Synthesis of hexagonal form of tungsten trioxide and electrochemical lithium insertion into the trioxide
The tungsten trioxide hydrate, WO 3 · yH 2O ( y = 0.8−1.1) with the hexagonal tungsten bronze (HTB) structure has been prepared by acidification of lithium tungstate solution with strong acid at a concentration of 0.5–1 M and at a temperature of 100 °C. On the other hand, hydrothermal synthesis of a...
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Veröffentlicht in: | Solid state ionics 1996, Vol.86, p.1443-1449 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The tungsten trioxide hydrate, WO
3 ·
yH
2O (
y = 0.8−1.1) with the hexagonal tungsten bronze (HTB) structure has been prepared by acidification of lithium tungstate solution with strong acid at a concentration of 0.5–1 M and at a temperature of 100 °C. On the other hand, hydrothermal synthesis of an acidified lithium tungstate solution at temperatures of 150–200 °C leads to the formation of
xLi
2O · WO
3 ·
yH
2O (
x = 0.25−0.30,
y = 0.6−0.8) having the HTB structure. The dehydration of WO
3 ·
yH
2O and
xLi
2O · WO
3 ·
yH
2O around 350 °C leads to the dehydrated trioxides, hexagonal WO
3 and
xLi
2O · WO
3 with the HTB structure, respectively. The tungsten trioxides prepared have been characterized by X-ray diffractometry, thermogravimetric analysis and electrochemical method. The cyclic voltammetric and galvanostatic measurements revealed that a reversible lithium intercalation into the crystal lattice of hexagonal WO
3 takes place with charge-discharge cycling. |
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ISSN: | 0167-2738 1872-7689 |
DOI: | 10.1016/0167-2738(96)00327-X |