This study investigates the critical relationship between the crystal phase, morphology, and photocatalytic activity of MnO2. The δ-MnO2 nanosheets, characterized by multiple exposed crystal planes forming junctions, exhibit optimized optical and electrical properties. Oxygen vacancy concentrations were observed in the order δ-MnO2 > γ-MnO2 > α-MnO2, with corresponding increases in band gap width from 1.38 eV (δ-MnO₂) to 1.68 eV (α-MnO₂). The δ-MnO2 nanosheets achieved over 80 % NO removal efficiency and effectively suppressed the production of NO2 byproducts, outperforming α-MnO2 nanorods and γ-MnO2 nanospheres. The adsorption energy of O₂ followed the trend δ-MnO2 > γ-MnO2 > α-MnO2, while the adsorption energy of NO was lowest on δ-MnO2, facilitating its interaction with reactive species such as •O2⁻ and •OH. For γ-MnO2, NO directly reacted with •O2⁻. The findings highlight the dependence of MnO2 photocatalytic performance on its crystal phase and morphology, with δ-MnO2 effectively inhibiting photogenerated electron-hole recombination due to its superior properties. This work presents a straightforward approach to designing high-performance transition metal photocatalysts through crystal phase and morphology control, offering valuable insights for future photocatalyst research.
Keywords: Catalyst; Crystal phase; NO; Photocatalysis.
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