scholarly journals Measuring Spin Relaxation Rates Using Satellite Exchange NMR Spectroscopy

2018 ◽  
Vol 57 (25) ◽  
pp. 7498-7502
Author(s):  
Gerard P. Robertson ◽  
Barbara Odell ◽  
Ilya Kuprov ◽  
Darren J. Dixon ◽  
Tim D. W. Claridge
2018 ◽  
Vol 130 (25) ◽  
pp. 7620-7624
Author(s):  
Gerard P. Robertson ◽  
Barbara Odell ◽  
Ilya Kuprov ◽  
Darren J. Dixon ◽  
Tim D. W. Claridge

1992 ◽  
Vol 06 (18) ◽  
pp. 1145-1150 ◽  
Author(s):  
Q. P. LI ◽  
ROBERT JOYNT

We study the experimental consequences of a gap function which is odd in energy. This type of gap may occur in high temperature superconductors. We show that nuclear spin relaxation experiments can be used to probe the "particle-hole parity" of a gap function. We find that an exponent α=1/3 which characterizes the energy dependence is in agreement with the currently available experimental data of both the nuclear spin relaxation rate (∝T(2-α)/α) and the electromagnetic penetration depth (∝T(1-α)/α).


2007 ◽  
Author(s):  
A. Reznitsky ◽  
A. Klochikhin ◽  
S. Permogorov ◽  
L. Tenishev ◽  
K. Mironenko ◽  
...  

2007 ◽  
Vol 105 (15-16) ◽  
pp. 2137-2151 ◽  
Author(s):  
H. Sato ◽  
V. Kathirvelu ◽  
A. Fielding ◽  
J. P. Blinco ◽  
A. S. Micallef ◽  
...  

2017 ◽  
Vol 231 (4) ◽  
Author(s):  
Yilin Shi ◽  
Richard W. Quine ◽  
George A. Rinard ◽  
Laura Buchanan ◽  
Sandra S. Eaton ◽  
...  

AbstractIn vivo oximetry by pulsed electron paramagnetic resonance is based on measurements of changes in electron spin relaxation rates of probe molecules, such as the triarylmethyl radicals. A series of experiments was performed at frequencies between 250 MHz and 1.5 GHz to assist in the selection of an optimum frequency for oximetry. Electron spin relaxation rates for the triarylmethyl radical OX063 as a function of radical concentration, salt concentration, and resonance frequency were measured by electron spin echo 2-pulse decay and 3-pulse inversion recovery in the frequency range of 250 MHz–1.5 GHz. At constant OX063 concentration, 1/T


2011 ◽  
Vol 1313 ◽  
Author(s):  
K. Arbi ◽  
I. Sobrados ◽  
M. Hoelzel ◽  
A. Kuhn ◽  
F. Garcia-Alvarado ◽  
...  

AbstractLithium mobility in LiM2(PO4)3 compounds, with M= Ge, Ti, Sn, Zr and Hf, has been investigated by 7Li Nuclear Magnetic Resonance (NMR) spectroscopy in the temperature range 100-500 K. From the analysis of 7Li NMR quadrupole interactions (CQ and η parameters), Li sites occupancy and exchange processes between structural sites have been studied. Below 250K, Li ions are preferentially located at M1 sites in rhombohedral phases, but occupy M12 sites in triclinic ones. At increasing temperatures, Li mobility has been deduced from spin-spin () and spin-lattice relaxation () rates. In this analysis, the presence of two relaxation mechanisms in plots has been associated with departures of conductivity from the Arrhenius behavior. At high temperatures, residence times at M12−T11−T11−T1 and M12 sites become similar and conductivity significantly increase. This superionic state can be achieved by enlarged order-disorder transformations in rhombohedral phases, or by sharp first order transitions in triclinic ones. Results described in the LiTi2(PO4)3 sample have been compared with those obtained in rhombohedral Li1+xTi2-xAlx(PO4)3 and LiTi2-xZrx(PO4)3 series showing respectively higher and lower conductivities. In the case of Li1.2Ti1.8Al0.2(PO4)3, displaying the highest reported conductivity, NMR results are discussed in relation with those obtained by Neutron Diffraction (ND) and Impedance Spectroscopy (IS). Diffusion coefficients determined by NMR Pulse Field Gradient (PFG) technique are similar to those deduced from Impedance Spectroscopy and NMR relaxation data.


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