摘要
In recent years, metal–semiconductor heterojunctions have been intensively researched in the field of photocatalysis due to the effective spatial separation of photo-induced electron-hole pairs. Here, the dual-functional copper (Cu 0 /Cu 2+ )-modified SrTiO 3-δ nanosheets (Cu/STCO) are successfully synthesized by a two-step route. First, Cu 2+ -doped SrTiO 3-δ (STCO) nanosheets are synthesized by a hydrothermal method and then Cu 0 nanoparticles (NPs) are in situ formed from the STCO under H 2 atmosphere at 500 °C. The optimized ratio 6 %-Cu/STCO photocatalyst exhibits the best photothermal catalytic performance for CO 2 reduction reaction (CO 2 RR) and H 2 evolution performance. The detailed characterization demonstrate that the Cu 2+ dopant extend the light absorption range and the in situ generated Cu 0 NPs effectively improve the separation ability of photogenerated charge carriers by forming the Schottky contact with STCO. The excited localized surface plasmon resonance (LSPR) effect of metallic Cu 0 in Cu/STCO shows a considerable catalysis performance even under 600 nm monochromatic light irradiation. The density functional theory (DFT) calculations suggest that the Cu/STCO diminishes the barrier of the rate-determining steps of the CO 2 RR and H 2 evolution thus perform the outstanding catalysis ability in two filed. This work presents the synergistic effect of Cu 0 and Cu 2+ on enhancing the photothermal catalytic performance for CO 2 RR and H 2 evolution and offers a novel strategy to synthesize the metal–semiconductor nanostructures for efficient harnessing of solar energy into fuel.
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