Nanostructured Fe2O3 and CuO composite electrodes for Li ion batteries synthesized and deposited in one step
► Iron and copper oxides as materials for negative electrodes for Li ion batteries. ► Precursor composed of dissolved metal salts in presence of PVdF binder successfully electrosprayed. ► Nanosized oxide particles directly and homogeneously dispersed with PVdF onto the electrode. ► Electrostatic spr...
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Published in: | Journal of power sources Vol. 196; no. 15; pp. 6425 - 6432 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
01-08-2011
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | ► Iron and copper oxides as materials for negative electrodes for Li ion batteries. ► Precursor composed of dissolved metal salts in presence of PVdF binder successfully electrosprayed. ► Nanosized oxide particles directly and homogeneously dispersed with PVdF onto the electrode. ► Electrostatic spray pyrolysis suitable for the direct production of nanocomposite electrode coatings.
Nanostructured composite electrodes based on iron and copper oxides for applications in Li-ion batteries are produced by Electrostatic spray pyrolysis (ESP). The electrodes are directly formed by electrospraying precursor solutions containing either iron or copper salts dissolved in N-methylpyrrolidone (NMP) together with polyvinylidene fluoride (PVdF) as binder. The morphology and the structure of the deposited electrodes are investigated by X-ray diffraction (XRD) and Transmission electron microscopy (TEM), which show that sub-micrometric deposits are formed as a composite of oxide nanoparticles of a few nanometers in a PVdF polymer matrix. Electrochemical characterization by cyclic voltammetry (CV) and galvanostatic charge–discharge tests demonstrate that the conversion reactions in these electrodes enable initial discharge capacities of about 800mAhg−1 and 1550mAhg−1 for CuO and Fe2O3, respectively. The capacity retention in both cases needs further improvements. |
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ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2011.03.066 |