Abstract

It is widely accepted that quadratic nonlinear processes, such as parametric generation or amplification, require the use of materials with a high degree of ordering. In some occasions, such ordering is found at a nanoscale, and in other cases, the order is at a micron scale. When such ordering is not intrinsic to the material, one may introduce a periodical distribution within the nonlinear material to, for instance, compensate the phase mismatch. In that event, the final material would be, in general, composed of two types of domains, distributed periodically across the entire material, one with a given nonlinear coefficient, and the other with the same coefficient with opposite sign. In principle, one would expect that small deviations from the adequate period, or some dispersion in the size of the domains, would lead to a cancellation of the coherent nonlinear process of three wave mixing. However, very recently, it was observed that with polycrystalline samples fabricated with a random orientation of zinc selenide (ZnSe) crystalline domains, when the average size of the domains was close to one coherence length (lcc), difference frequency generation grew linearly with the total length of the sample. Similar observations were reported some years ago from SBN needlelike crystalline domains and with the use of rotationally twinned crystals of ZnSe. In all these observations, the efficiency of the process seemed to be strongly linked to an average size of the domain close to the optimal value for quasi-phase matching with periodical inverted domains. In the present work, we study the process of phase matching to compensate the material dispersion in refractive index in materials where there is no structural ordering. We consider, here, one-dimensional (1-D) structures composed of planar layer domains with a well-defined orientation of the nonlinear susceptibility within the domain. Such domains, however, are randomly ordered and their thickness may vary with a Gaussian distribution around a given average size. In other words, the entire structure exhibits no ordering with respect to the orientation of the dipoles and the domains are allowed to have any possible thickness. Contrary to what one could expect, we observe that an increase in the amount of disorder is not necessarily detrimental with respect to the efficiency of a second harmonic generation (SHG) process. Moreover, the linear growth of the second harmonic (SH) intensity with respect to the number of domains is seen when the average size of the domains is close to one lc, but also, for any other average thickness of such domains. We are able to establish a clear link between the disorder inherent to the structure and the linear growth of the intensity with respect to the number of domains. It is also possible to obtain such type of nonlinear processes in random media where there is an index contrast between the several nonlinear domains. Recently significant progress has been made in the development in structured nonlinear materials. In the present paper we will review the performance of some of these nonlinear photonic materials that, eventually, could be implemented in a disordered configuration where the proposals of the present work could be experimentally tested

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