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Neodymium and erbium coordination environments in phosphate glasses - art. no. 104206

机译:磷酸盐玻璃中的钕和b配位环境-艺术没有。 104206

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The local structures of Nd3+ and Er3+ ions in two series of rare-earth (RE) phosphate glasses with nominal compositions xR(2)O(3)-(1-x) P2O5, where R=Nd and Er and 0.05less than or equal toxless than or equal to0.28, have been characterized by L-III-edge extended x-ray-absorption fine-structure spectroscopy (EXAFS). The RE coordination number depends on the R2O3 content, decreasing from 9.0 (10) oxygen nearest neighbors in ultraphosphate compositions (x<0.15) to 6.4 (9) oxygen nearest neighbors for the metaphosphate (x&SIM;0.25) compositions. The average Er-O bond distance decreases from 2.29 (1) to 2.23 (1) &ANGS;, and the average Nd-O bond distance decreases from 2.40 (1) to 2.37 (1) &ANGS; over the same compositional range. The changes in coordination environments are consistent with the conversion of isolated RE polyhedra to clustered RE polyhedra sharing common oxygens as the number of available terminal oxygens per RE ion decreases with increasing x. [References: 37]
机译:Nd3 +和Er3 +离子在两个标称成分为xR(2)O(3)-(1-x)P2O5的稀土(RE)磷酸盐玻璃系列中的局部结构,其中R = Nd和Er和0.05小于或等于或小于等于0.28的无毒气体已通过L-III边缘扩展X射线吸收精细结构光谱(EXAFS)进行了表征。 RE配位数取决于R 2 O 3含量,从超磷酸盐组合物中的氧最邻近(9.0(10))(x <0.15)降低为偏磷酸盐(x&SIM; 0.25)的6.4(9)最邻近的氧。平均Er-O键距从2.29(1)降低至2.23(1)&ANGS ;,平均Nd-O键距从2.40(1)降低至2.37(1)&ANGS;。在相同的成分范围内。配位环境的变化与分离的RE多面体向共享共有氧的聚簇RE多面体的转化一致,因为每个RE离子可用的末端氧的数量随x的增加而降低。 [参考:37]

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