Enhancing CO Selectivity in CO₂ Photoreduction via Local Hydrophobic Modifications in S-Scheme Heterojunctions.

Abstract

To address the challenge of competitive H₂O adsorption in photocatalytic CO₂ reduction, localized hydrophobicity-modified S-scheme heterojunctions (WS/o-CN) were synthesized by combining WS₂ and g-C₃N₄, which was modified by the addition of CTAB. Structural characterization and contact angle testing confirmed the formation of S-scheme heterojunctions and the specific structural role of CTAB. The optical, electrochemical properties, and gas adsorption capacity of the catalysts were analyzed, followed by <i>in situ</i> XPS and fs-TA tests to investigate the energy band structure and electron transfer paths. These results showed that localized hydrophobic modification reduces the surface proton concentration while maintaining efficient electron-hole separation in the S-scheme heterojunction. Testing the photocatalytic activity of WS/o-CN showed that the yield of CO reached 23.24 μmol g^-1 h^-1 with a high selectivity of 74.7%. Combined with molecular dynamics simulations and <i>in situ</i> DRIFTS tests, the results demonstrated that the introduction of the nonpolar long carbon chain CTAB effectively inhibits the adsorption of heterogeneous H₂O on the catalyst surface while enhancing the maximum adsorption of CO₂. The localized hydrophobicity reduces the proton concentration on the surface of g-C₃N₄, which in turn suppresses the absorption of photogenerated electrons by the HER reaction. This facilitates the efficient and selective conversion of CO₂ to CO. This study highlights a surface engineering strategy that couples electronic structure optimization with interfacial wettability control, providing valuable insights into the design of selective and efficient photocatalysts for CO₂-to-CO conversion.