Understanding the degradation behavior of azo dyes in photocatalytic wastewater treatment is of fundamental and practical importance for their application in textile-processing and other coloration industries.In this study,quantum chemistry,as density functional theory,was used to elucidate different degradation pathways ofazo pyridone dyes in a hydroxyl radical (HO·)-initiated photocatalytic system.A series of substituted azo pyridone dyes were synthesized by changing the substituent group in the para position of the benzene moiety,ranging from strong electron-donating to strong electron-withdrawing groups.The effect of dye molecular structure on the photocatalytic degradation reaction mechanism was analyzed and quantification of substituent effects on the thermodynamic and kinetics parameters was performed.Potential energy surface analysis revealed the most susceptible reaction site for the HO· attack.The calculated reaction barriers are found to be strongly affected by the nature of substituent group with a good correlation using Hammett σp constants and experimentally determined reaction rates.The stability of pre-reaction complexes and transition state complexes were analyzed applying the distortion-interaction model.The increased stability of the transition state complexes with the distancing from the substituent group has been established.