Exploring highly efficient and robust non-noble metal
catalysts
for VOC abatement is crucial but challenging. Mn-based perovskites
are a class of redox catalysts with good thermal stability, but their
activity in the catalytic combustion of light alkanes is insufficient.
In this work, we modulated the Mn–O bond strength in a Mn-based
perovskite via defect engineering, over which the catalytic activity
of propane combustion was significantly enhanced. It demonstrates
that the oxygen vacancy concentration and the Mn–O bond strength
can be efficiently modulated by finely tuning the Ni content in SmNi
x
Mn1–x
O3 perovskite catalysts (SN
x
M1–x
), which in turn can enhance the
redox ability and generate more active oxygen species. The SN0.10M0.90 catalyst with the lowest Mn–O bond
strength exhibits the lowest apparent activation energy, over which
the propane conversion rate increases by 3.6 times compared to that
on the SmMnO3 perovskite catalyst (SM). In addition, a
SN0.10M0.90/cordierite monolithic catalyst can
also exhibit a remarkable catalytic performance and deliver excellent
long-term durability (1000 h), indicating broad prospects in industrial
applications. Moreover, the promotional effect of Ni substitution
was further unveiled by density functional theory (DFT) calculations.
This work brings a favorable guidance for the exploration of highly
efficient perovskite catalysts for light alkane elimination.