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Fe3O4/Co3O4 core-shell nanocomposites modified structure and properties of heavy metal oxide diamagnetic glasses

机译:Fe3O4 / Co3O4核 - 壳纳米复合材料改性结构和重金属氧化物抗磁玻璃的性能

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摘要

Transition metal oxides nanomaterials are attractive for electrical, optical and magnetic applications due to their small polaron hopping, narrow band gap and strong spin-orbit interaction. Herein, 80 nm Fe3O4/Co3O4 core shell nanocomposites were synthesized and doped to heavy metal oxides glasses to evaluate the influence to glass structure, spectra and properties using varies characterization techniques. SEM, BET and XRD analysis confirm the successful synthesis of core-shell nanocomposites, and XPS, FT-IR and Raman spectra reveal the modification of CoO6 and CoO4 groups on glass frame BiO3, BiO6, PbO4 and BO3 units. UV-VIS spectra show a red-shift on cutoff wavelength with two absorption bands at 550 nm and 750 nm due to T-4(1g)(F) -> T-2(1g) (H) octahedral transition of Co2+ and T-5(2g) -> E-5(g) octahedral transition of Co3+ ions, respecitvely, which in turn contributed to electric conductivity. The evolution of Co2+ and Co3+ and their modification on glass induced changes on thermal, mechanical, magnetic and magneto optical properties.
机译:过渡金属氧化物纳米材料对于电气,光学和磁性应用具有吸引力,由于它们的小极化跳跃,窄带隙和强大的旋转轨道相互作用。这里,合成80nM Fe 3 O 4 / CO3O4核壳纳米复合材料并掺杂至重金属氧化物玻璃中,以评估对玻璃结构,光谱和性能的影响,使用各种表征技术。 SEM,BET和XRD分析证实了成功合成核 - 壳纳米复合材料,XPS,FT-IR和拉曼光谱显示COO6和COO4组在玻璃框架Bio3,Bio6,PbO4和Bo3单元上的改性。 UV-VIS光谱显示由于T-4(1g)(f)(f)(f)(f)(f) - > t-2(h)的CO2 +和t的八面体转变,在550nm和750nm处具有两个吸收带的截止波长。 -5(2g) - > E-5(g)CO 3 +离子的八面体转变,重新分配,这反过来导致电导率。 CO2 +和CO3 +的演变及其对热,机械,磁性和磁光性能的玻璃诱导变化的改性。

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