Picosecond strain pulses are a versatile tool for investigation of mechanical properties of meso-and nano-scale objects with high temporal and spatial resolutions. Generation of such pulses is traditionally realized via ultrafast laser excitation of a light-to-strain transducer involving thermoelastic, deformation potential, or inverse piezoelectric effects. These approaches unavoidably lead to heat dissipation and a temperature rise, which can modify delicate specimens, like biological tissues, and ultimately destroy the transducer itself limiting the amplitude of generated picosecond strain. Here we propose a non-thermal mechanism for generating picosecond strain pulses via ultrafast photo-induced first-order phase transitions (PIPTs). We perform experiments on vanadium dioxide VO 2 films, which exhibit a firstorder PIPT accompanied by a lattice change. We demonstrate that during femtosecond optical excitation of VO 2 the PIPT alone contributes to ultrafast expansion of this material as large as 0.45%, which is not accompanied by heat dissipation, and, for excitation density of 8 mJ cm −2 , exceeds the contribution from thermoelastic effect by a factor of five.
Exchange interactions determine the correlations between microscopic spins in magnetic materials. Probing the dynamics of these spin correlations on ultrashort length and time scales is, however, rather challenging, since it requires simultaneously high spatial and high temporal resolution. Recent experimental demonstrations of laser-driven two-magnon modes-zone-edge excitations in antiferromagnets governed by exchange couplingposed questions about the microscopic nature of the observed spin dynamics, the mechanism underlying its excitation, and their macroscopic manifestation enabling detection. Here, on the basis of a simple microscopic model, we derive the selection rules for cubic systems that describe the polarization of pump and probe pulses required to excite and detect dynamics of nearest-neighbor spin correlations and can be employed to isolate such dynamics from other magnetic excitations and magneto-optical effects. We show that laser-driven spin correlations contribute to optical anisotropy of the antiferromagnet even in the absence of spin-orbit coupling. In addition, we highlight the role of subleading anisotropy in the spin system and demonstrate that the dynamics of the antiferromagnetic order parameter occurs only in next-to-leading order, determined by the smallness of the magnetic anisotropy as compared to the isotropic exchange interactions in the system. We expect that our results will stimulate and support further studies of magnetic correlations on the shortest length and time scales.
We report on experimental picosecond acoustic studies of an ultrafast photoinduced insulator-to-metal and structural transition in VO2 nanostructures epitaxially grown on Al2O3 substrates with different orientations. Applying a pump-probe technique with combined excitation of a sample with picosecond strain and femtosecond laser pulses we demonstrate that dynamical strain of moderate amplitude of 0.1% has a pronounced impact on ultrafast photoinduced phase transition in VO2 nanohillocks. This enables novel path for controlling such transitions at picosecond and nanometer scales. Our experiments also allowed characterizing elastic and photo-elastic properties of the photo-induced metallic phase in VO2 and to relate them to the properties of the equilibrium phase. Furthermore, we demonstrate the generation of picosecond strain pulses upon laser-induced excitation of thin epitaxial VO2.
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