...
【24h】

Glass formation in and structural investigation of Li2S+GeS2+GeO2 composition using Raman and IR spectroscopy

机译:用拉曼光谱和红外光谱研究Li2S + GeS2 + GeO2的玻璃形成及结构研究

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Li2S + GeS2 + GeO2 ternary glasses have been prepared and a wide glass-forming range was obtained. The glass transition temperatures increase with the GeO2 concentration in the glasses. The vibrational modes of both bridging (Ge-S-Ge) and non-bridging (Ge-S-) sulfurs are observed in Raman and IR spectra of binary Li2S + GeS2 glasses. Additions of GeO2 to this binary glass increase the bridging oxygen band (Ge-O-Ge) at the expense of decreasing the bridging sulfur band (Ge-S-Ge), whereas the bands associated with the non-bridging sulfurs, (Ge-S-) remain constant in intensity up to high GeO2 concentrations. At higher concentrations of GeO2 ( >= 60%), the non-bridging oxygen band, which is not observed at low and intermediate GeO2 concentrations, appears and grows stronger. From these observations, it is suggested that the added lithium ions favor the non-bridging sulfur sites over the oxygen sites to form non-bridging sulfurs, whereas the added oxygen prefers the higher field strength Ge4+ cation to form bridging Ge-O-Ge bonds. The structural groups in the Li2S + GeS2 + GeO2 glasses that are consistent with results of Raman and IR spectra are described and are used to develop a structural model of these glasses. (c) 2005 Elsevier B.V. All rights reserved.
机译:已经制备了Li 2 S + GeS 2 + GeO 2三元玻璃,并且获得了宽的玻璃形成范围。玻璃化转变温度随玻璃中GeO2浓度的增加而增加。在二元Li2S + GeS2玻璃的拉曼光谱和红外光谱中观察到桥联(Ge-S-Ge)和非桥联(Ge-S-)硫的振动模式。向该二元玻璃中添加GeO2会增加桥接氧带(Ge-O-Ge),但以降低桥接硫带(Ge-S-Ge)为代价,而与非桥接硫相关的能带(Ge-在高GeO2浓度下,S-)的强度保持恒定。在较高的GeO2浓度(> = 60%)时,出现非桥连的氧带,该带在低和中等的GeO2浓度下未观察到并变得更强。从这些观察结果可以看出,所添加的锂离子优先于非桥接硫位点而不是氧位点形成非桥接硫,而所添加的氧气则倾向于较高场强的Ge4 +阳离子形成桥接的Ge-O-Ge键。 。描述了与拉曼光谱和红外光谱结果一致的Li2S + GeS2 + GeO2玻璃中的结构基团,并用于建立这些玻璃的结构模型。 (c)2005 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号