Journal
MATERIALS CHEMISTRY AND PHYSICS
Volume 143, Issue 3, Pages 952-962Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.matchemphys.2013.10.026
Keywords
Composite materials; Heat treatment; Electron microscopy; Powder diffraction
Categories
Funding
- Natural Science Foundation of China [61036009, 61177016, 21161160446]
- National High-Tech Research Development Program [2011AA03A110]
- Natural Science Foundation of Jiangsu Province [BK2010003]
- Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
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The synthesis of Bi4Ti3O12 and CuFe2O4 powders was achieved using a conventional solid-state reaction and the Sol-Gel method, respectively. A novel p-n heterojunction photocatalyst CuFe2O4/Bi4Ti3O12 was subsequently prepared through ball milling. The structures, morphologies, and optical properties of the photocatalysts were comprehensively characterized. The transmission electron microscopy (TEM) images showed a clear interface between CuFe2O4 and Bi4Ti3O12, indicating that a heterojunction between CuFe2O4 and Bi4Ti3O12 was formed during ball milling. In addition, the photocatalytic activity was evaluated based on the photocatalytic degradation of methyl orange (MO). The results indicated that the photocatalytic activity of the p-n heterojunction photocatalyst CuFe2O4/Bi4Ti3O12 was higher than that of Bi4Ti3O12 alone. The enhanced photocatalytic activity could be attributed to the formation of a heterojunction between CuFe2O4 and Bi4Ti3O12, which suppressed the recombination of photogenerated electron-hole pairs. We also investigated the effects of procedure time and dispersant (H2O) during ball milling on the photocatalytic activity. The mechanisms underlying the observed photocatalytic activity were also described based on the semiconductor energy band theory and p-n junction principle. Moreover, the analysis of the radical scavengers confirmed that center dot O-2(-) and h(+) were the primary reactive species to cause the degradation of the MO. (C) 2013 Elsevier B.V. All rights reserved.
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