稀土硼酸盐的红外吸收光谱

J.P. Laperches , P. Tarte
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引用次数: 138

摘要

研究了方解石、文石和水晶石结构的三价阳离子或稀土硼酸盐在1500 ~ 250 cm−1范围内的红外光谱。YBO3型稀土硼酸盐给出的红外模式不能与三重配相协调,而是指向硼的四重配,这一事实与这些硼酸盐所谓的钒矾体结构相矛盾。低频谱具有强烈的结构依赖性,并明显受三价阳离子配位数的影响。在这个区域观察到的强波段可能被分配到一个阳离子-氧振动,或者可能(对于方解石或文石型硼酸盐)一个硼酸阴离子的振动。我们的结果与最近在文献中发表的一些数据之间的一些显着差异被发现与虚假效应有关,例如样品的粒度测定和可能的取向效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectres d'absorption infrarouge de borates de terres rares

The infra-red spectra of either trivalent cations or rare-earth borates related to the calcite, the aragonite and the vaterite structures have been studied in the 1500-250 cm−1 region.

The infra-red pattern given by the rare-earth borates of the YBO3 type cannot be reconciled with a three-fold co-ordination, but instead points to a four-fold co-ordination of boron, a fact in contradiction with the alleged vaterite structure of these borates.

The low-frequency spectrum is strongly structure-dependent, and is clearly influenced by the co-ordination number of the trivalent cation. The strong band observed in this region may be assigned to a cation—oxygen vibration, or possibly (for the calcite or aragonite-type borates) to a libration of the borate anion. Some significant discrepancies between our results and some data recently published in the literature are found to be related to spurious effects, such as the granulometry of the sample and possibly orientation effects.

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