2015
DOI: 10.1016/j.electacta.2015.05.169
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The use of deuterated ethyl acetate in highly concentrated electrolyte as a low-cost solvent for in situ neutron diffraction measurements of Li-ion battery electrodes

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Cited by 14 publications
(15 citation statements)
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“…Yoshida et al [21] also showed that the atypically large salt concentration increased the oxidative stability of glyme solvents. Similarly, Petibon et al showed that NMC(442)/graphite cells with ester based electrolytes and large LiFSi concentration cycle quite well up to 4.4 V [22] and 4.7 V [23]. This change of reactivity was assigned to a peculiar solution structure [20,19], similarly to the findings of Nie et al [16].…”
Section: Introductionsupporting
confidence: 62%
“…Yoshida et al [21] also showed that the atypically large salt concentration increased the oxidative stability of glyme solvents. Similarly, Petibon et al showed that NMC(442)/graphite cells with ester based electrolytes and large LiFSi concentration cycle quite well up to 4.4 V [22] and 4.7 V [23]. This change of reactivity was assigned to a peculiar solution structure [20,19], similarly to the findings of Nie et al [16].…”
Section: Introductionsupporting
confidence: 62%
“…In this sense, a low-cost deuterated ethyl acetate based electrolyte suitable for in-situ neutron diffraction has been reported, showing comparable electrochemical performance and signalto-noise ratio of neutron diffraction patterns to more expensive conventional deuterated electrolytes [24]. Most importantly, the electrochemical performance of the in-situ cell should be similar to that of the real (commercial) battery, so that the structural information extracted can be directly compared to that found within the technological applications.…”
Section: In-situ Studiesmentioning
confidence: 99%
“…It may be possible to try using highly concentrated electrolyte solutions[27][28][29] to achieve these voltages in sodium-ion batteries in order to determine the mechanism at 5.3 V in the future. It should be noted that the computational calculations suggest that the V 4+ can be further desodiated to 5.3 V 13 but these voltages require specialised electrolytes and are not easily accessible at this stage.…”
mentioning
confidence: 99%