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Optical and structural characterization of quadruplet and quintuplet molybdenum-containing phosphate glasses

机译:四联体和五联体含钼磷酸盐玻璃的光学和结构表征

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In this work, vitreous samples were prepared in two series by normal melt-quenching technique and under controlled conditions. The amorphous nature of specimens was confirmed using XRD spectra. To perform FT-IR and UV-vis studies, the thin blown films were also prepared. Different ratios of transition metals are assumed to cause depolymerization of the phosphate glass network. Infrared spectra showed absorption bands related to characteristic bonds of phosphate. The P=O bond at about 1200 cm(-1) was observed, as a direct consequence of meta-phosphate bond group. The almost unchanged peak position and intensity of P=O bond (in the presence of two transition metal ions) indicated the glass modifying nature of transition metal oxides (TMOs). The spectra of two series are almost identical, except for 890-1100 cm(-1) range, which can be attributed to presence of second TMO in the first glass series. UV-vis spectra also showed that the absorption edge, optical band gap and Urbach energy of the prepared samples are highly dependent on the kind and percentage of their reagents. The most striking result of UV-vis measurements was increasing and decreasing of optical band gap in the first and the second series with MoO3 content, respectively. The shape of the absorption edge (a plot of (ahv)(1/2) versus hv) demonstrated the indirect nature of the band gap in the prepared specimens.
机译:在这项工作中,通过常规的熔融淬火技术并在受控条件下,将玻璃样品分为两个系列。使用XRD光谱确认了样品的非晶态性质。为了进行FT-IR和UV-vis研究,还制备了薄吹膜。假定不同比例的过渡金属引起磷酸盐玻璃网络的解聚。红外光谱表明吸收带与磷酸盐的特征键有关。观察到P = O键在大约1200 cm(-1),是偏磷酸键基团的直接结果。 P = O键的几乎不变的峰位置和强度(在两个过渡金属离子的存在下)表明过渡金属氧化物(TMO)的玻璃改性性质。除890-1100 cm(-1)范围外,两个系列的光谱几乎相同,这可以归因于第一个玻璃系列中第二个TMO的存在。紫外可见光谱还显示,所制备样品的吸收边,光学带隙和Urbach能量高度依赖于其试剂的种类和百分比。 UV-vis测量最显着的结果分别是在MoO3含量第一和第二系列中,光学带隙的增加和减小。吸收边缘的形状((ahv)(1/2)与hv的关系图)显示了所制备样品中带隙的间接性质。

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