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    <identifier>10.57760/sciencedb.35642</identifier>
    <datestamp>2026-05-07T11:05:09Z</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>2026-05-07</dc:date>
  <dc:title>Effect of t-ZrO2/m-ZrO2 Phase Interfaces on the Stability of Ni/Ca-ZrO2 Catalysts for CO2 Methanation</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.35642</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Nickel-based catalysts are considered among the most promising candidates for CO2 methanation; however, their tendency toward high-temperature sintering-induced deactivation remains a critical bottleneck for practical application. In this work, a series of Ni-based catalysts supported on mixed-phase t-ZrO2/m-ZrO2 nanocrystalline supports were firstly constructed via Ca doping and thermal treatment regulation. The catalyst calcined at 700 &amp;deg;C exhibited the best stability and low-temperature activity for CO2 methanation. Comprehensive characterizations, including XRD, BET, XPS, TEM, H2-TPR/TPD, and CO2-TPD, revealed that increasing calcination temperature enhanced the Ca-promoted phase transformation from m-ZrO2 to t-ZrO2 and facilitated grain growth of both zirconia phases. At a calcination temperature of 700 &amp;deg;C, t-ZrO2 and m-ZrO2 crystallites in the support were both small and comparable in size, favoring the formation of mixed-phase interfaces. The m/t-ZrO2 interphase boundaries provided anchoring sites for Ni nanoparticles, which is identified as the primary reason for the superior high-temperature anti-sintering performance of the catalyst calcined at 700 &amp;deg;C. In addition, these mixed-phase interfaces optimized the local electronic structure and enriched oxygen vacancy defects, thereby lowering the apparent activation energy for CO2 activation and endowing the 700 &amp;deg;C calcined catalyst with the highest low-temperature CO2 methanation activity. These findings demonstrate that constructing m/t-ZrO2 interphase boundaries through promoter engineering and thermal-treatment control is an effective strategy to stabilize Ni nanoparticles and enhance catalytic performance.</dc:description>
  <dc:subject>methanation; Ni/Ca-ZrO2 catalyst; sintering resistance; CO2</dc:subject>
  <dc:creator>Fu Yitian</dc:creator>
  <dc:creator>Li Jia</dc:creator>
  <dc:creator>Jiang Yanan</dc:creator>
  <dc:creator>Bai Yang</dc:creator>
  <dc:creator>Liu Yuan</dc:creator>
  <dc:rights>RESTRICTED</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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