<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2(10)</volume><submitter>Guo Y</submitter><pubmed_abstract>The lack of highly efficient, inexpensive catalysts severely hinders the large-scale application of electrochemical energy conversion technologies (e.g., electrochemical hydrogen evolution reaction (HER) for hydrogen production, metal-air batteries (Cathode: oxygen reduction reaction (ORR))). As a new class of nanomaterials with a high ratio of surface atoms and tunable composition and electronic structure, metal nanocluster (NCs) are promising candidates as catalysts. Herein, a novel catalyst using S,N-doped carbon matrix (NSCSs) is synthesized to efficiently stabilize high density and ultra-uniform ruthenium (Ru) nanoclusters (Ru@NSCSs) by small-molecule self-assembly pyrolysis approach. The obtained Ru@NSCSs catalyst exhibits outstanding HER activity in all pH conditions (especially with a low overpotential of 5 mV at a current density of 10 mA cm&lt;sup>-2&lt;/sup> in 1 m KOH) and excellent ORR performance (half-wave potential (&lt;i>E&lt;/i> &lt;sub>1/2&lt;/sub>) of 0.854 V in 0.1 m KOH). Based on the experimental investigations and theoretical calculations, it is discovered that the S-atom can modulate the electronic structure and optimization of redox states on the surficial sites of Ru NCs during the ORR process. This work provides a feasible strategy for understanding and regulating the metal-support interface of ultra-uniform nanoclusters catalysts.</pubmed_abstract><journal>Small science</journal><pagination>2200035</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11935901</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Coordination Engineering of Ultra-Uniform Ruthenium Nanoclusters as Efficient Multifunctional Catalysts for Zinc-Air Batteries.</pubmed_title><pmcid>PMC11935901</pmcid><pubmed_authors>Yin H</pubmed_authors><pubmed_authors>Huang C</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>He G</pubmed_authors><pubmed_authors>Yang B</pubmed_authors><pubmed_authors>Wu D</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Wang K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Coordination Engineering of Ultra-Uniform Ruthenium Nanoclusters as Efficient Multifunctional Catalysts for Zinc-Air Batteries.</name><description>The lack of highly efficient, inexpensive catalysts severely hinders the large-scale application of electrochemical energy conversion technologies (e.g., electrochemical hydrogen evolution reaction (HER) for hydrogen production, metal-air batteries (Cathode: oxygen reduction reaction (ORR))). As a new class of nanomaterials with a high ratio of surface atoms and tunable composition and electronic structure, metal nanocluster (NCs) are promising candidates as catalysts. Herein, a novel catalyst using S,N-doped carbon matrix (NSCSs) is synthesized to efficiently stabilize high density and ultra-uniform ruthenium (Ru) nanoclusters (Ru@NSCSs) by small-molecule self-assembly pyrolysis approach. The obtained Ru@NSCSs catalyst exhibits outstanding HER activity in all pH conditions (especially with a low overpotential of 5 mV at a current density of 10 mA cm&lt;sup>-2&lt;/sup> in 1 m KOH) and excellent ORR performance (half-wave potential (&lt;i>E&lt;/i> &lt;sub>1/2&lt;/sub>) of 0.854 V in 0.1 m KOH). Based on the experimental investigations and theoretical calculations, it is discovered that the S-atom can modulate the electronic structure and optimization of redox states on the surficial sites of Ru NCs during the ORR process. This work provides a feasible strategy for understanding and regulating the metal-support interface of ultra-uniform nanoclusters catalysts.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2025-07-05T03:04:31.829Z</modification><creation>2025-07-05T03:04:31.829Z</creation></dates><accession>S-EPMC11935901</accession><cross_references><pubmed>40212702</pubmed><doi>10.1002/smsc.202200035</doi></cross_references></HashMap>