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        <identifier>oai:figshare.com:article/33889768</identifier>
        <datestamp>2026-09-17T12:07:24Z</datestamp>
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          <dc:title>Table 1_Selective oxidation of glucose to gluconic acid by bimetallic catalysts.docx</dc:title>
          <dc:creator>Xiaoyang Liu (1815211)</dc:creator>
          <dc:creator>Jiajiang Zhou (25018678)</dc:creator>
          <dc:creator>Yafei Wang (438443)</dc:creator>
          <dc:creator>Haixin Guo (5265635)</dc:creator>
          <dc:subject>Functional Materials</dc:subject>
          <dc:subject>bimetallic catalysts</dc:subject>
          <dc:subject>biomass</dc:subject>
          <dc:subject>gluconic acid</dc:subject>
          <dc:subject>glucose oxidation</dc:subject>
          <dc:subject>Pt/NiO</dc:subject>
          <dc:description>&lt;p&gt;Selective aerobic oxidation of glucose to gluconic acid under alkali-free aqueous conditions is constrained by inefficient Pt utilization, particle aggregation, and poorly controlled metal-oxide interfaces. Herein, we develop a urea-assisted solvothermal strategy that integrates oxide-support screening, interfacial electronic regulation, and hierarchical pore engineering in Pt/MOx catalysts. Among eight oxide supports, Pt/NiO-U exhibited the highest activity. Comparative synthesis using NaOH and Na&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt; decoupled the structural role of urea from simple alkalinity, revealing that urea acts simultaneously as a slow-release pH regulator and a source of nitrogen-containing surface species. This multifunctional regulation generated highly dispersed Pt nanoparticles with an average diameter of 2.89 nm, modified the electronic environment of the Pt-NiO interface, and increased the availability of reactive surface oxygen species. N&lt;sub&gt;2&lt;/sub&gt; sorption further indicated a mesopore-dominated micro-meso-macroporous hierarchy spanning 1.72–148.55 nm, thereby coupling nanoscale active-site exposure with multiscale mass transport. At 100 °C under 1 MPa O&lt;sub&gt;2&lt;/sub&gt;, Pt/NiO-U achieved 100% glucose conversion and a gluconic acid yield of 92.5% without added soluble alkali, markedly outperforming the NaOH- and Na&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;-derived counterparts, which afforded yields of only 45.6% and 50.4%, respectively. Complete conversion with an 85.2% gluconic acid yield was also obtained at 80 °C within 1 h. The catalyst maintained complete conversion over five cycles, with a fifth-cycle yield of 79.3% and Pt and Ni leaching below 0.1%. These findings establish urea-assisted Pt-NiO interface engineering as a unified strategy for coordinating active-site dispersion, oxygen activation, and hierarchical mass transport in selective biomass oxidation.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-17T12:07:24Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fmats.2026.1943690.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Table_1_Selective_oxidation_of_glucose_to_gluconic_acid_by_bimetallic_catalysts_docx/33889768</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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