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Register a new userFemtosecond laser pulse train interaction with dielectric materials
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We investigate the interaction of trains of femtosecond microjoule laser pulses with dielectric materials by means of a multi-scale model. Our theoretical predictions are directly confronted with experimental observations in soda-lime glass. We show that due to the low heat conductivity, a significant fraction of the laser energy can be accumulated in the absorption region. Depending on the pulse repetition rate, the material can be heated to high temperatures even though the single pulse energy is too low to induce a significant material modification. Regions heated above the glass transition temperature in our simulations correspond very well to zones of permanent material modifications observed in the experiments.
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We show that a 1.13-GHz repetition rate optical pulse train with 0.70 fs high-frequency timing jitter (integration bandwidth of 17.5 kHz - 10 MHz, where the measurement instrument-limited noise floor contributes 0.41 fs in 10 MHz bandwidth) can be directly generated from a free-running, single-mode diode-pumped Yb:KYW laser mode-locked by single-walled carbon nanotube (SWCNT)-coated mirrors. To our knowledge, this is the lowest timing jitter optical pulse train with the GHz repetition rate ever measured. If this pulse train is used for direct sampling of 565-MHz signals (Nyquist frequency of the pulse train), the demonstrated jitter level corresponds to the projected effective-number-of-bit (ENOB) of 17.8, which is much higher than the thermal noise limit of 50-ohm load resistance (~14 bits).
We report enhanced broadband Terahertz (THz) generation and detailed characterization from the interaction of femtosecond two colour laser pulses with thin transparent dielectric tape target in ambient air. The proposed source is easy to implement, exhibits excellent scalability with laser energy. Spectral characterization using Fourier transform spectrometer reveals yield enhancement of more than 150 % in the THz region of 0.1 - 10 THz with respect to conventional two-colour laser plasma source in ambient air. Further, the source spectrum extends up to 40 THz with an enhancement of flux > 30 %. Experimental results, well supported with two-dimensional particle-in-cell simulations establishes that the transient photo-current produced by the asymmetric laser pulse interaction with air plasma as well as near solid density plasma formed on the tape surface is responsible for the enhanced terahertz generation. The source will be useful for the multidisciplinary activities and ongoing applications of the laboratory-based terahertz sources.
We present a comprehensive theoretical description for an irradiation of an ultrashort light pulse normally on thin materials based on first-principles time-dependent density functional theory. As the most elaborate scheme, we develop a microscopic description solving Maxwell equations for light electromagnetic fields and the time-dependent Kohn-Sham equation for electron dynamics simultaneously in the time domain using a common spatial grid. We call it the microscopic Maxwell-TDDFT scheme. We test this scheme for silicon thin films of various thickness, from a few atomic layers to a few tens of nm. We show that the microscopic Maxwell-TDDFT scheme provides a satisfactory description incorporating the electronic structure of thin films in the first-principles level, multiple reflections of the electromagnetic fields at the surfaces, and nonlinear light-matter interaction when the incident light pulse is strong. However, the calculation becomes expensive as the thickness increases. We then consider two limiting cases of extremely thin and sufficiently thick films and develop approximate schemes. For the extremely thin case including two-dimensional atomic-layered materials, a two-dimensional macroscopic electromagnetism is developed: a two-dimensional susceptibility is introduced for a weak field, while time evolution equation is derived for an intense field. For sufficiently thick films, the microscopic Maxwell-TDDFT scheme is expected to coincide with a description utilizing ordinary macroscopic electromagnetism. We numerically confirm it comparing the calculated results: For a weak field, a comparison is made with a description using the bulk dielectric susceptibility. For a strong field, a comparison is made with a multiscale Maxwell-TDDFT scheme which the authors group developed previously.
Controlling the directionality of spin waves is a key ingredient in wave-based computing methods such as magnonics. In this paper, we demonstrate this particular aspect by using an all-optical point-like source of continuous spin waves based on frequency comb rapid demagnetization. The emitted spin waves contain a range of k-vectors and by detuning the applied magnetic field slightly off the ferromagnetic resonance (FMR), we observe X-shaped caustic spin-wave patterns at $70^{circ}$ propagation angles as predicted by theory. When the harmonic of the light source approaches theFMR, the caustic pattern gives way to uniaxial spin-wave propagation perpendicular to the in-plane component of the applied field. This field-controlled propagation pattern and directionality of optically emitted short-wavelength spin waves provide additional degrees of freedom when designing magnonic devices.
Laser-induced manipulation of magnetism at the nanoscale is a rapidly growing research topic with potential for applications in spintronics. In this work, we address the role of the scattering cross section, thermal effects, and laser fluence on the magnetic, structural, and chemical stability of individual magnetic nanoparticles excited by single femtosecond laser pulses. We find that the energy transfer from the fs laser pulse to the nanoparticles is limited by the Rayleigh scattering cross section, which in combination with the light absorption of the supporting substrate and protective layers determines the increase in the nanoparticle temperature. We investigate individual Co nanoparticles (8 to 20 nm in size) as a prototypical model system, using x-ray photoemission electron microscopy and scanning electron microscopy upon excitation with single femtosecond laser pulses of varying intensity and polarization. In agreement with calculations, we find no deterministic or stochastic reversal of the magnetization in the nanoparticles up to intensities where ultrafast demagnetization or all-optical switching is typically reported in thin films. Instead, at higher fluences, the laser pulse excitation leads to photo-chemical reactions of the nanoparticles with the protective layer, which results in an irreversible change in the magnetic properties. Based on our findings, we discuss the conditions required for achieving laser-induced switching in isolated nanomagnets.
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