<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Yu J</submitter><pubmed_abstract>Earth-abundant electrocatalysts for the oxygen evolution reaction (OER) able to work in acidic working conditions are elusive. While many first-row transition metal oxides are competitive in alkaline media, most of them just dissolve or become inactive at high proton concentrations where hydrogen evolution is preferred. Only noble-metal catalysts, such as IrO&lt;sub>2&lt;/sub>, are fast and stable enough in acidic media. Herein, we report the excellent activity and long-term stability of Co&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub>-based anodes in 1 M H&lt;sub>2&lt;/sub>SO&lt;sub>4&lt;/sub> (pH 0.1) when processed in a partially hydrophobic carbon-based protecting matrix. These Co&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub>@C composites reliably drive O&lt;sub>2&lt;/sub> evolution a 10 mA cm&lt;sup>-2&lt;/sup> current density for >40 h without appearance</pubmed_abstract><journal>Nature communications</journal><pagination>4341</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9329283</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sustainable oxygen evolution electrocatalysis in aqueous 1 M H&lt;sub>2&lt;/sub>SO&lt;sub>4&lt;/sub> with earth abundant nanostructured Co&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub>.</pubmed_title><pmcid>PMC9329283</pmcid><pubmed_authors>Rogero C</pubmed_authors><pubmed_authors>Pena-Diaz M</pubmed_authors><pubmed_authors>Barja S</pubmed_authors><pubmed_authors>Arbiol J</pubmed_authors><pubmed_authors>Gimenez S</pubmed_authors><pubmed_authors>Spadaro MC</pubmed_authors><pubmed_authors>Galan-Mascaros JR</pubmed_authors><pubmed_authors>Gonzalez-Cobos J</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Garces-Pineda FA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sustainable oxygen evolution electrocatalysis in aqueous 1 M H&lt;sub>2&lt;/sub>SO&lt;sub>4&lt;/sub> with earth abundant nanostructured Co&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub>.</name><description>Earth-abundant electrocatalysts for the oxygen evolution reaction (OER) able to work in acidic working conditions are elusive. While many first-row transition metal oxides are competitive in alkaline media, most of them just dissolve or become inactive at high proton concentrations where hydrogen evolution is preferred. Only noble-metal catalysts, such as IrO&lt;sub>2&lt;/sub>, are fast and stable enough in acidic media. Herein, we report the excellent activity and long-term stability of Co&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub>-based anodes in 1 M H&lt;sub>2&lt;/sub>SO&lt;sub>4&lt;/sub> (pH 0.1) when processed in a partially hydrophobic carbon-based protecting matrix. These Co&lt;sub>3&lt;/sub>O&lt;sub>4&lt;/sub>@C composites reliably drive O&lt;sub>2&lt;/sub> evolution a 10 mA cm&lt;sup>-2&lt;/sup> current density for >40 h without appearance</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2026-05-09T15:30:39.098Z</modification><creation>2022-08-06T14:55:43.349Z</creation></dates><accession>S-EPMC9329283</accession><cross_references><pubmed>35896541</pubmed><doi>10.1038/s41467-022-32024-6</doi></cross_references></HashMap>