Construction of a novel supramolecular self‐assembly photocatalyst for full visible light spectrum photooxidation of phenol

The sluggish full visible light response of organic supramolecular catalysts is a challenge that greatly restricts their development in the photocatalytic field. Herein, we successfully fabricated a K, Cl‐codoped Bi2WO6/perylene‐diimide(PDI) catalyst with a novel, general, and facile ultrasound assisted water bath heating method. The UV adsorption onset of K, Cl‐codoped Bi2WO6/PDI is redshifted from 750 to 760 nm compared with that of the heterojunction of Bi2WO6/PDI. Under visible light, the phenol is thoroughly mineralized into CO2 and H2O, and the phenol degradation rate was three times higher than that of pure Bi2WO6/PDI. The electrons transfer from PDI to K‐ and Cl‐codoped Bi2WO6/PDI according to the charge density difference calculation. The built‐in potential of K‐ and Cl‐codoped Bi2WO6/PDI could increase from 2.09 to 5.54 eV. The excellent full visible light spectrum photooxidation of phenol is attributed to the suitably strong built‐in potential at the heterojunction between PDI and K, Cl‐codoped Bi2WO6. K, Cl‐codoped Bi2WO6/perylene‐diimide(PDI) catalyst was fabricated via ultrasound assisted water bath heating method. Under visible light, the phenol degradation rate was 3 times higher than that of pure Bi2WO6/PDI. The excellent full visible light spectrum photooxidation of phenol is attributed to the suitably strong built‐in potential at the heterojunction between PDI and K, Cl‐codoped Bi2WO6 (5.54 eV).