Observation of the two-photon transition enhanced first hyperpolarizability spectra in cinnamaldehyde derivatives: A femtosecond regime study

The application of nonlinear optical effects in optoelectronic devices is still scarce because the irradiance threshold necessary to induce a specific effect is very high. In this context, knowing the frequency-resolved first order molecular hyperpolarizability (beta) is essential to identifying regions where this response is intense enough to allow for applications in commercial devices. Thus, herein, we have determined the beta spectral dependence of five new push-pull cinnamylidene acetophenone derivatives using femtosecond laser-induced Hyper-Rayleigh Scattering (HRS). A considerable increase in beta values was observed in molecules. We found remarkable beta values in regions near the two-photon resonance, which are mediated by electron withdrawing and donating groups. This effect was mapped using wavelength-tunable femtosecond Z-scan technique. Furthermore, it was modeled in light of the sum-over-states approach for the second- and third-order nonlinearities. Finally, our outcomes suggest a strategy to obtain large beta values mediated by the 2PA transition.

Automated summary

The frequency-resolved first order molecular hyperpolarizability (beta) of five new push-pull cinnamylidene acetophenone derivatives was determined using femtosecond laser-induced Hyper-Rayleigh Scattering (HRS). Significant increase in beta values was observed in molecules, particularly in regions near the two-photon resonance mediated by electron withdrawing and donating groups. This effect was mapped using wavelength-tunable femtosecond Z-scan technique and modeled based on the sum-over-states approach for the second- and third-order nonlinearities. The results suggest a strategy to obtain large beta values mediated by the 2PA transition.