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Magnetic composite BiOCl-SrFe12O19: a novel p-n type heterojunction with enhanced photocatalytic activity
The magnetic composite BiOCl-SrFe 12 O 19 , a novel p-n type heterojunction was synthesized by hydrolysis with a medium temperature sintering method. The microstructure and magnetic properties of the prepared material were characterized by FTIR, XRD, SEM, TEM, HRTEM, SAED, and VSM. The results showe...
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Published in: | Dalton transactions : an international journal of inorganic chemistry 2014-02, Vol.43 (5), p.2211-222 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | The magnetic composite BiOCl-SrFe
12
O
19
, a novel p-n type heterojunction was synthesized by hydrolysis with a medium temperature sintering method. The microstructure and magnetic properties of the prepared material were characterized by FTIR, XRD, SEM, TEM, HRTEM, SAED, and VSM. The results showed the [001] facet of BiOCl with high photocatalytic activity was exposed in the BiOCl-SrFe
12
O
19
. The heterostructured BiOCl-SrFe
12
O
19
had better magnetic properties, contributing to its reuse and improvement in photocatalysis. Moreover, the composite was blessed with excellent photocatalytic activity and stability. In the BiOCl-SrFe
12
O
19
system, SrFe
12
O
19
not only inhibited the growth of BiOCl along the [001] direction to enhance the exposure of the [001] wafer, but also acted as a sensitizer absorbing light irradiation. The magnetic field generated from SrFe
12
O
19
made BiOCl, under light irradiation, produce more photo-induced electrons and holes and simultaneously hampered their recombination. For the first time we propose the possible mechanism of how to enhance photocatalytic activity by a magnetic field effect originating from the magnetic photocatalyst itself.
The structure and photocatalytic activity of the magnetic photocatalyst BiOCl-SrFe
12
O
19
were characterized. The high photocatalytic activity was interpreted by introducing the magnetic field effect for the first time. |
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ISSN: | 1477-9226 1477-9234 |
DOI: | 10.1039/c3dt52219a |