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Investigating structural properties and reaction mechanism of non-stoichiometric spinel LNMO via solid state NMR
In this study, 6,7 Li solid state nuclear magnetic resonance (ssNMR) has been used to characterize local disorder in LiNi 0.5 Mn 1.5 O 4 (LNMO) spinel cathodes and to understand their implications for the phase transformation mechanism during electrochemical cycling vs. lithium. By comparing NMR spe...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2023-11, Vol.11 (46), p.25612-25625 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | In this study, 6,7 Li solid state nuclear magnetic resonance (ssNMR) has been used to characterize local disorder in LiNi 0.5 Mn 1.5 O 4 (LNMO) spinel cathodes and to understand their implications for the phase transformation mechanism during electrochemical cycling vs. lithium. By comparing NMR spectra of LNMO samples with slightly varying transition metal stoichiometries, we demonstrate the high sensitivity of ssNMR in the indirect detection of transition metal order and its ability to identify disorder induced by stoichiometric variations. Secondly, we investigate the lithiation reaction mechanism of the non-stoichiometric transition metal-ordered LNMO spinel cathode by ex situ 7 Li NMR and highlight that its reaction process involves primarily two successive biphasic reactions. However, our results suggest that stoichiometrically induced transition metal disorder promotes a mixed solid solution and biphasic reaction mechanism. Besides an extended solid solution region, we evince that the biphasic reaction involves the presence of intermediate transient species that make it possible to bridge the miscibility gap between the Li 1 and Li 0.5 phases. These results go beyond our operando XRD results, underlining that local structural analysis by 7 Li ssNMR can provide valuable additional insights into the complex reaction mechanism that are difficult to access by other techniques. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/D3TA04649D |