<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Lin Q</submitter><pubmed_abstract>Osmium (Os), the least expensive member of the platinum-group metals, has emerged as a promising alternative to Pt-based catalysts for the hydrogen evolution reaction (HER). However, Os-based electrocatalysts still suffer from poor stability under acidic conditions, despite recent efforts to mitigate H* over-adsorption for improved intrinsic activity. Here, we design a porous CeO&lt;sub>2&lt;/sub> support that enables the atomic dispersion of Os, forming an Os single-atom catalyst (Os&lt;sub>SA&lt;/sub>-CeO&lt;sub>2&lt;/sub>). Unlike traditional flat-film supports, the porous CeO&lt;sub>2&lt;/sub> architecture prevents Os aggregation and achieves 100% interfacial anchoring of Os atoms. The resulting strong electronic coupling enables tight anchoring of Os and activates the CeO&lt;sub>2&lt;/sub> matrix with abundant oxy</pubmed_abstract><journal>Chemical science</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12908458</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Atomic-level interface engineering enables efficient and durable acidic hydrogen evolution of osmium at large current densities.</pubmed_title><pmcid>PMC12908458</pmcid><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Lin Q</pubmed_authors><pubmed_authors>Liang W</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Liao M</pubmed_authors><pubmed_authors>Song Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Atomic-level interface engineering enables efficient and durable acidic hydrogen evolution of osmium at large current densities.</name><description>Osmium (Os), the least expensive member of the platinum-group metals, has emerged as a promising alternative to Pt-based catalysts for the hydrogen evolution reaction (HER). However, Os-based electrocatalysts still suffer from poor stability under acidic conditions, despite recent efforts to mitigate H* over-adsorption for improved intrinsic activity. Here, we design a porous CeO&lt;sub>2&lt;/sub> support that enables the atomic dispersion of Os, forming an Os single-atom catalyst (Os&lt;sub>SA&lt;/sub>-CeO&lt;sub>2&lt;/sub>). Unlike traditional flat-film supports, the porous CeO&lt;sub>2&lt;/sub> architecture prevents Os aggregation and achieves 100% interfacial anchoring of Os atoms. The resulting strong electronic coupling enables tight anchoring of Os and activates the CeO&lt;sub>2&lt;/sub> matrix with abundant oxy</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T05:01:44.799Z</modification><creation>2026-07-09T13:10:29.942Z</creation></dates><accession>S-EPMC12908458</accession><cross_references><pubmed>41705039</pubmed><doi>10.1039/d5sc09741j</doi></cross_references></HashMap>