Under
xenon lamps, ZnFe2O4 (ZFO) has been
shown to be effective in removing uranium through photocatalysis.
However, its performance is still inadequate in low-light environments
due to low photon utilization and high electron–hole complexation.
Herein, S-doped hollow ZnFe2O4 microcubes (S
x
-H-ZFO, x = 1, 3, 6, 9) were synthesized
using the MOF precursor template method. The hollow morphology improves
the utilization of visible light by refracting and reflecting the
incident light multiple times within the confined domain. S doping
narrows the band gap and shifts the conduction band position negatively,
which enhances the separation, migration, and accumulation of photogenerated
charges. Additionally, S doping increases the number of adsorption
sites, ultimately promoting efficient surface reactions. Consequently,
S
x
-H-ZFO is capable of removing U(VI)
in low-light environments. Under cloudy and rainy weather conditions,
the photocatalytic rate of S3-H-ZFO was 100.31 μmol/(g·h),
while under LED lamps (5000 Lux) it was 72.70 μmol/(g·h).
More interestingly, a systematic mechanistic investigation has revealed
that S doping replaces some of the oxygen atoms to enhance electron
transfers and adsorption of O2. This process initiates
the formation of hydrogen peroxide, which reacts directly with UO2
2+ to form solid studtite (UO2)O2·2H2O. Additionally, the promising magnetic
separation capability of S
x
-H-ZFO facilitates
the recycling and reusability of the material. This work demonstrates
the potential of ZnFe2O4 extraction uranium
from nuclear wastewater.