Comparative Study of Li and Na Electrochemical Reactions with Iron Oxide Nanowires
Description
This study emphasizes optimization of Fe2O3 and Fe3O4 nanowire conversion electrodes by directly-growing them on current collectors, preparing them as single crystals, and coating their surfaces with conductive carbon coatings. The systems with the least polarization during Li-ion cycling are then tested as electrodes for Na-ion chemistry. Precipitation of nanograined material during the first cycle reduces the polarization associated with Li insertion upon subsequent cycles. After the first cycle, delithiation primarily contributes to polarization associated with the conversion reaction with lithiation occurring close to the equilibrium potential. The initial reduction reaction does not proceed to completion for Na chemistries. Electron microscopy reveals significant Na insertion that occurs along with the formation of defect networks. However, the results indicate that an insufficient amount is present to form critical nuclei necessary to induce the conversion reaction
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2013.12.007Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2013.12.007;
- PII
- S0013-4686(13)02441-9;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 118
- Journal Page Range
- p. 143-149
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46028105
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CRYSTALS; FERRITES; IRON OXIDES; NANOWIRES; POLARIZATION; PRECIPITATION; TRANSMISSION ELECTRON MICROSCOPY
- Descriptors DEC
- CHALCOGENIDES; ELECTRON MICROSCOPY; FERRIMAGNETIC MATERIALS; IRON COMPOUNDS; MAGNETIC MATERIALS; MATERIALS; MICROSCOPY; NANOSTRUCTURES; OXIDES; OXYGEN COMPOUNDS; SEPARATION PROCESSES; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.