4.7 Article

Photocatalytic CO2 reduction on Cu single atoms incorporated in ordered macroporous TiO2 toward tunable products

期刊

INORGANIC CHEMISTRY FRONTIERS
卷 9, 期 18, 页码 4753-4767

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qi01155g

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资金

  1. National Natural Science Foundation of China [21471004]
  2. Open Research Fund Program of Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province [SISPM-2021-02]
  3. Science Foundation of Zhejiang Sci-Tech University [17062002-Y]

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This study presents a Cu single-atom-incorporated photocatalyst that shows superior activity and selectivity in gas-solid and liquid-solid systems, mainly producing methane and ethylene, respectively.
The photocatalytic conversion of CO2 to hydrocarbons is a fascinating strategy to defuse the growing energy and environmental dilemmas, but there are great challenges in improving photocatalytic efficiency and tuning product selectivity. Both are of equal importance to increase the yield of the desired product and clarify the photocatalytic CO2 reduction mechanism. Herein, a Cu single-atom-incorporated three-dimensional-ordered macroporous TiO2 (Cu-0.01/3DOM-TiO2) photocatalyst was synthesized using a template-assisted in situ pyrolysis method. The Cu single atoms are uniformly anchored in a 3DOM TiO2 matrix, which not only broadens the light absorption range but also provides specific active sites for the adsorption and transformation of CO2 molecules. The photocatalytic CO2 reduction reaction was conducted in gas-solid and liquid-solid systems, respectively, to explore the effects of reaction modes on the CO2 conversion efficiency and product selectivity. The results indicate that the photocatalytic CO2 reduction reaction in gas-solid system mainly produces methane (CH4), with a high selectivity of 83.3% and a formation rate of 43.15 mu mol g(-1) h(-1). In contrast, the main product in the liquid-solid system is ethylene (C2H4), with a selectivity of 58.4% and a formation rate of 6.99 mu mol g(-1) h(-1). The Cu-0.01/3DOM-TiO2 photocatalyst shows superior activity and selectivity in the gas-solid system while favorably producing C2H4 in the liquid-solid system. The possible photocatalytic mechanisms of CO2 reduction in the two different reaction systems are discussed according to in situ infrared spectroscopy. This work provides some new information on promoting photocatalytic CO2 reduction to desirable products by the rational design of photocatalysts as well as tuning the reaction conditions.

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