Traditionally the study of dynamics of glass-forming materials has been focused on the structural α relaxation. However, in recent years experimental evidence has revealed that a secondary β relaxation belonging to a special class, called the Johari-Goldstein (JG) β relaxation, has properties strongly linked to the primary α relaxation. By invoking the principle of causality, the relation implies the JG β relaxation is fundamental and indispensable for generating the α relaxation, and the properties of the latter are inherited from the former. The JG β relaxation is observed together with the α relaxation mostly by dielectric spectroscopy. The macroscopic nature of the data allows the use of arbitrary or unproven procedures to analyze the data. Thus the results characterizing the JG β relaxation and the relation of its relaxation time τ_{β} to the α-relaxation time τ_{α} obtained can be equivocal and controversial. Coming to the rescue is the nuclear resonance time-domain-interferometry (TDI) technique covering a wide time range (10^{-9}-10^{-5}s) and a scattering vector q range (9.6-40nm^{-1}). TDI experiments have been carried out on four glass formers, ortho-terphenyl [M. Saito et al., Phys. Rev. Lett. 109, 115705 (2012)10.1103/PhysRevLett.109.115705], polybutadiene [T. Kanaya et al., J. Chem. Phys. 140, 144906 (2014)10.1063/1.4869541], 5-methyl-2-hexanol [F. Caporaletti et al., Sci. Rep. 9, 14319 (2019)10.1038/s41598-019-50824-7], and 1-propanol [F. Caporaletti et al., Nat. Commun. 12, 1867 (2021)10.1038/s41467-021-22154-8]. In this paper the TDI data are reexamined in conjunction with dielectric and neutron scattering data. The results show the JG β relaxation observed by dielectric spectroscopy is heterogeneous and comprises processes with different length scales. A process with a longer length scale has a longer relaxation time. TDI data also prove the primitive relaxation time τ_{0} of the coupling model falls within the distribution of the TDI q-dependent JG β-relaxation times. This important finding explains why the experimental dielectric JG β-relaxation times τ_{β}(T,P) is approximately equal to τ_{0}(T,P) as found in many glass formers at various temperature T and pressure P. The result, τ_{β}(T,P)≈τ_{0}(T,P), in turn explains why the ratio τ_{α}(T,P)/τ_{β}(T,P) is invariant to changes of T and pressure P at constant τ_{α}(T,P), the α-relaxation time.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1103/PhysRevE.104.015103 | DOI Listing |
PLoS Biol
January 2025
Department of Biomedical and Translational Sciences, Macon & Joan Brock Virginia Health Sciences at Old Dominion University, Norfolk, Virginia, United States of America.
Every heartbeat depends on cyclical contraction-relaxation produced by the interactions between myosin-containing thick and actin-based thin filaments (TFs) arranged into a crystalline-like lattice in the cardiac sarcomere. Therefore, the maintenance of thin filament length is crucial for myocardium function. The thin filament is comprised of an actin backbone, the regulatory troponin complex and tropomyosin that controls interactions between thick and thin filaments.
View Article and Find Full Text PDFJ Phys Chem A
January 2025
College of Physics Science and Technology, Yangzhou University, Yangzhou 225009, China.
Developing high-performance solar cells is a practical way to improve clean energy conversion efficiency. However, the performance of solar cells faces challenges such as fast carrier combination, poor stability, and limited solar light harvesting. Herein, we propose a strategy by decorating periodic holes in two-dimensional (2D) porous carbon-nitrogen (CN) materials with a zero-dimensional (0D) semiconducting (ZnO) cluster.
View Article and Find Full Text PDFJ Phys Chem B
January 2025
Department of Pharmaceutical Sciences, School of Pharmacy, West Virginia University, Morgantown, West Virginia 26506, United States.
measurement and mapping of oxygen levels within the tissues are crucial in understanding the physiopathological processes of numerous diseases, such as cancer, diabetes, or peripheral vascular diseases. Electron paramagnetic resonance (EPR) associated with biocompatible exogenous spin probes, such as Ox071 triarylmethyl (TAM) radical, is becoming the new gold standard for oxygen mapping in preclinical settings. However, these probes do not show tissue selectivity when injected systemically, and they are not cell permeable, reporting oxygen from the extracellular compartment only.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
Graduate School of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashiosaka, Osaka 577-8502, Japan.
Selective modification of chemically active sites on supports, such as steps, edges, and corners, with metal nanoparticles (NPs) is a challenging topic in the fields of catalysis and photocatalysis. However, the formation of site-selective, high-density metal NPs on a support has not yet been achieved. Radial ZnO mesocrystals composed of hexagonal nanowires (NWs) with {101̅0} sidewalls were synthesized by a simple solution-phase method.
View Article and Find Full Text PDFHeliyon
January 2025
Division of Polymer Chemistry, Department of Chemistry, Atomic Energy Commission, P.O. Box: 6091, Damascus, Syrian Arab Republic.
The degree of sulfonation (DS) is a key property of sulfonated polymers, as it significantly influences their swelling behaviour, conductivity and mechanical properties. Accurately determining the DS is essential for optimizing these materials for various applications. In this work, the DS of sulfonated poly (ether ether ketone) (SPEEK) was evaluated using a combination of analytical techniques, including titration, back titration, Fourier Transform Infrared (FTIR), Ultra-Violet (UV) and proton nuclear magnetic resonance (H NMR) spectroscopies, Thermogravimetric analysis (TGA), Rutherford backscattering (RBS) and particle induced X-ray emission (PIXE) analysis.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!