Phase Transition Mechanism Studied by1H and87Rb Spin-Lattice Relaxation Time in a RbHSO4Single Crystal

2001 ◽  
Vol 70 (12) ◽  
pp. 3708-3712 ◽  
Author(s):  
Ae Ran Lim ◽  
Jae Kap Jung ◽  
Hyun Min Park
1973 ◽  
Vol 51 (8) ◽  
pp. 781-786 ◽  
Author(s):  
Maria Wiszniewska ◽  
Robin L. Armstrong

Measurements of the 79Br nuclear quadrupole resonance frequency and spin–lattice relaxation time in a polycrystalline sample of (NH4)2PtBr6 from 4 to 450 K are reported. The frequency data indicate the occurrence of a structural phase transition at 58 K. The spin–lattice relaxation time data exhibit a distinct minimum, also at 58 K. The data are discussed in terms of a model previously introduced to account for phase transitions from cubic to tetragonal symmetry in R2MX6 compounds. A point charge calculation provides an explanation of the observed frequency splitting in terms of the alteration in the neighboring ion contribution to the electric field gradient at the 79Br nuclear sites. This alteration results from a small distortion of the cages defined by the NH4 ions and an accompanying rotation of the PtBr6 octahedra situated within these cages. The temperature dependences of two different average rotary lattice mode frequencies are deduced; in each case the observed behavior supports the hypothesis that it is the rotary lattice mode which softens thereby bringing about the change in structure.


1978 ◽  
Vol 39 (C6) ◽  
pp. C6-1215-C6-1216
Author(s):  
H. Ahola ◽  
G.J. Ehnholm ◽  
S.T. Islander ◽  
B. Rantala

1978 ◽  
Vol 56 (10) ◽  
pp. 1386-1389
Author(s):  
Marie D'Iorio ◽  
Robin L. Armstrong

The pressure-induced polymorphic phase transition at about 4 k bar in rubidium iodide was studied using nuclear magnetic resonance. The signature of the structural transition is a loss of echo intensity which presumably is due to an increase in the number of lattice defects as a result of the transition. The ratio of the spin–spin relaxation times of the iodine nuclei in the two phases is in agreement with the ratio predicted by a second moment calculation. The actual experimental values, however, are considerably smaller than the theoretical predictions signifying the migration of lattice defects. Estimates of the iodine spin–lattice relaxation time at atmospheric pressure indicate the necessity to include both an anharmonic Raman contribution and a covalency factor. The change in spin–lattice relaxation time with pressure as measured in the low pressure phase is dominated by the change in the lattice parameter. At the critical pressure the spin–lattice relaxation time decreases by a fractional amount which is approximately equal to the fractional volume change characterizing the transition. The pressure derivative of the spin–lattice relaxation time in the high pressure phase is nearly equal to that in the low pressure phase.


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