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Abstract
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In this work, the effect of Keggin polyoxometalates encapsulated in Keplerate {Mo72Fe30} shell (K shell) on the visible light-assisted catalase-like activity (H2O2 dismutation) of the resulting core−shell clusters PMo12@K, SiMo12@K, and BW12@ K was investigated. Superior photodismutation activity of PMo12@ K compared to that of K shell and two other core−shell clusters was discovered. The homogeneity of PMo12@K and its improved oxidative stability, increased redox potential, and reduced band gap caused by a synergistic effect between the Keplerate shell and Keggin core seem reasonable to explain such a superiority. The light-dependent photocatalytic performance of PMo12@K evaluated by action spectra revealed a maximum apparent quantum efficiency (AQY) at 400 nm, demonstrating the visible light-driven photocatalytic reaction. A first-order rate constant of 2 × 10−4 s −1 and activation energy of 108.8 kJ mol−1 alongside a turnover frequency of 0.036 s−1 and a total turnover number of up to ∼3800 approved the effective photocatalytic activity and improved the oxidative stability of PMo12@K. A nonradical photocatalytic mechanism through a Fe−OOH intermediate was proposed. Thus, the structure, optical activity, and oxidative stability of a host Keplerate-type nanocluster can be tuned significantly by encapsulation of a guest, like “cluster-in-cluster” structures, which opens the scope for introducing new visible light-sensitive hierarchical nanostructures.
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