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In a nonlinear three-wave mixing process, the interacting waves can accumulate an adiabatic geometric phase (AGP) if the nonlinear coefficient of the crystal is modulated in a proper manner along the nonlinear crystal. This concept was studied so far only for the case in which the pump wave is much stronger than the two other waves, hence can be assumed to be constant. Here we extend this analysis for the fully nonlinear process, in which all three waves can be depleted and we show that the sign and magnitude of the AGP can be controlled by the period, phase and duty cycle of the nonlinear modulation pattern. In this fully nonlinear interaction, all the states of the system can be mapped onto a closed surface. Specifically, we study a process in which the eigenstate of the system follows a circular rotation on the surface. Our analysis reveals that the AGP equals to the difference between the total phase accumulated along the circular trajectory and that along its vertical projection, which is universal for the undepleted (linear) and depleted (nonlinear) cases. Moreover, the analysis reveals that the AGPs in the processes of sum-frequency generation and difference-frequency generation have opposite chirality. Finally, we utilize the AGP in the fully nonlinear case for splitting the beam into different diffraction orders in the far field.
We implement a simple and powerful approach to characterize the domain distribution in the bulk of quadratic ferroelectric crystals via far-field second-harmonic spectroscopy. The approach is demonstrated in a lithium tantalate sample with periodic e
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