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    <identifier>10.57760/sciencedb.20982</identifier>
    <datestamp>2025-02-17T10:26:11Z</datestamp>
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  <dc:date>2025-02-17</dc:date>
  <dc:title>FeSAC</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.20982</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>In this study, we introduce time-of-flight secondary ion mass spectrometry (ToF-SIMS)&amp;nbsp;as a powerful and precise tool to identify the coordination structure of SACs. Using Fe SACs derived from biomass as a model system, we demonstrate that Fe adopts an Fe-N₂C₂&amp;nbsp;coordination rather than the commonly assumed Fe-N₄ configuration. Electron paramagnetic resonance (EPR) and M&amp;ouml;ssbauer spectroscopy further confirm the low-spin&amp;nbsp;nature of this Fe-N₂C₂ structure. This unique coordination endows our Fe@CS-8.8 catalyst with outstanding oxygen reduction reaction (ORR) activity, achieving a half-wave potential of 0.91 V vs. RHE, surpassing the benchmark Pt/C catalyst.&amp;nbsp;</dc:description>
  <dc:subject>FeC2N2;  zinc-air battery; active site; single atom catalyst</dc:subject>
  <dc:creator>Jianan Su</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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