Controlled engineering of Bi4O5Br2 and BiOBr via interactions imidazolium ionic liquids and medium during synthesis as a simple method for enhancement of photocatalytic activity - Publication - Bridge of Knowledge

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Controlled engineering of Bi4O5Br2 and BiOBr via interactions imidazolium ionic liquids and medium during synthesis as a simple method for enhancement of photocatalytic activity

Abstract

Ionic liquid-mediated synthesis of Bi4O5Br2 and BiOBr was carried out in non-polar solvents (glycerol, ethylene glycol) and a polar solvent (0.1 M mannitol). The effect of elongation of alkyl side chains (C4mim+, C8mim+, and C16mim+) of imidazolium ionic liquids, which act as a source of bromide and template, on the morphological, optical, and photocatalytic properties of materials was investigated. The crystallite size, morphology, particle size, energy bandgap, and exposure of (110), (001), and (102) facets were effectively tuned by selecting the proper ionic liquid–solvent system. The self-assembly of ILs and their role in forming Bi-based crystallites in non-polar and polar solvents differed. The most effective 5-fluorouracil was photooxidized over the samples prepared in C4mim+ – 0.1 M mannitol solution, while the best Cr(VI) photoreduction occurred with the sample formed in C4mim+ – glycerol. Molecular dynamics simulation correlated the length of alkyl side chains of imidazolium ILs with an increase in the number of “free” –OH groups of the solvent, which interacted with BiOBr nuclei during synthesis, fine-tuning its photocatalytic activity.

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Category:
Articles
Type:
artykuły w czasopismach
Published in:
Catalysis Science & Technology no. 14, pages 4968 - 4985,
ISSN: 2044-4753
Language:
English
Publication year:
2024
Bibliographic description:
Bielicka-giełdoń A., Wilczewska P., Ślusarz R., Terzyk A. P., Parnicka P., Szczodrowski K., Ryl J., Qi F., Siedlecka E.: Controlled engineering of Bi4O5Br2 and BiOBr via interactions imidazolium ionic liquids and medium during synthesis as a simple method for enhancement of photocatalytic activity// Catalysis Science & Technology -, (2025), s.4968-4985
DOI:
Digital Object Identifier (open in new tab) 10.1039/d4cy00500g
Sources of funding:
  • Free publication
Verified by:
Gdańsk University of Technology

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