Nearly 100% selective and visible-light-driven methane conversion to formaldehyde via. single-atom Cu and Wδ+

Abstract

Direct solar-driven methane (CH₄) reforming is highly desirable but challenging, particularly to achieve a value-added product with high selectivity. Here, we identify a synergistic ensemble effect of atomically dispersed copper (Cu) species and partially reduced tungsten (W^δ+), stabilised over an oxygen-vacancy-rich WO₃, which enables exceptional photocatalytic CH₄ conversion to formaldehyde (HCHO) under visible light, leading to nearly 100% selectivity, a very high yield of 4979.0 μmol·g⁻¹ within 2 h, and the normalised mass activity of 8.5 × 10⁶ μmol·g^-1_Cu·h⁻¹ of HCHO at ambient temperature. In-situ EPR and XPS analyses indicate that the Cu species serve as the electron acceptor, promoting the photo-induced electron transfer from the conduction band to O₂, generating reactive •OOH radicals. In parallel, the adjacent W^δ+ species act as the hole acceptor and the preferred adsorption and activation site of H₂O to produce hydroxyl radicals (•OH), and thus activate CH₄ to methyl radicals (•CH₃). The synergy of the adjacent dual active sites boosts the overall efficiency and selectivity of the conversion process.

Direct solar-driven methane (CH₄) reforming is highly desirable but challenging. Here, the synergy of atomic Cu species and partially reduced tungsten (W^δ+), stabilized over an oxygen-vacancy-rich WO₃, enables exceptional CH₄ conversion to formaldehyde (HCHO) under visible light.