Abstract
Supported metal catalysts of high intrinsic catalytic activities with significant mass and heat-transport properties are constructed via in situ synthesis based on the interfacial hydrothermal-oxidation/reductive-exolution (HO/RE) chemistry of Al metal substrates. The hydrothermal reaction of Al metal particles in an aqueous solution of Ni salt gives rise to the formation of NiAl-LDH@Al core-shell microstructure consisting of an Al core and a NiAl layered double hydroxide (LDH) shell with petal-like surface morphology. A reduction of the NiAl-LDH@Al leads to exolution of Ni atoms from the NiAl-LDH shell, developing fine Ni metal nanoparticles (NPs) with high surface dispersion and size uniformity. The mechanism of heterogeneous formation of MeAl-LDH (Me = hetero-metals) structures from Al metal substrate is suggested in detail. For CO2 methanation, the Ni/Al2O3@Al exhibits a three-fold greater turnover frequency (TOF) than the Ni/Al2O3 catalyst prepared by the conventional impregnation method, indicating the marked intrinsic catalytic properties of the Ni/Al2O3@Al catalyst.
Original language | English |
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Article number | 117461 |
Journal | Applied Catalysis A: General |
Volume | 594 |
DOIs | |
State | Published - 25 Mar 2020 |
Keywords
- CO methanation
- Core-shell catalyst
- Heat and mass transport
- In situ synthesis
- Supported metal catalyst