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
Hauptverfasser: Kumagai, Naoaki, Kumagai, Nobuko, Umetzu, Yoshio, Tanno, Kazuo, Pereira-Ramos, J.P.
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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.
ISSN:0167-2738
1872-7689
DOI:10.1016/0167-2738(96)00327-X