| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 180346 | Electrochemistry Communications | 2011 | 4 Pages |
First principles calculations are used to anticipate the electrochemistry of polyoxoanionic materials consisting of XO4 − yAy (A = F, N) groups. As an illustrative case, this work focuses on the effect of either N or F for O substitution upon the electrochemical properties of Li2FeSiO4. Within the Pmn21–Li2FeSiO4 structure, virtual models of Li2Fe22.5+SiO3.5N0.5 and Li1.5Fe2+SiO3.5F0.5 have been analyzed. We predict that the lithium deinsertion voltage associated to the Fe3+/Fe4+ redox couple is decreased by both substituents. The high theoretical specific capacity of Li2FeSiO4 (330 mAh/g) could be retained in N-substituted silicates thanks to the oxidation of N3− anions, whilst Li1.5Fe2+SiO3.5F0.5 has a lower specific capacity inherent to the F substitution. Substitution of N/F for O will respectively improve/worsen the electrode characteristics of Li2FeSiO4.
► The electrochemistry of polyoxoanionic materials consisting of XO4–yAy (A=F, N) groups is investigated by DFT methods. ► For the cathode material Li2FeSiO4, virtual models of Li2Fe22.5+SiO3.5N0.5 and Li1.5Fe2+SiO3.5F0.5 are investigated. ► It is found that the lithium deinsertion voltage of the Fe3+/Fe4+ redox couple is decreased by both substituents. ► Li2Fe22.5+SiO3.5N0.5 retains the high theoretical specific capacity of Li2FeSiO4 thanks to the oxidation of N3– anions. ► Substitution of N, F for O in will respectively improve/worsen the electrode characteristics of Li2FeSiO4.
