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    <identifier>10.57760/sciencedb.hjs.00512</identifier>
    <datestamp>2025-10-28T10:29:54Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-10-28</dc:date>
  <dc:title>In-situ Infrared Spectroscopy Reveals Electrocatalytic Mechanisms in Hydrogen Isotope Separation</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.hjs.00512</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>[Background] The separation of hydrogen isotopes (1H, 2H, 3H) is critically important for clean energy and nuclear applications. While electrolytic separation through selective hydrogen/deuterium evolution reactions (HER/DER) offers an environmentally benign approach, its efficiency remains constrained by insufficient understanding of the underlying electrocatalytic mechanisms. [Purpose] This study aimed to elucidate the fundamental mechanisms governing electrocatalytic hydrogen isotope separation by probing the dynamic evolution of surface adsorbates under operational conditions. [Methods] We developed an in-situ electrochemical analysis system coupling external reflection infrared absorption spectroscopy (ER-IRAS). This system was employed to investigate the dynamic evolution of surface adsorbates on Pt/C, Ru/C, PtRu/C, and PtNi/C catalysts during electrolysis. [Results] Our research yielded three key advances: (1) establishment of a comprehensive infrared spectral database identifying 33 characteristic vibrational modes of H/D adsorption species at electrocatalytic interfaces; (2) revelation of a dual-regulation mechanism where metal composition and applied potential synergistically control selectivity, with Pt-based and Ru-based catalysts exhibiting opposing potential-dependent behaviors; and (3) alloying, especially PtRu, boosts deuterium electrolysis selectivity by both tuning the active sites (electronic effect) and enhancing the transport channels (interfacial effect). [Conclusions] This work provides both fundamental insights and practical solutions: the developed in-situ spectroscopic methodology enables unprecedented observation of isotope-specific interfacial processes, while the alloying strategy offers a clear pathway for designing high-performance separation catalysts. These advances significantly propel the technological readiness for industrial implementation of electrolytic isotope separation.</dc:description>
  <dc:subject>Deuterium evolution reaction; Hydrogen evolution reaction; Catalytic selectivity; In situ infrared spectroscopy; H/D isotope discrimination</dc:subject>
  <dc:creator>刘苗苗</dc:creator>
  <dc:creator>倪源满</dc:creator>
  <dc:creator>刘翔</dc:creator>
  <dc:creator>静超</dc:creator>
  <dc:creator>林逍</dc:creator>
  <dc:creator>王建强</dc:creator>
  <dc:creator>张林娟</dc:creator>
  <dc:rights>RESTRICTED</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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