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Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy

[Image: see text] While solid-state NMR spectroscopic techniques have helped clarify the local structure and dynamics of ionic conductors, similar studies of mixed ionic–electronic conductors (MIECs) have been hampered by the paramagnetic behavior of these systems. Here we report high-resolution (17...

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Autores principales: Halat, David M., Dervişoğlu, Rıza, Kim, Gunwoo, Dunstan, Matthew T., Blanc, Frédéric, Middlemiss, Derek S., Grey, Clare P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025823/
https://www.ncbi.nlm.nih.gov/pubmed/27538437
http://dx.doi.org/10.1021/jacs.6b07348
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author Halat, David M.
Dervişoğlu, Rıza
Kim, Gunwoo
Dunstan, Matthew T.
Blanc, Frédéric
Middlemiss, Derek S.
Grey, Clare P.
author_facet Halat, David M.
Dervişoğlu, Rıza
Kim, Gunwoo
Dunstan, Matthew T.
Blanc, Frédéric
Middlemiss, Derek S.
Grey, Clare P.
author_sort Halat, David M.
collection PubMed
description [Image: see text] While solid-state NMR spectroscopic techniques have helped clarify the local structure and dynamics of ionic conductors, similar studies of mixed ionic–electronic conductors (MIECs) have been hampered by the paramagnetic behavior of these systems. Here we report high-resolution (17)O (I = 5/2) solid-state NMR spectra of the mixed-conducting solid oxide fuel cell (SOFC) cathode material La(2)NiO(4+δ), a paramagnetic transition-metal oxide. Three distinct oxygen environments (equatorial, axial, and interstitial) can be assigned on the basis of hyperfine (Fermi contact) shifts and quadrupolar nutation behavior, aided by results from periodic DFT calculations. Distinct structural distortions among the axial sites, arising from the nonstoichiometric incorporation of interstitial oxygen, can be resolved by advanced magic angle turning and phase-adjusted sideband separation (MATPASS) NMR experiments. Finally, variable-temperature spectra reveal the onset of rapid interstitial oxide motion and exchange with axial sites at ∼130 °C, associated with the reported orthorhombic-to-tetragonal phase transition of La(2)NiO(4+δ). From the variable-temperature spectra, we develop a model of oxide-ion dynamics on the spectral time scale that accounts for motional differences of all distinct oxygen sites. Though we treat La(2)NiO(4+δ) as a model system for a combined paramagnetic (17)O NMR and DFT methodology, the approach presented herein should prove applicable to MIECs and other functionally important paramagnetic oxides.
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spelling pubmed-50258232016-09-19 Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy Halat, David M. Dervişoğlu, Rıza Kim, Gunwoo Dunstan, Matthew T. Blanc, Frédéric Middlemiss, Derek S. Grey, Clare P. J Am Chem Soc [Image: see text] While solid-state NMR spectroscopic techniques have helped clarify the local structure and dynamics of ionic conductors, similar studies of mixed ionic–electronic conductors (MIECs) have been hampered by the paramagnetic behavior of these systems. Here we report high-resolution (17)O (I = 5/2) solid-state NMR spectra of the mixed-conducting solid oxide fuel cell (SOFC) cathode material La(2)NiO(4+δ), a paramagnetic transition-metal oxide. Three distinct oxygen environments (equatorial, axial, and interstitial) can be assigned on the basis of hyperfine (Fermi contact) shifts and quadrupolar nutation behavior, aided by results from periodic DFT calculations. Distinct structural distortions among the axial sites, arising from the nonstoichiometric incorporation of interstitial oxygen, can be resolved by advanced magic angle turning and phase-adjusted sideband separation (MATPASS) NMR experiments. Finally, variable-temperature spectra reveal the onset of rapid interstitial oxide motion and exchange with axial sites at ∼130 °C, associated with the reported orthorhombic-to-tetragonal phase transition of La(2)NiO(4+δ). From the variable-temperature spectra, we develop a model of oxide-ion dynamics on the spectral time scale that accounts for motional differences of all distinct oxygen sites. Though we treat La(2)NiO(4+δ) as a model system for a combined paramagnetic (17)O NMR and DFT methodology, the approach presented herein should prove applicable to MIECs and other functionally important paramagnetic oxides. American Chemical Society 2016-08-19 2016-09-14 /pmc/articles/PMC5025823/ /pubmed/27538437 http://dx.doi.org/10.1021/jacs.6b07348 Text en Copyright © 2016 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Halat, David M.
Dervişoğlu, Rıza
Kim, Gunwoo
Dunstan, Matthew T.
Blanc, Frédéric
Middlemiss, Derek S.
Grey, Clare P.
Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy
title Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy
title_full Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy
title_fullStr Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy
title_full_unstemmed Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy
title_short Probing Oxide-Ion Mobility in the Mixed Ionic–Electronic Conductor La(2)NiO(4+δ) by Solid-State (17)O MAS NMR Spectroscopy
title_sort probing oxide-ion mobility in the mixed ionic–electronic conductor la(2)nio(4+δ) by solid-state (17)o mas nmr spectroscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025823/
https://www.ncbi.nlm.nih.gov/pubmed/27538437
http://dx.doi.org/10.1021/jacs.6b07348
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