Self-assembly of TiO2/ZIF-8 nanocomposites for varied photocatalytic CO2reduction with H2O vapor induced by different synthetic methods

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Abstract

Photoreduction of carbon dioxide (CO2) provides an effective perspective for solving the energy crisis and environmental problems. Herein, two types of composite photocatalysts (TiO2/ZIF-8) based on ZIF-8 and TiO2have been designed and synthesized with the help of the grinding method and the solid-synthesis method. Both composite photocatalysts are employed for the photocatalytic reduction of CO2. In composite photocatalysts prepared by the grinding method, ZIF-8 particles are distributed on the surface of TiO2, and provide extra available spaces for storing CO2, which is beneficial for improving their photoreduction performances. As a result, an enhanced CO formation rate of 21.74 μmol g−1h−1with a high selectivity of 99% is obtained for this family of composite photocatalystsviathe solid-gas mode without photosensitizers and sacrificial agents. For comparison, the other family of composite photocatalysts synthesizedviathe solid-synthesis method possesses structures similar to ZIF-8, where TiO2is encapsulated inside the framework of ZIF-8. This structural feature obstructs the contact between the active sites of TiO2and CO2, and leads to lower activities. The best CO formation rate of this family is only 10.67 μmol g−1h−1with 90% selectivity. Both the structural features of the two families of photocatalysts are described to explain their differences in photoreduction performances. The experimental finding reveals that different synthetic approaches indeed result in diversified structures and varied photocatalytic performances. This work affords a new scalable and efficient approach for the rational design of efficient photocatalysts in the area of artificial photosynthesis.

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Zou, Y. H., Wang, H. N., Meng, X., Sun, H. X., & Zhou, Z. Y. (2021). Self-assembly of TiO2/ZIF-8 nanocomposites for varied photocatalytic CO2reduction with H2O vapor induced by different synthetic methods. Nanoscale Advances, 3(5), 1455–1463. https://doi.org/10.1039/d0na00814a

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