In this article, the effects of 6 MeV energy of X-ray radiation on polycarbonate polymeric lms were investigated. The induced alterations are assessed using several methodologies: FTIR spectroscopy, contact angle measurements, surface roughness assessment, UV/Vis spectroscopy, and luminescence emission spectroscopy. As well, using the basic sets in the ground state of the polycarbonate structure, the vibrational analysis has been carried out using the density functional theory (DFT). The FTIR spectra display that the X-ray irradiation produces surface chemical alterations in the irradiated lms due to successive degradation mechanisms due to the decrease in the detected band peaks. The basis sets that were calculated using the DFT method are in good agreement with the experimentally observed spectra.The frontier molecular orbital energies are used to assess the molecule's energy gap (HOMO-LUMO). The value of the frontier energy gap re ects the chemical reactivity and intermolecular charge transfer that take place within the molecule. The surface wettability behaviors were amended due to the decrease in the contact angle values of irradiated lms. This leads to an increase in the surface roughness and surface free energy. X-ray irradiation can enhance the surface goodness of polycarbonate lms and control their surface properties to be used in biocompatibility applications. The optical properties of irradiated lms show modi cations in the studied optical parameters. The absorbance spectra exhibited a shift in the absorption edge of the irradiated samples compared with the pristine one. This shift indicates the decreases in the band gap energy of irradiated samples. For direct transitions, the band gap decreased from 4.03 to 3.125 eV, and for indirect transitions, it decreased from 3.5 0 to 2.65 eV. This result was attributable to the formation of defects and the creation of complex charge transfer due to Xray irradiation. The photoluminescence emission spectra show that the peak intensities are obviously in uenced by increasing the irradiation doses. This is attributable to the band-band transition, donor/acceptor pairs, and bound to free transition, which correlated to the received absorbed dose.of oxidation products, polar components, creation of ionic chemical species, gaseous and water molecules production, loss of volatile fragments and the generation of free radicals that can cause scission and/or cross-linking mechanisms [11][12][13]. The two mechanisms are reliant on the polymer's nature and the environmental conditions, and consequently, scissioning and crosslinking are competing phenomena. Moreover, the natural behaviors of these changes in the irradiated polymeric lms depend on the interfering factors, like the composition of the polymer and its molecular weight, and also on the types of radiation and its energy [14][15][16]. Polymers are gaining popularity due to their numerous advantages, including ease of processing, and several degrees of elasticity or stiffness. They are also more affordable overall d...