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  Silica-supported Au@hollow-SiO2 particles with outstanding catalytic activity prepared via block copolymer template approach

Shajkumar, A., Nandan, B., Sanwaria, S., Albrecht, V., Libera, M., Lee, M.-H., et al. (2017). Silica-supported Au@hollow-SiO2 particles with outstanding catalytic activity prepared via block copolymer template approach. Journal of Colloid and Interface Science, 491, 246-254. doi:10.1016/j.jcis.2016.12.051.

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Shajkumar, Aruni1, Autor
Nandan, Bhanu1, Autor
Sanwaria, Sunita1, Autor
Albrecht, Victoria1, Autor
Libera, Marcin1, Autor
Lee, Myong-Hoon1, Autor
Auffermann, Gudrun2, Autor           
Stamm, Manfred1, Autor
Horechyy, Andriy1, Autor
Affiliations:
1External Organizations, ou_persistent22              
2Gudrun Auffermann, Inorganic Chemistry, Max Planck Institute for Chemical Physics of Solids, Max Planck Society, ou_1863432              

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 Zusammenfassung: Catalytically active Au@hollow-SiO2 particles embedded in porous silica support (Au@hollow-SiO2@PSS) were prepared by using spherical micelles from poly(styrene)-block-poly(4-vinyl pyridine) block copolymer as a sacrificial template. Drastic increase of the shell porosity was observed after pyrolytic removal of polymeric template because the stretched poly(4-vinyl pyridine) chains interpenetrating with silica shell acted as an effective porogen. The embedding of Au@hollow-SiO2 particles in porous silica support prevented their fusion during pyrolysis. The catalytic activity of Au@hollow-SiO2@PSS was investigated using a model reaction of catalytic reduction of 4-nitrophenol and reductive degradation of Congo redazo-dye. Significantly, to the best of our knowledge, Au@hollow-SiO2@PSS catalyst shows the highest activity among analogous systems reported till now in literature. Such high activity was attributed to the presence of multiple pores within silica shell of Au@hollow-SiO2 particles and easy accessibility of reagents to the catalytically active sites of the ligand-free gold surface through the porous silica support. (C) 2016 Elsevier Inc. All rights reserved.

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Sprache(n): eng - English
 Datum: 2017-01-102017-01-10
 Publikationsstatus: Erschienen
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 Ort, Verlag, Ausgabe: -
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 Identifikatoren: DOI: 10.1016/j.jcis.2016.12.051
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Titel: Journal of Colloid and Interface Science
  Kurztitel : J. Colloid Interface Sci.
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Amsterdam etc. : Elsevier Inc.
Seiten: - Band / Heft: 491 Artikelnummer: - Start- / Endseite: 246 - 254 Identifikator: ISSN: 0021-9797
CoNE: https://pure.mpg.de/cone/journals/resource/954927606757