The design of a micro-/nanoreactor is of great significance
for
catalytic ozonation, which can achieve effective mass transfer and
expose powerful reaction species. Herein, the mesoporous carbon with
atomic Fe–N4 sites embedded in the ordered carbon
nanochannels (Fe–N4/CMK-3) was synthesized by the
hard-template method. Fe–N4/CMK-3 can be employed
as nanoreactors with preferred electronic and geometric catalytic
microenvironments for the internal catalytic ozonation of CH3SH. During the CH3SH oxidation process, the mass transfer
coefficient of the Fe–N4/CMK-3 confined system with
sufficient O3 transfer featured a level of at least 1.87
× 10–5, which is 34.6 times that of the Fe–N4/C–Si unconfined system. Detailed experimental studies
and theoretical calculations demonstrated that the anchored atomic
Fe–N4 sites and nanoconfinement effects regulated
the local electronic structure of the catalyst and promoted the activation
of O3 molecules to produce atomic oxygen species (AOS)
and reactive oxygen species (ROS), eventually achieving efficient
oxidation of CH3SH into CO2/SO4
2–. Benefiting from the high diffusion rate and the
augmentation of AOS/ROS, Fe–N4/CMK-3 exhibited an
excellent poisoning tolerance, along with high catalytic durability.
This contribution provides the proof-of-concept strategy for accelerating
catalytic ozonation of sulfur-containing volatile organic compounds
(VOCs) by combining confined catalysis and atomic catalysts and can
be extended to the purification of other gaseous pollutants.