arXiv subjects

Chii-Dong Lin

Publications and source records attributed to Chii-Dong Lin.

5 recordsLinked to original sources

arXiv2025

Strong-Field Photoelectron Interferometry with Near-Single-Cycle Yb Lasers

The concept of using photoelectron interferometry in short laser fields to probe electron dynamics and target structures was introduced more than two decades ago. However, the quality of experimental data has remained insufficient for quantitative analysis, largely due to the instability of few-cycle Ti:Sa laser pulses, the current workhorse of short pulses. Here, we report the first systematic strong-field ionization experiments performed with industrial-grade, carrier-envelope-phase (CEP) stabilized, near-single-cycle Yb lasers. By measuring photoelectron momentum distributions in the direct-ionization regime, we show that single-cycle cosine-shaped pulses can separate and enhance both spider-leg and fishbone holographic structures. The spider-leg structure enables extraction of the electron scattering phase from the Ar atomic potential-information typically accessible only through attosecond metrology, while the fishbone structure reveals the orbital-parity contrast between Ar atoms and nitrogen molecules. Our measurements are quantitatively reproduced by both semiclassical Herman-Kluk-propagator and \textit{ab initio} simulations, paving the way for precision studies of electron-molecule scattering with widely accessible industrial-grade lasers.

physics.atom-ph↗

arXiv2025

Bright 25-attosecond light pulses reach the one atomic unit of time

Generating ever-shorter and brighter light pulses has long been a central pursuit in ultrafast science, as it benchmarks our ability to create and manipulate the coherence on the intrinsic timescale of sub-atomic electron motion. The current state-of-the-art in attosecond pulse generation reaches durations of 40-50 attoseconds (1 as = $10^{-18}$ seconds), produced via high-order harmonic generation (HHG) driven by secondary mid-infrared light sources. However, these sources often suffer from low stability and poor HHG conversion efficiency. In this work, we demonstrate the generation of 25$\pm$2 attosecond light pulses, a new world record for the shortest light pulse, driven by a post-compressed, industrial-grade Yb-based laser system. The resulting high-harmonic spectrum spans photon energies from 50 eV to 320 eV, covering the carbon K-edge, with a calibrated photon flux exceeding $10^{12}$ photons per second, approximately three orders of magnitude higher than previous studies. The pulse duration was characterized using an angle-resolved photoelectron streaking camera on helium atoms and systematically optimized through the use of dielectric filters of varying thicknesses to compensate the attochirp. Our study reaches the threshold of one atomic unit of time (24.2 attoseconds), the boundary between atomic and ionic physics, opening the door to resolving exciting ionic quantum dynamics with tabletop lasers.

physics.atom-ph↗

arXiv2025

Optical Interference Effect in Strong-field Electronic Coherence Spectroscopy

We have investigated strong-field-induced electronic coherences in argon and molecular nitrogen ions created by high-intensity, few-cycle infrared laser pulses. This is a step toward the long-sought goal of strong-field coherent control in molecular chemistry. We employed high-intensity, few-cycle infrared laser pulses in a pump-probe setup to investigate a recent prediction that electronic coherences in nitrogen molecules change the ion yields vs. pump-probe delay. [Yuen and Lin, Phys. Rev. A 109, L011101 (2024)]. The predicted coherence signals in molecular nitrogen could not be resolved above the optical interference of the pump and probe pulses; a simultaneous measurement clearly resolved the induced cation fine-structure coherence in strong-field-ionized argon. The results of our comparison with simulations suggest that optical interference effects manifest differently in each ionic species and must be carefully accounted for when interpreting experimental data. We found that nonsequential double ionization in the low-intensity region of the focal volume can reduce the visibility of coherence generated by two-pulse sequential ionization, and we quantify the importance of pulse shape and spectral characteristics for isolating the desired coherence signals.

physics.atom-ph↗

arXiv2020

Laser-induced electron diffraction of the ultrafast umbrella motion in ammonia

Visualizing molecular transformations in real-time requires a structural retrieval method with Ångström spatial and femtosecond temporal atomic resolution. Imaging of hydrogen-containing molecules additionally requires an imaging method that is sensitive to the atomic positions of hydrogen nuclei, with most methods possessing relatively low sensitivity to hydrogen scattering. Laser-induced electron diffraction (LIED) is a table top technique that can image ultrafast structural changes of gas-phase polyatomic molecules with sub-Ångström and femtosecond spatiotemporal resolution together with relatively high sensitivity to hydrogen scattering. Here, we image the umbrella motion of an isolated ammonia molecule (NH$_3$) following its strong field ionization. Upon ionization of a neutral ammonia molecule, the ammonia cation (NH$_3^+$) undergoes an ultrafast geometrical transformation from a pyramidal ($Φ_{HNH} = 107 ^\circ$) to planar ($Φ_{HNH}=120^\circ$) structure in approximately 8 femtoseconds. Using LIED, we retrieve a near-planar ($Φ_{HNH}=117 \pm 5^\circ$) field-dressed NH$_3^+$ molecular structure $7.8-9.8$ femtoseconds after ionization. Our measured field-dressed NH$_3^+$ structure is in excellent agreement with our calculated equilibrium field dressed structure using quantum chemical ab initio calculations.

physics.chem-ph↗

arXiv2015

Imaging an aligned polyatomic molecule with laser-induced electron diffraction

Laser-induced electron diffraction is an evolving tabletop method, which aims to image ultrafast structural changes in gas-phase polyatomic molecules with sub-Ångström spatial and femtosecond temporal resolution. Here, we provide the general foundation for the retrieval of multiple bond lengths from a polyatomic molecule by simultaneously measuring the C-C and C-H bond lengths in aligned acetylene. Our approach takes the method beyond the hitherto achieved imaging of simple diatomic molecules and is based upon the combination of a 160 kHz mid-IR few-cycle laser source with full three-dimensional electron-ion coincidence detection. Our technique provides an accessible and robust route towards imaging ultrafast processes in complex gas phase molecules with atto- to femto-second temporal resolution.

physics.atom-ph↗