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We present an optical technique based on ultrafast photoacoustics to precisely determine the local temperature distribution profile in liquid samples in contact with a laser heated optical transducer. This ultrafast pump-probe experiment uses time-domain Brillouin scattering (TDBS) to locally determine the light scattering frequency shift. As the temperature influences the Brillouin scattering frequency, the TDBS signal probes the local laser-induced temperature distribution in the liquid. We demonstrate the relevance and the sensitivity of this technique for the measurement of the absolute laser-induced temperature gradient of a glass forming liquid prototype, glycerol, at different laser pump powers - i.e. different steady state background temperatures. Complementarily, our experiments illustrate how this TDBS technique can be applied to measure thermal diffusion in complex multilayer systems in contact to a surrounding liquid.
Time-domain Brillouin scattering uses ultrashort laser pulses to generate coherent acoustic pulses of picoseconds duration in a solid sample and to follow their propagation in order to image material inhomogeneities with sub-optical depth resolution.
We demonstrate the use of the micro-Brillouin light scattering (micro-BLS) technique as a local temperature sensor for magnons in a Permalloy thin film and phonons in the glass substrate. A systematic shift in the frequencies of two thermally excited
Brillouin light scattering spectroscopy from so-called standing spin waves in thin magnetic films is often used to determine the magnetic exchange constant. The data analysis of the experimentally determined spin-wave modes requires an unambiguous as
A simple theory is developed for an interpretation of the time-domain Brillouin scattering experiments where the coherent acoustic pulse and the probe light pulse beams are propagating at an angle to each other. The directivity pattern of their acous
Although ultrafast manipulation of magnetism holds great promise for new physical phenomena and applications, targeting specific states is held back by our limited understanding of how magnetic correlations evolve on ultrafast timescales. Using ultra