A simple preparation of carbon doped porous Bi2O3 with enhanced visible-light photocatalytic activity

Carbon doped bismuth oxide with a porous structure was prepared by calcination of bismuth nitrate in glycol solution. The as-prepared samples show enhanced visible-light photocatalytic activity. [Display omitted] •C-doped Bi2O3 with a porous structure is obtained by a simply calcination of Bi(NO3)3...

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Bibliographic Details
Published inJournal of alloys and compounds Vol. 608; pp. 44 - 48
Main Authors Dai, Gaopeng, Liu, Suqin, Liang, Ying
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 25.09.2014
Elsevier
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Summary:Carbon doped bismuth oxide with a porous structure was prepared by calcination of bismuth nitrate in glycol solution. The as-prepared samples show enhanced visible-light photocatalytic activity. [Display omitted] •C-doped Bi2O3 with a porous structure is obtained by a simply calcination of Bi(NO3)3 in glycol.•The C-doped Bi2O3 exhibited much higher photocatalytic activity than the pure Bi2O3.•Carbon was incorporated into the lattice of Bi2O3 lattice. Carbon doped bismuth oxide (Bi2O3) with a porous structure is obtained by a simply calcination of bismuth nitrate pentahydrate (Bi(NO3)3⋅5H2O) in glycol solution. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV–Vis absorption spectroscopy. The photocatalytic activity was evaluated by the photocatalytic degradation of methyl orange (MO) in an aqueous solution under visible-light radiation (λ>420nm). The results show that carbon was incorporated into the lattice of Bi2O3. The absorption intensity of C-doped Bi2O3 increases in the region of 450–530nm and the absorption edge has an obvious shift to long wavelength. The C-doped Bi2O3 exhibited much higher photocatalytic activity than the pure one due to the synergetic effects of the porous structure and the improved absorption in the visible-light region.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2014.04.097