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Electrochemical and spectrophotometric study on trivalent neodymium ion in molten binary mixtures of LiCl and alkali earth chlorides

机译:氯化锂与碱土金属氯化物熔融二元混合物中三价钕离子的电化学和分光光度研究

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The thermodynamic stability of Nd(III) complexes was studied by electrochemical techniques for molten binary mixtures composed of LiCl and an alkali earth chloride, CaCl_2, SrCl_2, or BaCl_2 at 923 K. The Gibbs free energy change of formation of Nd(III) in the melts was determined. The obtained values showed a good correlation with the polarizing power of solvent cations. The Nd(III) complex was more stable in the melts with low polarizing power. The electronic absorption spectrum of the hypersensitive f-f transition of Nd~(3+) was investigated to obtain information about the structural change of the NdCl63- complex. The estimated oscillator strength of the ~4G_(5/2),~2G_(7/2) ← ~4I_(9/2) transition and the degree of the energy splitting in electronic energy levels showed different trends upon the polarizing power for each of added alkali earth chloride. This indicates that the coordination environments further from second neighbors could have significant impact on the electronic energy levels of Nd(III) in the mixtures including alkali earth cations.
机译:通过电化学技术研究了Lid和碱土金属氯化物,CaCl_2,SrCl_2或BaCl_2组成的熔融二元混合物在923 K时Nd(III)配合物的热力学稳定性。确定熔体。所获得的值与溶剂阳离子的极化能力显示出良好的相关性。 Nd(III)络合物在熔体中具有较低的极化能力,稳定性更高。研究了Nd〜(3+)的超敏f-f跃迁的电子吸收光谱,以获得有关NdCl63-配合物结构变化的信息。 〜4G_(5/2),〜2G_(7/2)←〜4I_(9/2)跃迁的估计振荡器强度以及电子能级的能量分裂程度在每种情况下的极化功率上显示出不同的趋势加入碱土金属氯化物。这表明远离第二邻居的配位环境可能会对包括碱土金属阳离子的混合物中Nd(III)的电子能级产生重大影响。

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