Nanostructured CuO thin film electrodes prepared by spray pyrolysis: a simple method for enhancing the electrochemical performance of CuO in lithium cells
Nanostructured CuO thin films were prepared by using a spray pyrolysis method, copper acetate as precursor and stainless steel as substrate. The textural and structural properties of the films were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction...
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Veröffentlicht in: | Electrochimica acta 2004-10, Vol.49 (26), p.4589-4597 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Nanostructured CuO thin films were prepared by using a spray pyrolysis method, copper acetate as precursor and stainless steel as substrate. The textural and structural properties of the films were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The SEM images revealed thorough coating of the substrate and thickness of 450–1250
nm; the average particle size as determined from the AFM images ranged from 30 to 160
nm. The XRD patterns revealed the formation of CuO alone and the XPS spectra confirmed the presence of Cu
2+ as the main oxidation state on the surface. The films were tested as electrodes in lithium cells and their electrochemical properties evaluated from galvanostatic and step potential electrochemical spectroscopy (SPES) measurements. The discharge STEP curves exhibited various peaks consistent with the processes CuO ⇔ Cu
2O ⇔ Cu and with decomposition of the electrolyte, a reversible process in the light of the AFM images. The best electrode exhibited capacity values of 625
Ah
kg
−1 over more than 100 cycles. This value, which involves a CuO ⇔ Cu reversible global reaction, is ca. 50% higher than that reported for bulk CuO. The nanosize of the particles and the good adherence of the active material to the substrate are thought to be the key factors accounting for the enhanced electrochemical activity found. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2004.05.012 |