<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chung CW</submitter><funding>National Tsing Hua University</funding><funding>National Science and Technology Council</funding><pagination>1073-1097</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12628007</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(2)</volume><pubmed_abstract>Recent advances in magnetically enhanced (electro)catalysis have disclosed the potential of magnetic fields to modulate reaction kinetics and catalytic performance. Herein, a combination of alternating magnetic field (AMF) as a physical stimulus, reduced graphene oxide (rGO) as a magneto-sensitizer, single-atom Fe on rGO (FeSA:rGO) as the catalytic active site, and H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> as a dual reductant and oxidant demonstrated a proof-of-concept magneto-catalytic process that is thermodynamically driven solely by magneto-voltaic activity. Upon application of an AMF to electroconductive FeSA:rGO, AMF-induced charge separation led to formation of low-lying electron holes (&lt;i>E&lt;/i> &lt;sub>HOMO&lt;/sub> = 2.41/2.43 eV) and excited electrons (&lt;i>E&lt;/i> &lt;sub>LUMO&lt;/sub> = -0.65/-0.57 eV), whic</pubmed_abstract><journal>Chemical science</journal><pubmed_title>Magneto-voltaic activity of single-atom iron on reduced graphene oxide for magneto-catalytic conversion of H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; into O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;.</pubmed_title><pmcid>PMC12628007</pmcid><funding_grant_id>110-2622-M-007-002</funding_grant_id><funding_grant_id>112-2628-M-007-004-MY4</funding_grant_id><funding_grant_id>114-2218-E-007-012</funding_grant_id><funding_grant_id>109Q2711E1</funding_grant_id><funding_grant_id>109-2622-M-007-003-CC2</funding_grant_id><funding_grant_id>113-2218-E-007-014</funding_grant_id><funding_grant_id>109-2628-M-007-003-MY3</funding_grant_id><funding_grant_id>110Q2513E1</funding_grant_id><pubmed_authors>Chen CL</pubmed_authors><pubmed_authors>Lai YC</pubmed_authors><pubmed_authors>Chi CC</pubmed_authors><pubmed_authors>Huang CC</pubmed_authors><pubmed_authors>Chen HT</pubmed_authors><pubmed_authors>Dhanthala Chittibabu DK</pubmed_authors><pubmed_authors>Chen YC</pubmed_authors><pubmed_authors>Lu MY</pubmed_authors><pubmed_authors>Apfel UP</pubmed_authors><pubmed_authors>Liang JG</pubmed_authors><pubmed_authors>Iffland L</pubmed_authors><pubmed_authors>Chen JL</pubmed_authors><pubmed_authors>Chan TS</pubmed_authors><pubmed_authors>Chung CW</pubmed_authors><pubmed_authors>Huang JY</pubmed_authors><pubmed_authors>Lu TT</pubmed_authors><pubmed_authors>Lu YR</pubmed_authors><pubmed_authors>Lin ZH</pubmed_authors><pubmed_authors>Dayao LA</pubmed_authors><pubmed_authors>Chou HH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Magneto-voltaic activity of single-atom iron on reduced graphene oxide for magneto-catalytic conversion of H&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt; into O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;.</name><description>Recent advances in magnetically enhanced (electro)catalysis have disclosed the potential of magnetic fields to modulate reaction kinetics and catalytic performance. Herein, a combination of alternating magnetic field (AMF) as a physical stimulus, reduced graphene oxide (rGO) as a magneto-sensitizer, single-atom Fe on rGO (FeSA:rGO) as the catalytic active site, and H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub> as a dual reductant and oxidant demonstrated a proof-of-concept magneto-catalytic process that is thermodynamically driven solely by magneto-voltaic activity. Upon application of an AMF to electroconductive FeSA:rGO, AMF-induced charge separation led to formation of low-lying electron holes (&lt;i>E&lt;/i> &lt;sub>HOMO&lt;/sub> = 2.41/2.43 eV) and excited electrons (&lt;i>E&lt;/i> &lt;sub>LUMO&lt;/sub> = -0.65/-0.57 eV), whic</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T19:47:59.863Z</modification><creation>2026-06-04T03:11:40.117Z</creation></dates><accession>S-EPMC12628007</accession><cross_references><pubmed>41268518</pubmed><doi>10.1039/d5sc05275k</doi></cross_references></HashMap>