摘要
Rapid charge separation and transfer is the key scientific problem in photocatalysis. The construction of S-scheme heterojunction is one of the effective strategies to promote charge separation and maintain the strong redox properties. Herein, the NiO, K0.2WO3, and NiWO4ternary double S-scheme K0.2WO3/NiO/NiWO4heterojunction (W/NiO) was created by a one-step molten salt method. Ultraviolet-visible (UV-Vis) diffuse reflectance spectra, photoluminescence (PL) spectra, photoelectrochemistry tests, and other analyses revealed that the double S-scheme heterostructure broadened the spectral response range of NiO and promoted its separation of photocarriers. Compared with pristine NiO, the modified double S-scheme heterojunction enhanced the surface adsorption of water molecules and the accumulation of intermediate product of HCOO−, and optimized the CO2reduction system, realizing the improved CO yield of 373 μmol·g−1·h−1in Ru(byp)32+/ethanolamine of CO2reduction system. This study indicates that double S-scheme heterojunction could facilitate efficient photogenerated charge transfer and separation, thereby achieving high activity and selectivity for CO2photoreduction. Our work provides a reference for the one-step construction of double S-scheme heterojunction.
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