Correlative Imaging of Motoneuronal Cell Elasticity by Pump and Probe Spectroscopy.

Because of their role of information transmitter between the spinal cord and the muscle fibers, motor neurons are subject to physical stimulation and mechanical property modifications. We report on motoneuron elasticity investigated by time-resolved pump and probe spectroscopy. A dual picosecond geometry simultaneously probing the acoustic impedance mismatch at the cell-titanium transducer interface and acoustic wave propagation inside the motoneuron is presented. Such noncontact and nondestructive microscopy, correlated to standard atomic force microscopy or a fluorescent labels approach, has been carried out on a single cell to address some physical properties such as bulk modulus of elasticity, dynamical longitudinal viscosity, and adhesion.

Generation and detection of acoustic solitons in crystalline slabs by laser ultrasonics.

Acoustic solitons have been recently observed in different systems (Si, Sapphire, MgO, alpha-quartz). Such acoustic waves could lead to sub-picosecond acoustic pulses. In this paper, we report on the formation of acoustic solitons in a GaAs crystalline slab. A short picosecond acoustic pulse is generated by absorption of a femtosecond laser pulse in an aluminum thin film deposited on one side of the slab. This strain pulse travels through the sample up to the opposite side where it is detected by a time delayed laser pulse reflected by an aluminum transducer. We use interferometric detection to measure independently the real and imaginary parts of the relative change in optical reflectivity induced by the acoustic pulse. We find that, at low temperature and with a laser pump pulse energy of 10 nJ, an acoustic soliton clearly separates from the acoustic pulse in GaAs slab. The soliton shape is compared with numerical simulations for different excitation conditions. From the very unique properties of solitons, we infer a soliton pulse duration of about 2.3 ps which corresponds to a spatial extent of only 12 nm.

Nonadiabatic alignment of asymmetric top molecules: rotational revivals.

The rotational revival structure of asymmetric top molecules, following irradiation by an intense picosecond laser pulse, is explored theoretically and experimentally. Numerically we solve nonperturbatively for the rotational dynamics of a general asymmetric top subject to a linearly polarized intense pulse, and analyze the dependence of the dynamical alignment on the field and system parameters. Experimentally we use time-resolved photofragment imaging to measure the alignment of two molecules with different asymmetry, iodobenzene, and iodopentafluorobenzene. Our numerical results explain the experimental observations and generalize them to other molecules. The rotational revival structure of asymmetric tops differs qualitatively from the intensively studied linear top case. Potentially it provides valuable structural information about molecules.

Observation of enhanced field-free molecular alignment by two laser pulses.

We show experimentally that field-free alignment of iodobenzene molecules, induced by a single, intense, linearly polarized 1.4-ps-long laser pulse, can be strongly enhanced by dividing the pulse into two optimally synchronized pulses of the same duration. For a given total energy of the two-pulse sequence the degree of alignment is maximized with an intensity ratio of 1:3 and by sending the second pulse near the time where the alignment created by the first pulse peaks.

Nonadiabatic alignment of asymmetric top molecules: field-free alignment of iodobenzene.

Nonadiabatic laser alignment of an asymmetric top molecule is studied using the combination of a quantum dynamical theory and time-resolved photofragment imaging experiments. In particular, the degree of alignment of iodobenzene, induced by an intense, linearly polarized picosecond laser pulse, is calculated and measured. Pronounced alignment is obtained under field-free conditions.