4.7 Article

Steering interfacial charge kinetics: Synergizing cocatalyst roles of Ti3C2Mx (MXene) and NCDs for superior photocatalytic performance over TiO2

期刊

APPLIED SURFACE SCIENCE
卷 599, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2022.154001

关键词

NCDs; Photocatalysis; Synergizing cocatalyst; Steering charge kinetics

资金

  1. National Natural Science Foundation of China
  2. Guangdong Basic and Applied Basic Research Foundation
  3. Characteristics Innovation Project of Guangdong Province University
  4. Youth Innovation Project of Guangdong Province University
  5. COVID-19 Epidemic Prevention and Control Project [21802019]
  6. Innovation and Entrepreneurship Training Project of Wuyi University [2022A1515010009, 2020A1515110427]
  7. Open Project Program of Guangdong Provincial Key Laboratory of Hydrogen Energy Technology [2019KTSCX185]
  8. Research Fund Program of Guangdong Provincial Key Lab of Green Chemical Product Technology [2020KQNCX088]
  9. Research Fund Program of Key Laboratory of Fuel Cell Technology of Guangdong Province [2020FKZX02]
  10. Education Department of Guangdong Province [2020CX18]
  11. Science and Technology Development Fund (FDCT) from Macau SAR [20191010-001]
  12. Research & Development Office at University of Macau [GC202108]
  13. Shenzhen-Hong Kong -Macao Science and Technology Research Programme from Shenzhen
  14. [2020KSYS004]
  15. [0081/2019/AMJ]
  16. [0154/2019/A3]
  17. [0102/2019/A2]
  18. [MYRG2018-00003-IAPME]
  19. [SGDX20210823103803017]

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This study fabricates 0D/2D/2D NCDs/TiO2/Ti3C2Mx photocatalyst via hydrothermal route for the first time and explores the synergistic effect of MXene and NCDs in enhancing the photocatalytic performance of TiO2 nanosheets. The results show that the photocatalytic hydrogen evolution and tetracycline hydrochloride degradation of 0.1 NCDs/TiO2/Ti3C2Mx-12 h are significantly higher than those of TiO2. The surface termination dominated electronic property of MXene and the synergistic interfacial charge kinetics steering play crucial roles in the photocatalytic enhancement.
Steering the kinetics of photoexcited electron-hole pairs to achieve the elongated lifetime of carrier is one of key strategies to enhance the photocatalytic performance. Here, 0D/2D/2D NCDs/TiO2/Ti3C2Mx photocatalyst is fabricated for the first time via hydrothermal route, the mixed group terminated MXene (Ti3C2Mx, M =-O, -OH,-F) and N-doped carbon dots (NCDs) are exploited as an electron acceptor and hole mediator, respectively, enhancing the photocatalytic activity of TiO2 nanosheets by steering interfacial charge kinetics. The photo catalytic hydrogen evolution and tetracycline hydrochloride (TC) degradation of 0.1 NCDs/TiO2/Ti3C2Mx-12 h are ~ 4 and 9 times higher than those of TiO2, respectively. UPS and DFT calculation results determine that the work function (phi) of Ti3C2Mx as 4.16 eV and 3.63 eV, respectively, which are larger than that of bare Ti3C2 (phi = 3.55 eV), while the work function of TiO2 and NCDs are 3.98 and 3.09 eV, respectively. The results of charge transfer dynamics reveal that the photocatalytic enhancement of NCDs/TiO2/Ti3C2Mx is dominantly attributed to the synergizing cocatalyst roles of Ti3C2Mx (MXene) and NCDs. The insight into the surface termination dominated electronic property of MXene and synergistic steering the interfacial charge kinetics is an effective way to fabricate high performance MXene-based photocatalysts.

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