Nat. Inst. For R&D of Isotopic and Molec. Technologies, 400293 Cluj-Napoca, Romania.
Spectrochim Acta A Mol Biomol Spectrosc. 2013 Feb;102:414-8. doi: 10.1016/j.saa.2012.09.051. Epub 2012 Oct 13.
Glasses from xCuO⋅(100-x)[7GeO(2)⋅3PbO(2)⋅0.05Al(2)O(3)] system where x=0, 1, 5, 10, 20 and 30 mol% CuO were studied by FT-IR, UV-VIS and ESR spectroscopy in order to obtain information about the structural correlations and the relationship between structure and optical properties in these materials. The analyses of these IR spectra reveal that the accommodation of the network with the excess of oxygen ions is possible by the depolymerization of the germanate network in shorter chains, especially ortho- and/or pyrogermanate structural units. UV-VIS absorption spectrum of the sample with x=1% CuO begins with a rising absorption band situated at about 250 nm. This band can be assigned to the GeOGe wrong bonds such as the Ge(+2) centers. Optical study is performed to calculate the refractive index and optical band gap using UV-VIS spectra in the wavelength range 250-1,000 nm. The increase in optical band is explained on the basis of the average bond energy of the system and the number of non-bridging oxygen ions. ESR spectra of CuO substituted samples are characterized by broad peaks probably because of the formation of Cu(+2)-Ge(+2) exchange pairs which are weakly coupled though the oxygen atom.
研究了 xCuO⋅(100-x)[7GeO(2)⋅3PbO(2)⋅0.05Al(2)O(3)] 系统(其中 x=0、1、5、10、20 和 30mol%CuO)的玻璃,通过傅里叶变换红外光谱、紫外可见光谱和电子顺磁共振光谱,以获取关于结构相关性以及这些材料中结构与光学性质之间关系的信息。这些红外光谱的分析表明,通过较短链中锗酸盐网络的解聚,可以实现网络与过量氧离子的适应,特别是邻位和/或焦锗酸盐结构单元。x=1%CuO 的样品的紫外可见吸收光谱从位于约 250nm 的上升吸收带开始。该带可以归因于 GeOGe 错误键,例如 Ge(+2)中心。进行光学研究以使用 250-1000nm 波长范围内的紫外可见光谱计算折射率和光学带隙。光学带隙的增加是基于系统的平均键能和非桥氧离子的数量来解释的。CuO 取代样品的 ESR 谱特征是宽峰,可能是由于 Cu(+2)-Ge(+2)交换对的形成,尽管通过氧原子弱耦合,但这些交换对是弱耦合的。