Improved photo-dechlorination at polar photocatalysts K3B6O10X (X = Cl, Br) by halogen atoms-modulated polarization

Abstract

The contamination of chlorophenols in water has been considered as an urgent environmental issue. In this study, two polar photocatalysts with a similar structure, K₃B₆O₁₀Br (KBB) and K₃B₆O₁₀Cl (KBC) were synthesized through a high temperature solid phase method and applied for the effective mineralization and removal of the chlorophenols. More than 92.0% of 2-chlorophenols can be fully degraded within 16 min under UV light irradiation, which is six times faster than the commercial P25 TiO₂ catalyst. The out-of-center distortions capability of the XK₆ octahedrons is greatly influenced by X (X = Cl and Br) atoms. The magnitude of the out-of-center distortion of KBC and KBB were 0.137 and 0.027, respectively. A better photocatalytic activity performance was therefore observed for KBC due to its higher spontaneous polarization ability and facile charge separation process. Kelvin probe force microscopy (KPFM) experiments further proved KBC has a larger surface potential change before and after the light irradiation. Reactive species capture experiments confirmed the role of radicals in the order of ˙O₂⁻ > e⁻ > h⁺ > ˙OH.