Nickel is one of the most attractive catalytically active
species
for methane reforminga crucial process for producing liquid
fuels and methanol, and the use of nanoporous materials to support
nickel is usually necessary. Impregnation is the commonly used method
to incorporate nickel into a porous support. In this work, we incorporate
catalytically active nickel into a highly porous cerium(IV)-based
metal–organic framework (MOF) by utilizing either the conventional
impregnation or the self-limiting post-synthetic modification, and
the nanosized MOF-derived ceria-supported nickel is prepared by carbonizing
the nickel-incorporated Ce-based MOFs. The crystallinity, porosity,
nanostructural morphology, and surface properties of each MOF and
MOF-derived materials are characterized, and as a demonstration, the
MOF-derived catalysts are used for the bi-reforming of methane (BRM).
The catalytic activity at various temperatures is examined, and the
long-term stability of MOF-derived catalysts for BRM is investigated
at 600 °C. The presence of MOF-derived carbon is necessary to
initiate the BRM at a lower temperature, and compared to the conventional
impregnation, the use of post-synthetic modification to install the
spatially separated nickel sites in the parent MOF can effectively
retard the agglomeration of nickel in the final MOF-derived catalyst
during the long-term BRM. Findings here suggest that the use of post-synthetic
modification to install the catalytically active species in MOFs is
beneficial for designing the MOF-derived catalysts that are more resistive
to sintering.
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