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Herein, we develop an ultrafast magnetic\u2010field\u2010enabled quench (MFEQ) strategy to synthesize a series of M\n                    <jats:sub>1<\/jats:sub>\n                    \/G\u2010FeO\n                    <jats:sub>x<\/jats:sub>\n                    (M\u2550Ni, Fe, Co, Ir, Ru, and Pt) SACs within a few seconds. Using Ni\n                    <jats:sub>1<\/jats:sub>\n                    \/G\u2010FeO\n                    <jats:sub>x<\/jats:sub>\n                    as a proof of concept, this method leverages the rapid quenching of thermally incandescent Fe foam into an Ni\u2010containing ethanol solution, triggering simultaneous graphene formation and Ni anchoring. The Ni\n                    <jats:sub>1<\/jats:sub>\n                    \/G\u2010FeO\n                    <jats:sub>x<\/jats:sub>\n                    catalyst shows exceptional alkaline oxygen evolution reaction (OER) performance, operating at 200\u00a0mV for 10\u00a0mA cm\n                    <jats:sup>\u22122<\/jats:sup>\n                    and sustaining 105\u00a0mA cm\n                    <jats:sup>\u22122<\/jats:sup>\n                    for 330\u00a0h without degradation. Notably, the Ni\n                    <jats:sub>1<\/jats:sub>\n                    \/G\u2010FeO\n                    <jats:sub>x<\/jats:sub>\n                    \u2010catalyzed anion exchange membrane water electrolysis (AEMWE) device exhibits a low voltage of 1.86\u00a0V at 1.0 A cm\n                    <jats:sup>\u22122<\/jats:sup>\n                    and 600\u00a0h long\u2010term stability. Density functional theory (DFT) calculations and experiments reveal that the strong electronic interactions between Ni\n                    <jats:sub>1<\/jats:sub>\n                    \/G and FeO\n                    <jats:sub>x<\/jats:sub>\n                    contribute to the optimized electronic structure and reduced energy barrier. Techno\u2010economic analysis (TEA) highlights the superior energy efficiency of the MFEQ method, which requires only US$19.2 in energy expenditure to synthesize 1\u00a0kg of SACs. This work provides new insights into the ultrafast fabrication of SACs.\n                  <\/jats:p>","DOI":"10.1002\/anie.2977516","type":"journal-article","created":{"date-parts":[[2026,7,8]],"date-time":"2026-07-08T11:03:39Z","timestamp":1783508619000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Magnetic\u2010Field\u2010Enabled Ultrafast Quench Synthesis of Single\u2010Atom Catalysts for Efficient Anion Exchange Membrane Water Electrolysis"],"prefix":"10.1002","volume":"65","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0898-5292","authenticated-orcid":false,"given":"Shenghua","family":"Chen","sequence":"first","affiliation":[{"name":"School of Chemistry, National Innovation Platform (Center) For Industry\u2010Education Integration of Energy Storage Technology, School of Chemical Engineering and Technology Xi'an Jiaotong University  Xi'an P. R. 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