Abstract
Herein, the promising properties of open-structured NaV3O8 as a cathode material for Zn-ion batteries (ZIBs) are investigated. First-principles calculations predict the insertion of Zn2+ (0.74 Å) in NaV3O8 with an interlayer distance of ≈7 Å, enabling delivery of a high discharge capacity of 353 mAh g−1 at 70 mA g−1 (0.2 C) for 300 cycles in the operating window of 0.3−1.5 V in 1 m Zn(CF3SO3)2 aqueous solution. Operando synchrotron X-ray diffraction, X-ray absorption near edge structure spectroscopy, and first-principles calculations validate the insertion of Zn2+ into the NaV3O8 structure within the operation range. Moreover, operando synchrotron X-ray diffraction and operando Raman spectroscopy reveal the formation of layered zinc hydroxytriflate (Zn5(OH)8(CF3SO3)2∙xH2O) as a side reaction below 0.8 V on discharge (reduction) and its dissolution into the electrolyte above 0.8 V on charge (oxidation). The formation of the Zn hydroxytriflate interfacial layer increases the charge-transfer activation energy from 15.5 to 48 kJ mol−1, leading to kinetics fade below 0.8 V. The findings reveal the charge-storage mechanism for NaV3O8, which may also be applicable to other vanadate cathodes, providing new insights for the investigation and design of ZIBs.
| Original language | English |
|---|---|
| Article number | 2001595 |
| Journal | Advanced Energy Materials |
| Volume | 10 |
| Issue number | 40 |
| DOIs | |
| State | Published - 1 Oct 2020 |
| Externally published | Yes |
Keywords
- batteries
- intercalation
- operando
- vanadate
- zinc