The diethyl carbonate, DEC, is an ester that is used as a solvent in Li-ion batteries, but its behavior under ionizing radiation was unknown. The transient optical absorption spectra, the decay kinetics, and the influence of various scavengers have been studied by using the picosecond laser-triggered electron accelerator ELYSE. In neat DEC, the intense near-IR (NIR) absorption spectrum is assigned to the solvated electron. It is overlapped in the visible range by another transient but longer-lived and less intense band that is assigned to the oxidized radical DEC(-H). The solvated electron molar absorption coefficients and radiolytic yield evolution from 25 ps, the geminate recombination kinetics, and the rate constants of electron transfer reactions to scavengers are determined. The radiolytic mechanism, indicating a certain radioresistance of DEC, is compared with that for other solvents.

The experimental detection of short picosecond photoacoustic response induced by femtosecond laser pump radiation deeply penetrating in GaAs and generating long acoustic strain pulse is reported. It is demonstrated that it is possible, in this case, to achieve high-frequency coherent acoustic phonon monitoring in semiconductors as efficiently as in the case of metals where the penetration depth of pump radiation is shorter and the generated acoustic strain pulse is short itself. The physical origin of such monitoring of high-frequency acoustic phonons is discussed thanks to a detailed analysis of the spectral transformation functions of both the generation process ͑opto-acoustic transformation͒ and the detection process ͑acousto-optic transformation͒. We show that it is possible to tune the detection process from a narrowband to a broadband spectrum detection process. In particular, the broadband detection process is achieved with a proper choice of the probe wavelength permitting efficient coupling between the acoustic field and the probe electromagnetic wave only in a nanometric thin region near semiconductor surface. Efficient broadband acousto-optic detection results in the short pulsed photoacoustic responses in transient optical reflectivity even when long acoustic pulses are generated, because of sufficient sensitivity to high-frequency coherent phonons even weakly contributing to the total acoustic field. These results indicate the opportunity to broaden the range of the substrate materials and pump laser frequencies that can be used in high-frequency coherent phonon spectroscopy of the materials and nanostructures.