Boron‐Doped Diamond for Hydroxyl Radical and Sulfate Radical Anion Electrogeneration, Transformation, and Voltage‐Free Sustainable Oxidation

Boron‐doped diamond‐based electrochemical advanced oxidation processes (BDD‐EAOPs) have attracted much attention. However, few systematic studies concerning the radical mechanism in BDD‐EAOPs have been published. In situ electron paramagnetic resonance spectrometry is used to confirm that SO 4 •− is directly electrogenerated from SO 4 2− . Then, excess SO 4 •− dimerizes to form S 2 O 8 2− and accumulates in the BDD‐EAOP system. But no S 2 O 8 2− accumulates at pH = 10 owing to the rapid transformation of SO 4 •− and S 2 O 8 2− . Above the overpotential of water oxidation, • OH is electrogenerated and cooperated with SO 4 •− . In the power‐off phase, the accumulated S 2 O 8 2− can be reactivated to SO 4 •− via specific degradation intermediates to achieve sustainable degradation. Di‐ n ‐butyl phthalate (DnBP), a typical endocrine disruptor, is selected as a model contaminant. Surprisingly, 99.8% of DnBP (initial concentration of 1 mg L −1 ) is removed, using an intermittent power supply strategy with a periodic 10 min power‐on phase at a duty ratio of 1:2, reducing the electrical energy consumption (1.8 kWh m −3 ) by more than 30% compared with continuous power supply consumption. These radical electrogeneration transformation mechanisms reveal an important new strategy for sustainable oxidation, especially for in situ water restoration, and are expected to provide a theoretical basis for BDD applications.