Study on the synthesis of heterostructure MoS2/TiO2 material for photocatalytic degradation of 2,4-dichlorophenoxyacetic acid

Authors

  • Nguyen Hoang Hao Vinh University Author
  • Dao Thi Tuan Faculty of Chemistry, Hanoi National University of Education Author
  • Phung Thi Lan Faculty of Chemistry, Hanoi National University of Education Author
  • Nguyen Thi Mo Faculty of Chemistry, Hanoi National University of Education Author
  • Nguyen Ngoc Ha Faculty of Chemistry, Hanoi National University of Education Author
  • Nguyen Thi Thu Ha Faculty of Chemistry, Hanoi National University of Education Author
  • Le Minh Cam Faculty of Chemistry, Hanoi National University of Education Author

DOI:

https://doi.org/10.51316/jca.2021.059

Keywords:

2,4-D, heterostructure, nanoflower MoS2, nanowire TiO2

Abstract

Nanoflower MoS2, nanowire TiO2(NNW) and 3D MoS2/TiO2 nano-heterostructure have been synthesized successfully by simple typical hydrothermal reaction method followed by 200oC calcination under an argon atmosphere. The prepared samples are characterized in detail by XRD, FESEM, UV-vis DRS, EDX and BET. The results suggest that the TiO2 NNW is successfully coupled with MoS2 to form the heterojunction nanostructure. The hybrid heterostructures can effectively utilize visible-light and solar energy to degrade 2,4-dichlorophenoxyacetic acid (2,4-D). The degradation rate of 2,4-D is as high as 99%. The improved photocatalytic activity owes to the decreased band-gap and the heterosurface properties of MoS2/TiO2, promoting the electron-hole pairs separation and absorption capacity to visible light. This work presents a facile approach for fabricating the MoS2/TiO2 heterostructures for efficient photocatalytic 2,4-D solution, which will facilitate the development of designing photo catalysts applied in environment and energy.

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References

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Published

30-10-2021

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How to Cite

Study on the synthesis of heterostructure MoS2/TiO2 material for photocatalytic degradation of 2,4-dichlorophenoxyacetic acid . (2021). Vietnam Journal of Catalysis and Adsorption, 10(3), 113-120. https://doi.org/10.51316/jca.2021.059

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