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    Jin Zhang, Yuefeng Lu, Ruiyi Wang, Xincheng Li, Dingkai Wang, Meiling Liu, Yuefeng Wang, Zhanfeng Zheng. Ru/TiO2 catalyst modified by phosphate ion: realizing specific transformation of CO2 hydrogenation products[J]. Chinese Journal of Chemical Physics .
    Citation: Jin Zhang, Yuefeng Lu, Ruiyi Wang, Xincheng Li, Dingkai Wang, Meiling Liu, Yuefeng Wang, Zhanfeng Zheng. Ru/TiO2 catalyst modified by phosphate ion: realizing specific transformation of CO2 hydrogenation products[J]. Chinese Journal of Chemical Physics .

    Ru/TiO2 catalyst modified by phosphate ion: realizing specific transformation of CO2 hydrogenation products

    • Regulation of the CO2 hydrogenation process to obtain highly selective target products is a challenging and important research topic. In this study, we report the key role of PO43- anions modified on the Ru/TiO2 catalyst surface in regulating the CO2 hydrogenation process. Ion chromatography, XRD, XPS and TEM confirmed the successful preparation of the Ru/TiO2 catalyst modified by PO43- anions. The original Ru/TiO2 catalyst showed poor catalytic activity in CO2 hydrogenation, and the main hydrogenation product was CO. With the Ru/TiO2 catalyst modified by PO43- anions, the conversion of CO2 clearly improved, and the hydrogenation product changed from CO to CH4. XPS characterization and DFT theoretical calculations confirmed that the modified PO43- anions acted mainly on the Ru metal site on the Ru/TiO2 catalyst surface, effectively regulating the surface electronic properties of the Ru metal, which affected the conversion efficiency of CO2. In addition, CO-TPD and DRIFTS characterization revealed that the adsorption of CO intermediates improved after the Ru metal surface was modified with PO43- anions, which was beneficial for further CO hydrogenation and the formation of CH4 products. Our work expands the research strategies of anion-modified metal-based catalysts that regulate the hydrogenation performance of CO2 and provides a new direction for further understanding the influence mechanism of the catalyst surface structure on hydrogenation performance.
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