4.7 Article

0D/3D Bi3TaO7/ZnIn2S4 heterojunction photocatalyst towards degradation of antibiotics coupled with simultaneous H2 evolution: In situ irradiated XPS investigation and S-scheme mechanism insight

期刊

APPLIED SURFACE SCIENCE
卷 596, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2022.153444

关键词

Photocatalysis; Degradation; S-scheme mechanism; Bi3TaO7; ZnIn2S4; H-2 evolution

资金

  1. National Natural Science Foun-dation of China [52104254, 52003079]
  2. Natural Science Foundation of Hubei Province [2021CFB242, 2021CFB569]
  3. Research Project of Hubei Provincial Department of Education [Q20202501, Q20212502]

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Photocatalytic pollutant degradation coupled hydrogen generation via water splitting utilizing solar energy is a promising method for addressing environmental pollution and energy shortage. However, the limited utilization efficiency of solar energy and quick recombination of photogenerated carriers have hindered its application. In this study, a 0D Bi3TaO7 nanodots-decorated 3D ZnIn2S4 nanoflowers photocatalyst was synthesized for efficient simultaneous photocatalytic degradation of antibiotics and hydrogen generation. The relationship between S-scheme heterojunction photocatalysts and photocatalytic pollutant degradation coupled hydrogen evolution will be discussed, along with a careful examination of the interfacial transfer mechanism.
Photocatalytic pollutant degradation coupled hydrogen generation via water splitting utilizing solar energy is a highly promising method for solving the problems of environment pollution and energy shortage. However, restricted utilization efficiency of solar energy and quick recombination of photogenerated carriers of catalysts have restricted its application in photocatalytic pollutant degradation coupled hydrogen evolution. In this work, we synthesized a 0D Bi3TaO7 nanodots-decorated 3D ZnIn2S4 nanoflowers photocatalyst using a simple two-step solvothermal method. The simultaneously photocatalytic degradation of antibiotics (tetracycline) coupled with hydrogen generation was efficiently realized over the resultant S-scheme ZnIn2S4/Bi3TaO7 composites. The relationship between S-scheme heterojunction photocatalysts and photocatalytic pollutant degradation coupled hydrogen evolution will be discussed. As a result, optimized ZB20 composite achieves highly efficient TC degradation rate >90% after ten cycles coupled with simultaneous H2 evolution (13.7 mu mol g-1h- 1) with Pt cocatalyst. Furthermore, interfacial transfer mechanism of S-scheme heterojunction photocatalysts will be carefully examined combining in-situ characterization techniques and DFT study.

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