Yuan Bing, Aitken Bruce G, Sen Sabyasachi
Division of Materials Science and Engineering, University of California at Davis, Davis, California 95616, USA.
Science and Technology Division, Corning Inc., Corning, New York 14831, USA.
J Chem Phys. 2022 Sep 21;157(11):114503. doi: 10.1063/5.0107799.
A fundamental and much-debated issue in glass science is the existence and nature of liquid-liquid transitions in glass-forming liquids. Here, we report the existence of a novel reentrant structural transition in a S-rich arsenic sulfide liquid of composition AsS. The nature of this transition and its effect on viscosity are investigated in situ using a combination of differential scanning calorimetry and simultaneous Raman spectroscopic and rheometric measurements. The results indicate that, upon heating significantly above its glass transition temperature (261 K), the constituent S sulfur chains in the structure of the supercooled liquid first undergo a S⇌S chain-to-ring conversion near ∼383 K, which is exothermic in nature. Further heating above 393 K alters the equilibrium to shift in the opposite direction toward an endothermic ring-to-chain conversion characteristic of the well-known λ-transition in pure sulfur liquid. This behavior is attributed to the competing effects of enthalpy of mixing and conformational entropy of ring and chain elements in the liquid. The existence of reentrant structural transitions in glass-forming liquids could provide important insights into the thermodynamics of liquid-liquid transitions and may have important consequences for harnessing novel functionalities of derived glasses.
玻璃科学中一个基本且备受争议的问题是玻璃形成液体中液-液转变的存在及其性质。在此,我们报告了在富硫的硫化砷液体(成分AsS)中存在一种新型的折返结构转变。利用差示扫描量热法、同步拉曼光谱和流变测量相结合的方法,对这种转变的性质及其对粘度的影响进行了原位研究。结果表明,在加热到显著高于其玻璃化转变温度(261 K)时,过冷液体结构中的组成硫链首先在约383 K附近经历S⇌S链到环的转变,这本质上是放热的。进一步加热到393 K以上会使平衡向相反方向移动,朝着纯硫液体中著名的λ转变所特有的吸热环到链的转变方向发展。这种行为归因于液体中混合焓以及环和链元素的构象熵的竞争效应。玻璃形成液体中折返结构转变的存在可能为液-液转变的热力学提供重要见解,并可能对利用衍生玻璃的新功能产生重要影响。