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    In-Situ Immobilization of H<sub>5</sub>PMo<sub>10</sub>V<sub>2</sub>O<sub>40</sub> on Protonated Graphitic Carbon Nitride under Hydrothermal Conditions: A Highly Efficient and Reusable Catalyst for Hydroxylation of Benzene

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    A novel heterogeneous catalyst was prepared by in situ immobilization of H<sub>5</sub>PMo<sub>10</sub>V<sub>2</sub>O<sub>40</sub> (PMo<sub>10</sub>V<sub>2</sub>) on protonated g-C<sub>3</sub>N<sub>4</sub> (pg-C<sub>3</sub>N<sub>4</sub>) under hydrothermal conditions. The results of Ī¶ potential, PL, FT-IR, XRD, and XPS indicated that PMo<sub>10</sub>V<sub>2</sub> was immobilized on the protonated Cī—øNī—»C of CN heterocycles. XPS and EPR confirmed the presence of V<sup>4+</sup> in the catalyst due to electronic interaction between PMo<sub>10</sub>V<sub>2</sub> and pg-C<sub>3</sub>N<sub>4</sub>. The textural and morphology properties of the catalyst were characterized by N<sub>2</sub> adsorptionā€“desorption, SEM, and TEM. PMo<sub>10</sub>V<sub>2</sub>/pg-C<sub>3</sub>N<sub>4</sub> showed excellent catalytic performance with 25.8% benzene conversion and 99.7% selectivity to phenol in the hydroxylation of benzene to phenol. The excellent catalytic performance of PMo<sub>10</sub>V<sub>2</sub>/pg-C<sub>3</sub>N<sub>4</sub> could be attributed to high dispersion of PMo<sub>10</sub>V<sub>2</sub> on pg-C<sub>3</sub>N<sub>4</sub>, the presence of V<sup>5+</sup>/V<sup>4+</sup> redox pairs, and the cooperative benzene-activation capability of g-C<sub>3</sub>N<sub>4</sub>. The PMo<sub>10</sub>V<sub>2</sub>/pg-C<sub>3</sub>N<sub>4</sub> catalyst can be easily recycled without loss of activity
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