4.8 Article

2D/2D/2D heterojunction of Ti3C2 MXene/MoS2 nanosheets/TiO2 nanosheets with exposed (001) facets toward enhanced photocatalytic hydrogen production activity

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 246, Issue -, Pages 12-20

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2019.01.051

Keywords

Photocatalytic H-2 production; Exposed active facet; Ti3C2 MXene; MoS2 nanosheets; TiO2 nanosheets

Funding

  1. National Natural Science Foundation of China [51872173]
  2. Taishan Scholarship of Young Scholars
  3. Natural Science Foundation of Shandong Province [ZR2017JL020]
  4. Taishan Scholarship of Climbing Plan [tspd20161006]
  5. Key Research and Development Program of Shandong Province [2018GGX102028]

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Exposing the highly active facets and hybridizing the photocatalyst with appropriate cocatalysts with right placement have been regarded as a powerful approach to high performance photocatalysts. Herein, TiO2 nanosheets (NSs) are in situ grown on highly conductive Ti3C2 MXene and then MoS2 NSs are deposited on the (101) facets of TiO2 NSs with mainly exposed high-active (001) facets through a two-step hydrothermal method. And a unique 2D-2D-2D structure of Ti3C2@TiO2@MoS2 composite is achieved. With an optimized MoS2 loading amounts (15 wt%), the Ti3C2@TiO2@MoS2 composite shows a remarkable enhancement in the photocatalytic H-2 evolution reaction compared with Ti3C2@TiO2 composite and TiO2 NS. It also shows good stability under the reaction condition. This arises from: (i) the in situ growth of TiO2 NSs construct strong interfacial contact with excellent electronic conductivity of Ti3C2, which facilitates the separation of carriers; (ii) the coexposed (101) and (001) facets can form a surface heterojunction within single TiO2 NS, which is beneficial for the transfer and separation of charge carriers; and (iii) the MoS2 NSs are deposited on the electrons-rich (101) facets of TiO2 NSs, which not only effectively reduces the charge carriers recombination rate by capturing photoelectrons, but also makes TiO2 NSs expose more highly active (001) facets to afford high-efficiency photogeneration of electron-hole pairs.

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