Synthesis of tailored WO3 and WOx (2.9 < x < 3) nanoparticles by adjusting the combustion conditions in a H2/O2/Ar premixed flame reactor

被引:19
作者
Gupta, Anoop [1 ]
Ifeacho, Pascal [1 ]
Schulz, Christof [1 ,2 ]
Wiggers, Hartmut [1 ,2 ]
机构
[1] Univ Duisburg Essen, Inst Combust & Gasdynam IVG, D-47057 Duisburg, Germany
[2] Univ Duisburg Essen, Ctr NanoIntegrat Duisburg Essen CeNIDE, D-47057 Duisburg, Germany
关键词
Premixed flame; Tungsten oxide; Nanoparticle synthesis; Particle size and morphology; Stoichiometry tuning; CHEMICAL-VAPOR-DEPOSITION; THERMAL EVAPORATION; THIN-FILMS; OXIDE; PARTICLES; BEHAVIOR;
D O I
10.1016/j.proci.2010.06.162
中图分类号
O414.1 [热力学];
学科分类号
070201 [理论物理];
摘要
Flame synthesis of WO3 and WOx (2.9 < x < 3) nanoparticles is carried out by adding a dilute concentration of WF6 as precursor in a low-pressure H-2/O-2/Ar premixed flame reactor. The reactor is equipped with molecular-beam sampling and particle mass spectroscopy (PMS) to determine particle composition and sizes as a function of height above burner. Varying the H-2/O-2 ratio allowed us to tune the stoichiometry of the product. With a H-2/O-2 ratio of 0.67 white colored stoichiometric WO3 is formed, whereas the H-2/O-2 ratio >0.8 yields blue colored non-stoichiometric WOx (2.9 < x < 3) nanoparticles. The size of nanoparticles can be controlled by varying the residence time in the high-temperature zone of the reactor as observed by molecular-beam sampling with subsequent analysis using PMS. Transmission electron microscopy (TEM) images of as-synthesized nanoparticles show that particles are non-agglomerated and have an almost spherical morphology. The X-ray diffraction (XRD) pattern of the as-synthesized material indicates that the powders exhibit poor crystallinity, however, subsequent thermal annealing of the sample in air changes its structure from amorphous to crystalline phase. It is observed that particles with sub-stoichiometric composition (WOx) show higher conductivity compared to the stoichiometric WO3 sample. (C) 2010 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1883 / 1890
页数:8
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