Oxygen vacancy plays an important
role in catalytic oxidation of
formaldehyde (HCHO), but the inherent drawback of its thermodynamic
instability causes the deactivation of catalysts. Hence, improving
the thermodynamic stability of oxygen vacancy is a crux during HCHO
oxidation. Here, a novel and simple nitrogen doping of MnO2/C catalyst is designed for HCHO oxidation at room temperature. The
surface lattice oxygen of MnO2 will be activated by nitrogen-doping,
which acts as active sites for HCHO oxidation and solves the thermodynamic
instability issue of oxygen vacancy. Furthermore, carbon is doped
with nitrogen to promote electron transfer and accelerate the HCHO
oxidation process. Therefore, the catalytic activity and stability
of the catalyst can be significantly promoted, which can completely
remove ∼1 ppm HCHO in the tank within 3 h, and remains highly
active after 5 cycles at room temperature (RH = 55%). In addition,
the excellent removal performance over the prepared catalyst is also
attributed to abundant surface oxygen species, amorphous crystallinity,
and low reduction temperature. In situ diffuse reflectance infrared
Fourier transform spectrometry (DRIFTS) and density functional theory
(DFT) calculations reveal the reaction mechanism of HCHO. This strategy
provides crucial enlightenment for designing novel Mn-based catalysts
for application in the HCHO oxidation field.