High-Efficiency Photooxidation of Methane to the C1 Product

The efficient conversion of methane (CH4) to high-value-added chemicals using a photocatalyst at room temperature and pressure faces great challenges compared to harsh reaction conditions. However, achieving this efficient conversion would yield substantial cost advantages and hold immense potential for development. Here, we demonstrate the enhanced photocatalytic conversion efficiency of CH4 at room temperature and pressure conditions without requiring any oxidant through the construction of a bimetal Ag-Cu-loaded brookite TiO2 photocatalyst. The C1 products were ultimately obtained with 100% selectivity and a yield of 936 mu mol<middle dot>g-1<middle dot>h-1. The performance exceeds that of similar research by tens of times. The high selectivity of this system is attributed to the optimal number of <middle dot>OH, which strikes a balance between excess and deficiency. Ag effectively enhances electron transport in the photocatalytic reaction process on a dual active site photocatalyst, while Cu significantly improves the selectivity of the C1 products. In this system, the hydroxyl radical (<middle dot>OH) activates CH4 to generate the methyl radical (<middle dot>CH3), which then binds with the lattice oxygen of TiO2, breaking the Ti-O bond and resulting in the formation of *OCH3. The *OCH3 undergoes further conversion to CH3OH, which is subsequently oxidized to HCHO by <middle dot>OH. This work presents a cost-effective and highly efficient approach for directly oxidizing CH4 into valuable chemicals, ensuring superior selectivity.