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Marina Kveder

Publications and source records attributed to Marina Kveder.

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Embedded electron spin decoherence as indicator of the matrix material structure

In this work the problem of characterizing matrix material structure from embedded electron spin decoherence is studied both theoretically and experimentally. Theoretical calculation using nuclear spin bath model and cluster correlation expansion method shows that the positions of decoherence time scale extremums among single crystal orientations of the matrix material coincide with those of the nearest neighbour proton dipolar couplings. This finding is confirmed by single crystal pulsed EPR experiment performed on $γ$-irradiated malonic acid (MA). Electron spin decoherence decay profile in polycrystalline matrix material is obtained from the orientation dependence as an average over sampled orientations on a Fibonacci grid. In addition, it is pointed out theoretically that a further removal of crystal ordering in the nuclear spin bath can reduce decoherence time scale from the polycrystalline value. This prediction is verified experimentally by the Hahn echo time decay scale in a new amorphous polymorph of MA, obtained for the first time by mechanical milling. Thus the embedded electron spin decoherence can be viewed as a quantitative indicator for studying structures and/or structure changes of the matrix material.

cond-mat.mtrl-sci

Low temperature electron-spin relaxation in the crystalline and glassy states of solid ethanol

X-band electron paramagnetic resonance (EPR) spectroscopy was used to study the spectral properties of a nitroxide spin probe in ethanol glass and crystalline ethanol, at 5 - 11.5 K. The different anisotropy of molecular packing in the two host matrices was evidenced by different rigid limit values for maximal hyperfine splitting in the signal of the spin probe. The significantly shorter phase memory time, , for the spin probe dissolved in crystalline ethanol, as compared to ethanol glass, was discussed in terms of contribution from spectral diffusion. The effect of low-frequency dynamics was manifested in the temperature dependence of and in the difference between the data measured at different spectral positions. This phenomenon was addressed within the framework of the slow-motional isotropic diffusion model [S. Lee, and S. Z. Tang, Phys. Rev. B 31, 1308 (1985)] predicting the spin probe dynamics within the millisecond range, at very low temperatures. The shorter spin-lattice relaxation time of the spin probe in ethanol glass was interpreted in terms of enhanced energy exchange between the spin system and the lattice in the glass matrix due to boson peak excitations.

cond-mat.soft

Electron spin-lattice relaxation in solid ethanol: the effect of nitroxyl radical hydrogen bonding and matrix disorder

The electron spin-lattice relaxation of TEMPO and TEMPONE was measured at temperatures between 5 and 80 K in crystalline and glassy ethanol using X-band electron paramagnetic resonance spectroscopy. The experimental data at the lowest temperatures studied were explained in terms of electron-nuclear dipolar interaction between the paramagnetic center and the localized excitations, whereas at higher temperatures low-frequency vibrational modes from the host matrix and Raman processes should be considered. The strong impact of hydrogen bonding between the dopant molecule and ethanol host on the spin relaxation was observed in ethanol glass whereas in crystalline ethanol both paramagnetic guest molecules behaved similarly.

physics.chem-ph