“…All patterns of pure MoO 3 and mixed oxide samples a‐d showed a group of sharp diffractions of orthorhombic MoO 3 (α‐MoO 3 , JCPDS#35‐0609) at 2θ=12.77, 23.31, 25.75, 27.30, 29.43, 33.75, 35.45, 39.32, 46.51 and 49.37° which correspond to (020), (110), (040), (021), (130), (111), (041), (060), (061) and (002) crystal facets (α‐MoO 3 , JCPDS#35‐0609). [ 20 , 21 ] On the other hand, the XRD pattern of CdO clearly displayed five very strong diffraction peaks at 2θ=33.07° (111), 38.34° (200), 55.30° (220), 65.96° (311) and 69.26° (222) which belong to face‐centred system (Monteponite CdO, JCPDS # 5‐0640) as shown in Figure 1 e.[ 22 , 23 ] Three distinct diffraction peaks can be observed in patterns b‐d of mixed MoO 3 ‐CdO samples at 2θ=29.25° (112), 31.99° (004) and 34.38° (200), which could be related to the formation of tetragonal phase CdMoO 4 in these mixtures (JCPDS # 07–0209). [ 24 , 25 , 26 ] The crystallite size of the obtained different phases in these samples, that is, α‐MoO 3 , CdO and CdMoO 4 , was calculated using the Scherrer equation.…”