Abstract
We report on 1H NMR measurements of spin–lattice and spin–spin relaxation times in hydrogen molecules confined in nanocavities of the a-Si–H thin films. We found that the 1H spin–spin relaxation time T2 and the spin–lattice relaxation times T1 and T1ρ in the laboratory and rotating frames, respectively, exhibit anisotropic behavior as functions of the angle between the film growth direction and the applied magnetic field. This effect is caused by the dipole–dipole interaction of nuclear spins of hydrogen molecules experiencing restricted diffusion in ellipsoid-like nanocavities. The experimental results are analyzed within the framework of the previously developed theory. The analysis allows determining the distribution of nanocavities over orientations in the film under study. Similar phenomena can occur in various materials containing nanocavities and in nanoporous compounds of various origins in which molecular diffusion occurs and to which the above approach is applicable.
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Acknowledgements
We are grateful to Profs. J. Baugh and N.A. Sergeev for helpful discussion. This research was supported by a grant from the United States—Israel Binational Science Foundation (BSF), Jerusalem, Israel (No. 2019033), and in part by a R01 grant from the National Institutes of Health (NIH) of the United States (#69047).
Funding
This research was funded by a grant from the United States—Israel Binational Science Foundation (BSF), Jerusalem, Israel (No. 2019033), and by a grant from the National Institutes of Health in the United States (AR 069047).
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All the authors contributed to the concept and design of the study. AMP carried out experiments. GBF, VS, and YX made data processing, compiled a computer program, and took part in the calculations. PRiC grew the films and made their characterization. All the authors read and approved the final version of the manuscript.
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Panich, A.M., Furman, G.B., Sokolovsky, V. et al. Anisotropic Spin–Lattice and Spin–Spin Relaxations in Hydrogen Molecules Trapped in Non-Spherical Nanocavities. Appl Magn Reson 54, 371–381 (2023). https://doi.org/10.1007/s00723-022-01515-6
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DOI: https://doi.org/10.1007/s00723-022-01515-6