SearcharxivSearch

arXiv subjects

Uri Arieli

Publications and source records attributed to Uri Arieli.

4 recordsLinked to original sources

Shaping Ultrafast Pulses for Enhanced Resonant Nonlinear Interactions

Coherent control with shaped ultrafast pulses is a powerful approach for steering nonlinear light-matter interactions. Previous studies in quantum control have shown that, beyond transform-limited pulses, those with antisymmetric spectral phases can drive nonresonant multiphoton transitions with comparable efficiency. However, in resonant multiphoton transitions, the material's spectral-phase response introduces dispersion that degrades nonlinear efficiency. Pre-shaping the pulse to compensate for the material's impulse response can restore and enhance nonlinear interactions beyond the transform-limited case. Yet, is this the only spectral phase that can yield such enhancement? Here, we study sub-10 fs single-pulse four-wave mixing in resonant plasmonic nanostructures using arctangent spectral-phase-shaped pulses. We uncover two distinct enhancement regimes: one compensating for material dispersion, and a counterintuitive regime where the arctangent phase induces an antisymmetric polarization response, driving constructive multiphoton pathway interference. Our theoretical analysis provides clear physical explanation for both phenomena. Notably, it predicts that both enhancement mechanisms scale exponentially with harmonic order, offering a powerful strategy for dramatically enhancing high-order harmonic generation in resonant systems.

physics.optics

Shaping Exciton Polarization Dynamics in 2D Semiconductors by Tailored Ultrafast Pulses

The ultrafast formation of strongly bound excitons in two-dimensional semiconductors provide a rich platform for studying fundamental physics as well as developing novel optoelectronic technologies. While extensive research has explored the excitonic coherence, many-body interactions, and nonlinear optical properties, the potential to study these phenomena by directly controlling their coherent polarization dynamics has not been fully realized. In this work, we use a sub-10fs pulse shaper to study how temporal control of coherent exciton polarization affects the generation of four-wave mixing in monolayer WSe2 under ambient conditions. By tailoring multiphoton pathway interference, we tune the nonlinear response from destructive to constructive interference, resulting in a 2.6-fold enhancement over the four-wave mixing generated by a transform-limited pulse. This demonstrates a general method for nonlinear enhancement by shaping the pulse to counteract the temporal dispersion experienced during resonant light-matter interactions. Our method allows us to excite both 1s and 2s states, showcasing a selective control over the resonant state that produces nonlinearity. By comparing our results with theory, we find that exciton-exciton interactions dominate the nonlinear response, rather than Pauli blocking. This capability to manipulate exciton polarization dynamics in atomically thin crystals lays the groundwork for exploring a wide range of resonant phenomena in condensed matter systems and opens up new possibilities for precise optical control in advanced optoelectronic devices.

physics.optics

Coherent Control of the Non-instantaneous Nonlinear Power-law Response in Resonant Nanostructures

We experimentally demonstrate coherent control of the nonlinear response of optical second harmonic generation in resonant nanostructures beyond the weak-field regime. Contrary to common perception, we show that maximizing the intensity of the pulse does not yield the strongest nonlinear power-law response. We show this effect emerges from the temporally asymmetric photo-induced response in a resonant mediated non-instantaneous interaction. We develop a novel theoretical approach which captures the photoinduced nonlinearities in resonant nanostructures beyond the two photon description and give an intuitive picture to the observed non-instantaneous phenomena.

physics.optics

Deep Learning for Design and Retrieval of Nano-photonic Structures

Our visual perception of our surroundings is ultimately limited by the diffraction limit, which stipulates that optical information smaller than roughly half the illumination wavelength is not retrievable. Over the past decades, many breakthroughs have led to unprecedented imaging capabilities beyond the diffraction-limit, with applications in biology and nanotechnology. In this context, nano-photonics has revolutionized the field of optics in recent years by enabling the manipulation of light-matter interaction with subwavelength structures. However, despite the many advances in this field, its impact and penetration in our daily life has been hindered by a convoluted and iterative process, cycling through modeling, nanofabrication and nano-characterization. The fundamental reason is the fact that not only the prediction of the optical response is very time consuming and requires solving Maxwell's equations with dedicated numerical packages. But, more significantly, the inverse problem, i.e. designing a nanostructure with an on-demand optical response, is currently a prohibitive task even with the most advanced numerical tools due to the high non-linearity of the problem. Here, we harness the power of Deep Learning, a new path in modern machine learning, and show its ability to predict the geometry of nanostructures based solely on their far-field response. This approach also addresses in a direct way the currently inaccessible inverse problem breaking the ground for on-demand design of optical response with applications such as sensing, imaging and also for plasmon's mediated cancer thermotherapy.

physics.optics