Spatio-temporal focusing of an ultrafast pulse through a multiply scattering medium.

Pulses of light propagating through multiply scattering media undergo complex spatial and temporal distortions to form the familiar speckle pattern. There is much current interest in both the fundamental properties of speckles and the challenge of spatially and temporally refocusing behind scattering media. Here we report on the spatially and temporally resolved measurement of a speckle field produced by the propagation of an ultrafast optical pulse through a thick strongly scattering medium. By shaping the temporal profile of the pulse using a spectral phase filter, we demonstrate the spatially localized temporal recompression of the output speckle to the Fourier-limit duration, offering an optical analogue to time-reversal experiments in the acoustic regime. This approach shows that a multiply scattering medium can be put to profit for light manipulation at the femtosecond scale, and has a diverse range of potential applications that includes quantum control, biological imaging and photonics.

Controlling the polarization eigenstate of a quantum dot exciton with light.

We demonstrate optical control of the polarization eigenstates of a neutral quantum dot exciton without any external fields. By varying the excitation power of a circularly polarized laser in microphotoluminescence experiments on individual InGaAs quantum dots we control the magnitude and direction of an effective internal magnetic field created via optical pumping of nuclear spins. The adjustable nuclear magnetic field allows us to tune the linear and circular polarization degree of the neutral exciton emission. The quantum dot can thus act as a tunable light polarization converter.

Time-dependent photoionization of azulene: competition between ionization and relaxation in highly excited states.

Pump-probe photoionization has been used to map the relaxation processes taking place from highly vibrationally excited levels of the S(2) state of azulene, populated directly or via internal conversion from the S(4) state. Photoelectron spectra obtained by 1+2(') two-color time-resolved photoelectron imaging are invariant (apart from in intensity) to the pump-probe time delay and to the pump wavelength. This reveals a photoionization process which is driven by an unstable electronic state (e.g., doubly excited state) lying below the ionization potential. This state is postulated to be populated by a probe transition from S(2) and to rapidly relax via an Auger-like process onto highly vibrationally excited Rydberg states. This accounts for the time invariance of the photoelectron spectrum. The intensity of the photoelectron spectrum is proportional to the population in S(2). An exponential energy gap law is used to describe the internal conversion rate from S(2) to S(0). The vibronic coupling strength is found to be larger than 60+/-5 microeV.

Factorization of numbers with the temporal Talbot effect: optical implementation by a sequence of shaped ultrashort pulses.

We report on the successful operation of an analogue computer designed to factor numbers. Our device relies solely on the interference of classical light and brings together the field of ultrashort laser pulses with number theory. Indeed, the frequency component of the electric field corresponding to a sequence of appropriately shaped femtosecond pulses is determined by a Gauss sum which allows us to find the factors of a number.

Quantum state measurement using coherent transients.

We present the principle and experimental demonstration of time resolved quantum state holography. The quantum state of an excited state interacting with an ultrashort chirped laser pulse is measured during this interaction. This has been obtained by manipulating coherent transients created by the interaction of femtosecond shaped pulses and rubidium atoms.

Femtosecond spectral electric field reconstruction using coherent transients.

We have implemented a new approach for measuring the time-dependent intensity and phase of ultrashort optical pulses. It is based on the interaction between shaped pulses and atoms, leading to coherent transients.

Realization of a time-domain Fresnel lens with coherent control.

Perturbative chirped pulse excitation leads to oscillations of the excited state amplitude. These coherent transients are governed by interferences between resonant and off-resonant contributions. Control mechanisms in both frequency and time domain are used to modify these dynamics. First, by applying a phase step in the spectrum, we manipulate the phase of the oscillations. By direct analogy with Fresnel zone lenses, we then conceive highly phase-amplitude modulated pulse shapes that slice destructive interferences out of the excitation time structure and enhance the final population.