arXiv subjects

P. Wen

Publications and source records attributed to P. Wen.

4 recordsLinked to original sources

arXiv2016

Relaxation decoupling in metallic glassy state

Upon cooling, glass-forming liquids experience a two-step relaxation associated to the cage rattling and the escape from the cage, and the following decoupling between the \b{eta}- and the α-relaxations. The found decoupling behaviors have greatly changed the face of glassy physics and materials studies. Here we report a novel dynamic decoupling that the relaxation function changes gradually from a single-step to a two-step form as temperature declines through the stress relaxation of various metallic glasses in a broad time and temperature range below glass transition temperature (Tg). Such a two-step relaxation is unexpected in glassy state and reveals a decoupling of dynamic modes arising from two different mechanisms: a faster one exhibiting ballistic-like feature, and a slower one associated with a broader distribution of relaxation times typical of subdiffusive atomic motion. This first observation of two-step dynamics in metallic glassy state points to a far richer-than-expected scenario for glass relaxation.

cond-mat.dis-nn↗

arXiv2016

Rejuvenation of metallic glasses under high pressure

Modulating energy states of metallic glasses (MGs) is significant in understanding the nature of glasses and control their properties. In this study, we show that rejuvenation in enthalpy can be achieved and preserved in bulk MGs by using high pressure (HP) annealing, which is a controllable method to continuously alter the energy states of MGs. Contrary to the decrease in enthalpy by conventional annealing at ambient pressure, such rejuvenation can occur and be enhanced by increasing both of annealing temperature and pressure. By using double aberration corrected scanning transmission electron microscopy, it is revealed that the rejuvenation, which is attributed to coupling effect of high pressure and high temperature, originates from the microstructural change that involves "negative flow units" with a higher atomic packing density compared to that of the elastic matrix of MGs. The results demonstrate that HP annealing is an effective way to rejuvenate MGs into higher energy states, and it may assist in understanding the microstructural origin of the rejuvenation in MGs.

cond-mat.mtrl-sci↗

arXiv2016

Correlations Between Local Elastic Heterogeneities and Overall Elastic Properties in Metallic Glasses

The common notion suggests that metallic glasses (MGs) are a homogeneous solid at the macroscopic scale; however, recent experiments and simulations indicate that MGs contain nano-scale elastic heterogeneities. Despite the fundamental importance of these findings, a quantitative understanding is still lacking for the local elastic heterogeneities intrinsic to MGs. On the basis of Eshelby's theory, here we develop a micromechanical model that correlates the properties of the local elastic heterogeneities, being very difficult to measure experimentally, to the measurable overall elastic properties of MGs, such as shear/bulk modulus and Poisson's ratio. Our theoretical modeling is verified by the experimental data obtained from various MGs annealed to different degrees. Particularly, we revealed that the decrease of Poisson's ratio upon annealing of MGs is associated with a much large shear softening over hydrostatic-pressure softening, and $vice$ $versa$ in local elastic inhomogeneities. The relative extent of the bulk versus shear modulus softens is extracted for different MGs, and is found to closely depend on the specific composition and their ductility. The implication of our results on the Poisson's ratio criterion on the ductility as well as the aging dynamics in MGs is discussed.

cond-mat.mtrl-sci↗

arXiv2011

The Excess Heat Capacity in Glass-forming Liquid Systems Containing Molecules

The excess heat capacity at glass transition temperature in two types of glass-forming systems of [xNaNO3\cdot(1-x)KNO3]60[Ca(NO3)2]40 (0 \leq x \leq 1) and Ca(NO3)2\cdotyH2O (4 \leq y \leq 13) is studied. In the former system, with the replacement of K+ cation with Na+ cation, the excess heat capacity is almost invariable around 65.1 J\cdotmol-1\cdotK-1, while the excess increases by 38.9 J\cdotmol-1\cdotK-1 with the increasing per molar H2O content in latter system. A quantitative description of the excess heat capacity is built up with the consideration of atomic and molecular translational motion in the glass-forming systems. This finding might offer further understanding to the glass transition.

cond-mat.stat-mech↗