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Autor(en) / Beteiligte
Titel
Surface plasmon resonance enhanced visible-light-driven photocatalytic activity in Cu nanoparticles covered Cu2O microspheres for degrading organic pollutants
Ist Teil von
  • Applied surface science, 2016-03, Vol.366, p.120-128
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2016
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • •Cu NPs introduce the SPR and result in an increase of visible light absorption.•The photocatalytic activity of Cu2O/Cu improves greatly due to the SPR effect.•A dark catalytic activity is observed stemming from the Fenton-like reaction.•The •O2− and •OH radicals contribute to the photocatalytic process.•The •OH radicals contribute to the dark catalytic process. Micron-sized Cu2O with different coverage of Cu nanoparticles (NPs) on the sphere has been synthesized by a redox procedure. The absorption spectra show that Cu NPs induce the surface plasmon resonance (SPR) at the wavelength of ∼565nm. Methylene blue (MB) photodegrading experiments under visible-light display that the Cu2O–Cu–H2O2 system exhibits a superior photocatalytic activity to Cu2O–H2O2 or pure H2O2 with an evident dependency on Cu coverage. The maximum photodegradation rate is 88% after visible-light irradiating for 60min. The role of the Cu NPs is clarified through photodegradation experiments under 420nm light irradiation, which is different from the SPR wavelength of Cu NPs (∼565nm). By excluding the SPR effect, it proves that Cu SPR plays a key role in the photodegradation. Besides, a dark catalytic activity is observed stemming from the Fenton-like reaction with the aid of H2O2. The radical quenching experiments indicate that both •O2− and •OH radicals contribute to the photocatalysis, while the dark catalysis is only governed by the •OH radicals, leading to a lower activity comparing with the photocatalysis. Therefore, with introducing Cu NPs and H2O2, the Cu2O-based photocatalytic activity could be significantly improved due to the SPR effect and dark catalysis.
Sprache
Englisch
Identifikatoren
ISSN: 0169-4332
eISSN: 1873-5584
DOI: 10.1016/j.apsusc.2015.12.238
Titel-ID: cdi_proquest_miscellaneous_1793277334

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