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Details

Autor(en) / Beteiligte
Titel
Controlled synthesis of rh-In2O3 nanostructures with different morphologies for efficient photocatalytic degradation of oxytetracycline
Ist Teil von
  • Applied surface science, 2019-01, Vol.464, p.115-124
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2019
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • [Display omitted] •Two different rh-In2O3 nanostructures were prepared by controlling reactive condition.•The both rh-In2O3 samples are mesoporous materials with narrower band gaps.•The two prepared rh-In2O3 nanostructures are used to degrade OTC for the first time.•The both obtained rh-In2O3 show better photocatalytic activities than a commercial In2O3. Two rhombohedral corundum-type In2O3 (rh-In2O3) nanostructures were successfully prepared through solvothermal synthesis of InOOH precursors combined with post-annealing treatment. One is a unique and monodisperse urchin-like rh-In2O3 with three dimensional structures; another is a small size rod-like rh-In2O3 with two dimensional nanostructures. The morphological difference of the two InOOH precursors was mainly controlled by sodium dodecyl sulfonate (SDS) which acted as a soft template during the synthesis. The measurements of X-ray photoelectron spectroscopy, nitrogen adsorption and optical absorption indicated that the both obtained rh-In2O3 nanostructures are mesoporous materials which may possess oxygen vacancies and narrower band gaps. The photocatalytic activities of as-prepared urchin-like and rod-like rh-In2O3 were investigated by degrading oxytetracycline (OTC) under ultraviolet light irradiation. Compared with a commercial In2O3, the two above rh-In2O3 nanostructures exhibited an absolute superiority on photo-degrading OTC. Furthermore, the probable photocatalytic reaction mechanism was discussed and proposed according to radical trapping experiment and the detection of degradation intermediates.
Sprache
Englisch
Identifikatoren
ISSN: 0169-4332
eISSN: 1873-5584
DOI: 10.1016/j.apsusc.2018.08.057
Titel-ID: cdi_crossref_primary_10_1016_j_apsusc_2018_08_057

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