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Magnetic and magneto-optical quenching in (Mn2+, Sr2+) metaphosphate glasses

机译:(Mn 2 + ,Sr 2 + )偏磷酸盐玻璃的磁淬和磁光淬火

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Transition metal ions such as Mn2+, Fe2+, or Co2+ provide an interesting alternative to rare earth dopants in optically active glasses. In terms of their magneto-optical properties, they are not yet very well exploited. Here, we report on the effect of Mn2+ on Faraday rotation in a metaphosphate glass matrix along the join MnxSr1-x(PO3)2 with x = 0...1. Mn2+ shows small optical extinction in the visible spectral range and, compared to other transition metal ions, a high effective magnetic moment. At high Mn- levels, however, the magneto-optical activity of Mn2+ is strongly quenched due to ionic clustering. The magnetic properties of the heavily Mn2+-loaded phosphate matrix are dominated by a superexchange interaction in the Mn2+-O-Mn2+ bridge with antiparallel spin alignment between Mn2+ and O2- species. The apparent paramagnetic potential of Mn2+ species can therefore not be exploited at room temperature.
机译:诸如Mn2 +,Fe2 +或Co2 +的过渡金属离子为光学活性玻璃中的稀土掺杂剂提供了有趣的替代方法。就其磁光特性而言,它们尚未得到很好的利用。在这里,我们报道了Mn2 +对偏磷酸盐玻璃基体中沿着MnxSr1-x(PO3)2的x = 0 ... 1的法拉第旋转的影响。 Mn2 +在可见光谱范围内显示出小的消光性,并且与其他过渡金属离子相比,具有很高的有效磁矩。但是,在高Mn-含量下,由于离子簇聚,Mn2 +的磁光活性被强烈淬灭。 Mn2 +重载磷酸盐基体的磁性由Mn2 + -O-Mn2 +桥中的超交换相互作用以及Mn2 +和O2-物种之间的反平行自旋排列决定。因此,在室温下无法利用Mn2 +物质的表观顺磁势。

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