Laminar membranes assembled by ultrathin cobalt-copper oxide nanosheets for nanoconfined catalytic degradation of contaminants.

[Display omitted] • Nanoconfinement catalysis is implemented within Co-Cu ONS membrane nanochannels. • Co-Cu ONS membrane achieves ∼ 100% removal of organic pollutants within 86 ms. • The degradation rate is 103−5 times faster compared with the best state-of-the-art. • Oxygen vacancies facilitate electron transfer between metal cations and PMS. • DFT calculations illustrate the mechanism of nanoconfinement catalysis. Practical applications for the degradation of organic contaminants by conventional batch-mode heterogeneous advanced oxidation processes remain elusive due to mass-transfer limitations of short-lived reactive oxygen species (ROS). Nanoconfinement catalysis has received increasing attention because of enhanced reaction efficiency and mass and electron transfer. Here, we implemented the concept of nanoconfinement catalysis using a two-dimensional membrane. Ultrathin cobalt-copper oxide nanosheets (Co-Cu ONS) rich in active sites and oxygen vacancies were prepared through a facile solution reduction method. The assembled Co-Cu ONS membrane with active sites confined within membrane nanochannels spontaneously activates peroxymonosulfate and facilitates the generation of ROS and the redox cycles of metal cations. Therefore, an ultimate degradation efficiency (∼100%), ultrafast (∼86 ms) decomposition of organic pollutants, and excellent catalytic stability (greater than120 h) were achieved. The degradation rate is 103−5 times faster than the best state-of-the-art. This approach offers an attractive alternative for water purification with membrane-based nanoconfinement catalysts. [ABSTRACT FROM AUTHOR]