Natural sunlight-driven oxidation of Mn2+(aq) and heterogeneous formation of Mn oxides on hematite

The oxidation of dissolved Mn2+(aq) plays a critical role in driving manganese cycles and regulating the fate of essential elements and contaminants in environmental systems. Based on sluggish oxidation rate, abiotic processes have been considered less effective oxidation pathway for manganese oxidation in environmental systems. Interestingly, a recent study (Jung et al., 2021) has shown that the rapid photochemical oxidation of Mn2+(aq) could be a feasible scenario to uncover the potential significance of abiotic Mn2+(aq) oxidation. Nevertheless, the significance of photochemical oxidation of Mn2+(aq) under natural sunlight exposure remains unclear. Here, we demonstrate the rapid photocatalytic oxidation of Mn2+(aq) and the heterogeneous growth of tunnel-structured Mn oxides under simulated freshwater and seawater conditions in the presence of natural sunlight and hematite. The natural sunlight-driven photocatalytic oxidation of Mn2+(aq) by hematite showed kinetic constants of 1.02 h−1 and 0.342 h−1 under freshwater and seawater conditions, respectively. The natural sunlight-driven photocatalytic oxidation rates are quite comparable to the results obtained from the previous laboratory test using artificial sunlight, which has ∼4.5 times stronger light intensity. It is likely because of ∼5.5 times larger light exposure area in the natural sunlight-driven photocatalytic oxidation than that of the laboratory test using artificial sunlight. We also elucidate the roles of cation species in controlling the oxidation rate of Mn2+(aq) and the crystalline structure of Mn oxide products. Specifically, in the presence of large amounts of cations, the oxidation rate of Mn2+(aq) was slower likely because of competitive adsorption. Furthermore, our findings highlight that Mg2+ contributes significantly to the formation of large-tunneled Mn oxides. These results illuminate the importance of abiotic photocatalytic processes in controlling the redox chemistry of Mn in real environmental aqueous systems on the oxidation of Mn2+(aq), and provide an environmentally sustainable approach to effectively remediate water contaminated with Mn2+(aq) using natural sunlight. [Display omitted] •Hematite rapidly oxidizes Mn2+(aq) under natural sunlight condition.•Heterogeneous nucleation of the oxidized Mn2+(aq) forms tunneled Mn(III/IV) oxides.•Mg2+(aq) plays a crucial role in the photocatalytic oxidation of Mn2+(aq).•Sunlight-driven photocatalysis effectively remediates Mn2+(aq)-cont