<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang X</submitter><funding>National Natural Science Foundation of China</funding><funding>National Natural Science Foundation of China (National Science Foundation of China)</funding><pagination>2649</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11258313</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Hydrogen peroxide photosynthesis suffers from insufficient catalytic activity due to the high energy barrier of hydrogen extraction from H&lt;sub>2&lt;/sub>O. Herein, we report that mechanochemically synthesized keto-form anthraquinone covalent organic framework which is able to directly synthesize H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> (4784 μmol h&lt;sup>-1&lt;/sup> g&lt;sup>-1&lt;/sup> at λ > 400 nm) from oxygen and alkaline water (pH = 13) in the absence of any sacrificial reagents. The strong alkalinity resulted in the formation of OH&lt;sup>-&lt;/sup>(H&lt;sub>2&lt;/sub>O)&lt;sub>n&lt;/sub> clusters in water, which were adsorbed on keto moieties within the framework and then dissociated into O&lt;sub>2&lt;/sub> and active hydrogen, because the energy barrier of hydrogen extraction was largely lowered. The produced hydrogen reacted with </pubmed_abstract><journal>Nature communications</journal><pubmed_title>Keto-anthraquinone covalent organic framework for H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> photosynthesis with oxygen and alkaline water.</pubmed_title><pmcid>PMC11258313</pmcid><funding_grant_id>52070128, 22206125, 22376138</funding_grant_id><pubmed_authors>Cheng S</pubmed_authors><pubmed_authors>Wen X</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Zhou B</pubmed_authors><pubmed_authors>Long M</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Chen C</pubmed_authors><pubmed_authors>Miao J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Keto-anthraquinone covalent organic framework for H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> photosynthesis with oxygen and alkaline water.</name><description>Hydrogen peroxide photosynthesis suffers from insufficient catalytic activity due to the high energy barrier of hydrogen extraction from H&lt;sub>2&lt;/sub>O. Herein, we report that mechanochemically synthesized keto-form anthraquinone covalent organic framework which is able to directly synthesize H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> (4784 μmol h&lt;sup>-1&lt;/sup> g&lt;sup>-1&lt;/sup> at λ > 400 nm) from oxygen and alkaline water (pH = 13) in the absence of any sacrificial reagents. The strong alkalinity resulted in the formation of OH&lt;sup>-&lt;/sup>(H&lt;sub>2&lt;/sub>O)&lt;sub>n&lt;/sub> clusters in water, which were adsorbed on keto moieties within the framework and then dissociated into O&lt;sub>2&lt;/sub> and active hydrogen, because the energy barrier of hydrogen extraction was largely lowered. The produced hydrogen reacted with </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T03:19:51.292Z</modification><creation>2025-04-04T03:19:51.292Z</creation></dates><accession>S-EPMC11258313</accession><cross_references><pubmed>38531862</pubmed><doi>10.1038/s41467-024-47023-y</doi></cross_references></HashMap>