Controlled Synthesis, Mechanism and Degradation Property of Birnessite-MnO2 Nanoflowers and Nanoflakes.

Birnessite-MnO2 nanoflakes were synthesized via an aqueous oxidation method at 90 °C using Mn(CH3COO)2, NaOH, and KMnO4. The samples' morphology, crystalline structure, and optical property were determined by field emission scanning electron microscopy, X-ray powder diffraction and UV-Vis spectrophotometry. The birnessite-MnO2 nanoflakes were converted to KxMn8O16 and Mn suboxides following a decrease in the concentration of KMnO4 in the reaction. The amount of NaOH in the reaction determined the type of precursor. Without NaOH, the precursor was converted from Mn(OH)2 to Mn2+ (from Mn(CH3COO)2), thereby enabling the synthesis of birnessite-MnO2 nanoflowers. The formation mechanism of birnessite-MnO2 nanoflowers and nanoflakes was clarified via the corresponding simulated crystal structures. Evaluation of the synthesized samples confirmed that the birnessite-MnO2 nanoflakes and nanoflowers exhibited excellent degradation properties.

Aqueous Synthesis of Mn3O4 Nanoparticle@MnOOH Nanobelt Heterostructures.

A combined heterostructures with Mn3O4 nanoparticles attached to MnOOH nanobelts were prepared via an aqueous oxidation method at 90 °C with H2O2 as oxidant. The crystalline structures and morphologies of the as-prepared samples were detected by X-ray powder diffraction (XRD), field emission scanning electron microscope (FESEM) and high resolution transmission electron microscope (HRTEM) analysis, and the forming mechanism of Mn3O4@MnOOH nanomaterials was discussed. Crystalline composition and morphologies of samples changed with reaction time and crystallinity of Mn(OH)2 precursor. ß-MnOOH nanoplates can be obtained in the initial reaction, then it transformed to γ-MnOOH nanobelts and/or Mn3O4 nanoparticles as reaction time increasing. The ratio of Mn3O4 in Mn3O4@MnOOH nanomaterials increased with the better crystallinity of Mn(OH)2 precursor. The as-prepared Mn3O4@MnOOH nanomaterials with varied compositions were used for degradation of Rhodamine B (RhB) in acid condition. The degradation reactions carried out in acid condition without stimulated light sources. The results showed that the manganese heterostructures had good activity based on synergy of Mn3O4 and MnOOH nanocrystals.