Loading…
Phase transformation and precipitation behavior of niobium component out of niobium-doped anatase-type TiO2 nanoparticles synthesized via hydrothermal crystallization
The precipitation behavior of niobium component out of niobium-doped anatase-type TiO 2 and structural change in the course of heating were investigated. The samples were directly formed under hydrothermal conditions at 240 °C for 5 h in the presence of aqueous ammonia via crystallization from co-pr...
Saved in:
Published in: | Journal of materials science 2009-11, Vol.44 (22), p.6135-6143 |
---|---|
Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The precipitation behavior of niobium component out of niobium-doped anatase-type TiO
2
and structural change in the course of heating were investigated. The samples were directly formed under hydrothermal conditions at 240 °C for 5 h in the presence of aqueous ammonia via crystallization from co-precipitates that were obtained from precursor solutions of TiOSO
4
and NbCl
5
. The as-prepared niobium-doped anatase-type titania nanoparticles showed bluish color and absorption in the visible region, which was confirmed to be due to the presence of Ti(III) in the solid solutions using electron paramagnetic resonance measurement. The niobium-doped anatase-type titania existed stably without an appearance of any other phases after heating up to 500 °C for 1 h. In the course of heating at 500–800 °C, continual and clear decrease in the lattice parameters
a
0
and
c
0
of the anatase was observed, which was followed by the precipitation of Nb
2
O
5
and TiNb
2
O
7
out of the niobium-doped anatase, but the anatase phase was maintained without anatase-to-rutile phase transformation up to 850–1,000 °C. The anatase-to-rutile phase transformation was gradually retarded when the niobium content increased. |
---|---|
ISSN: | 0022-2461 1573-4803 |
DOI: | 10.1007/s10853-009-3848-2 |