Synergistic Elimination of Chlorophenols Using a Single-Atom Nickel with Single-Walled Carbon Nanotubes: The Roles of Adsorption, Hydrodechlorination, and the Electro-Fenton Process.

Electrocatalytic degradation enables the efficient treatment of chlorinated pollutants (COPs); however, its application has been significantly hindered by the large amounts of unsafe intermediate products. In this study, we present a single-atom nickel with single-walled carbon nanotubes (SWCNTs) as an electrochemical reactor for the complete elimination of chlorophenols. Distinct products and reductive mechanisms were observed for Ni-N-C compared to Cu-N-C. Ni-N-C incorporation has a novel degradation pathway for efficient chlorophenol degradation involving hydrodechlorination and the electro-Fenton process. Most importantly, the weak adsorption between the chlorophenols and the SWCNTs promoted their dechlorination by the attached active atomic hydrogen (H*) formed on the Ni-N-C. Meanwhile, the SWCNTs improved the reduction of O to HO, which was subsequently decomposed by Ni-N-C to form hydroxyl radicals (·OH) for phenol oxidation. As a result, the degradation rate of 4-chlorophenol was increased by 5 and 10 times compared with those of the Ni-N-C and SWCNTs alone, respectively. The first-order reaction rate constant was 2.7 h, and the metal mass kinetics constant was 1956.5 ming. Aromatic COPs containing benzene rings could be degraded, but chloroacetic acids could not. This study demonstrates a new design for multifunctional electrochemical degradation that functions via dechlorination and the ·OH activation mechanism.