<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Tan L</submitter><pubmed_abstract>Proton exchange membrane water electrolysis (PEMWE) is a cornerstone technology for carbon-neutral hydrogen production, yet its scalability is constrained by the intrinsic activity-stability trade-off of oxygen evolution reaction (OER) electrocatalysts. To overcome this challenge, we design a Ru/RuO&lt;sub>2&lt;/sub> heterostructure by integrating metallic Ru to modulate the d-orbital electron density of RuO&lt;sub>2&lt;/sub>. The metallic Ru domains suppress lattice oxygen migration (LOM) while enhancing electron delocalization. The e&lt;sub>g&lt;/sub> orbital filling shifts the Ru 4d-band center downward, reducing the adsorption strength of reaction intermediates (*OH, *O, and *OOH). The optimized Ru/RuO&lt;sub>2&lt;/sub> electrocatalyst achieves an overpotential of 181 mV at 10 mA cm&lt;sup>-2&lt;/sup> in 0.5 M H&lt;su</pubmed_abstract><journal>Chemical science</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12822733</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Dopant-free stabilization of ruthenium oxide &amp;lt;i&amp;gt;via&amp;lt;/i&amp;gt; metallic Ru-induced d-orbital modulation for acidic water electrolysis.</pubmed_title><pmcid>PMC12822733</pmcid><pubmed_authors>Tan L</pubmed_authors><pubmed_authors>Tian J</pubmed_authors><pubmed_authors>Su T</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Lin C</pubmed_authors><pubmed_authors>Zhu L</pubmed_authors><pubmed_authors>Faiza M</pubmed_authors><pubmed_authors>Luo W</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Wu X</pubmed_authors><pubmed_authors>Song Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dopant-free stabilization of ruthenium oxide &amp;lt;i&amp;gt;via&amp;lt;/i&amp;gt; metallic Ru-induced d-orbital modulation for acidic water electrolysis.</name><description>Proton exchange membrane water electrolysis (PEMWE) is a cornerstone technology for carbon-neutral hydrogen production, yet its scalability is constrained by the intrinsic activity-stability trade-off of oxygen evolution reaction (OER) electrocatalysts. To overcome this challenge, we design a Ru/RuO&lt;sub>2&lt;/sub> heterostructure by integrating metallic Ru to modulate the d-orbital electron density of RuO&lt;sub>2&lt;/sub>. The metallic Ru domains suppress lattice oxygen migration (LOM) while enhancing electron delocalization. The e&lt;sub>g&lt;/sub> orbital filling shifts the Ru 4d-band center downward, reducing the adsorption strength of reaction intermediates (*OH, *O, and *OOH). The optimized Ru/RuO&lt;sub>2&lt;/sub> electrocatalyst achieves an overpotential of 181 mV at 10 mA cm&lt;sup>-2&lt;/sup> in 0.5 M H&lt;su</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T21:36:28.895Z</modification><creation>2026-06-05T03:11:24.738Z</creation></dates><accession>S-EPMC12822733</accession><cross_references><pubmed>41573120</pubmed><doi>10.1039/d5sc08602g</doi></cross_references></HashMap>