arXiv subjects

Yanwei Xiong

Publications and source records attributed to Yanwei Xiong.

6 recordsLinked to original sources

arXiv2026

Reconstruction of missing low-angle scattering in two-dimensional diffraction signal

Anisotropic two-dimensional diffraction signals encode additional structural information, including atom-pair angular distributions, beyond conventional isotropic scattering. However, experimental constraints such as beam stops result in missing low-angle scattering data, which limits accurate real-space reconstruction. We develop an iterative algorithm to recover the missing low-angle signal in two-dimensional diffraction patterns. The method transforms between momentum-transfer and real-space domains using coupled Fourier and Abel transforms, while enforcing real-space support constraints to suppress reconstruction artifacts. Importantly, the algorithm requires only minimal a priori knowledge of the molecular structure, namely the approximate shortest and longest internuclear distances. We demonstrate accurate reconstruction of the missing signal using both simulated data and experimental diffraction patterns from laser-aligned trifluoroiodomethane (CF3I) molecules, enabling improved real-space structural retrieval from incomplete diffraction data. Our results remove a fundamental experimental limitation in ultrafast diffraction and establish a general route toward complete structural retrieval from incomplete scattering data.

physics.chem-ph↗

arXiv2025

Retrieval of missing small-angle scattering data in gas-phase diffraction experiments

We report an iterative algorithm to retrieve accurate real space information from gas phase ultrafast diffraction measurements with missing data at low momentum transfer. The algorithm operates in a manner similar to phase retrieval algorithms which transform signals back and forth between the signal domain and the Fourier transform domain and apply constraints to retrieve the missing phase. Our algorithm retrieves missing data that is not accessible experimentally by applying a real-space constraint that requires only an approximate a-priori knowledge of the shortest and longest internuclear distances in the molecule. We demonstrate successful retrieval of the missing data in simulated data and in experimentally measured electron diffraction signals of photo-dissociated iodobenzene molecules.

physics.chem-ph↗

arXiv2025

Ultrafast electron diffractive imaging of the dissociation of pre-excited molecules

Gas phase ultrafast electron diffraction (GUED) has become a powerful technique to directly observe the structural dynamics of photoexcited molecules. GUED reveals information about the nuclear motions that is complementary to the information on the electronic states provided by spectroscopic measurements. GUED experiments so far have utilized a single laser pulse to excite the molecules and an electron pulse to probe the dynamics. This limits the excited states which can be studied to only those that can be reached by absorption of a photon from the ground state or in some cases simultaneous absorption of multiple photons. A broader class of experiments and dynamics can be accessed using two time-delayed laser pulses to access unexplored regions of the potential energy surfaces. As a proof-of-principle experiment using a double excitation, we studied the photodissociation of trifluoroiodomethane molecules that are pre-excited with an infrared (800 nm) femtosecond laser pulse before photo-dissociation is triggered with an ultraviolet (266 nm) femtosecond laser pulse. We have observed significant differences in the dissociation dynamics, with pre-excitation resulting in a slower dissociation process. This new capability can offer new insights on the evolution of nuclear wavepackets in regions of the excited potential energy surface which are inaccessible in single photon excitation. We present a methodology to carry out the measurement, analyze and interpret the data that could be applied to a broad class of experiments.

physics.chem-ph↗

arXiv2025

Ultrafast dynamics of ferroelectric polarization of NbOI$_{2}$ captured with femtosecond electron diffraction

Two-dimensional (2D) ferroelectric materials like NbOI$_{2}$ have garnered significant interest, yet their temporal response and synergetic interaction with light remain underexplored. Previous studies on the polarization of oxide ferroelectrics have relied on time-resolved optical second harmonic generation or ultrafast X-ray scattering. Here, we probe the laser-induced polarization dynamics of 2D NbOI$_{2}$ nanocrystals using ultrafast transmission electron diffraction and deflectometry. The deflection of the electron pulses is directly sensitive to the changes in the polarization, while the diffraction signal captures the structural evolution. Excited with a UV laser pulse, the polarization of NbOI$_{2}$ is initially suppressed for two picoseconds, then it recovers and overshoots, leading to a transiently enhanced polarization persisting for over 200 ps. This recovery coincides with coherent acoustic phonon generation, triggering a piezoresponse in the NbOI$_{2}$ nanocrystals. Our results offer a new method for sensing the ferroelectric order parameter in femtosecond time scales.

cond-mat.mtrl-sci↗

arXiv2023

Monitoring the evolution of relative product populations at early times during a photochemical reaction

Identifying multiple rival reaction products and transient species formed during ultrafast photochemical reactions and determining their time-evolving relative populations are key steps towards understanding and predicting photochemical outcomes. Yet, most contemporary ultrafast studies struggle with clearly identifying and quantifying competing molecular structures/species amongst the emerging reaction products. Here, we show that mega-electronvolt ultrafast electron diffraction in combination with ab initio molecular dynamics calculations offer a powerful route to determining time-resolved populations of the various isomeric products formed after UV (266 nm) excitation of the five-membered heterocyclic molecule 2(5H)-thiophenone. This strategy provides experimental validation of the predicted high (~50%) yield of an episulfide isomer containing a strained 3-membered ring within ~1 ps of photoexcitation and highlights the rapidity of interconversion between the rival highly vibrationally excited photoproducts in their ground electronic state.

physics.chem-ph↗

arXiv2021

Quantum state tomography of molecules by ultrafast diffraction

Ultrafast electron diffraction and time-resolved serial crystallography are the basis of the ongoing revolution in capturing at the atomic level of detail the structural dynamics of molecules. However, most experiments employ the classical "ball-and-stick" depictions, and the information of molecular quantum states, such as the density matrix, is missing. Here, we introduce a framework for the preparation and ultrafast coherent diffraction from rotational wave packets of molecules, and we establish a new variant of quantum state tomography for ultrafast electron diffraction to characterize the molecular quantum states. The ability to reconstruct the density matrix of molecules of arbitrary degrees of freedom will provide us with an unprecedentedly clear view of the quantum states of molecules, and enable the visualization of effects dictated by the quantum dynamics of molecules.

quant-ph↗