Abstract
Highly base-free catalytic of biomass-derived feedstock into value-added chemical is of great interest in catalysis but remains a challenge. Herein, a hollow nanocatalyst composed of Au nanoparticles as the core and Zn/Ni bimetallic metal-organic frameworks (MOFs) functionalized with the -NH2 ligand as the shell (Au@Zn/Ni-MOF-2-NH2) is fabricated through a straightforward one-pot hydrothermal method for a highly efficient, selective, and base-free synthesis of d-xylonic acid by the catalytic oxidation of d-xylose. Experimental and theoretical results confirmed the key role of hollow core-shell Au@Zn/Ni-MOF-2-NH2 in providing in-depth synergistic effects between the Au nanoparticles and the porous MOF and further facilitating the transport of reactant and product molecules, triggering a noticeably impressive turnover frequency value of 76.53 h-1 for d-xylonic acid generation, outperforming the bare Au nanocatalyst by 306 times. The highly integrated structure of Au@Zn/Ni-MOF-2-NH2 is stable for recycled use during the oxidation process, which further demonstrates the superior availability of such a bimetallic MOF-based hollow core-shell heterogeneous nanocatalyst.
Original language | English (US) |
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Pages (from-to) | 5396-5403 |
Number of pages | 8 |
Journal | ACS Sustainable Chemistry and Engineering |
Volume | 10 |
Issue number | 17 |
DOIs | |
State | Published - May 2 2022 |
Keywords
- core-shell
- d-xylose oxidation
- density functional theory
- hollow nanostructure
- metal-organic frameworks
ASJC Scopus subject areas
- General Chemistry
- Environmental Chemistry
- General Chemical Engineering
- Renewable Energy, Sustainability and the Environment