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Springer proceedings in physics

Resonant Optical Kerr Response with Ultrashort Decay Time by Nonlocal Wave Coupling of Light and Excitons

Masayoshi Ichimiya, Takayuki Umakoshi, Hiroyuki Murata, Takashi Kinoshita, Hajime Ishihara, Masaaki Ashida

Published Jan 1, 2015• 0 citations
Publisher
DOI
10.1007/978-3-319-13242-6_85

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We observe ultrafast and large nonlinear optical responses of a semiconductor thin film where excitons are weakly confined and their center-of-mass motion is quantized. The observed degenerate four-wave mixing (DFWM) signal of a GaAs double-hetero-structure layer exhibits an anomalous thickness-dependence, and is much enhanced at the thickness of 110nm. The decay time of the response is the order of ps, which depends on the thickness of the layer and on the number of the layer. These phenomena are elucidated by the theory of the nonlocal interaction between excitonic states and the light beyond the long wavelength approximation regime. The enhancement at the thickness is due to the size-resonant enhancement of the internal field with a nano-scale spatial structure, where the second quantized level of the exciton center-of-mass motion mainly contributes to the large response at the thickness. We, furthermore, demonstrate ultrafast response in a reflective type nonlinear polarization rotation switch with the 110nm thick three double-hetero. The signal intensity of 20% for the reflective pulse was obtained at a pump intensity of 10nJ/cm2, and the decay time is 1.5ps at low temperatures. These results provide a novel design of a semiconductor structure in order to obtain both large and ultrafast nonlinear response that is suitable for device application.
We investigate the response of photonic crystal (PC) atoms with Kerr nonlinearity to the excitation of ultrashort optical pulses. Surprisingly, it is found that PC atoms with sharp resonant peaks in frequency spectrum (or with large quality factors) can respond to ultrashort pulses very rapidly when Kerr nonlinearity is introduced. More interestingly, the response time under high-power densities can be even shorter than the duration of the pump pulse. It is revealed that the nonlinearity induced broadening of dynamical frequency spectrum is responsible for the ultrafast response time, implying the possibility of ultrafast all-optical switching.