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Synergistic effect of Fe2O3 and CeO2 co-modified titanate nanosheet heterojunction on enhanced photocatalytic degradation
CeO 2 and Fe 2 O 3 co-modified titanate nanosheet (Fe 2 O 3 /CeO 2 @TNS) was prepared by one-pot hydrothermal method; the photocatalyst exhibited large surface area with CeO 2 and Fe 2 O 3 particles well dispersed on the surface. The results of XRD, BET, and Raman proved that the CeO 2 and Fe 2 O 3...
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Published in: | Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2017-09, Vol.19 (9), p.1, Article 325 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | CeO
2
and Fe
2
O
3
co-modified titanate nanosheet (Fe
2
O
3
/CeO
2
@TNS) was prepared by one-pot hydrothermal method; the photocatalyst exhibited large surface area with CeO
2
and Fe
2
O
3
particles well dispersed on the surface. The results of XRD, BET, and Raman proved that the CeO
2
and Fe
2
O
3
introduced in the TNS influenced its structure evolution from 3D to 2D. The modification resulted in a shift of the absorption edge toward a longer wavelength and the band gap reduced to 2.87 eV. The three-component systems performed excellent photocatalytic activity and cycle stability on phenol and methyl blue (MB) solution under sunlight; nearly total phenol and MB were degraded in dozens of minutes. And the reaction rate constant (
K
) of Fe
2
O
3
/CeO
2
@TNS on phenol degradation was 1.77, 3.25, 4.88, and 13-fold of Fe
2
O
3
@TNS, CeO
2
@TNS, bare TNS, and P25, respectively. The enhanced photocatalytic activity could be ascribed to the efficient separation of photogenerated pairs through the formation of tandem n-n-n heterojunction among the three-component systems. This work will be useful for the design of other tandem n-n-n heterojunction photocatalytic systems for application in energy conversion and environmental remediation.
Graphical abstract
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ISSN: | 1388-0764 1572-896X |
DOI: | 10.1007/s11051-017-4013-5 |