Short-pulse-induced solute migration in the CHClO + 1,2 dichloroethane solution.

Using the Z-scan technique with 532 nm 19 ps laser pulses separated by two time intervals τ's (0.1 s and 1.0 s) sandwiching the mass diffusion time constant of the CHClO + 1,2 dichloroethane solution, we investigate short-pulse-induced solute migration in the sample by measuring its transmittance change with τ variation.

Shrinkage of picosecond laser beam by plasma reflection in super-resolution near-field structure of SiN/Sb/SiN thin film.

The transmittive and reflective Z-scan technique is used with a 10 Hz, frequency doubled, Q-switched, and mode-locked Nd:YAG laser to verify that the reflectivity of the super-resolution near-field structure of an SiN/Sb/SiN thin film increases as incident intensity decreases. This intensity-dependent reflection, called nonlinear reflection, reflects a TEM(00) mode laser beam more strongly at its periphery than at its center and so shrinks the transmitted laser beam. The observed nonlinear reflection is attributed to laser-induced change of carrier densities in Sb, to justify quantitatively the experimental results.

Kramers-Kronig relation between nonlinear absorption and refraction of C(60) and C(70).

Using the Z-scan technique with 532 nm 16 picosecond laser pulses, we observe reverse saturable absorption and positive nonlinear refraction of toluene solutions of both C(60) and C(70). By deducting the positive Kerr nonlinear refraction of the solvent, we notice that the solute molecules contribute to nonlinear refraction of opposite signs: positive for C(60) and negative for C(70). Attributing nonlinear absorption and refraction of both solutes to cascading one-photon excitations, we illustrate that they satisfy the Kramers-Kronig relation.

Solute migration caused by excited state absorptions.

Using the Z-scan technique, we find that migration of chloroaluminum phthalocyanine in liquid ethanol can be induced by the absorption of a 19 ps laser pulse with energy exceeding a threshold but not by that of a 2.8 ns pulse depositing more energy at the solute molecules. Considering each solute molecule as an oscillator confined within a potential well, we explain, in accordance with the five-energy-band model, that solute molecules excited by a 19 ps pulse retain more translational excess energy to overcome the potential well barrier compared with those excited by a 2.