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Mixed samarium valences effect in Faraday rotation glasses: Structure, optical, magnetic and magneto-optical properties

机译:在法拉第旋转眼镜中混合钐价效应:结构,光学,磁性和磁光性能

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摘要

Sm2+ ions are attractive in high density memory applications due to its spectral hole burning property. In this study, for the first time, the influence of mixed valence states of Sm ions to magnetic and magneto optical property of diamagnetic glasses were studied. The chemical valence states of Sm and their modification on glass structure, optical absorption, luminescence, magnetic and Faraday rotation performances were characterized using X-ray Photoelectron Spectroscopy (XPS), X-Ray diffraction, Ultraviolet-visible (UV-Vis), Fourier Transform Infrared (FT-IR), Raman spectra and vibrating-sample magnetization (VSM) measurements, respectively. Characteristic emission peaks due to D-5(0)-> F-7(0) and D-5(0)-> F-7(1) transitions of Sm2+ and (5)G(5/2)-> H-6(7/2), (5)G(5/2)-> H-6(9/2) transitions of Sm3+ ions were detected in luminescence spectra, indicating the reduction of Sm3+ to Sm2+. XPS analysis on Sm3d core-level spectra demonstrated the co-existence of Sm2+ and Sm3+ and their evolution was Sm2O3 content-dependent. Optical absorption of H-6(5/2)->(4)G(5/2), F-6(11/2), F-6(9/2), F-6(7/2), F-6(5/2) transitions of Sm3+ ions were observed in UV-VIS spectra, however, the absorption peaks of Sm2+ were covered by the stronger absorption of Pb2+ and Bi3+ ions in the UV region. The refractive index, optical cutoff wavelength and band gap of glasses were changed by the incorporation of highly polarizable Sm ions. Due to the different magnetic ordering of Sm2+ and Sm3+ ions, glass doped with 1%Sm2O3 presented diamagnetic nature while glasses doped with higher Sm2O3 exhibited paramagnetic behavior, and the Faraday rotation property also was greatly influenced by magnetization susceptibility. 1%Sm2O3 doped glasses presented the strongest magnetization and biggest Verdet constant of 0.1886 min/G.cm at 633 nm. Several influence factors to Verdet constant such as non-bridging oxygen structure, wavelength, refractive index, magnetic susceptibility and temperature were discussed.
机译:由于其光谱孔燃烧性,SM2 +离子在高密度存储器应用中具有吸引力。在本研究中,研究了SM离子的混合价状态对磁性玻璃磁性和磁光性的影响。使用X射线光电子谱(XPS),X射线衍射,紫外线(UV-VI),傅立叶,SM的SM的化学价值,光学吸收,发光,磁性和法拉第旋转性能对玻璃结构,光学吸收,发光,磁性和法拉第旋转性能进行了特征。分别变换红外(FT-IR),拉曼光谱和振动样磁化(VSM)测量。由于D-5(0) - > F-7(0)和D-5(0) - > F-7(1)转变为SM2 +和(5/2) - > H引起的特征发射峰-6(7/2),(5)g(5/2) - > H-6(9/2)在发光光谱中检测SM3 +离子的转变,表明SM3 +降低SM2 +。 SM3D核心级光谱的XPS分析显示SM2 +和SM3 +的共存,它们的进化是SM2O3含量依赖性。 H-6(5/2) - >(4)G(5/2),F-6(11/2),F-6(9/2),F-6(7/2)的光学吸收,在UV-Vis光谱中观察到SM3 +离子的F-6(5/2)转变,然而,SM2 +的吸收峰被UV区域中的Pb2 +和Bi3 +离子的较强吸收覆盖。通过掺入高度极化的SM离子来改变眼镜的折射率,光学截止波长和带隙。由于SM2 +和SM3 +离子的不同磁排序,掺杂1%SM2O3的玻璃呈现了抗磁性性质,而掺杂更高的SM2O3的眼镜表现出顺磁性行为,并且法拉第旋转性能也受到磁化敏感性的大大影响。 1%SM2O3掺杂眼镜呈现最强的磁化,最大的磁化和最大的verdet常数为0.1886 min / g.cm,在633nm处。讨论了诸如非桥接氧结构,波长,折射率,磁敏感度和温度的诸如非桥接氧结构的若干影响因素。

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