4.6 Article

Fabrication of Z-Scheme TiO2/SnS2/MoS2 ternary heterojunction arrays for enhanced photocatalytic and photoelectrochemical performance under visible light

期刊

JOURNAL OF SOLID STATE CHEMISTRY
卷 307, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jssc.2021.122737

关键词

TiO2/SnS2/MoS2; Photocatalysis; Photoelectrochemistry; Z-scheme

资金

  1. Anhui Provincial Natural Science Foundation [1808085ME130]
  2. National Natural Science Foundation of China [51702003]
  3. Provincial Foundation for Excellent Young Talents of Colleges and Universities of Anhui Prov-ince [gxyq2019023, KJ2018A0094]
  4. Doctoral foundation of Anhui University of science and technology

向作者/读者索取更多资源

Z-scheme TiO2/SnS2/MoS2 ternary heterojunction arrays synthesized by a hydrothermal technique exhibit enhanced photocatalytic and photoelectrochemical performance due to their unique microstructure and band alignment.
In the current work, Z-scheme TiO2/SnS2/MoS2 ternary heterojunction arrays were synthesised on a fluorine-doped tin oxide conductive glass by using a facile hydrothermal technique. The microstructures, energy band structures, and photocatalytic performances of TiO2, TiO2/SnS2, and TiO2/MoS2 were investigated. The results revealed that for methylene blue, ternary TiO2/SnS2/MoS2 exhibited considerably enhanced photocatalytic efficiency (similar to 79%) and the optimal transient current density (similar to 0.92 mA/cm(2)) under visible-light irradiation; these two values were four and eight times higher than those exhibited by TiO2, respectively. The highly improved photocatalytic and photoelectrochemical performance could be attributed to the unique microstructure and band alignment of TiO2/SnS2/MoS2. These attributes can be explained as follows: (i) the large specific surface area offers numerous active sites, (ii) the modulation of the narrow-band SnS2 and MoS2 broadens visible-light response, and (iii) the Z-scheme heterojunction effectively restricts the bulk recombination and spatially separates the photogenerated electron-hole (e(-)-h(+)) pairs.

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