Thermodynamic behavior and related phase transitions in SeTeSn and SeTeSnM (M = Ge, In, Pb, and Sb) chalcogenide glass ceramics

IF 1.9
Kaushal Kumar Sarswat , Ishu Sharma , Neeraj Mehta
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Abstract

This study addresses the critical need for a deeper thermodynamic understanding of chalcogenide glass–ceramic systems by investigating Se76Te20Sn2 and Se78Te20Sn2M2 (M = Ge, In, Pb, Sb) alloys. Although previous research has focused on thermal stability and crystallization behavior, limited attention has been given to the systematic analysis of specific heat behavior and its kinetic correlations near the glass transition temperature (Tg). While prior studies have emphasized thermal stability and crystallization, this work focuses on the composition-dependent evolution of specific heat (Cp) across the glass transition temperature (Tg). Differential scanning calorimetry (DSC) was employed under non-isothermal conditions to evaluate the specific heat (Cp) and derive associated thermodynamic parameters: enthalpy (H), entropy (S), and Gibbs free energy (G).
Two novel kinetic–thermodynamic correlations were identified: (i) a linear relationship between the rate of conversion change Δ(dα/dT) and logβ, and (ii) a direct correlation between the specific heat jump (ΔCp) and logβ. These results offer new insights into how heating rate influences thermal transitions. The thermodynamic profiles of Cp, H, S, and G exhibit continuous transition characteristics, indicating that Tg functions as a dynamic threshold rather than a sharp boundary. This work contributes to a deeper understanding of glass transition phenomena and provides a framework for tailoring phase-change behavior in functional chalcogenide materials.

Abstract Image

SeTeSn和SeTeSnM (M = Ge, in, Pb, Sb)硫系玻璃陶瓷的热力学行为及相关相变
本研究通过研究Se76Te20Sn2和Se78Te20Sn2M2 (M = Ge, In, Pb, Sb)合金,解决了对硫系玻璃陶瓷体系更深入的热力学理解的关键需求。虽然以往的研究主要集中在热稳定性和结晶行为上,但对玻璃化转变温度(Tg)附近比热行为及其动力学相关性的系统分析关注有限。虽然先前的研究强调热稳定性和结晶性,但本研究的重点是在玻璃化转变温度(Tg)上比热(Cp)的成分依赖演化。采用差示扫描量热法(DSC)在非等温条件下计算比热(Cp),并得出相关的热力学参数:焓(H)、熵(S)和吉布斯自由能(G)。发现了两个新的动力学-热力学相关性:(i)转换变化率Δ(dα/dT)与logβ之间的线性关系,以及(ii)比热跳(ΔCp)与logβ之间的直接关系。这些结果为加热速率如何影响热转变提供了新的见解。Cp、H、S和G的热力学分布呈现连续转变特征,表明Tg是一个动态阈值,而不是一个尖锐的边界。这项工作有助于更深入地了解玻璃化转变现象,并为定制功能硫系材料的相变行为提供了一个框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
3.10
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