Synergistic Features of Superoxide Molecule Anchoring and Charge Transfer on Two-Dimensional Ti3C2Tx MXene for Efficient Peroxymonosulfate Activation.

Abstract

The heterogeneous Fenton-like process is regarded as a promising approach to produce reactive oxygen species for water purification and environmental remediation. Here, we report a simple and rational strategy for the design of an efficient catalyst by reducing the dimensionality instead of changing the composition or structure. Based on theoretical and experimental evidence, considerable active sites were exposed on the low-dimensional Ti3C2Tx monolayer surface and showed outstanding reactivity toward peroxymonosulfate activation, which was mainly because of the superior compatibility between the highest occupied molecular orbital of catalysts and lowest unoccupied molecular orbital of Oxone. Stimulated emission depletion super-resolution microscopy innovatively provided visual insights into the spatiotemporal heterogeneous activation process and revealed that the unilaminar Ti3C2Tx nanosheet exhibited preferable reaction dynamics relative to its inert bulk counterpart, with an aqueous 2,4-dichlorophenoxyacetic acid degradation rate ∼376 times higher than that when using bulk Ti3C2Tx as the activator.