“…Figure d visualizes the superiority of BTO-H in RhB degradation at the fixed time point of 30 min. There are many materials factors that may affect these data, including phase assemblage, impurities (viz., heterojunction formation), crystallinity, crystallite size, electronic band alignment, recombination time, BET surface area, [V O •• ], and blockage of active sites . Accordingly, the present work suggests that the catalytic performance (dye degradation) is associated with the following: - The reduced E g and shift in E f , which are caused by increased defect concentrations (Ti 3+ , Ti 2+ , Ti 0 , V O •• ) and optimized by H 2 reduction, result in band alignment that establishes conditions favorable for dye degradation
- The shallow energy level established by the high E f and associated lowering of the CBM enhances charge carrier separation by promoting the diffusion of electrons to the surface, thereby reducing recombination with holes and facilitating higher carrier concentrations and efficient charge transfer across the grain surface.
- The increased BET surface area and associated [V O •• ] are optimized by H 2 reduction, thereby providing more active sites for catalytic reaction, although there may be mitigation by blockage of active sites by species dissolved in the water.
- The application of mechanical vibration leads to a displacement of charges (and possibly adsorbed species), thereby inducing the piezoelectric potential that facilitates surface reactions.
- The ultrasonic irradiation and resultant external stress induce the reduced band gap and band bending that shifts the conduction band closer to the HER band potential and the valence band further away from the OER band potential.
- It also is possible that multivalent Ti itself can act as an heterojunction structure to improve electron mobility and reduce charge transfer resistance, both of which are beneficial to the catalytic activity.
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