The high-pressure behavior of layered V2O5 is investigated using in si
tu Raman spectroscopy in a diamond anvil cell. Upon compression, the m
ode associated with the vanadyl V = O double bond at 997 cm(-1) soften
s and vanishes at about 10 GPa. Above 7 GPa, additional modes appear i
n the V-O stretching region, at lower wavenumbers than the V = O stret
ching oscillation. Such a behavior is interpreted as a pressure-induce
d five-to-six coordination change around the V5+ cations, leading to a
three-dimensional V2O5 lattice. Upon decompression, intermediate phas
es are recovered.