of 0.71 in a continuous flow cell with an estimated minimum work of 35 kJ&lt;sub>e&lt;/sub> per mole of CO&lt;sub>2&lt;/sub> from 15% CO&lt;sub>2&lt;/sub>. Further exploration using ambient air (410 ppm CO&lt;sub>2&lt;/sub> in the presence of 20% oxygen) as a feed gas shows electron utilization of 0.38 in a continuous flow cell to provide an estimated minimum work of 65 kJ&lt;sub>e&lt;/sub> per mole of CO&lt;sub>2&lt;/sub>.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-04T11:33:35.965Z</modification><creation>2025-04-04T11:33:35.965Z</creation></dates><accession>S-EPMC9852473</accession><cross_references><pubmed>36658126</pubmed><doi>10.1038/s41467-023-35866-w</doi></cross_references></HashMap>