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Table · dataset · 2026

Table 1_Selective oxidation of glucose to gluconic acid by bimetallic catalysts.docx

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<p>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.

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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<sub>2</sub>CO<sub>3</sub> 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.

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N<sub>2</sub> 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<sub>2</sub>, 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<sub>2</sub>CO<sub>3</sub>-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.</p>

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