By anchoring MoS2 nanosheets onto FeS2 derived
from different MIL-100(Fe) precursors, a series of FeS2@MoS2-x samples featuring sulfur vacancies
(SVs) were prepared as efficient peroxymonosulfate (PMS) activators
to degrade sulfamethoxazole (SMX) from aqueous solution. Benefiting
from the strongly reductive sulfur species (S2– and
S2
2–), enriched Mo(IV) sites, and abundant
SVs, 40 μM SMX was completely removed by the FeS2@MoS2-2/PMS system in 7 min (0.2 g/L FeS2@MoS2-2, 0.25 mM PMS). The k
obs obtained
by FeS2@MoS2-2 was 0.598 min–1, which was 5.8 and 51.1 times higher than that of FeS2 (0.103 min–1) and MoS2 (0.012 min–1), respectively. Quenching experiments, electron paramagnetic
resonance (EPR) analysis, and 18O isotope labeling tests
evidenced the involvement of radical (•OH, SO4
•–) and non-radical (1O2, FeIV = O) pathways in the FeS2@MoS2-2/PMS system, and MoS2 anchoring enormously
enhanced the contribution of non-radicals to 45.5%. In addition, SVs
possessed favorable affinity toward PMS and dissolved oxygen (DO),
promoting continuous production of reactive active species. The degradation
pathways of SMX were unveiled as well. The satisfactory recyclability,
stability, and universality enabled FeS2@MoS2-2 to serve as a promising candidate for PMS activation. This study
provides a novel strategy to construct sulfur vacancy-featuring Fe-based
sulfide catalysts using MIL-100(Fe) as sacrificial templates for activating
PMS to treat refractory organic-polluted water.