In situ turning defects of exfoliated Ti(3)C(2) MXene into Fenton-like catalytic active sites

Controllable in situ formation of nanoclusters with discrete active sites is highly desirable in heterogeneous catalysis. Herein, a titanium oxide–based Fenton-like catalyst is constructed using exfoliated Ti(3)C(2) MXene as a template. Theoretical calculations reveal that a redox reaction between the surface Ti-deficit vacancies of the exfoliated Ti(3)C(2) MXene and H(2)O(2) molecules facilitates the in situ conversion of surface defects into titanium oxide nanoclusters anchoring on amorphous carbon (TiO(x)@C). The presence of mixed-valence Ti(δ+) (δ = 0, 2, 3, and 4) within TiO(x)@C is confirmed by X-ray photoelectron spectroscopy (XPS) and X-ray absorption fine structure (XAFS) characterizations. The abundant surface defects within TiO(x)@C effectively promote the generation of reactive oxygen species (ROS) leading to superior and stable Fenton-like catalytic degradation of atrazine, a typical agricultural herbicide. Such an in situ construction of Fenton-like catalysts through defect engineering also applies to other MXene family materials, such as V(2)C and Nb(2)C.