Organic-inorganic hybrid films combine the basic properties of organic and inorganic materials and offer special advantages that enhance optical, thermal and mechanical properties. We have studied the temperature dependent photoluminescence (PL) of nanocrystalline gamma-CuCl hybrid films from 15K to room temperature in order to investigate the electronic transitions of the hybrid films. The I impurity bound exciton peak is the most intense emission peak at 15 K but the peak intensity decreases rapidly with increasing temperature due to the low binding energy of this exciton bound to an impurity center and above 80 K all three excitonic and biexcitonic peaks, except the Z(3) free exciton emission peak disappeared. The biexciton emission peak intensity follows a quadratic dependency on power in the excitation power range <10 kWcm(-2). The integrated Z(3) excitonic PL intensity is almost independent of the temperature below 80 K, while above 100 K the PL emission intensity decreases rapidly. Thermal quenching of the Z(3) free exciton PL emission in hybrid films has been observed. The full width at half maximum (FWHM) of the free exciton peak was investigated as a function of temperature and was explained by a theoretical model which considers the scattering of excitons with acoustic phonons and longitudinal optical phonons. The FWHM of the Z3 free exciton emission peak increases with increasing temperature, and a value of similar to 76 meV was deduced for the FWHM at room temperature, which is comparatively better than ZnO (106 meV) and GaN (100 meV) nanostructures. The Z(3) free exciton energy of the hybrid films exhibits a blue shift of 3 meV at 15 K compared to the bulk CuCl samples which may be due to a dead layer effect near the CuCl nanocrystal surface. The exciton energy also presents a blue shift of similar to 41 meV with increasing temperature from 15 K to room temperature. The results obtained for the gamma-CuCl hybrid films are comparable to those of vacuum evaporated and sputtered CuCl films reported in the literature. (C) 2014 Elsevier B.V. All rights reserved.