<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang J</submitter><funding>National Key R&amp;D Program of China</funding><funding>European Union's Horizon 2020 research and innovation programme</funding><funding>National Key Research and Development Program of China</funding><funding>Natural Science Foundation of Jiangsu Province</funding><funding>CRC 1415</funding><pagination>e202209486</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9804859</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(39)</volume><pubmed_abstract>Ruthenium (Ru) has been theoretically considered a viable alkaline hydrogen evolution reaction electrocatalyst due to its fast water dissociation kinetics. However, its strong affinity to the adsorbed hydroxyl (OH&lt;sub>ad&lt;/sub> ) blocks the active sites, resulting in unsatisfactory performance during the practical HER process. Here, we first reported a competitive adsorption strategy for the construction of SnO&lt;sub>2&lt;/sub> nanoparticles doped with Ru single-atoms supported on carbon (Ru SAs-SnO&lt;sub>2&lt;/sub> /C) via atomic galvanic replacement. SnO&lt;sub>2&lt;/sub> was introduced to regulate the strong interaction between Ru and OH&lt;sub>ad&lt;/sub> by the competitive adsorption of OH&lt;sub>ad&lt;/sub> between Ru and SnO&lt;sub>2&lt;/sub> , which alleviated the poisoning of Ru sites. As a consequence, the Ru SAs-</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>Competitive Adsorption: Reducing the Poisoning Effect of Adsorbed Hydroxyl on Ru Single-Atom Site with SnO&lt;sub>2&lt;/sub> for Efficient Hydrogen Evolution.</pubmed_title><pmcid>PMC9804859</pmcid><funding_grant_id>No. BK20220369</funding_grant_id><funding_grant_id>GrapheneCore3: 881603</funding_grant_id><funding_grant_id>No. 417590517</funding_grant_id><funding_grant_id>2021YFA1502700</funding_grant_id><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Feng X</pubmed_authors><pubmed_authors>Chen G</pubmed_authors><pubmed_authors>Sun D</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Fan C</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Competitive Adsorption: Reducing the Poisoning Effect of Adsorbed Hydroxyl on Ru Single-Atom Site with SnO&lt;sub>2&lt;/sub> for Efficient Hydrogen Evolution.</name><description>Ruthenium (Ru) has been theoretically considered a viable alkaline hydrogen evolution reaction electrocatalyst due to its fast water dissociation kinetics. However, its strong affinity to the adsorbed hydroxyl (OH&lt;sub>ad&lt;/sub> ) blocks the active sites, resulting in unsatisfactory performance during the practical HER process. Here, we first reported a competitive adsorption strategy for the construction of SnO&lt;sub>2&lt;/sub> nanoparticles doped with Ru single-atoms supported on carbon (Ru SAs-SnO&lt;sub>2&lt;/sub> /C) via atomic galvanic replacement. SnO&lt;sub>2&lt;/sub> was introduced to regulate the strong interaction between Ru and OH&lt;sub>ad&lt;/sub> by the competitive adsorption of OH&lt;sub>ad&lt;/sub> between Ru and SnO&lt;sub>2&lt;/sub> , which alleviated the poisoning of Ru sites. As a consequence, the Ru SAs-</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2026-03-17T16:01:25.578Z</modification><creation>2025-04-04T21:04:35.353Z</creation></dates><accession>S-EPMC9804859</accession><cross_references><pubmed>35862112</pubmed><doi>10.1002/anie.202209486</doi></cross_references></HashMap>