Dyre Jeppe C
"Glass and Time", IMFUFA, Dept. of Sciences, Roskilde University, P.O. Box 260, DK-4000 Roskilde, Denmark.
J Phys Chem Lett. 2024 Feb 15;15(6):1603-1617. doi: 10.1021/acs.jpclett.3c03308. Epub 2024 Feb 2.
This perspective article reviews arguments that glass-forming liquids are different from those of standard liquid-state theory, which typically have a viscosity in the mPa·s range and relaxation times on the order of picoseconds. These numbers grow dramatically and become 10 - 10 times larger for liquids cooled toward the glass transition. This translates into a qualitative difference, and below the "solidity length" which is roughly one micron at the glass transition, a glass-forming liquid behaves much like a solid. Recent numerical evidence for the solidity of ultraviscous liquids is reviewed, and experimental consequences are discussed in relation to dynamic heterogeneity, frequency-dependent linear-response functions, and the temperature dependence of the average relaxation time.
这篇观点文章回顾了一些观点,即玻璃形成液体不同于标准液态理论中的液体,标准液态理论中的液体通常粘度在毫帕秒范围内,弛豫时间在皮秒量级。对于朝着玻璃化转变冷却的液体,这些数值会急剧增大,增大到10 - 10倍。这转化为一种质的差异,并且在玻璃化转变时大约为一微米的“固态长度”以下,玻璃形成液体的行为更像固体。本文回顾了超粘性液体固态性的最新数值证据,并讨论了与动态非均匀性、频率依赖线性响应函数以及平均弛豫时间的温度依赖性相关的实验结果。