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    <responseDate>2026-10-14T14:51:10Z</responseDate>
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    <identifier>10.57760/sciencedb.37652</identifier>
    <datestamp>2026-02-24T17:38:46Z</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>2026-02-24</dc:date>
  <dc:title>Phase-dependent of ZrO2 supported palladium catalysts for high-efficiency ethane combustion</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.37652</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Supported palladium catalysts have shown remarkable activity in the catalytic combustion of anthropogenic short-chain alkanes; however, the influence of the support crystal phase on catalytic behavior remains insufficiently elucidated. Herein, we systematically unveil the polymorphic effect of ZrO2 support (monoclinic ZrO2: m-ZrO2; tetragonal ZrO2: t-ZrO2; and hybrid phase of monoclinic and tetragonal ZrO2: h-ZrO2) on the catalytic performance of Pd species for ethane combustion. Among these materials, Pd/m-ZrO2 delivers an exceptional specific reaction rate of 6.49 nmolꞏm-2ꞏs-1 at 260 &amp;deg;C, representing 1.5- and 11-fold enhancement over Pd/h-ZrO2 and Pd/t-ZrO2 counterparts. Mechanistic investigations reveal that this superiority stems from a tripartite synergy governed by support polymorphism: (i) robust metal‒support interactions (MSIs) not only epitaxially stabilize highly dispersed PdOx clusters but also downshift the Pd d-band center to an optimal energy level; (ii) Phase-induced charge transfer at the Pd/m-ZrO2 interface lowers the oxygen vacancy formation energy, thereby accelerating the Mars-van Krevelen (MvK) redox cycle via enhanced lattice oxygen mobility; (iii) Abundant Lewis acid sites on Pd/m-ZrO2 facilitates the polarization and cleavage of C&amp;ndash;H bonds (the rate-determining step). Furthermore, the robust Pd&amp;ndash;Zr interfacial bonding endows Pd/m-ZrO2 with exceptional water resistance by mitigating hydroxyl poisoning. This work provides molecular-level insights into how support polymorphism orchestrates EMSIs and surface reactivity, establishing a design paradigm for efficient alkane abatement catalysts.</dc:description>
  <dc:subject>Pd/ZrO2 catalysts; Support polymorphism‌; Ethane combustion‌; Electronic metal‒support interactions; C-H bond activation</dc:subject>
  <dc:creator>段培高</dc:creator>
  <dc:creator>陈磊</dc:creator>
  <dc:creator>练冬金</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-sa/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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