Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered Solids

Materials often contain minor heterogeneous phases that are difficult to characterize yet nonetheless significantly influence important properties. Here we describe a solid-state NMR strategy for quantifying minor heterogenous sample regions containing dilute, essentially uncoupled nuclei in materia...

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Main Authors: Brennan J. Walder, Todd M. Alam
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:International Journal of Molecular Sciences
Subjects:
CFx
Online Access:https://www.mdpi.com/1422-0067/21/11/3938
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spelling doaj-2bd4c539421e4eaba3990759e41f377b2020-11-25T03:46:31ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-05-01213938393810.3390/ijms21113938Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered SolidsBrennan J. Walder0Todd M. Alam1Sandia National Laboratories, Department of Organic Materials Science, Albuquerque, NM 87185, USASandia National Laboratories, Department of Organic Materials Science, Albuquerque, NM 87185, USAMaterials often contain minor heterogeneous phases that are difficult to characterize yet nonetheless significantly influence important properties. Here we describe a solid-state NMR strategy for quantifying minor heterogenous sample regions containing dilute, essentially uncoupled nuclei in materials where the remaining nuclei experience heteronuclear dipolar couplings. NMR signals from the coupled nuclei are dephased while NMR signals from the uncoupled nuclei can be amplified by one or two orders of magnitude using Carr-Meiboom-Purcell-Gill (CPMG) acquisition. The signal amplification by CPMG can be estimated allowing the concentration of the uncoupled spin regions to be determined even when direct observation of the uncoupled spin NMR signal in a single pulse experiment would require an impractically long duration of signal averaging. We use this method to quantify residual graphitic carbon using <sup>13</sup>C CPMG NMR in poly(carbon monofluoride) samples synthesized by direct fluorination of carbon from various sources. Our detection limit for graphitic carbon in these materials is better than 0.05 mol%. The accuracy of the method is discussed and comparisons to other methods are drawn.https://www.mdpi.com/1422-0067/21/11/3938solid-state NMRquantitative NMRCPMGlayered carboncarbon monofluorideCFx
collection DOAJ
language English
format Article
sources DOAJ
author Brennan J. Walder
Todd M. Alam
spellingShingle Brennan J. Walder
Todd M. Alam
Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered Solids
International Journal of Molecular Sciences
solid-state NMR
quantitative NMR
CPMG
layered carbon
carbon monofluoride
CFx
author_facet Brennan J. Walder
Todd M. Alam
author_sort Brennan J. Walder
title Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered Solids
title_short Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered Solids
title_full Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered Solids
title_fullStr Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered Solids
title_full_unstemmed Quantification of Uncoupled Spin Domains in Spin-Abundant Disordered Solids
title_sort quantification of uncoupled spin domains in spin-abundant disordered solids
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-05-01
description Materials often contain minor heterogeneous phases that are difficult to characterize yet nonetheless significantly influence important properties. Here we describe a solid-state NMR strategy for quantifying minor heterogenous sample regions containing dilute, essentially uncoupled nuclei in materials where the remaining nuclei experience heteronuclear dipolar couplings. NMR signals from the coupled nuclei are dephased while NMR signals from the uncoupled nuclei can be amplified by one or two orders of magnitude using Carr-Meiboom-Purcell-Gill (CPMG) acquisition. The signal amplification by CPMG can be estimated allowing the concentration of the uncoupled spin regions to be determined even when direct observation of the uncoupled spin NMR signal in a single pulse experiment would require an impractically long duration of signal averaging. We use this method to quantify residual graphitic carbon using <sup>13</sup>C CPMG NMR in poly(carbon monofluoride) samples synthesized by direct fluorination of carbon from various sources. Our detection limit for graphitic carbon in these materials is better than 0.05 mol%. The accuracy of the method is discussed and comparisons to other methods are drawn.
topic solid-state NMR
quantitative NMR
CPMG
layered carbon
carbon monofluoride
CFx
url https://www.mdpi.com/1422-0067/21/11/3938
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