Catalytic
conversion of a biomass derivative (levulinic acid, LA)
to a high value-added product (γ-valerolactone, GVL) has attracted
much attention, in which the control of catalytic selectivity plays
an important role. Herein, a stepwise method was developed to prepare
Co-MoO
x
catalysts via topological transformation (calcination reduction) from layered
double hydroxide (Mo/CoAl-LDH) precursors. X-ray diffraction, high-resolution
transmission electron microscopy, and hydrogen temperature-programmed
reduction demonstrate the formation of MoO
x
-decorated Co structures of Co-MoO
x
samples.
Remarkably, the sample that is reduced at 500 °C is featured
with the most abundant interfacial Coδ+
(denoted as Co-MoO
x
-500), which
exhibits an excellent catalytic performance toward the hydrodeoxygenation
(HDO) reaction of several biomass-derived platform molecules (furfural,
FAL; succinic acid, SA; 5-hydroxymethyl-furfural, HMF; and levulinic
acid, LA). Especially, this optimal catalyst displays a high yield
(99%) toward the HDO reaction of LA to GVL, which stands at the highest
level among non-noble metal catalysts. The combination of in situ FT-IR characterization and theoretical calculation
further confirms that interfacial Coδ+
sites in Co-MoO
x
-500 act as adsorption
active sites for the polarization of a CO bond in an LA molecule,
which simultaneously promotes CO hydrogenation and CO
cleavage. Moreover, the MoO
x
overlayer
suppresses the formation of byproducts by covering the Co0 sites. This work offers a cost-effective and efficient catalyst,
which can be potentially applied in catalytic conversion of biomass-derived
platform molecules.