Temperature dependence studies of NQR frequencies of halogens and also of quadrupolar relaxation times of chlorine nuclei in ammonium hexahalotellurates(IV)

1989 ◽  
Vol 93 (1) ◽  
pp. 13-18 ◽  
Author(s):  
Yoshihiro Furukawa ◽  
Daiyu Nakamura
Keyword(s):  
Temperature Dependence ◽  
Relaxation Times ◽  
Quadrupolar Relaxation

scholarly journals A Study of Anonic Motions in Solid Rubidiumand Cesium Tetrachloroaurates(III)by Measuring the Temperature Dependence of Chlorine Nuclear Quadrupolar Relaxation Times

1989 ◽  
Vol 44 (2) ◽  
pp. 125-130 ◽  
Author(s):  
Atsushi Ishikawa ◽  
Tetsuo Asaji ◽  
Daiyu Nakamura ◽  
Ryuichi Ikeda
Keyword(s):  
Temperature Dependence ◽  
Complex Anion ◽  
Lattice Vibration ◽  
Relaxation Times ◽  
Potential Wells ◽  
Square Planar ◽  
Temperature Dependences ◽  
Cesium Salts ◽  
Quadrupolar Relaxation ◽  
Diagonal Axis

Abstract The temperature dependences of 35Cl NQR frequencies and 35Cl nuclear quadrupolar relaxation times T1Q and T2Q were determined above 82K for Rb[AuCl4] and CsfAuClJ up to ca. 340 and 320 K, respectively. Below these temperatures two 35Cl NQR frequencies were observed for each complex whereas no resonance could be detected above the respective temperatures. For both complexes, T1Q observed below ca. 270 K was interpreted as mainly determined by the rotary lattice vibration around the pseudo-C4(C4) axis and each Cl-Au-Cl diagonal axis of the square planar complex anion, whereas T1q observed above ca. 270 K was definitely shown to be determined through the reorientation of the anions about their C′4 axis. The activation energies for the C′4 reorientation of the anions was evaluated to be 71 and 53 kJ mol-1 for the rubidium and cesium salts, respectively. The anionic dynamics are discussed by assuming the motion of the anions within and out of the C4 potential wells at lower and higher temperatures, respectively.

Bonded Hydrogen and Trapped H2 in a-Si1−xGex:H Alloys

1989 ◽  
Vol 149 ◽  
Author(s):  
E. J. Vanderheiden ◽  
G. A. Williams ◽  
P. C. Taylor ◽  
F. Finger ◽  
W. Fuhs
Keyword(s):  
Temperature Dependence ◽  
Molecular Hydrogen ◽  
Relaxation Times ◽  
Lattice Relaxation ◽  
Spin Lattice Relaxation ◽  
Spin Lattice ◽  
H Nmr ◽  
Local Environments

ABSTRACT1H NMR has been employed to study the local environments of bonded hydrogen and trapped molecular hydrogen (H2) in a series of a-Si1−xGex:H alloys. There is a monotonic decrease of bonded hydrogen with increasing x from ≈ 10 at. % at x = 0 (a-Si:H) to ≈ 1 at. % at x = 1 (a-Ge:H). The amplitude of the broad 1H NMR line, which is attributed to clustered bonded hydrogen, decreases continuously across the system. The amplitude of the narrow 1H NMR line, which is attributed to bonded hydrogen essentially randomly distributed in the films, decreases as x increases from 0 to ≈ 0.2. From x = 0.2 to x ≈ 0.6 the amplitude of the narrow 1H NMR line is essentially constant, and for x ≥ 0.6 the amplitude decreases once again. The existence of trapped H2 molecules is inferred indirectly by their influence on the temperature dependence of the spin-lattice relaxation times, T1. Through T1, measurements it is determined that the trapped H2 concentration drops precipitously between x = 0.1 and x = 0.2, but is fairly constant for 0.2 ≤ x ≤ 0.6. For a-Si:H (x = 0) the H2 concentration is ≈ 0.1 at. %, while for x ≥ 0.2 the concentration of H2 is ≤ 0.02 at. %.

Temperature Dependence of Dynamic Properties of Elastomers. Relaxation Distributions

1952 ◽  
Vol 25 (4) ◽  
pp. 720-729 ◽  
Author(s):  
John D. Ferry ◽  
Edwin R. Fitzgerald ◽  
Lester D. Grandine ◽  
Malcolm L. Williams
Keyword(s):  
Distribution Function ◽  
Temperature Dependence ◽  
Dynamic Properties ◽  
Relaxation Times ◽  
Dynamic Mechanical Properties ◽  
Relaxation Processes ◽  
The Real ◽  
Reduced Frequency ◽  
Dynamic Rigidity ◽  
Composite Curve

Abstract By the use of reduced variables, the temperature dependence and frequency dependence of dynamic mechanical properties of rubberlike materials can be interrelated without any arbitrary assumptions about the functional form of either The definitions of the reduced variables are based on some simple assumptions regarding the nature of relaxation processes. The real part of the reduced dynamic rigidity, plotted against the reduced frequency, gives a single composite curve for data over wide ranges of frequency and temperature; this is true also for the imaginary part of the rigidity or the dynamic viscosity. The real and imaginary parts of the rigidity, although independent measurements, are interrelated through the distribution function of relaxation times, and this relation provides a check on experimental results. First and second approximation methods of calculating the distribution function from dynamic data are given. The use of the distribution function to predict various types of time-dependent mechanical behavior is illustrated.

Molecular Motions and Phase Transitions in Solid CH3NH3PbX3 (X = C1, Br, I) as Studied by NMR and NQR

1991 ◽  
Vol 46 (3) ◽  
pp. 240-246 ◽  
Author(s):  
Qiang Xu ◽  
Taro Eguchi ◽  
Hirokazu Nakayama ◽  
Nobuo Nakamura ◽  
Michihiko Kishita
Keyword(s):  
Phase Transitions ◽  
Temperature Dependence ◽  
Relaxation Times ◽  
Lattice Relaxation ◽  
Molecular Motions ◽  
Isotropic Reorientation ◽  
Higher Temperature ◽  
Successive Phase

AbstractThe temperature dependence of 35C1, 81Br, and 127I NQR frequencies and 1Hspin-lattice relaxation times (T1) for CH3NH3PbX3 (X = Cl, Br, I) was measured through the successive phase transitions in these solids. The isotropic reorientation of the CH3NH3 ions takes place in the higher-temperature phases (tetragonal [I4/mcm] and cubic) of the three salts (Ea= 11 kJ mol -1). T1's in the lowest-temperature phases (orthorhombic) indicate that the cations undergo correlated C3-reorientation in the chloride (Ea = 5.45 kJ mol -1)and in the iodide (Ea = 5.80 kJ mol -1, whereas correlated (Ea = 2.40 kJ mol-1) and uncorrected (Ea = 7.50 kJ mol-1) C3- reorientations are excited in the bromide. It is also revealed that the rotational tunneling of the cations governs T1 at lowtemperature region in the orthorhombic phases of these salts

scholarly journals The Dynamic Properties of 5Cb Filled with Aerosil Particles Investigated by Pcs

1999 ◽  
Vol 559 ◽  
Author(s):  
F.M. Aliev ◽  
M. Kreuzer ◽  
Yu.P. Panarin
Keyword(s):  
Liquid Crystal ◽  
Temperature Dependence ◽  
Relaxation Process ◽  
Nematic Liquid Crystal ◽  
Broad Spectrum ◽  
Dynamic Properties ◽  
Relaxation Times ◽  
Correlation Spectroscopy ◽  
Relaxation Processes ◽  
Optoelectronic Application

ABSTRACTNematic liquid crystal filled with Aerosil particles, a prospective composite material for optoelectronic application, has been investigated by static light scattering and Photon Correlation Spectroscopy (PCS). The Aerosil particles in filled nematic liquid crystals (FN) form a network structure with LC domains about 2500 Å in size with a random distribution of the director orientation of each domain.We found that the properties of 5CB are considerably affected by the network. The N-I phase transition in filled 5CB was found to be smeared out and depressed. PCS experiments show that two new relaxation processes appear in filled 5CB in addition to the director fluctuation process in bulk. The slow relaxation process, with a broad spectrum of relaxation times, is somewhat similar to the slow decay, which is observed in confined nematic liquid crystal.The middle frequency process was assigned to the director fluctuations in the surface layer formed at the particle-LC interface. The decay function describing this relaxation process is a stretched exponential (β ≍ 0.7). The temperature dependence of the relaxation times of the middle frequency obeys the Vogel-Rilcher law. Such a temperature dependence, accompanied by a broad spectrum of relaxation times suggests that the dynamics of the director fluctuations near the Aerosil particle-LC interface is glass-like.

The Influence of Boundary Conditions and Surface Layer Thickness on Dielectric Relaxation of Liquid Crystals Confined in Cylindrical Pores

2000 ◽  
Vol 651 ◽  
Author(s):  
Z. Nazario ◽  
G. P. Sinha ◽  
F.M. Aliev
Keyword(s):  
Liquid Crystal ◽  
Boundary Conditions ◽  
Temperature Dependence ◽  
Layer Thickness ◽  
Dielectric Spectroscopy ◽  
Relaxation Times ◽  
Thin Layers ◽  
Short Axis ◽  
Librational Mode ◽  
Cylindrical Pores

AbstractDielectric spectroscopy was applied to investigate the dynamic properties of liquid crystal octylcyanobiphenyl (8CB) confined in 2000 Å cylindrical pores of Anopore membranes with homeotropic and axial (planar) boundary conditions on the pore walls. Homeotropic boundary conditions allow the investigation of the librational mode in 8CB by dielectric spectroscopy. We found that the dynamics of the librational mode is totally different from the behavior observed in investigations of relaxation due to reorientation of molecules around their short axis. The interpretation of the temperature dependence of relaxation times and of the dielectric strength of the librational mode needs the involvement of the temperature dependence of orientational order parameter. For samples with axial boundary conditions, layers of LCs with different thickness were obtained on the pore walls as a result of controlled impregnation of porous matrices with 8CB from solutions of different liquid crystal concentration. The process due to rotation of molecules around their short axis with single relaxation time observed for bulk 8CB is replaced by a process with a distribution of relaxation times in thin layers. This relaxation process broadens with decreasing layer thickness.

Relaxation Phenomena of MgCuZn Ferrites

2009 ◽  
Vol 421-422 ◽  
pp. 521-524
Author(s):  
Taku Murase ◽  
Hidenobu Umeda
Keyword(s):  
Resonance Frequency ◽  
Temperature Dependence ◽  
Relative Permeability ◽  
Loss Factor ◽  
Relaxation Times ◽  
Activation Energies ◽  
Relaxation Phenomenon ◽  
Relaxation Phenomena ◽  
Infinite Temperature

The decrease of initial relative permeability at 103-106Hz is observed in MgCuZn or MnMgCuZn ferrites. By measuring the temperature dependence of loss factor, the gradual deterioration of initial relative permeability is attributed to a relaxation phenomenon. The relaxation phenomena of MnMgCuZn ferrites occur in the condition of the stoichiometoric composition and the higher sintering temperatures. The activation energies of the relaxation phenomena are calculated to be 0.3-1.0eV. The relaxation times at infinite temperature are calculated to be 10-12-10-16 second. The initial relative permeability of MgCuZn or MnMgCuZn ferrites with the relaxation phenomena is higher than the value calculated from the resonance frequency and Snoek’s limit law.

Temperature Dependence of Proton Relaxation Times in Aqueous Solutions of Paramagnetic Ions

1959 ◽  
Vol 30 (4) ◽  
pp. 950-956 ◽  
Author(s):  
Robert A. Bernheim ◽  
Thomas H. Brown ◽  
H. S. Gutowsky ◽  
D. E. Woessner
Keyword(s):  
Aqueous Solutions ◽  
Temperature Dependence ◽  
Relaxation Times ◽  
Proton Relaxation ◽  
Paramagnetic Ions
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