Preparation of F-doped titania nanoparticles with a highly thermally stable anatase phase by alcoholysis of TiCl4

被引:40
|
作者
Lv, Yingying [3 ,4 ]
Yu, Leshu [1 ,2 ,4 ]
Huang, Heyong [3 ]
Liu, Hailong [3 ]
Feng, Yuying [3 ]
机构
[1] Nanjing Univ, Key Lab Mesoscop Chem MOE, Nanjing 210093, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Nanjing 210093, Peoples R China
[3] Nanjing Normal Univ, Anal & Testing Ctr, Dept Chem & Environm Sci, Nanjing 210097, Peoples R China
[4] Shangrao Normal Univ, Dept Chem, Shangrao 334001, Peoples R China
基金
中国博士后科学基金;
关键词
Ceramics; High-temperature alloys; Oxide materials; Sintering; Phase transitions; X-ray diffraction; PHOTOCATALYTIC PROPERTIES; DIOXIDE NANOPARTICLES; 001; FACETS; TIO2; LIGHT; TRANSFORMATION; DEGRADATION; PERCENTAGE; NANOSHEETS; SURFACE;
D O I
10.1016/j.apsusc.2009.07.098
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pure anatase is a metastable phase and inclined to (transform) be transformed into rutile structure under heating over than 500 degrees C, which limits its suitability for high-temperature applications. Hitherto much research efforts have been made to increase the stability temperature of anatase structure. However, metallic doping usually introduced metallic oxides into titania at high temperature, and many nonmetallic doping are not competent for increasing the stability temperature of anatase structure up to 900 degrees C. In this study, F-doped anatase TiO2 nanoparticles were conveniently prepared via the alcoholysis of TiCl4 and the as-prepared product shows very high stability temperature up to 1000 degrees C before being transformed into rutile structure phase. On the basis of XPS results of F-doped titania annealed at different temperature, it is learned that the F atoms were anchored on the crystal planes of anatase in favor of decreasing the energy faces of anatase and stabilizing the anatase structure till annealed at 1300 degrees C all the anatase were transformed into rutile phase. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:9548 / 9552
页数:5
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