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Visible-Light-Induced Photocatalytic Activity of Stacked MXene Sheets of Y2CF2

  • Kazuhiko Maeda*
    Kazuhiko Maeda
    Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1-NE-2, Ookayama, Meguro-ku, Tokyo 152-8550, Japan
    *E-mail: [email protected] (K.M.).
  • Haruki Wakayama
    Haruki Wakayama
    Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1-NE-2, Ookayama, Meguro-ku, Tokyo 152-8550, Japan
  • Yasuhito Washio
    Yasuhito Washio
    Materials Research Center for Element Strategy, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8503, Japan
  • Asako Ishikawa
    Asako Ishikawa
    Materials Research Center for Element Strategy, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8503, Japan
  • Megumi Okazaki
    Megumi Okazaki
    Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1-NE-2, Ookayama, Meguro-ku, Tokyo 152-8550, Japan
  • Hiroko Nakata
    Hiroko Nakata
    Department of Chemistry, School of Science, Tokyo Institute of Technology, 2-12-1-NE-2, Ookayama, Meguro-ku, Tokyo 152-8550, Japan
  • , and 
  • Satoru Matsuishi*
    Satoru Matsuishi
    Materials Research Center for Element Strategy, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama 226-8503, Japan
    *E-mail: [email protected] (S.M.).
Cite this: J. Phys. Chem. C 2020, 124, 27, 14640–14645
Publication Date (Web):June 10, 2020
https://doi.org/10.1021/acs.jpcc.0c03072
Copyright © 2020 American Chemical Society

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    Abstract

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    Transition metal carbides, nitrides, and carbonitrides (MXenes) are emerging two-dimensional (2D) materials, with a variety of applications, such as heterogeneous catalysis, due to their metallic conductivity and resulting charge transport properties. However, the semiconductor photocatalysis of MXene-related materials has not been experimentally demonstrated. Here, we show that stacked MXene sheets of Y2CF2 behave as an n-type semiconductor, with a 1.9 eV band gap and a rather negative conduction band potential of approximately −2.1 V versus Ag/AgNO3. In the presence of triethanolamine as an electron donor, Y2CF2 exhibits the ability to reduce protons into H2 under visible light. However, Y2CF2 is not very stable during the photoreaction, even in the presence of triethanolamine, undergoing oxidative degradation to form fluorocarbon and carbonate species due primarily to the high-energy valence band formed by C 2p orbitals.

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    • Additional characterization and photoreaction data (Tables S1 and S2 and Figures S1 and S2) (PDF)

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