Formation of Mn3O4 nanobelts through the solvothermal process and their photocatalytic property

被引:51
作者
Ahmed, Khalid Abdelazez Mohamed [1 ,2 ]
Huang, Kaixun [3 ]
机构
[1] Al Neelain Univ, Fac Sci & Technol, Dept Chem, POB 12702, Khartoum, Sudan
[2] Taif Univ, Fac Sci & Educ, Dept Chem, POB 888, At Taif 5700, Saudi Arabia
[3] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Wuhan 430074, Hubei, Peoples R China
关键词
Manganese oxide; Solvothermal; Nanobelts; Diphenylthiocarbazone; MAGNETIC-PROPERTIES; OXIDE NANOBELTS; NANOWIRES; OXIDATION; NANOSTRUCTURES; PERFORMANCE; ELECTRODE; NANORODS; CATALYST; GROWTH;
D O I
10.1016/j.arabjc.2014.08.014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hausmannite Mn3O4 nanobelts were synthesized from manganese acetate and potassium hydroxide precursors in the presence of melamine-ethanol-distill water via the reflux and solvothermal methods. X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) spectroscopes confirm the composition of the as-prepared product. Field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), selected area electron diffraction (SA-ED), high resolution transmission electron microscopy (HR-TEM) and N-2 adsorption-desorption isotherm results showed that the as-fabricated sample exhibits a nanosized belt-like crystal, single crystalline, tetragonal phase structure and high BET surface area. The effects of the reaction conditions such as melamine amount, solvent ratios and reaction time on the morphology of the products were studied. The band gap of the as-synthesized products was calculated via diffuse reflectance spectral analysis and their activity of catalytic oxidation was evaluated by degradation of diphenylthiocarbazone under visible-light irradiation. GC-MS instrument was used to monitor the temporal course of the catalytic reaction. The results showed that the degradation efficiency of diphenylthiocarbazone catalyzed by Mn3O4 nanobelts was higher than that which had been prepared in particle and sheet-like nanocrystals. (C) 2014 King Saud University. Production and hosting by Elsevier B.V. All rights reserved.
引用
收藏
页码:429 / 439
页数:11
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