“…Despite this, the Raman spectrum is typical of α‐V 2 O 5 , with its main features at 147, 285, 305, 405, 702, and 995 cm −1 , whereas the monoclinic VO 2 phase has a set of strong well-resolved bands, located at 194, 224, 262, 310, 387, and 612 cm −1 46 . Among these, the mode at 147 cm −1 (ω o(2) ) is associated with the in‐phase oscillation of vanadium (shear-like distortions), the band at 702 cm −1 (ω v-o(2)-v) ) is assigned to the asymmetric stretching of V–O (2) –V bridges, and the highest intensity feature at 995 cm −1 (ω v=o(1) ) corresponds to the stretching vibrations of V=O (1) vanadyl bonds in V 2 O 5 28 , 36 , 44 , 46 . Besides, the low-energy peaks at 194 and 224 cm −1 (ω v1 and ω v2 ) correspond to the motion of vanadium atoms along the c‐axis of the VO 2 crystal (stretching motion of V–V dimers), while the high-energy one at 612 cm −1 (ω o ) is associated with the V–O vibrations 32 , 36 , 46 .…”