Experimental and Computational Study on U(VI) Sorption Mechanisms of Single-Layered Ti3C2TX Nanosheets

Environmental contamination by U(VI) from radioactive wastewater has become a challenging concern in the development of nuclear energy. A highly efficient recovery of U(VI) from wastewater is essential for environmental remediation and can mitigate the depletion of conventional uranium resources. This study describes the synthesis of single-layered Ti3C2TX nanosheets by chemical exfoliation using ultrasonography. The single-layered structure promoted a high sorption capacity of 3.20 mmol/g for U(VI) (distribution constant K-d > 10(4) mL/g) and excellent selectivity in mine wastewater that contained numerous coexisting ions. Fragmentation of the Ti3C2TX nanosheets from micron-scale to nanoscale upon uranyl sorption was detected by small-angle X-ray scattering and transmission electron microscopy. Extended X-ray absorption fine structure spectroscopy, X-ray photoelectron spectroscopy, and density functional theory calculations demonstrated that uranyl groups coordinated with the terminal -OH and -F on the surface of the Ti3C2TX nanosheets. These findings provide imperative insights into the design and application of nanomaterials to effectively treat uranium-contaminated wastewater.