Kaseman Derrick C, Hung Ivan, Lee Kathleen, Kovnir Kirill, Gan Zhehong, Aitken Bruce, Sen Sabyasachi
Division of Materials Science, University of California at Davis , Davis, California 95616, United States.
J Phys Chem B. 2015 Feb 5;119(5):2081-8. doi: 10.1021/jp5123618. Epub 2015 Jan 27.
The short-range structure, connectivity, and chemical order in As(x)Te(100-x) (25 ≤ x ≤ 65) glasses are studied using high-resolution two-dimensional projection magic-angle-turning (pjMAT) (125)Te nuclear magnetic resonance (NMR) spectroscopy. The (125)Te pjMAT NMR results indicate that the coordination of Te atoms obeys the 8-N coordination rule over the entire composition range. However, in strong contrast with the analogous glass-forming As-S and As-Se chalcogenides, significant violation of chemical order is observed in As-Te glasses over the entire composition range in the form of homopolar As-As (Te-Te) bonds, even in severely As (Te)-deficient glasses. The speciation of the Te coordination environments can be explained with the dissociation reaction model As2Te3 → 2As + 3Te(II), characterized by a dissociation constant that is independent of glass composition. These structural characteristics can be attributed to the high metallicity of Te and the strong energetic similarity between the Te-Te, Te-As, and As-As bonds, and they are consistent with the monotonic and often nearly linear variation of physical properties observed in telluride glasses as a function of the Te content.
利用高分辨率二维投影魔角旋转(pjMAT)(125)Te核磁共振(NMR)光谱研究了As(x)Te(100-x)(25≤x≤65)玻璃中的短程结构、连通性和化学有序性。(125)Te pjMAT NMR结果表明,在整个成分范围内,Te原子的配位遵循8-N配位规则。然而,与类似的玻璃形成硫属化物As-S和As-Se形成强烈对比的是,在整个成分范围内,即使在严重缺乏As(Te)的玻璃中,As-Te玻璃也以同极As-As(Te-Te)键的形式出现了明显的化学有序性违反。Te配位环境的物种形成可以用离解反应模型As2Te3→2As+3Te(II)来解释,其特征是离解常数与玻璃成分无关。这些结构特征可归因于Te的高金属性以及Te-Te、Te-As和As-As键之间强烈的能量相似性,并且它们与碲化物玻璃中观察到的物理性质随Te含量的单调且通常近乎线性的变化一致。