4.7 Article

Co-MOF as an electron donor for promoting visible-light photoactivities of g-C3N4 nanosheets for CO2 reduction

期刊

CHINESE JOURNAL OF CATALYSIS
卷 41, 期 3, 页码 514-523

出版社

SCIENCE PRESS
DOI: 10.1016/S1872-2067(19)63497-2

关键词

Co-MOF; g-C3N4 nanosheets; Charge separation; Visible-light photoactivity; Photocatalytic CO2 conversion

资金

  1. National Natural Science Foundation of China [21871079,21501052]
  2. Outstanding Youth Project of Natural Science Foundation of Heilongjiang Province [YQ2019B006]

向作者/读者索取更多资源

A possible mechanism for boosting the visible-light photoactivities of graphitic carbon nitride (g-C3N4) nanosheets for CO2 reduction via coupling with the electron donor Co-metal-organic framework (MOF) is proposed in this study. Specifically, Co-MOF as an electron donor is capable of transferring the photogenerated electrons in the lowest unoccupied molecular orbital (LUMO) to the conduction band of g-C3N4 to facilitate charge separation. As expected, the prepared Co-MOF/g-C3N4 nanocomposites display excellent visible-light-driven photocatalytic CO2 reduction activities. The CO production rate of 6.75 mu mol g(-1)h(-1) and CH4 evolution rate of 5.47 mu mol g(-1) h(-1) are obtained, which are approximately 2 times those obtained with the original g-C3N4 under the same conditions. Based on a series of analyses, it is shown that the introduction of Co-MOF not only broadens the range of visible-light absorption but also enhances the charge separation, which improves the photocatalytic activity of g-C3N4 to a higher level. In particular, the hydroxyl radical (center dot OH) experiment was operated under 590 nm (single-wavelength) irradiation, which further proved that the photogenerated electrons in the LUMO of Co-MOF can successfully migrate to g-C3N4. This work may provide an important strategy for the design of highly efficient g-C3N4-based photocatalysts for CO2 reduction. (C) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

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