A novel hydrolytic reaction to morphology-controlled TiO2 micro/nanostructures for enhanced photocatalytic performancesElectronic supplementary information (ESI) available. See DOI: 10.1039/c5ra04524j
Different TiO 2 micro/nanostructures have been hydrothermally prepared through controlling the hydrolysis and nucleation rate of Ti 4+ ions by urea and H 2 O 2 in a (NH 4 ) 2 TiF 6 aqueous solution. Anatase TiO 2 nanorods with diameters of 10-30 nm and lengths up to 300-500 nm were evolved from the...
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Zusammenfassung: | Different TiO
2
micro/nanostructures have been hydrothermally prepared through controlling the hydrolysis and nucleation rate of Ti
4+
ions by urea and H
2
O
2
in a (NH
4
)
2
TiF
6
aqueous solution. Anatase TiO
2
nanorods with diameters of 10-30 nm and lengths up to 300-500 nm were evolved from the intermediate monoclinic H
2
Ti
5
O
11
·3H
2
O in the presence of H
2
O
2
and urea, whereas TiO
2
core-shell nanospheres with diameters of 300-500 nm were obtained with the sole assistance of urea
via
the Ostwald ripening effect and TiO
2
microspheres with diameters of about 1-2 μm were formed in the presence of only H
2
O
2
. Photocatalytic degradation of Rhodamine B (RhB) has been used to evaluate their activities. The results indicate that the anatase TiO
2
nanorods have superior photocatalytic efficiency to the core-shell nanospheres and microspheres counterparts owing to their larger specific surface area and higher yield of &z.rad;OH radicals. This work not only offers a simple and promising route to the controllable synthesis of various TiO
2
architectures, but also provides new insight for improving the photocatalytic performance of TiO
2
through morphological engineering, which will have potential applications in environmental remediation.
TiO
2
nanorods, core-shell nanospheres, and microspheres were prepared
via
tuning the hydrolysis and nucleation rate of Ti
4+
ions. Superior photocatalytic efficiency of TiO
2
nanorods attributes to large surface area and high ⋅OH radical productivity. |
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ISSN: | 2046-2069 |
DOI: | 10.1039/c5ra04524j |