Abstract

The wavelength dependence of the third-order nonlinear optical susceptibilities, χ(3), of the Au:TiO2 composite films with Au concentration varying from 15% to 60% (volume fraction), was measured by a degenerate four-wave mixing (DFWM) technique using a probe laser with a pulse width of 200 fs. It was found that, with the wavelength of the probe laser close to the surface plasmon resonance (∼680 nm), both the χ(3) and the figure of merit, χ(3)/α (α is optical absorption coefficient) were significantly enhanced. The maximum value of the χ(3) was 6×10−7 esu and occurred at an Au concentration of about 38%. Femtosecond time-resolved DFWM measurements revealed that the response time of the optical nonlinearity in the Au:TiO2 films is extremely fast. The time-resolved DFWM results suggest that the main physical mechanism involved in the optical nonlinearity in Au:TiO2 films on the femtoseconds time scale is the interband electric–dipole transition, and the hot electron excitation only partially contributes to the χ(3) on the femtosecond time scale and it becomes dominant only in the picosecond region.

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