Influence of reaction conditions on the electrochemical-hydrothermal synthesis of two ammonium vanadium phosphates: (NH4)2VO(HPO4)2·H2O and (NH4)2VO(V0.88P1.12O7)

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Lumei Liu, Xiqu Wang, Ranko Bontchev, Kent Ross and Allan J. Jacobson


Abstract

The new phase (NH4)2VO(HPO4)2·H2O, 1, has been synthesized by hydrothermal electrocrystallization at 100[thin space (1/6-em)]°C. 1 is triclinic, space group P1 with Z=2, a=7.2499(8), b=8.1244(9), c=8.6529(9) Å, α=73.472(2), β=80.085(2), γ=85.077(2)° and V=480.94(9) Å3. When the reaction temperature is increased to 110[thin space (1/6-em)]°C, 1 is completely transformed into the known compound (NH4)2VO(V0.88P1.12O7), 2. The layered compound NH4VOPO4·xH2O, 3, a new example of the well-known MxVOPO4·xH2O phase has also been prepared by the same technique.


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