1. Chemically bonded CdS/Bi2MoO6 Z-scheme heterojunction synergises with strong internal electric field for photocatalytic CO2 reduction.
- Author
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Wu, Yinting, Xiao, Jianyu, Yuan, Jie, Wang, Liang, Luo, Songyu, Zhang, Zizhong, Fu, Xianzhi, and Dai, Wenxin
- Subjects
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FOURIER transform infrared spectroscopy , *X-ray photoelectron spectroscopy , *ELECTRIC fields , *CHEMICAL reduction , *SURFACE charges , *KELVIN probe force microscopy - Abstract
Properly designed interfacial electric fields between CdS and Bi 2 MoO 6 can effectively promote carrier separation and then enhance photocatalytic CO 2 reduction. [Display omitted] • CdS/Bi 2 MoO 6 composite materials were synthesized by in-situ growth method. • CdS/Bi 2 MoO 6 exhibits excellent photocatalytic CO 2 reduction performance. • Properly designed interfacial electric fields and interfacial chemical bonds can effectively promote carrier separation. • The photo-corrosion is effectively suppressed in this photocatalytic system. Constructing strong interfacial electric fields to enhance the surface charge transport kinetics is an effective strategy for promoting CO 2 conversion. Herein, we present the fabrication of CdS-Bi 2 MoO 6 Z-scheme heterojunctions with a robust internal electric field (IEF) using an in situ growth technique, establishing chemical bonding between the components. The IEF at the interface can offer an impetus for the segregation and transportation of photogenerated carriers, while the Cd-O chemical bonding mode acts as a rapid conduit for these carriers, thereby reducing the charge transfer distance. As a result, the Z-scheme charge transfer is accelerated due to the synergistic influence of these two factors. Therefore, the optimized CdS/Bi 2 MoO 6 Z-scheme heterojunction possesses significantly enhanced dynamic carrier mobility, thus promoting the conversion of CO 2 to CO without the need for additional co-catalysts or sacrificial agents. This optimization yields a remarkable CO selectivity of up to 97%. Meanwhile, the expedited Z-scheme charge transfer mechanism is validated through X-ray photoelectron spectroscopy, Kelvin probe force microscopy, and in situ diffuse reflectance infrared Fourier transform spectroscopy. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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