Highly selective capture of cesium (Cs+) from
complex
aqueous solutions has become increasingly important owing to its (133Cs) indispensable role in some cutting-edge technologies
and the environmental mobility of radioactive nuclide (137Cs) from nuclear wastewater. Herein, we report the development of
cation-intercalated lamellar MoS2 as an effective Cs+ adsorbent with the advantages of facile synthesis and highly
tunable layer spacing. Two types of cations, including Na+ and NH4
+, were employed for the intercalations
between adjacent layers of MoS2. The results demonstrated
that the adsorption capacity of the NH4
+-intercalated
material (M-NH4
+, 134 mg/g) for Cs+ clearly outperformed the others due to higher loading percentages
of cations and larger layer spacing. The cesium partition coefficients
for M-NH4
+ in the presence of 100-fold competing
ions all exceed 1 × 103 mL/g. A simulated complex
aqueous solution containing 15.37 mg/L Cs+ and highly excess
of competing ions Li+, Na+, K+, Mg2+, and Ca2+ (20–306 times higher) was introduced
to prove the practical application potential using our best-performing
M-NH4
+, showing a good to excellent partition
ability of Cs+ among other cations, especially for Cs/K
and Cs/Na with separation factors of 58 and 212, respectively. The
adsorption and selectivity mechanisms were clearly elucidated using
various advanced techniques, such as scanning electron microscopy
(SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD),
X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. These
results revealed that the good selectivity for Cs+ can
be ascribed to the differences in Lewis acidities, hydration energy,
cation sizes, and in particular, the divergence of coordination modes
which was successfully achieved after tuning the layer distance via
the cation intercalation strategy. In addition, the material has fast
kinetics (<30 min), wide range of pH tolerance (4–10), and
good reusability. Overall, our studies point out that the tunable
lamellar MoS2-based materials are promising adsorbents
for Cs+ capture and separation.