Covalent organic framework with sulfonic acid functional groups for visible light-driven CO2 reduction
Wanrong Li1, Qian Wang1, Fuzhi Cui1
1College of Chemistry and Chemical Engineering, State Key Laboratory of Chemo/Biosensing and Chemometrics, Advanced Catalytic Engineering Research Center of the Ministry of Education, Hunan University Changsha 410082 P. R. China guofangjiang@hnu.edu.cn.
Abstract:
In this study, a covalent organic framework (TpPa-SO3H) photocatalyst with sulfonic acid function groups was synthesized using a solvothermal method. The morphologies and structural properties of the as-prepared composites were characterized by X-ray diffraction, infrared spectroscopy, ultraviolet-visible diffuse reflectance spectroscopy, X-ray photoelectron spectroscopy, N2 adsorption-desorption measurements, and field emission scanning electron microscopy. An electrochemical workstation was used to test the photoelectric performance of the materials. The results show that TpPa-SO3H has -SO3H functional groups and high photocatalytic performance for CO2 reduction. After 4 h of visible-light irradiation, the amount of CO produced is 416.61 μmol g-1. In addition, the TpPa-SO3H photocatalyst exhibited chemical stability and reusability. After two testing cycles under visible light irradiation, the amount of CO produced decreased slightly to 415.23 and 409.15 μmol g-1. The XRD spectra of TpPa-SO3H were consistent before and after the cycles. Therefore, TpPa-SO3H exhibited good photocatalytic activity. This is because the introduction of -SO3H narrows the bandgap of TpPa-SO3H, which enhances the visible light response range and greatly promotes the separation of photogenerated electrons.
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