Activation of O2 over three-dimensional manganese oxide nanoprisms under ambient conditions towards oxidative removal of aqueous organics

Three-dimensional nanomaterials are generally beneficial to catalytic performance because of their larger specific surface area, more exposed active sites, enhanced mass transfer and shorter diffusion distance between reactants and catalysts. In this study, a bimetallic doping strategy was developed for the synthesis of three-dimensional alpha-phase manganese oxide (Ce-Bi-OMS-2) with nanoprism structural morphology for the first time. The doping component and dosage both affected the size, morphology, crystal phase and textural properties of Ce-Bi-OMS-2. The 3D material could efficiently activate O-2 under ambient conditions and further be used as the catalyst to degrade bisphenol A at 66.8% degradation rate with a rate constant of 0.0179 min(-1) under standard conditions. Moreover, a degradation rate of 99% and mineralization rate of 67% for bisphenol A were realized under optimal conditions. XPS, radical quenching experiments and EPR suggested that O-2(-) was mainly responsible for the degradation, and OH and O-1(2) played secondary dominant roles. Further investigations indicated that structural dimension, enhanced specific surface area (147 m(2) g(-1)) and rich surface oxygen vacancies contributed to the good catalytic performance. This work not only provides a novel and facile doping strategy for the construction of a 3D nanostructured material but also demonstrates the activation of O-2 over a 3D catalyst for the degradation of aqueous organic pollutants.

Automated summary

A novel bimetallic doping strategy was developed for the synthesis of three-dimensional manganese oxide (Ce-Bi-OMS-2) with nanoprism structural morphology. The structural dimension, enhanced specific surface area, and rich surface oxygen vacancies contributed to the good catalytic performance. This study demonstrates the activation of O-2 over a 3D catalyst for the degradation of aqueous organic pollutants.