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NMR longitudinal relaxation enhancement in metal halides by heteronuclear polarization exchange during magic-angle spinning. / Shmyreva, A.A.; Safdari, M.; Furó, I.; Dvinskikh, S.V.

в: Journal of Chemical Physics, Том 144, № 22, 2016, стр. 224201_1-5.

Результаты исследований: Научные публикации в периодических изданияхстатья

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Shmyreva, AA, Safdari, M, Furó, I & Dvinskikh, SV 2016, 'NMR longitudinal relaxation enhancement in metal halides by heteronuclear polarization exchange during magic-angle spinning', Journal of Chemical Physics, Том. 144, № 22, стр. 224201_1-5. https://doi.org/10.1063/1.4953540

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Author

Shmyreva, A.A. ; Safdari, M. ; Furó, I. ; Dvinskikh, S.V. / NMR longitudinal relaxation enhancement in metal halides by heteronuclear polarization exchange during magic-angle spinning. в: Journal of Chemical Physics. 2016 ; Том 144, № 22. стр. 224201_1-5.

BibTeX

@article{7b32f59c393d49d2bb38e093edb32833,
title = "NMR longitudinal relaxation enhancement in metal halides by heteronuclear polarization exchange during magic-angle spinning",
abstract = "{\textcopyright} 2016 Author(s).Orders of magnitude decrease of 207Pb and 199Hg NMR longitudinal relaxation times T1 upon magic-angle-spinning (MAS) are observed and systematically investigated in solid lead and mercury halides MeX2 (Me = Pb, Hg and X = Cl, Br, I). In lead(ii) halides, the most dramatic decrease of T1 relative to that in a static sample is in PbI2, while it is smaller but still significant in PbBr2, and not detectable in PbCl2. The effect is magnetic-field dependent but independent of the spinning speed in the range 200-15 000 Hz. The observed relaxation enhancement is explained by laboratory-frame heteronuclear polarization exchange due to crossing between energy levels of spin-1/2 metal nuclei and adjacent quadrupolar-spin halogen nuclei. The enhancement effect is also present in lead-containing organometal halide perovskites. Our results demonstrate that in affected samples, it is the relaxation data recorded under non-spinning conditions that characterize the local properties at the metal sites. A pract",
author = "A.A. Shmyreva and M. Safdari and I. Fur{\'o} and S.V. Dvinskikh",
year = "2016",
doi = "10.1063/1.4953540",
language = "English",
volume = "144",
pages = "224201_1--5",
journal = "Journal of Chemical Physics",
issn = "0021-9606",
publisher = "American Institute of Physics",
number = "22",

}

RIS

TY - JOUR

T1 - NMR longitudinal relaxation enhancement in metal halides by heteronuclear polarization exchange during magic-angle spinning

AU - Shmyreva, A.A.

AU - Safdari, M.

AU - Furó, I.

AU - Dvinskikh, S.V.

PY - 2016

Y1 - 2016

N2 - © 2016 Author(s).Orders of magnitude decrease of 207Pb and 199Hg NMR longitudinal relaxation times T1 upon magic-angle-spinning (MAS) are observed and systematically investigated in solid lead and mercury halides MeX2 (Me = Pb, Hg and X = Cl, Br, I). In lead(ii) halides, the most dramatic decrease of T1 relative to that in a static sample is in PbI2, while it is smaller but still significant in PbBr2, and not detectable in PbCl2. The effect is magnetic-field dependent but independent of the spinning speed in the range 200-15 000 Hz. The observed relaxation enhancement is explained by laboratory-frame heteronuclear polarization exchange due to crossing between energy levels of spin-1/2 metal nuclei and adjacent quadrupolar-spin halogen nuclei. The enhancement effect is also present in lead-containing organometal halide perovskites. Our results demonstrate that in affected samples, it is the relaxation data recorded under non-spinning conditions that characterize the local properties at the metal sites. A pract

AB - © 2016 Author(s).Orders of magnitude decrease of 207Pb and 199Hg NMR longitudinal relaxation times T1 upon magic-angle-spinning (MAS) are observed and systematically investigated in solid lead and mercury halides MeX2 (Me = Pb, Hg and X = Cl, Br, I). In lead(ii) halides, the most dramatic decrease of T1 relative to that in a static sample is in PbI2, while it is smaller but still significant in PbBr2, and not detectable in PbCl2. The effect is magnetic-field dependent but independent of the spinning speed in the range 200-15 000 Hz. The observed relaxation enhancement is explained by laboratory-frame heteronuclear polarization exchange due to crossing between energy levels of spin-1/2 metal nuclei and adjacent quadrupolar-spin halogen nuclei. The enhancement effect is also present in lead-containing organometal halide perovskites. Our results demonstrate that in affected samples, it is the relaxation data recorded under non-spinning conditions that characterize the local properties at the metal sites. A pract

U2 - 10.1063/1.4953540

DO - 10.1063/1.4953540

M3 - Article

VL - 144

SP - 224201_1-5

JO - Journal of Chemical Physics

JF - Journal of Chemical Physics

SN - 0021-9606

IS - 22

ER -

ID: 7954473