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Physical property changes associated with glass transition in chalcogenide glasses.

机译:与硫属化物玻璃中的玻璃化转变有关的物理性质变化。

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High purity chalcogenide glasses were prepared in the binary Ge-Se and ternary Ge-Sb-Se systems by vacuum melting of pre-distilled samples. To understand the effects of average coordination number, {dollar}langle {lcub}rm r{rcub}rangle{dollar}, on glass-forming capability, connectivity and rigidity percolation properties such as thermal expansion coefficient, molar volume, heat capacity, viscosity, hardness, elastic modulus, acoustic attenuation and isothermal compressibility were studied as a function of {dollar}langle {lcub}rm r{rcub}rangle{dollar} in chalcogenide glasses. In the early eighties, Phillips proposed the constraint theory for covalent glasses, suggesting that ideal glass-forming condition should occur when the number of constraints match the degrees of freedom. This condition is satisfied at {dollar}langle {lcub}rm r{rcub}rangle{dollar} = 2.4 for covalent glasses. Most of the earlier experiments, in this field, to support Phillips' constraint theory of an existing percolation threshold at {dollar}langle {lcub}rm r{rcub}rangle{dollar} = 2.4 concentrated on locating extremum behavior either in glassy state properties or in liquid state properties of chalcogenide glasses and, hence, were inconclusive. The present work shows that the configurational contributions to the thermal expansion, heat capacity and isothermal compressibility, in addition to the molar volume, show distinct minima at {dollar}langle {lcub}rm r{rcub}rangle{dollar} = 2.4, suggesting a minimization in structural rearrangements during liquid to glass transition. We believe that if such a liquid possesses minimized accessible configurations in the supercooled liquid region it ought to display a poor crystallization tendency. Thus the key to the problem of percolation threshold is embodied in configurational changes associated with glass transition. A thermodynamic argument based on free energy is put forth to correlate constraint theory with ease of glass-forming ability. The study of thermodynamic order parameters indicates maximized connectivity for the glass at {dollar}langle {lcub}rm r{rcub}rangle{dollar} = 2.4. This renders additional support to the hypothesis that ease of glass-forming ability is associated with a balance between constraints and degrees of freedom in a glass-forming system.
机译:通过对预蒸馏样品进行真空熔融,在二元Ge-Se和三元Ge-Sb-Se系统中制备了高纯度硫属化物玻璃。要了解平均配位数{dollar} langle {lcub} rm r {rcub} rangle {dollar}对玻璃形成能力,连接性和刚度渗流特性(如热膨胀系数,摩尔体积,热容,粘度)的影响研究了硫族化物玻璃中硬度,弹性模量,声衰减和等温压缩率与{r}的关系。八十年代初,菲利普斯提出了共价玻璃的约束理论,认为当约束的数量与自由度匹配时,理想的玻璃形成条件应该出现。对于共价眼镜,满足以下条件:{rm} = 2.4。该领域中的大多数较早的实验都支持Phillips的约束理论,即在{dollar} langle {lcub} rm r {rcub} rangle {dollar} = 2.4时的现有渗透阈值集中在玻璃态属性中确定极值行为或硫属化物玻璃的液态特性,因此尚无定论。目前的工作表明,除了摩尔体积外,对热膨胀,热容和等温压缩性的构型贡献还显示出在{dollar} langle {lcub} rm r {rcub} rangle {dollar} = 2.4时的明显最小值。在液体过渡到玻璃的过程中结构重排最小化。我们相信,如果这种液体在过冷的液体区域中具有最小的可及构型,那么它应该显示出不良的结晶趋势。因此,渗滤阈值问题的关键体现在与玻璃化转变相关的构型变化中。提出了基于自由能的热力学论点,以将约束理论与易于形成玻璃的能力联系起来。对热力学有序参数的研究表明,玻璃在{美元}角度{rcub} rm r {rcub}角度{美元} = 2.4时具有最大的连通性。这为玻璃形成能力的简易性与玻璃形成系统中约束与自由度之间的平衡相关联的假设提供了额外的支持。

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