4.2 Article

Enhanced photocatalytic degradation of lindane using metal-semiconductor Zn@ZnO and ZnO/Ag nanostructures

期刊

JOURNAL OF ENVIRONMENTAL SCIENCES
卷 74, 期 -, 页码 107-115

出版社

SCIENCE PRESS
DOI: 10.1016/j.jes.2018.02.014

关键词

Zn@ZnO; ZnO/Ag; Lindane; Pulsed laser ablation in liquid; Photocatalysis

资金

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2016R1D1A1B03934376]
  2. Korea government (MSIP) [2017M2B2A9A02049940, 2017R1A41014595]
  3. National Research Foundation of Korea [21A20151513130, 2016R1D1A1B03934376] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

To achieve enhanced photocatalytic activity for the degradation of lindane, we prepared metal-semiconductor composite nanoparticles (NPs). Zn@ZnO core-shell (CS) nanocomposites, calcined ZnO, and Ag-doped ZnO (ZnO/Ag) nanostructures were prepared using pulsed laser ablation in liquid, calcination, and photodeposition methods, respectively, without using surfactants or catalysts. The as-prepared catalysts were characterized by using X-ray diffraction (XRD), field-emission scanning electron microscopy, high-resolution transmission electron microscopy, ultraviolet-visible (UV-vis) spectroscopy, and photoluminescence spectroscopy. In addition, elemental analysis was performed by energy dispersive X-ray spectroscopy. The obtained XRD and morphology results indicated good dispersion of Zn and Ag NPs on the surface of the ZnO nanostructures. Investigation of the photocatalytic degradation of lindane under UV-vis irradiation showed that Zn@ZnO CS nanocomposites exhibit higher photocatalytic activity than the other prepared samples. The maximum degradation rate of lindane was 99.5% in 40 min using Zn@ZnO CS nanocomposites. The radical trapping experiments verified that the hydroxyl radical (center dot OH) was the main reactive species for the degradation of lindane. (c) 2017 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.

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