Low-temperature
catalytic oxidation of propane on Pt-based catalysts
is of paramount importance but remains a major challenge for the emission
control of volatile organic compounds (VOCs). Here, we report the
promoting effects of doped WO
x
on 0.5
wt % Pt/ZrO2 catalysts for propane oxidation, which strongly
depended on the crystal structure of ZrO2. Among them,
0.5 wt % Pt/WO
x
/t-ZrO2 shows
the highest catalytic activity, the T
90 is 216 °C, which is about 155 and 80 °C lower than that
of Pt/t-ZrO2 and Pt/WO
x
/m-ZrO2, respectively, and the turnover frequency (TOF) of Pt/WO
x
/t-ZrO2 at 190 °C is about 3
times that of Pt/WO
x
/m-ZrO2. Multicharacterization results show that compared with Pt/WO
x
/m-ZrO2, doped WO
x
can be highly dispersed on t-ZrO2 and form the
solid solution-like (Zr1–x
W
x
O2+x/2) nanolayer
structure at the catalyst surface, which produces additional strong
Brønsted acid sites and metallic Pt (Pt0) sites via
an electron transfer from W to Pt on Pt/WO
x
/t-ZrO2. The synergistic effect of Pt0 and
strong acidity at the Pt–Zr1–x
W
x
O2+x/2 interface facilitates the rapid removal of surface intermediates
including carboxylate and CO generated during the reaction and promotes
C3H8 oxidation on Pt/WO
x
/t-ZrO2. This work highlights a direction for the design
of high-efficiency metal oxide-modified Pt/ZrO2 nanoscale
catalysts by changing the crystal structure of the ZrO2 support for the removal of VOCs.