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Details

Autor(en) / Beteiligte
Titel
Fabrication of a novel 3D E-Fe2O3-Pi-MoS2 film with highly enhanced carrier mobility and photoelectrocatalytic activity
Ist Teil von
  • Electrochimica acta, 2020-03, Vol.337, p.135748, Article 135748
Ort / Verlag
Oxford: Elsevier Ltd
Erscheinungsjahr
2020
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • A novel 3D E-Fe2O3-Pi-MoS2 film was fabricated for water oxidation and environmental remediation. The nonmetal doping with phosphorus and vertically oriented MoS2 nanosheets were successfully constructed on Fe2O3 substrate, and the electrochemical modification further enhanced its photoelectrocatalytic (PEC) activity. The photocurrent density of E-Fe2O3-Pi-MoS2 for water oxidation was 30 times or 19.4 times higher than that of Fe2O3 under visible light or UV–vis light illumination at 0.45 V vs. Ag/AgCl, respectively. E-Fe2O3-Pi-MoS2 film also showed excellent PEC activity for phenol degradation (93.73%) and good stability. Hydroxyl radicals and holes were main active species. The remarkable activity of E-Fe2O3-Pi-MoS2 film could be attributed to the synergistic effects of nonmetal doping with phosphorous, vertically oriented MoS2 nanosheets fabrication and the electrochemical modification treatment, which significantly improved the charge transfer and enhanced the separation efficiency of photogenerated carriers. This work provides an effective, environmentally friendly, and low-cost semiconductor materials for sustainable energy and environmental application. [Display omitted] •E-Fe2O3-Pi-MoS2 film was synthesized by impregnation and hydrothermal method.•The nonmetal-P and vertically oriented MoS2 were constructed on Fe2O3 film.•A facile electrochemical treatment leads to remarkably enhanced PEC performance.•Enhanced carrier mobility and slower recombination rate were achieved.•E-Fe2O3-Pi-MoS2 film exhibited excellent PEC activity and stability.
Sprache
Englisch
Identifikatoren
ISSN: 0013-4686
eISSN: 1873-3859
DOI: 10.1016/j.electacta.2020.135748
Titel-ID: cdi_proquest_journals_2441577598

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