Structural investigation of SnO2 catalytic nanoparticles doped with F and Sb

被引:4
|
作者
Parlinska-Wojtan, Magdalena [1 ]
Sowa, Roman [1 ]
Pokora, Monika [2 ]
Martyla, Agnieszka [2 ]
Lee, Kug-Seung [3 ]
Kowal, Andrzej [2 ,4 ,5 ,6 ]
机构
[1] Univ Rzeszow, Ctr Innovat & Technol Transfer, Rzeszow, Poland
[2] Gen Res Inst Nonferrous Met, Cent Lab Batteries & Cells, Poznan, Poland
[3] Pohang Inst Sci & Technol, Pohang Accelerator Lab, Pohang 790600, South Korea
[4] Univ East Sarajevo, Ctr Synth & Characterizat Nanomat, Sarajevo, Bosnia & Herceg
[5] Ceram Branch, Inst Power Engn, Res Inst, Boguchwala, Poland
[6] Univ Rzeszow, Ctr Microelect & Nanotechnol, Rzeszow, Poland
关键词
SnO2; nanoparticles; electron microscopy; Sb doping of SnO2; mesoporous structure; GAS-SENSING PROPERTIES; TIN OXIDE; ELECTROCATALYSTS; NANOCRYSTALS; ALCOHOL;
D O I
10.1002/sia.5384
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
Structural and morphological properties of pure and F-doped or Sb-doped particles of tin oxide were studied by X-ray diffraction and transmission electron microscopy (TEM). A typical polycrystalline diffraction pattern corresponding to the tetrahedral phase was obtained for all the particles independently of the doping. No peaks matching any antimony oxide phase were observed; thus, it is probable that Sb replaces Sn in the tin oxide lattice. Doping with antimony results in a lattice parameter increase of the SnO2/Sb phase, which might be related to the geometrical distortion of the lattice due to the replacement of Sn by Sb. Moreover, the SnO2/Sb sample exhibited a preferential orientation in the (110) and (101) planes. The TEM analysis showed that all the tin oxide particles are agglomerated and form aggregates and networks leading to a mesoporous structure with different pore sizes. The particles have a spherical shape and sizes between 5 and 20 nm in average. All particles were well crystallized with nicely visible lattice fringes in the high-resolution HRTEM images. Copyright (C) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:1090 / 1093
页数:4
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