A novel compound [(CH 3CH 2) 4N] 4[(La 12 (OH) 12 MoO 29 )] was synthesized by hydrothermal reaction. The single crystal X ray diffraction shows that the compound crystallized in the monoclinic space group C2/c ; a =2...A novel compound [(CH 3CH 2) 4N] 4[(La 12 (OH) 12 MoO 29 )] was synthesized by hydrothermal reaction. The single crystal X ray diffraction shows that the compound crystallized in the monoclinic space group C2/c ; a =2 5729(4) nm, b =1 4318(1) nm, c =2 1217(4) nm, β =111 56(1)°, V =6 8235(7) nm 3, Z =4, R =0 0751. The basic building blocks of the crystal structure included one MoO 5 hexahedron and twelve LaO 6 octahedra which shared a common edge to form a [(La 12 (OH) 12 MoO 29 )] 4- unit. These units were held together by the [(CH 3CH 2) 4N] + ions.展开更多
In this research, cerium （III） nitrate hexahydrate （Ce（NO3）3·6H2O） and ammonium molybdate tetrahydrate （（NH4）6Mo7O24·4H2O） with Ce3＋-to-Mo6＋ molar ratio of 2：3 were dissolved in 40 ml different ...In this research, cerium （III） nitrate hexahydrate （Ce（NO3）3·6H2O） and ammonium molybdate tetrahydrate （（NH4）6Mo7O24·4H2O） with Ce3＋-to-Mo6＋ molar ratio of 2：3 were dissolved in 40 ml different solvents of deionized （DI） water, polyethylene glycol （PEG） and ethylene glycol （EG） to form different solutions which were followed by adjusting pH from the traditional values to 7.0 and 10.0 with 1 mol.L-1 sodium hydroxide （NaOH）. Subsequently, the solutions were processed by 270-W microwave-hydrother- mal/solvothermal method. Phase, morphology, vibrational modes and photonic properties were fully characterized by X-ray powder diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, Fourier transform infrared spectroscopy （FTIR）, Raman spectrophotometry, ultraviolet-visible （UV-Vis） absorption and photoluminescence （PL） spectroscopy. The as-synthe-sized products were pure cerium molybdenum oxide （Ce2（MoO4）3） of nanoparticles clustered together as nano- plates in DI water and PEG solvents, and of spindle-like nanoparticles in EG solvent, including the presence of Ce-O-H mode and MoO4 units. The results show that direct energy gaps of the first two have the same value of 2.30 eV, and that of the last is 2.80 eV, including their blue emission at the same wavelength of 488 nm.展开更多
基金Supported by the National Natural Science Foundation of China(No.2 0 1710 10 )
文摘A novel compound [(CH 3CH 2) 4N] 4[(La 12 (OH) 12 MoO 29 )] was synthesized by hydrothermal reaction. The single crystal X ray diffraction shows that the compound crystallized in the monoclinic space group C2/c ; a =2 5729(4) nm, b =1 4318(1) nm, c =2 1217(4) nm, β =111 56(1)°, V =6 8235(7) nm 3, Z =4, R =0 0751. The basic building blocks of the crystal structure included one MoO 5 hexahedron and twelve LaO 6 octahedra which shared a common edge to form a [(La 12 (OH) 12 MoO 29 )] 4- unit. These units were held together by the [(CH 3CH 2) 4N] + ions.
基金financially supported by Thailand's Office of the Higher Education Commission through the National Research University Project for Chiang Mai University
文摘In this research, cerium （III） nitrate hexahydrate （Ce（NO3）3·6H2O） and ammonium molybdate tetrahydrate （（NH4）6Mo7O24·4H2O） with Ce3＋-to-Mo6＋ molar ratio of 2：3 were dissolved in 40 ml different solvents of deionized （DI） water, polyethylene glycol （PEG） and ethylene glycol （EG） to form different solutions which were followed by adjusting pH from the traditional values to 7.0 and 10.0 with 1 mol.L-1 sodium hydroxide （NaOH）. Subsequently, the solutions were processed by 270-W microwave-hydrother- mal/solvothermal method. Phase, morphology, vibrational modes and photonic properties were fully characterized by X-ray powder diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, Fourier transform infrared spectroscopy （FTIR）, Raman spectrophotometry, ultraviolet-visible （UV-Vis） absorption and photoluminescence （PL） spectroscopy. The as-synthe-sized products were pure cerium molybdenum oxide （Ce2（MoO4）3） of nanoparticles clustered together as nano- plates in DI water and PEG solvents, and of spindle-like nanoparticles in EG solvent, including the presence of Ce-O-H mode and MoO4 units. The results show that direct energy gaps of the first two have the same value of 2.30 eV, and that of the last is 2.80 eV, including their blue emission at the same wavelength of 488 nm.
