In situ synchrotron powder X-ray diffraction study of formation and growth of yttrium and ytterbium aluminum garnet nanoparticles in sub- and supercritical water

被引:15
|
作者
Norby, Peter [1 ,2 ]
Jensen, Kirsten M. O. [1 ,2 ]
Lock, Nina [1 ,2 ]
Christensen, Mogens [1 ,2 ]
Iversen, Bo B. [1 ,2 ]
机构
[1] Aarhus Univ, Ctr Mat Crystallog, Dept Chem, Langelandsgade 140, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, INANO, DK-8000 Aarhus C, Denmark
基金
新加坡国家研究基金会;
关键词
LOW-TEMPERATURE SYNTHESIS; HYDROTHERMAL SYNTHESIS; BATIO3; NANOPARTICLES; RAPID SYNTHESIS; PHOSPHOR; NANOCRYSTALS; PARTICLES; RADIATION; SIZE; ZIRCONIA;
D O I
10.1039/c3ra41854e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The formation and growth of yttrium and ytterbium aluminium garnet (Y3-xYbxAl5O12, x = 0.0-3.0) nanoparticles in sub- and supercritical water have been followed by in situ synchrotron powder X-ray diffraction. At a pressure of 256 bar the formation of crystalline garnet nanoparticles occurs within seconds when the temperature is above 300 degrees C, and it takes place through an intermediate phase of (Y/Yb)(4)O(NO3)(OH)(9). Below the critical point of water (T-c = 374 degrees C, P-c = 221 bar), AlOOH crystallizes simultaneously with the garnet phase, and it is observed that both very rapid heating of the reactants and supercritical conditions are necessary to achieve phase pure YAG. Thus, under supercritical conditions YAG forms directly within the time resolution of the experiments (5 s). The particle growth is dependent on the Yb content, the Yb source and the synthesis temperature, and the crystallite size decreases from 35 nm for pure Y3Al5O12 to 20 nm for Y2.4Yb0.6Al5O12. After initial particle formation, growth is much slower in sub-critical water than in supercritical water.
引用
收藏
页码:15368 / 15374
页数:7
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