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Autor(en) / Beteiligte
Titel
Facile hydrothermal synthesis and continuously improved sonophotocatalytic performance of PO4-doped Bi2WO6 nanoplates
Ist Teil von
  • Journal of alloys and compounds, 2024-06, Vol.988, Article 174245
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2024
Link zum Volltext
Quelle
Elsevier ScienceDirect Journals Complete
Beschreibungen/Notizen
  • The doping of ionic group composed of various atoms can play a great role in regulating electronic structure, optimizing light absorption capacity, and enhancing the catalytic performance of semiconductor catalysts. Herein, we took a urea-precipitate assisting hydrothermal route for preparing PO4-doped Bi2WO6 nanoplates and discussed the effect of the ionic group doping on the sonophotocatalytic performance toward the degradation of pollutant. The result of the X-ray photoelectron spectrometer (XPS) measurements revealed that abundant oxygen vacancies were formed in PO4-doped Bi2WO6 owing to the incorporation of the ionic group, which would contribute to the regulation of electronic structure and activated carriers’ migration rate. The sonophotocatalytic activity toward the removal of tetracycline hydrochloride (TCH) was investigated under visible-light coupling with ultrasonic irradiation. The results showed that PO4-doped Bi2WO6 nanoplates possessed higher sonophotocatalytic degradation rate than pure Bi2WO6. More interestingly, the TCH removal efficiency was continuously improved over PO4-doped Bi2WO6 nanoplates with the assistance of the sulfate radical-mediated technique. Based on the comprehensive discussion and analysis, a possible enhancement mechanism of the sonophotocatalytic behavior was proposed for PO4-doped Bi2WO6 nanoplates catalyst in the presence of peroxymonosulfate. •PO4-doped Bi2WO6 nanoplates were successfully prepared.•The PO4 doping induced the formation of more oxygen vacancy.•The synergistic effect contributed to continuous enhancement of catalytic performance.
Sprache
Englisch
Identifikatoren
ISSN: 0925-8388
eISSN: 1873-4669
DOI: 10.1016/j.jallcom.2024.174245
Titel-ID: cdi_elsevier_sciencedirect_doi_10_1016_j_jallcom_2024_174245

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