Immobilization and photo catalytic properties of phthalocyanines anchored to the surface of Si-MCM-41 and SBA-15

Research output: Contribution to journalArticleResearchpeer review

Authors

  • O. Bartels
  • D. Wöhrle
  • J. Caro
  • M. Wark

External Research Organisations

  • University of Bremen
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Details

Original languageEnglish
Pages (from-to)2884-2892
Number of pages9
JournalStudies in Surface Science and Catalysis
Volume154 C
Publication statusE-pub ahead of print - 2 Sept 2007

Abstract

Tetrasulfo-phthalocyanine dye molecules acting as singlet oxygen generators for photo-oxidations were immobilized in mesoporous Si-MCM-41 or SBA-15 molecular sieves. The extraction stable fixation was achieved by either covalent or ionic bonding in the pores of differently modified hosts. Modification of the mesoporous hosts Si-MCM-41 or SBA-15 with N-trimethoxysilyl-propyl-N,N,N- trimethylammonium chloride provides a material that is suitable for ionic grafting of negatively charged dyes, which exhibit less aggregation compared with covalently grafted dyes. In addition, the grafting procedure is simplified. The obtained composite materials show photo-catalytic activity in the oxidation of sulfide anions in aqueous solutions. Since the photo-oxidation is most active in the region of pH 8-10 the use of SBA-15 as carrier is highly preferable due to its thicker pore walls providing an improved stability in basic media. However, photo bleaching of the photo-sensitizer itself is a serious problem.

Keywords

    Functionalization, Photo-oxidation, Phthalocyanine, SBA-15, Si-MCM-41, Sulfides

ASJC Scopus subject areas

Cite this

Immobilization and photo catalytic properties of phthalocyanines anchored to the surface of Si-MCM-41 and SBA-15. / Bartels, O.; Wöhrle, D.; Caro, J. et al.
In: Studies in Surface Science and Catalysis, Vol. 154 C, 02.09.2007, p. 2884-2892.

Research output: Contribution to journalArticleResearchpeer review

Bartels, O, Wöhrle, D, Caro, J & Wark, M 2007, 'Immobilization and photo catalytic properties of phthalocyanines anchored to the surface of Si-MCM-41 and SBA-15', Studies in Surface Science and Catalysis, vol. 154 C, pp. 2884-2892. https://doi.org/10.1016/s0167-2991(04)80568-8
Bartels, O., Wöhrle, D., Caro, J., & Wark, M. (2007). Immobilization and photo catalytic properties of phthalocyanines anchored to the surface of Si-MCM-41 and SBA-15. Studies in Surface Science and Catalysis, 154 C, 2884-2892. Advance online publication. https://doi.org/10.1016/s0167-2991(04)80568-8
Bartels O, Wöhrle D, Caro J, Wark M. Immobilization and photo catalytic properties of phthalocyanines anchored to the surface of Si-MCM-41 and SBA-15. Studies in Surface Science and Catalysis. 2007 Sept 2;154 C:2884-2892. Epub 2007 Sept 2. doi: 10.1016/s0167-2991(04)80568-8
Bartels, O. ; Wöhrle, D. ; Caro, J. et al. / Immobilization and photo catalytic properties of phthalocyanines anchored to the surface of Si-MCM-41 and SBA-15. In: Studies in Surface Science and Catalysis. 2007 ; Vol. 154 C. pp. 2884-2892.
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abstract = "Tetrasulfo-phthalocyanine dye molecules acting as singlet oxygen generators for photo-oxidations were immobilized in mesoporous Si-MCM-41 or SBA-15 molecular sieves. The extraction stable fixation was achieved by either covalent or ionic bonding in the pores of differently modified hosts. Modification of the mesoporous hosts Si-MCM-41 or SBA-15 with N-trimethoxysilyl-propyl-N,N,N- trimethylammonium chloride provides a material that is suitable for ionic grafting of negatively charged dyes, which exhibit less aggregation compared with covalently grafted dyes. In addition, the grafting procedure is simplified. The obtained composite materials show photo-catalytic activity in the oxidation of sulfide anions in aqueous solutions. Since the photo-oxidation is most active in the region of pH 8-10 the use of SBA-15 as carrier is highly preferable due to its thicker pore walls providing an improved stability in basic media. However, photo bleaching of the photo-sensitizer itself is a serious problem.",
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AU - Wöhrle, D.

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AU - Wark, M.

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