Loading…
Anodic behaviour and X-ray photoelectron spectroscopy of ternary tin oxides
The compounds SrSnO 3, BaSnO 3 and Ca 2SnO 4 have been synthesized by solid-state and/or sol–gel methods, characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) and their electrochemical properties studied as cathodes versus Li metal i...
Saved in:
Published in: | Journal of power sources 2005-01, Vol.139 (1), p.250-260 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The compounds SrSnO
3, BaSnO
3 and Ca
2SnO
4 have been synthesized by solid-state and/or sol–gel methods, characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) and their electrochemical properties studied as cathodes versus Li metal in the range 0.005–1.0
V. ASnO
3 (A = Sr, Ba), adopt the perovskite structure whereas Ca
2SnO
4 has the Sr
2PbO
4 structure. The discharge capacities (mAh
g
−1) (moles of equivalent Li) on the 20th cycle at a current rate of 30
mA
g
−1 are: SrSnO
3 (solid-state) (144 (1.4)), SrSnO
3 (sol–gel) (222 (2.1)), BaSnO
3 (solid-state) (190 (2.2)), BaSnO
3 (sol–gel) (156 (1.8)) and Ca
2SnO
4 (247 (2.4)). The SrSnO
3 (sol–gel) with nano-particle morphology displays better galvanostatic cycling performance than SrSnO
3 (solid-state). The cycling behaviour of SrSnO
3 and BaSnO
3 is inferior to that of Ca
2SnO
4 and CaSnO
3, which demonstrates that ‘Ca’ is superior as a matrix element than Sr or Ba. The inferior electrochemical performance of Ca
2SnO
4 in comparison to CaSnO
3 reveals that the higher Ca:Sn ratio in the former is not advantageous and the perovskite structure is preferable to that of Sr
2PbO
4 structure. The coulombic efficiencies are >98% in all cases. Cyclic voltammetry (CV) compliments the observed cycling behaviour. |
---|---|
ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2004.06.057 |