The Synthesis of α-MoO3 by Ethylene Glycol

被引:80
作者
Chiang, Tzu Hsuan [1 ]
Yeh, Hung Che [1 ]
机构
[1] Natl United Univ, Dept Energy Engn, Miaoli 36003, Taiwan
来源
MATERIALS | 2013年 / 6卷 / 10期
关键词
ethylene glycol; molybdenum trioxide; crystallization; sintering; X-RAY PHOTOELECTRON; MOLYBDENUM TRIOXIDE; MOO3; NANOSTRUCTURES; ELECTROCHROMIC PROPERTIES; FIELD-EMISSION; OXIDE; OXIDATION; ACID; TEMPERATURE; PERFORMANCE;
D O I
10.3390/ma6104609
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
This study investigated the use of ethylene glycol to form alpha-MoO3 (molybdenum trioxide) from ammonium molybdate tetrahydrate at various sintering temperatures for 1 h. During the sintering process, the morphologies of the constituents were observed using scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy was used to explain the reaction process. In this work, the results obtained using X-ray photoelectron spectroscopy (XRD) demonstrated that, when the molybdenum trioxide powder was treated thermally at 300 degrees C, the material exhibited crystallinity. The peaks were indexed to correspond with the (110), (040), (021), (111), and (060) crystallographic planes, and the lattice parameters of a, b, and c were about 3.961, 13.876, and 3.969 angstrom. Using these observations, we confirmed that orthorhombic alpha-MoO3 was formed for sintering temperatures from 300 to 700 degrees C. Pattern images were obtained by the selected area electron diffraction pattern (SAED) technique, and the d distance of the high resolution transmission electron microscopy (HRTEM) images were almost 0.39 and 0.36 nm, and the Mo 3d(5/2), Mo 3d(3/2), and O 1s of X-ray photoelectron spectroscopy (XPS) were located at 233.76, 237.03, and 532.19 eV, which also demonstrated that alpha-MoO3 powder had been synthesized.
引用
收藏
页码:4609 / 4625
页数:17
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