Abstract
Considering that CO2 is a harmful greenhouse gas, the effective conversion of this compound to high-value hydrocarbons is highly desirable, but also challenging. Herein, we synthesize a series of Cu- and Ag-modified TiO2 (B phase) photocatalysts, and we analyze their efficiency in catalyzing the photoreduction of CO2 in the presence of H2O and simulated solar irradiation. The obtained results show that the TiO2(B) catalyst modified with 1% Ag and 0.5% Cu has the best photoreduction performance, with CO and CH4 yields of 860 and 410 μmol/g, respectively, after for 3 h of reaction. Based on CO2-TPD testing, Cu enhances the photocatalytic activity of TiO2(B) by adsorbing and activating CO2. Meanwhile, the Ag nanoparticles increase the absorption of visible light through surface plasmonic resonance effect (SPR), and they transfer electrons to the TiO2(B) nanosheets. The transferred electrons migrate to the Cu particles where they reduce the adsorbed and activated CO2. This study provides an effective method for improving the photocatalytic CO2 reduction performance of TiO2(B)-based catalysts.
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Acknowledgements
This work was financially supported by the Foundation of Jiangsu Key Laboratory for Biomass Energy and Material (JSBEM202001), National Natural Science Foundation of China (No. 22078057, No. 21576050 and No. 51602052), Fundamental Research Funds for the Central Universities of China (No. 3207045403, 3207045409, 3207046414), Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), Zhongying Young Scholars of Southeast University, Applied Basic Research Program of Suzhou (SYG202026), Postgraduate Research and Practice Innovation Program of Jiangsu Province (SJCX20_0014, SJCX20_0015), and Innovation Platform Project Supported by Jiangsu Province of China (6907041203).
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Li, N., Geng, D. & Zhou, J. Ag and Cu Nanoparticles Synergistically Enhance Photocatalytic CO2 Reduction Activity of B Phase TiO2. Catal Lett 152, 124–138 (2022). https://doi.org/10.1007/s10562-021-03618-4
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DOI: https://doi.org/10.1007/s10562-021-03618-4