“…Zinc Oxide ZnO, where the location of the vibrational modes located at 105, 385, 445, 585 and 663 cm -1 are associated with the vibrational active modes of the Wurtzite phase of ZnO (Ruiz et al, 2011) the dominant peak at 445 cm -1 is attributed to high-frequency phonons from oxygen atoms (Fletcher et al, 2014), and E1 (LO) mode at 585 cm -1 is associated with interstitial zinc and oxygen vacancies, the E2 L peak at 105 cm -1 is associated with the vibrations of the zinc (Scepanovic et al, 2009), the vibrational mode E2 high -E2 low at 337 cm -1 is associated with multifononic processes (Londoño-Calderón et al, 2012) and finally the vibrational mode A 1 TO at 385 cm -1 is associated with intrinsic defects (Sundara Venkatesh et al, 2016), for the ZnS the additional presence of two resonant raman lines is observed in 217 and 350 cm -1 that correspond to the active vibrational modes of the ZnS, the spectrum shows the dominant peak in 350 cm -1 identified as a mode T2 (LO) of first order [20] (Milekhin et al, 2012), the LO mode in 217 cm -1 is attributed to the second order of raman scattering (Fairbrother et al, 2014). The heterostructure ZnO/ZnS/CuS locates the characteristic peaks that are associated with the presence of ZnO, ZnS and CuS and the appearance of the new peak that denotes the presence of the coveline phase of CuS at 165 cm -1 and 465 cm -1 (Baert et al, 2013). The photocatalytic test was performed with the degradation of MB (methylene blue), and MO (methyl orange).…”