No Arabic abstract
Modern nonlinear optical materials allow light of one wavelength be efficiently converted into light at another wavelength. However, designing nonlinear optical materials to operate with ultrashort pulses is difficult, because it is necessary to match both the phase velocities and group velocities of the light. Here we show that self-organized nonlinear gratings can be formed with femtosecond pulses propagating through nanophotonic waveguides, providing simultaneous group-velocity matching and quasi-phase-matching for second harmonic generation. We record the first direct microscopy images of photo-induced nonlinear gratings, and demonstrate how these waveguides enable simultaneous $chi^{(2)}$ and $chi^{(3)}$ nonlinear processes, which we utilize to stabilize a laser frequency comb. Finally, we derive the equations that govern self-organized grating formation for femtosecond pulses and explain the crucial role of group-velocity matching. In the future, such nanophotonic waveguides could enable scalable, reconfigurable nonlinear optical systems.
Coherent broadband excitation of plasmons brings ultrafast photonics to the nanoscale. However, to fully leverage this potential for ultrafast nanophotonic applications, the capacity to engineer and control the ultrafast response of a plasmonic system at will is crucial. Here, we develop a framework for systematic control and measurement of ultrafast dynamics of near-field hotspots. We show deterministic design of the coherent response of plasmonic antennas at femtosecond timescales. Exploiting the emerging properties of coupled antenna configurations, we use the calibrated antennas to engineer two sought-after applications of ultrafast plasmonics: a subwavelength resolution phase shaper, and an ultrafast hotspot switch. Moreover, we demonstrate that mixing localized resonances of lossy plasmonic particles is the mechanism behind nanoscale coherent control. This simple, reproducible and scalable approach promises to transform ultrafast plasmonics into a straightforward tool for use in fields as diverse as room temperature quantum optics, nanoscale solid state physics and quantum biology.
Rare-earth doped nanocrystals are emerging light sources used for many applications in nanotechnology enabled by human ability to control their various optical properties with chemistry and material science. However, one important optical problem -- polarisation of photoluminescence -- remains largely out of control by chemistry methods. Control over photoluminescence polarisation can be gained via coupling of emitters to resonant nanostructures such as optical antennas and metasurfaces. However, the resulting polarization is typically sensitive to position disorder of emitters, which is difficult to mitigate. Recently, new classes of disorder-immune optical systems have been explored within the framework of topological photonics. Here we explore disorder-robust topological arrays of Mie-resonant nanoparticles for polarisation control of photoluminescence of nanocrystals. We demonstrate polarized emission from rare-earth-doped nanocrystals governed by photonic topological edge states supported by zigzag arrays of dielectric resonators. We verify the topological origin of polarised photoluminescence by comparing emission from nanoparticles coupled to topologically trivial and nontrivial arrays of nanoresonators.
Multimode fibres (MMFs) are attracting interest for complex spatiotemporal dynamics, and for ultrafast fibre sources, imaging and telecommunications. This new interest is based on three key properties: their high spatiotemporal complexity (information capacity), the important role of disorder, and complex intermodal interactions. To date, phenomena in MMFs have been studied only in limiting cases where one or more of these properties can be neglected. Here we study MMFs in a regime in which all these elements are integral. We observe a spatial beam-cleaning process preceding spatiotemporal modulation instability. We show that the origin of these processes is a universal unstable attractor in graded-index MMFs. Both the self-organization of the attractor, as well as its instability, are caused by intermodal interactions characterized by cooperating disorder, nonlinearity and dissipation. The demonstration of a disorder-enhanced nonlinear process in MMF has important implications for telecommunications, and the multifaceted complexity of the dynamics showcases MM waveguides as ideal laboratories for many topics and applications in complexity science.
Diffusion of heat in metals is a fundamental process which is crucial for a variety of applications of metal nanostructures. Surprisingly, however, {em ultrafast} heat diffusion received only limited attention so far. Here, we show that heat diffusion can be made faster than $e-ph$ energy transfer rate, in which case, it dominates the spatio-temporal dynamics of the temperature. This enables the metals to overcome the conventional limitations of the nonlinear optical response of materials - it can be simultaneously fast and strong. As a specific example, we identify the underlying (femtosecond and few picosecond) time scales responsible for the generation and erasure of optically-induced transient Bragg gratings in thin metal films. Further, we show that heat diffusion gives rise to a significant nonlocal thermo-optic nonlinearity - it affects also the nonlinear optical response such that the overall change of the permittivity (hence, reflectivity of the transient grating) has a significant dependence also on the illumination period rather than only on the illumination intensity.
Recent advancements in computational inverse design have begun to reshape the landscape of structures and techniques available to nanophotonics. Here, we outline a cross section of key developments at the intersection of these two fields: moving from a recap of foundational results to motivation of emerging applications in nonlinear, topological, near-field and on-chip optics.