Abstract
Virtually all intercalation compounds exhibit significant changes in unit cell volume as the working ion concentration varies. NaxFePO4 (0 < x < 1, NFP) olivine, of interest as a cathode for sodium-ion batteries, is a model for topotactic, high-strain systems as it exhibits one of the largest discontinuous volume changes (∼17% by volume) during its first-order transition between two otherwise isostructural phases. Using synchrotron radiation powder X-ray diffraction (PXD) and pair distribution function (PDF) analysis, we discover a new strain-accommodation mechanism wherein a third, amorphous phase forms to buffer the large lattice mismatch between primary phases. The amorphous phase has short-range order over ∼1nm domains that is characterized by a and b parameters matching one crystalline end-member phase and a c parameter matching the other, but is not detectable by powder diffraction alone. We suggest that this strain-accommodation mechanism may generally apply to systems with large transformation strains.
| Original language | English |
|---|---|
| Pages (from-to) | 1696-1702 |
| Number of pages | 7 |
| Journal | Nano Letters |
| Volume | 17 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 8 2017 |
Keywords
- batteries
- olivines
- operando
- pair-distribution function
- Phase transformations
- sodium iron phosphate
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