arXiv subjects

David Ayuso

Publications and source records attributed to David Ayuso.

At least 19 recordsLinked to original sources

arXiv2026

Roadmap on Attosecond Science

Twenty-five years have passed since the first experimental demonstration of attosecond pulses, marking the advent of our ability to resolve and control electron motion in real time. What began as a technological breakthrough - generating the shortest flashes ever produced - has evolved into a powerful approach for probing and steering electronic dynamics in atoms, molecules, and solids. This roadmap, authored by leading experts in the field, surveys the recent rapid progress in the generation and characterization of attosecond pulses, emerging attosecond measurement and control techniques, and their expanding range of applications. It reviews current and future developments in attosecond light sources, including novel laser technologies, waveform synthesizers, new schemes for high-order harmonic generation, attosecond pulse generation at free-electron lasers, and structured light. Advances in attosecond measurement methodologies are also discussed, encompassing all-attosecond pump-probe spectroscopy, attosecond four-wave mixing, attosecond microscopy, spectroscopy with light transients, and attosecond interferometry. Furthermore, the roadmap addresses applications of attosecond spectroscopy to reveal electron dynamics in molecules and condensed matter systems from both theoretical and experimental perspectives, and highlights emerging directions at the interface with quantum optics and quantum entanglement. Overall, this work aims to serve as a comprehensive resource for navigating the evolving landscape of attosecond science.

physics.optics↗

arXiv2026

A beat wave approach to harmonic generation in chiral media

We extend the beat-wave framework for laser harmonic generation - where spectra form regular lattices in Fourier space - to the nonlinear response of isotropic chiral media driven by locally chiral light. We represent the enantio-sensitive response of the medium by a chiral zero-frequency (DC) mode derived from the transverse spin density induced by structured or focused fields. Beating between this DC mode and the driving electromagnetic modes yields alternating chiral and achiral contributions on a regular harmonic lattice. We derive a general criterion for when chiral and achiral pathways overlap at the same harmonic and generate enantio-sensitive interference that survives spatial or angular integration (global chirality), versus when enantio-sensitivity remains confined to spatially varying patterns (local chirality). We apply the criterion to published configurations of synthetic chiral light, including OAM-carrying bicircular fields and crossed multicolour beams, and show that it reproduces and clarifies their reported global-chirality and beam-bending regimes.

physics.optics↗

arXiv2025

Non-Dichroic Enantio-Sensitive Chiroptical Spectroscopy

Chiroptical effects using circularly polarized light produce signals that change sign when switching either molecular handedness (enantiosensitivity) or the light helicity (circular dichroism). Here, we break this enantiosensitive-and-dichroic paradigm by measuring a new type of chiroptical signal which is enantiosensitive but not dichroic. We photoionize chiral molecules using a strong laser field and detect the three-dimensional photoelectron momentum distribution. The non-dichroic, enantiosensitive asymmetry is encoded in octupolar and higher multipolar terms in the photoelectron angular distribution, which appear in multiphoton ionization with elliptically polarized fields or cross polarized two-color fields. The robustness of the enantiosensitivity with respect to the relative phase between the vectorial components of the ionizing field represents an example of symmetry protection, and opens unexplored opportunities for imaging ultrafast dynamics in chiral molecules, such as enantiosensitive photoelectron spectroscopy with bright squeezed vacuum states.

physics.chem-ph↗

arXiv2025

Theory of Non-Dichroic Enantio-Sensitive Chiroptical Spectroscopy

We show that the photoelectron angular distributions produced by elliptical and cross-polarized two-color laser fields interacting with randomly oriented chiral molecules decompose into four irreducible representations of the $D_{2h}$ point group. One of these ($A_u$) corresponds to a non-dichroic enantiosensitive (NoDES) contribution. This NoDES contribution has opposite sign for opposite enantiomers but remains invariant under reversal of the field ellipticity, enabling chirality detection that is robust against variations of the relative phase between orthogonal field components. We propose a protocol to isolate this component using only two velocity-map imaging projections and validate it through numerical simulations. Our calculations, performed in the two-photon resonantly-enhanced ionization, multi-photon, and strong-field ionization regimes with cross-polarized two-color fields show that the NoDES signal reaches about 1\% of the energy-resolved ionization yield, comparable to photoelectron circular dichroism and much larger than standard magnetic-dipole chiroptical effects. NoDES spectroscopy thus provides a symmetry-protected and phase-robust route to probe molecular chirality on the ultrafast time scale. The experimental confirmation of our theory is presented in the companion paper [L. Fede et al., arXiv:2512.19062 (2025)].

physics.chem-ph↗

arXiv2024

Geometry of chiral temporal structures I: Physical effects

In non-relativistic physics, the concepts of geometry and topology are usually applied to characterize spatial structures or structures in momentum space. We introduce the concept of temporal geometry, which encompasses the geometric and topological properties of temporal shapes, i.e. trajectories traced by the tip of a time-dependent vector in vector space. We apply it to vectors describing ultrafast electron currents or induced polarization in chiral molecules. The central concepts of temporal geometry - Berry curvature and Berry connection - emerge as ubiquitous features of photoexcited, non-equilibrium, chiral electron dynamics. We demonstrate that the Berry curvature and Berry connection (i) rely on the polarization properties of light pulses, (ii) can be introduced for multiphoton processes, and (iii) control enantio-sensitive geometric observables via non-equilibrium electronic dynamics excited by tailored laser fields. Our findings may open a way to ultrafast, topologically non-trivial, and enantio-sensitive chemical dynamics.

quant-ph↗

arXiv2024

Chiral topological light for detecting robust enantio-sensitive observables

The topological response of matter to electromagnetic fields is a property in high demand in materials design and metrology due to its robustness against noise and decoherence, stimulating recent advances in ultrafast photonics. Embedding topological properties into the enantio-sensitive optical response of chiral molecules could therefore enhance the efficiency and robustness of chiral optical discrimination. Here we achieve such a topological embedding by introducing the concept of chiral topological light~-- a light beam which displays chirality locally, with an azimuthal distribution of its handedness described globally by a topological charge. The topological charge is mapped onto the azimuthal intensity modulation of the non-linear optical response, where enantio-sensitivity is encoded into its spatial rotation. The spatial rotation is robust against intensity fluctuations and imperfect local polarization states of the driving field. Our theoretical results show that chiral topological light enables detection of percentage-level enantiomeric excesses in randomly oriented mixtures of chiral molecules, opening a way to new, extremely sensitive and robust chiro-optical spectroscopies with attosecond time resolution.

physics.optics↗

arXiv2024

Ultrafast TACOS -- Terahertz-Assisted Chiro-Optical Spectroscopy

We bring together the advantages of terahertz (THz) and optical spectroscopies to introduce TACOS (Terahertz-Assisted Chiro-Optical Spectroscopy), a novel approach for ultrafast and highly efficient imaging of molecular chirality and control over chiral electronic dynamics. We show how, using a THz pulse, we can induce a transient electronic orientation in a medium of randomly oriented chiral molecules that breaks the isotropy of the molecular sample. This symmetry breaking twists the nonlinear response of the medium to an ultrashort linearly polarised optical pulse in a highly enantiosensitive manner. As a result, the medium emits elliptically polarised light at new optical frequencies that records the molecular handedness via purely electric-dipole interactions. The long wavelength and period of the THz pulse enable both spatial coherence across the sample and a substantial degree of electronic orientation over the duration of the ultrashort optical pulse. TACOS does not require optical carrier-envelope phase stability or working in vacuum, and it creates exciting avenues for ultrafast and highly efficient chiral sensing and manipulation.

physics.optics↗

arXiv2024

Capturing electron-driven chiral dynamics in UV-excited molecules

Molecular chirality is a key design property for many technologies including bioresponsive imaging, circularly polarized light detection and emission, molecular motors and switches. Imaging and manipulating the primary steps of transient chirality is therefore central for controlling numerous physical, chemical and biological properties that arise from chiral molecules in response to external stimuli. So far, the manifestation of electron-driven chiral dynamics in neutral molecules has not been demonstrated at their intrinsic timescale. Here, we use time-resolved photoelectron circular dichroism (TR-PECD) with an unprecedented instrument response function of 2.9 fs to image the dynamics of coherent electronic motion activated by prompt UV-excitation in neutral chiral molecules, disclosing its impact on the molecular chiral response. We find that electronic beatings between Rydberg states lead to periodic modulations of the chiroptical response on the few-femtosecond timescale, showing a sign inversion in less than 10 fs. Calculations including both the molecular UV-excitation and subsequent photoionization confirm this interpretation and provide further evidence that the combination of the resulting photoinduced chiral current with a circularly polarized probe pulse realizes an enantio-selective filter of molecular orientations upon photoionization, opening up a route towards enantio-selective charge-directed reactivity.

physics.chem-ph↗

arXiv2023

All-optical coherent control of chiral electronic transitions for highly enantioselective photochemistry

Enantioselective photochemistry provides access to unique molecular structures and functions, with deep implications for fundamental science and industrial applications. Current methods for highly enantioselective photochemistry critically rely on chiral sensitisers, as circularly polarised light on its own yields vanishingly weak enantioselectivity. Here, we introduce a quantum control strategy to drive highly enantioselective electronic excitations in randomly oriented samples using a pulsed ($\sim$22 fs) IR laser and two of its harmonics, in the absence of intermediate resonances. Our approach addresses electronic transitions, does not require chiral sensitisers, or cold molecules, or long electronic coherence times, is relevant for liquid-phase samples, and remains effective over interaction regions extending across many laser wavelengths, even in the presence of dispersion. We show how, by 3D shaping the field's polarisation over the interaction region, we can achieve enantioselective coherent control over electronic population transfer. Our ab-initio simulations in the chiral molecule carvone yield a selectivity of $\sim$30 % in the populations of the first excited electronic state, three orders-of-magnitude higher than what is possible with circularly polarised light ($\sim$0.01 %). These results bring all-optical enantioselective photochemistry into the realm of practical applications.

physics.chem-ph↗

arXiv2023

Ultrafast control over chiral sum-frequency generation

We introduce an ultrafast all-optical approach for efficient chiral recognition which relies on the interference between two low-order nonlinear processes which are ubiquitous in nonlinear optics: sum-frequency generation and third-harmonic generation. In contrast to traditional sum-frequency generation, our approach encodes the medium's handedness in the intensity of the emitted harmonic signal, rather than in its phase, and it enables full control over the enantiosensitive response. We show how, by sculpting the sub-optical-cycle oscillations of the driving laser field, we can force one molecular enantiomer to emit bright light while its mirror twin remains dark, thus reaching the ultimate efficiency limit of chiral sensitivity via low-order nonlinear light-matter interactions. Our work paves the way for ultrafast and highly efficient imaging and control of the chiral electronic clouds of chiral molecules using lasers with moderate intensities, in all states of matter: from gases to liquids to solids, with molecular specificity and on ultrafast timescales.

physics.optics↗

arXiv2022

Tilting light's polarization plane to spatially separate the nonlinear optical response of chiral molecules on ultrafast timescales

Distinguishing between the left- and right-handed versions of a chiral molecule (enantiomers) is vital, but also inherently difficult. Traditional optical methods using elliptically or circularly polarized light rely on weak linear effects which arise beyond the electric-dipole approximation, posing major limitations for time resolving ultrafast chiral molecular dynamics. Here we show how, by tilting the plane of polarization of an ultrashort burst of intense elliptically polarized light, towards its propagation direction, we can turn the light field into a highly efficient chiro-optical tool. This "forward tilting" can be achieved by focusing the beam tightly, creating structured light which exhibits a nontrivial polarization pattern in space. We demonstrate that our structured field allows us to realize an interferometer for efficient chiral recognition that separates the nonlinear optical response of left- and right-handed molecules in space. Our work provides a simple, yet highly efficient, way of spatially structuring the polarization of light to image molecular chirality, with extreme enantio-sensitivity and on ultrafast time scales.

physics.optics↗

arXiv2022

Structuring the local handedness of synthetic chiral light: global chirality versus polarization of chirality

Synthetic chiral light enables ultrafast and highly efficient imaging of molecular chirality. Unlike standard circularly polarized light, the handedness of synthetic chiral light does not rely on the spatial structure of the light field: it is encoded locally, in the chiral trajectory that the tip of the electric-field vector draws in time, at each point in space. Being locally chiral, already within the electric-dipole approximation, synthetic chiral light is a highly efficient chiral photonic reagent. Synthetic chiral light that is locally and globally chiral allows us to selectively quench the nonlinear response of a selected molecular enantiomer while maximizing it in its mirror twin at the level of total signal intensities. Synthetic chiral light that exhibits polarization of chirality allows us to realize a chiral version of Young's double-slit experiment that leads to enantio-sensitive light bending. Here we connect these two new concepts and show how one can structure the local and global handedness of synthetic chiral light in space, and how these local and global properties are imprinted in the enantio-sensitive response of the chiral molecules, creating new opportunities for ultrafast, all-optical and highly efficient imaging of molecular chirality.

physics.optics↗

arXiv2022

Ultrafast chirality: the road to efficient chiral measurements

Today we are witnessing the electric-dipole revolution in chiral measurements. Here we reflect on its lessons and outcomes, such as the perspective on chiral measurements using the complementary principles of "chiral reagent" and "chiral observer", the hierarchy of scalar, vectorial and tensorial observables, the new properties of the chiro-optical response in the ultrafast and non-linear domains, and the geometrical magnetism associated with the chiral response in photoionization. The electric-dipole revolution is a landmark event. It has opened routes to extremely efficient enantio-discrimination with a family of new methods. These methods are governed by the same principles but work in vastly different regimes -- from microwaves to optical light; they address all molecular degrees of freedom -- electronic, vibrational and rotational, and use flexible detection schemes, i.e. detecting photons or electrons, making them applicable to different chiral phases, from gases to liquids to amorphous solids. The electric-dipole revolution has also enabled enantio-sensitive manipulation of chiral molecules with light. This manipulation includes exciting and controlling ultrafast helical currents in vibronic states of chiral molecules, enantio-sensitive control of populations in electronic, vibronic and rotational molecular states, and opens the way to efficient enantio-separation and enantio-sensitive trapping of chiral molecules. The word "perspective" has two meanings: "outlook" and "point of view". In this perspective article, we have tried to cover both meanings.

physics.optics↗

arXiv2021

Geometric fields and new enantio-sensitive observables in photoionization of chiral molecules

Chiral molecules are instrumental for molecular recognition in living organisms. Distinguishing between two opposite enantiomers, the mirror twins of the same chiral molecule, is both vital and challenging. Photoelectron circular dichroism (PECD), an extremely sensitive probe of molecular chirality via photoionization, outperforms standard optical methods by many orders of magnitude. Here we show that the physical origin of PECD in chiral molecules is linked to the concept of geometric magnetism, which enables a broad class of phenomena in solids including the anomalous electron velocity, the Hall effect, and related topological phenomena. We uncover the geometric field in molecular photoionization, which leads to a new class of enantio-sensitive observables emerging due to ultrafast excitation of chiral electronic or vibronic currents prior to ionization. Next, we introduce the first member of this new class: enantio-sensitive orientation of chiral molecules via photoionization. This effect opens new routes to both enantio-separation and imaging of chiral dynamics on ultrafast time scales. Our work suggests that geometric fields in photoionization provide the bridge between the two geometrical properties, chirality and topology.

physics.chem-ph↗

arXiv2021

New opportunities for ultrafast and highly enantio-sensitive imaging and control of chiral nuclear dynamics: towards enantio-selective attochemistry

The recently introduced synthetic chiral light [D. Ayuso et al, Nat. Photon. 13, 866-871 (2019)] has opened up new opportunities for ultrafast and highly efficient imaging and control of chiral matter. Here we show that the giant enantio-sensitivity enabled by such light could be exploited to probe chiral nuclear rearrangements during chemical reactions in an highly enantio-sensitive manner. Using a state-of-the-art implementation of time-dependent density functional theory, we explore how the nonlinear response of the prototypical chiral molecule H2O2 changes as a function of its dihedral angle, which defines its handedness. The macroscopic intensity emitted from randomly oriented molecules at even harmonic frequencies (of the fundamental) depends strongly on this nuclear coordinate. Because of the ultrafast nature of such nonlinear interactions, the direct mapping between chiral dichroism and nuclear geometry provides a way to probe chiral nuclear dynamics at their natural time scales. Our work paves the way for ultrafast and highly efficient imaging of enantio-sensitive dynamics in more complex chiral systems, including biologically relevant molecules.

physics.chem-ph↗

arXiv2021

Giant chiro-optical response in high harmonic generation

High harmonic generation (HHG) records the ultrafast electronic response of matter to light, encoding key properties of the interrogated quantum system, such as chirality. The first implementation of chiral HHG [Cireasa et al. Nat. Phys. 11, 654 (2015)] relied on the weak electronic response of a medium of randomly oriented chiral molecules to the magnetic component of an elliptically polarized wave, yielding relatively weak chiro-optical signals. Here we show that elliptically polarized light can drive a strong chiral response in chiral molecules via purely electric-dipole interactions -- the magnetic component of the wave does not participate at all. This giant chiro-optical response, which remains hidden in standard HHG experiments, can be mapped into the macroscopic far-field signal using a non-collinear configuration, creating new opportunities for bringing the electric-dipole "revolution" to HHG.

physics.optics↗

arXiv2020

Ultrafast optical rotation for extremely sensitive enantio-discrimination

Sculpting sub-cycle temporal structures of optical waveforms allows one to image and even control electronic clouds in atoms, molecules and solids. Here we show how the transverse spin component arising upon spatial confinement of such optical waveforms enables extremely efficient chiral recognition and control of ultrafast chiral dynamics. When an intense few-cycle, linearly polarized laser pulse is tightly focused into a medium of randomly oriented chiral molecules, the medium generates light which is elliptically polarized, with opposite helicities and opposite rotations of the polarization ellipse in media of opposite handedness. In contrast to conventional optical activity of chiral media, this new nonlinear optical activity is driven by purely electric-dipole interactions and leads to giant enantio-sensitivity in the near VIS-UV domain, where optical instrumentation is readily available. Adding a polarizer turns rotation of the polarization ellipse into highly enantio-sensitive intensity of the nonlinear-optical response. Sub-cycle optical control of the incident light wave enables full control over the enantio-sensitive response. The proposed all-optical method not only enables extremely efficient chiral discrimination, but also ultrafast imaging and control of chiral dynamics with commercially available optical technology.

physics.optics↗

arXiv2020

Polarization of chirality

It has been long recognized that the spatial polarization of the electronic clouds in molecules, and the spatial arrangements of atoms into chiral molecular structures, play crucial roles in physics, chemistry and biology. However, these two fundamental concepts - chirality and polarization - have remained unrelated so far. This work connects them by introducing and exploring the concept of polarization of chirality. We show that, like charge, chirality, or handedness, can be polarized, and that such polarization leads to fundamental consequences, demonstrated here using light. First, we analyze how chirality dipoles and higher-order chirality multipoles manifest in experimental observables. Next, we show how to create chirality-polarized optical fields of alternating handedness in space. Despite being achiral, these racemic space-time light structures interact differently with chiral matter of opposite handedness, and the chirality dipole of light controls and quantifies the strength of the enantio-sensitive response. Using nonlinear interactions, we can make a medium of randomly oriented chiral molecules emit light to the left, or to the right, depending on the molecular handedness and on the chirality dipole of light. The chiral dichroism in emission direction reaches its highest possible value of 200%. Our work opens the field of chirality polarization shaping of light and new opportunities for efficient chiral discrimination and control of chiral and chirality-polarized light and matter on ultrafast time scales.

physics.optics↗