In this article we show the fabrication by a dry approach at mild temperature (< 150 ºC) of a photoluminescence white light emitting hybrid layer. The white light emitter is obtained by evaporation of two photoluminescent small molecules, a blue (1,3,5-triphenyl-2-pyrazoline TPP) and an orange (rubrene) dye within the porous of a SiO 2 host film fabricated by glancing angle deposition (GLAD). Fluorescencence (Föster) resonant energy transfer between the two organic dyes allows the emission of the combined system upon excitation of the TPP molecule at wavelength of 365 nm. The distribution of the organic molecule within the host layer is analysed as a function of the substrate temperature and vacuum conditions and the required conditions for the white emission determined by finely controlling the TPP:Rubrene ratio. The full vacuum processing of the hybrid layers provides a straightforward route for the incorporation of the white light emitters as optical defect within one-dimensional Bragg microcavities. As consequence, directional emission of the system is achieved which allows the development of wide-range in situ tunable photoluminescent devices.