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Register a new userEvidence of diffusive fractal aggregation of TiO2 nanoparticles by femtosecond laser ablation at ambient conditions
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The specific mechanisms which leads to the formation of fractal nanostructures by pulsed laser deposition remain elusive despite intense research efforts, motivated mainly by the technological interest in obtaining tailored nanostructures with simple and scalable production methods. Here we focus on fractal nanostructures of titanium dioxide, $TiO_2$, a strategic material for many applications, obtained by femtosecond laser ablation at ambient conditions. We model the fractal formation through extensive Monte Carlo simulations based on a set of minimal assumptions: irreversible sticking and size independent diffusion. Our model is able to reproduce the fractal dimensions and the area distributions of the nanostructures obtained in the experiments for different densities of the ablated material. The comparison of theory and experiment show that such fractal aggregates are formed after landing of the ablated material on the substrate surface by a diffusive mechanism. Finally we discuss the role of the thermal conductivity of the substrate and the laser fluence on the properties of the fractal nanostructures. Our results represent an advancement towards controlling the production of fractal nanostructures by pulsed laser deposition.
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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.
Fast fabrication of micro-optical elements for generation of optical vortex beams based on the q-plate design is demonstrated by femtosecond (fs) laser ablation of gold film on glass. Q-plates with diameter of ~0.5 mm were made in ~1 min using galvanometric scanners with writing speed of 5 mm/s. Period of gratings of 0.8 micrometers and groove width of 250 nm were achieved using fs-laser ablation at 343 nm wavelength. Phase and intensity analysis of optical vortex generators was carried out at 633 nm wavelength and confirmed the designed performance. Efficiency of spin-orbital conversion of the q-plates made by ablation of 50-nm-thick film of gold was ~3%. Such gratings can withstand thermal annealing up to 800C. They can be used as optical vortex generators using post-selection of polarisation.
Quantum technology relies on proper hardware, enabling coherent quantum state control as well as efficient quantum state readout. In this regard, wide-bandgap semiconductors are an emerging material platform with scalable wafer fabrication methods, hosting several promising spin-active point defects. Conventional readout protocols for such defect spins rely on fluorescence detection and are limited by a low photon collection efficiency. Here, we demonstrate a photo-electrical detection technique for electron spins of silicon vacancy ensembles in the 4H polytype of silicon carbide (SiC). Further, we show coherent spin state control, proving that this electrical readout technique enables detection of coherent spin motion. Our readout works at ambient conditions, while other electrical readout approaches are often limited to low temperatures or high magnetic fields. Considering the excellent maturity of SiC electronics with the outstanding coherence properties of SiC defects the approach presented here holds promises for scalability of future SiC quantum devices.
Magnetic skyrmions present interesting physics due to their topological nature and hold significant promise for future information technologies. A key barrier to realizing skyrmion devices has been stabilizing these spin structures under ambient conditions. In this manuscript, we exploit the tunable magnetic properties of amorphous Fe/Gd mulitlayers to realize skyrmion lattices which are stable over a large temperature and magnetic field parameter space, including room temperature and zero magnetic field. These hybrid skyrmions have both Bloch-type and Neel-type character and are stabilized by dipolar interactions rather than Dzyaloshinskii-Moriya interactions, which are typically considered required for the generation of skyrmions. Small angle neutron scattering (SANS) was used in combination with soft X-ray microscopy to provide a unique, multi-scale probe of the local and long-range order of these structures. These results identify a pathway to engineer controllable skyrmion phases in thin film geometries which are stable at ambient conditions.
Manipulation of magnetization with ultrashort laser pulses is promising for information storage device applications. The dynamic of the magnetization response depends on the energy transfer from the photons to the spins during the initial laser excitation. A material of special interest for magnetic storage is FePt nanoparticles , on which optical writing with optical angular momentum was demonstrated recently by Lambert et al., although the mechanism remained unclear. Here we investigate experimentally and theoretically the all-optical switching of FePt nanoparticles. We show that the magnetization switching is a stochastic process. We develop a complete multiscale model which allows us to optimize the number of laser shots needed to write the magnetization of high anisotropy FePt nanoparticles in our experiments. We conclude that only angular momentum induced optically by the inverse Faraday effect will provide switching with one single femtosecond laser pulse.
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