Abstract
The layered V2O5 cathode exhibits appealing features of multiple electron redox processes and versatile cation-storage capacities. However, the huge volume respiration induces structural collapse and limits its commercial-scale deployment. Herein, a scalable water-bath strategy is developed to tailor the (001) spacing of the bulk V2O5 from the original 4.37 Å to its triple value (14.2 Å). The intercalated polyaniline (PANI) molecules act as pillars in the V2O5 interlayer, thus affording the abundant storage sites and enhanced cation diffusivities of Li+, Na+, or hydrated Zn2+. Upon various cations (de-)intercalation, transmission-mode operando X-ray diffraction is employed to document the zero-strain behavior of the PANI-intercalated V2O5. This scalable intercalation-polymerization strategy, coupled with the compatibility study of the ionic radius and the c-lattice for the layered structure, enables the rational engineering of the intercalation-type cathodes toward facile reaction kinetics.
| Original language | English |
|---|---|
| Article number | 2100164 |
| Journal | Advanced Functional Materials |
| Volume | 31 |
| Issue number | 22 |
| DOIs | |
| State | Published - 26 May 2021 |
Keywords
- interlayer spacing
- lattice breathing
- operando X-ray diffraction
- scalable strategy
- vanadium pentoxide
- zero-strain behavior
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