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Artykuły w czasopismach na temat "Dense Glassy Systems"

1

Mandal, Rituparno, Pranab Jyoti Bhuyan, Madan Rao, and Chandan Dasgupta. "Active fluidization in dense glassy systems." Soft Matter 12, no. 29 (2016): 6268–76. http://dx.doi.org/10.1039/c5sm02950c.

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Dense soft glasses show strong collective caging behavior at sufficiently low temperatures. Using numerical simulations, we show that the introduction of activity can induce cage breaking and fluidization in a model of soft glass. The glass phase disappears beyond a critical value of the activity.
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Berthier, Ludovic, Elijah Flenner, and Grzegorz Szamel. "Glassy dynamics in dense systems of active particles." Journal of Chemical Physics 150, no. 20 (2019): 200901. http://dx.doi.org/10.1063/1.5093240.

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Yang, Junjie, Anjana Samarakoon, Sachith Dissanayake, et al. "Spin jam induced by quantum fluctuations in a frustrated magnet." Proceedings of the National Academy of Sciences 112, no. 37 (2015): 11519–23. http://dx.doi.org/10.1073/pnas.1503126112.

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Since the discovery of spin glasses in dilute magnetic systems, their study has been largely focused on understanding randomness and defects as the driving mechanism. The same paradigm has also been applied to explain glassy states found in dense frustrated systems. Recently, however, it has been theoretically suggested that different mechanisms, such as quantum fluctuations and topological features, may induce glassy states in defect-free spin systems, far from the conventional dilute limit. Here we report experimental evidence for existence of a glassy state, which we call a spin jam, in the vicinity of the clean limit of a frustrated magnet, which is insensitive to a low concentration of defects. We have studied the effect of impurities on SrCr9pGa12-9pO19 [SCGO(p)], a highly frustrated magnet, in which the magnetic Cr3+ (s = 3/2) ions form a quasi-2D triangular system of bipyramids. Our experimental data show that as the nonmagnetic Ga3+ impurity concentration is changed, there are two distinct phases of glassiness: an exotic glassy state, which we call a spin jam, for the high magnetic concentration region (p>0.8) and a cluster spin glass for lower magnetic concentration (p<0.8). This observation indicates that a spin jam is a unique vantage point from which the class of glassy states of dense frustrated magnets can be understood.
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Godfrin, P. D., P. Falus, L. Porcar, et al. "Dynamic properties of different liquid states in systems with competing interactions studied with lysozyme solutions." Soft Matter 14, no. 42 (2018): 8570–79. http://dx.doi.org/10.1039/c8sm01678j.

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Normalized MSDs and simulation snapshots (including only particles in a percolated cluster) are shown for percolated and locally glassy systems. Particles in locally dense regions (with 6 or more neighbors) contributing to locally glassy behavior are blue. All other particles are red and made smaller for clarity.
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El-Eskandarany, M. Sherif, and Naser Ali. "Synthesizing of Novel Bulk (Zr67Cu33)100−xWx(x; 5–30 at%) Glassy Alloys by Spark Plasma Sintering of Mechanically Alloyed Powders." Molecules 25, no. 8 (2020): 1906. http://dx.doi.org/10.3390/molecules25081906.

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Metallic glassy alloys with their short-range order have received considerable attention since their discovery in 1960’s. The worldwide interest in metallic glassy alloys is attributed to their unique mechanical, physical, and chemical properties, which cannot be found together in long-range order alloys of the same compositions. Traditional preparation methods of metallic glasses, such as rapid solidification of melts, always restrict the formation of glassy alloys with large atomic fraction (above 3–5 at%) of high melting point metals (Ta, Mo, W). In this study, (Zr67Cu33)100−xWx(x; 5–30 at%) metallic glassy alloys were fabricated through a mechanical alloying approach, which starts from the elemental powders. This system shows excellent glass forming ability in a wide range of W (0 ≤ x ≥ 30 at%). We have proposed a spark plasma sintering technique to prepare nearly full-dense large sized (20 × 20 mm) bulk metallic glassy alloys. The as-consolidated bulk metallic glassy alloys were seen to possess high thermal stability when compared with the other metallic glassy systems. This is implied by their high glass transition temperature (722–735 K), wide range of supercooled liquid region (39 K to over 100 K), and high values of crystallization temperature (761 K to 823 K). In addition, the fabricated ternary systems have revealed high microhardness values.
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El-Eskandarany, Mohamed Sherif, Naser Ali, and Maryam Saeed. "Glass-Forming Ability and Soft Magnetic Properties of (Co75Ti25)100−xFex (x; 0–20 at.%) Systems Fabricated by SPS of Mechanically Alloyed Nanopowders." Nanomaterials 10, no. 5 (2020): 849. http://dx.doi.org/10.3390/nano10050849.

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Due to their outstanding mechanical properties and soft magnetic characteristics, cobalt-based metallic glassy alloys have stimulated much interesting research. These metastable ferromagnetic materials possess very small magnetocrystalline anisotropy, and almost zero magnetostriction. They reveal low coercivity, extremely low core loss, moderate saturation polarization, and very high magnetism. Despite these attractive physical behaviors, Co-based metallic glasses are difficult to obtain by the melting/casting and conventional rapid solidification techniques due to their poor glass-forming ability. In the present study, we succeed in preparing (Co75Ti25)100−xFex (x; 0–20 at.%) metallic glassy powders, using a mechanical alloying approach. The end product of the as-prepared powders was consolidated into full dense cylinders with large-diameter and thickness (2 × 2 cm), using spark plasma sintering technique. The results have shown that the consolidation step did not lead to any undesired crystallizations or phase transformations, and the as-consolidated buttons maintained their unique short-range order structure. These bulk metallic glassy systems possessed high glass-transition and crystallization temperatures, suggesting their high thermal stability. However, they showed low values of the reduced glass-transition temperatures, indicating that this system is difficult to prepare by the conventional way of preparations.
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Vergadou, Niki, and Doros N. Theodorou. "Molecular Modeling Investigations of Sorption and Diffusion of Small Molecules in Glassy Polymers." Membranes 9, no. 8 (2019): 98. http://dx.doi.org/10.3390/membranes9080098.

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With a wide range of applications, from energy and environmental engineering, such as in gas separations and water purification, to biomedical engineering and packaging, glassy polymeric materials remain in the core of novel membrane and state-of the art barrier technologies. This review focuses on molecular simulation methodologies implemented for the study of sorption and diffusion of small molecules in dense glassy polymeric systems. Basic concepts are introduced and systematic methods for the generation of realistic polymer configurations are briefly presented. Challenges related to the long length and time scale phenomena that govern the permeation process in the glassy polymer matrix are described and molecular simulation approaches developed to address the multiscale problem at hand are discussed.
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Lehmkühler, Felix, Birgit Hankiewicz, Martin A. Schroer, et al. "Slowing down of dynamics and orientational order preceding crystallization in hard-sphere systems." Science Advances 6, no. 43 (2020): eabc5916. http://dx.doi.org/10.1126/sciadv.abc5916.

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Despite intensive studies in the past decades, the local structure of disordered matter remains widely unknown. We show the results of a coherent x-ray scattering study revealing higher-order correlations in dense colloidal hard-sphere systems in the vicinity of their crystallization and glass transition. With increasing volume fraction, we observe a strong increase in correlations at both medium-range and next-neighbor distances in the supercooled state, both invisible to conventional scattering techniques. Next-neighbor correlations are indicative of ordered precursor clusters preceding crystallization. Furthermore, the increase in such correlations is accompanied by a marked slowing down of the dynamics, proving experimentally a direct relation between orientational order and sample dynamics in a soft matter system. In contrast, correlations continuously increase for nonequilibrated, glassy samples, suggesting that orientational order is reached before the sample slows down to reach (quasi-)equilibrium.
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Черепанов, В. В., А. Г. Щурик та Р. А. Миронов. "Оптические свойства отечественного сетчатого стеклоуглерода и его основы". Журнал технической физики 128, № 4 (2020): 548. http://dx.doi.org/10.21883/os.2020.04.49206.224-19.

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The paper presents the results of experimental studies and mathematical modeling of the optical properties of glassy carbon and domestic reticulated foam materials based on it. Since the optical properties of the surface are studied on dense samples, dense samples were previously created, identical in physical properties to glassy carbon - the basis of highly porous cellular carbon materials. From the experimentally measured the spectral hemispherical reflectivity of the surface of the samples under its normal illumination and by the Kramers-Kronig relations the spectra of optical constants of glassy carbon - the refractive indices and absorption, as well as a number of their derivative characteristics were determined. For them, simple approximating relations are given in the paper. The obtained spectral data was incorporated into the previously developed optical statistical simulation model of ultra-porous reticulated foam materials, which is based on a rigorous electromagnetic theory and allows you to take into account both the features of their microstructure and physical processes that occur in such systems at different spa-tial and temporal scales. The results of the calculation of local spectra, the scattering phase function, and radiation thermal conductivity are presented for the reticulated glassy carbon foam, which has wide prospects for use as a structural and heat-shielding material. Some additional features of the mathematical model are demonstrated also.
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10

Debets, Vincent E., and Liesbeth M. C. Janssen. "Active glassy dynamics is unaffected by the microscopic details of self-propulsion." Journal of Chemical Physics 157, no. 22 (2022): 224902. http://dx.doi.org/10.1063/5.0127569.

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Recent years have seen a rapid increase of interest in dense active materials, which, in the disordered state, share striking similarities with the conventional passive glass-forming matter. For such passive glassy materials, it is well established (at least in three dimensions) that the details of the microscopic dynamics, e.g., Newtonian or Brownian, do not influence the long-time glassy behavior. Here, we investigate whether this still holds true in the non-equilibrium active case by considering two simple and widely used active particle models, i.e., active Ornstein-Uhlenbeck particles (AOUPs) and active Brownian particles (ABPs). In particular, we seek to gain more insight into the role of the self-propulsion mechanism on the glassy dynamics by deriving a mode-coupling theory (MCT) for thermal AOUPs, which can be directly compared to a recently developed MCT for ABPs. Both theories explicitly take into account the active degrees of freedom. We solve the AOUP- and ABP-MCT equations in two dimensions and demonstrate that both models give almost identical results for the intermediate scattering function over a large variety of control parameters (packing fractions, active speeds, and persistence times). We also confirm this theoretical equivalence between the different self-propulsion mechanisms numerically via simulations of a polydisperse mixture of active quasi-hard spheres, thereby establishing that, at least for these model systems, the microscopic details of self-propulsion do not alter the active glassy behavior.
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