arXiv subjects

Chao Lian

Publications and source records attributed to Chao Lian.

At least 19 recordsLinked to original sources

arXiv2026

A Unified Heterogeneous Implementation of Numerical Atomic Orbitals-Based Real-Time TDDFT within the ABACUS Package

We present a unified heterogeneous computing framework for real-time time-dependent density functional theory (RT-TDDFT) based on numerical atomic orbitals (NAOs), implemented in the ABACUS package. We introduce three co-designed abstraction layers, including unified data containers, unified linear algebra operators, and unified grid integration interfaces. These layers collectively accelerate the two most demanding parts of NAO-based RT-TDDFT: explicit real-time wavefunction propagation and real-space grid operations such as Hamiltonian construction and force evaluation under external fields. We validate the method by computing optical properties for systems ranging from finite molecules to periodic solids, showing excellent agreement with standard benchmarks. Performance evaluations on bulk silicon demonstrate that a single GPU can achieve substantial wall-clock speedup over a fully utilized dual-socket CPU node. Furthermore, distributed multi-GPU strong-scaling tests confirm high parallel efficiency over tens of GPUs. This work establishes a high-performance, portable platform for large-scale first-principles simulations of ultrafast electron dynamics.

cond-mat.mtrl-sci↗

arXiv2026

Ultrafast Laser Induces Macroscopic Symmetry-Breaking of Diamond Color Centers

The negatively charged nitrogen-vacancy center is a leading quantum platform due to its excellent spin coherence and stable interactions. Understanding its ultrafast dynamics is crucial for quantum applications but presents significant challenges for both experimental characterization and atomic-scale modeling. Here, we employ real-time time-dependent density functional theory to investigate the coupled electron-phonon-spin dynamics in negatively charged nitrogen-vacancy centers. Laser excitation promotes minority-spin electrons within 100~fs, establishing a $C_{3v}$-symmetry breaking charge ordering. Subsequently, ionic motion on the potential energy surface of the excited electrons generates both symmetric oscillations of carbon-nitrogen bonds and dynamic Jahn-Teller distortions with a $C_{3v}$-symmetry breaking. These distortions subsequently induce nonlocal coherent phonons in the diamond lattice, which propagate with the $C_{3v}$-symmetry breaking at the sound velocity ($\sim$2~Å/fs). Our simulations provide direct time-resolved visualization of these processes, offering novel insights into the microscopic interplay of electrons, phonons, and spins in nitrogen-vacancy centers.

cond-mat.mtrl-sci↗

arXiv2026

Reversable phase transitions in ferroic two-dimensional Nb2O2I4 through optically excited coherent phonons

We investigate optically induced phase transitions in the two-dimensional (2D) ferroelectric (FE) material Nb2O2I4 using real-time time-dependent density functional theory (rt-TDDFT). Our results demonstrate that tailored laser pulses can activate specific coherent phonon modes. Specifically, the anharmonic atomic distortions of the A1-1 and A1-2 modes at the Γ-point facilitate the reversal of in-plane polarization. By fine-tuning laser parameters, additional phonon modes at both the Y and Γ points are excited. The resulting nonequilibrium atomic dynamics enable the formation of previously unreported ferroic phases, including three antiferroelectric (AFE) phases and one ferrielectric (FiE) phase. Notably, these optically induced phases can be reverted to the initial FE state using appropriate techniques. This controllable reversibility among multiple ferroic phases positions 2D Nb2O2I4 as a highly promising candidate for next-generation electronic storage applications.

cond-mat.mtrl-sci↗

arXiv2024

Topological polarons in halide perovskites

Halide perovskites emerged as a revolutionary family of high-quality semiconductors for solar energy harvesting and energy-efficient lighting. There is mounting evidence that the exceptional optoelectronic properties of these materials could stem from unconventional electron-phonon couplings, and it has been suggested that the formation of polarons and self-trapped excitons could be key to understanding such properties. By performing first-principles simulations with unprecedented detail across the length scales, here we show that halide perovskites harbor a uniquely rich variety of polaronic species, including small polarons, large polarons, and charge density waves, and we explain a variety of experimental observations. We find that these emergent quasiparticles support topologically nontrivial phonon fields with quantized topological charge, making them the first non-magnetic analog of the helical Bloch points found in magnetic skyrmion lattices.

cond-mat.mtrl-sci↗

arXiv2024

Neutralization of low energy Na$^{+}$ scattered from InAs(001)

The neutralization probability of low energy Na$^{+}$ ions scattered from In- and As-rich InAs(001) surfaces is measured by time-of-flight spectroscopy. It is found that the neutralization probability for projectiles scattered from As sites is larger than from In sites for both types of surfaces. A modification of the resonant charge transfer model is proposed in which a freezing contour that follows the atomic structure is combined with molecular dynamics and density functional theory. Together, these approaches show that the neutralization of alkali projectiles scattered from a compound solid material is determined by multiple factors, particularly the surface atomic and electronic structures. This model is applicable to any system in which the surface potential is inhomogeneous, such as compound materials and adsorbate-covered surfaces.

cond-mat.mtrl-sci↗

arXiv2024

Theory of excitonic polarons: From models to first-principles calculations

Excitons are neutral excitations that are composed of electrons and holes bound together by their attractive Coulomb interaction. The electron and the hole forming the exciton also interact with the underlying atomic lattice, and this interaction can lead to a trapping potential that favors exciton localization. The quasi-particle thus formed by the exciton and the surrounding lattice distortion is called excitonic polaron. Excitonic polarons have long been thought to exist in a variety of materials, and are often invoked to explain the Stokes shift between the optical absorption edge and the photo-luminescence peak. However, quantitative ab initio calculations of these effects are exceedingly rare. In this manuscript, we present a theory of excitonic polarons that is amenable to first-principles calculations. We first apply this theory to model Hamiltonians for Wannier excitons experiencing Fröhlich or Holstein electron-phonon couplings. We find that, in the case of Fröhlich interactions, excitonic polarons only form when there is a significant difference between electron and hole effective masses. Then, we apply this theory to calculating excitonic polarons in lithium fluoride ab initio. The key advantage of the present approach is that it does not require supercells, therefore it can be used to study a variety of materials hosting either small or large excitonic polarons. This work constitutes the first step toward a complete ab initio many-body theory of excitonic polarons in real materials.

cond-mat.mtrl-sci↗

arXiv2024

Excitonic polarons and self-trapped excitons from first-principles exciton-phonon couplings

Excitons consist of electrons and holes held together by their attractive Coulomb interaction. Although excitons are neutral excitations, spatial fluctuations in their charge density couple with the ions of the crystal lattice. This coupling can lower the exciton energy and lead to the formation of a localized excitonic polaron, or even a self-trapped exciton in the presence of strong exciton-phonon interactions. Here, we develop a theoretical and computational approach to compute excitonic polarons and self-trapped excitons from first principles. Our methodology combines the many-body Bethe-Salpeter approach with density-functional perturbation theory, and does not require explicit supercell calculations. As a proof of concept, we demonstrate our method for a compound of the halide perovskite family.

cond-mat.mtrl-sci↗

arXiv2023

Electron-phonon physics from first principles using the EPW code

EPW is an open-source software for $\textit{ab initio}$ calculations of electron-phonon interactions and related materials properties. The code combines density functional perturbation theory and maximally-localized Wannier functions to efficiently compute electron-phonon coupling matrix elements on ultra-fine Brillouin zone grids. This data is employed for predictive calculations of temperature-dependent properties and phonon-assisted quantum processes in bulk solids and low-dimensional materials. Here, we report on significant new developments in the code that occurred during the period 2016-2022, namely: a transport module for the calculation of charge carrier mobility and conductivity under electric and magnetic fields within the $\textit{ab initio}$ Boltzmann transport equation; a superconductivity module for the calculation of critical temperature and gap structure in phonon-mediated superconductors within the $\textit{ab initio}$ anisotropic multi-band Eliashberg theory; an optics module for calculations of phonon-assisted indirect transitions; a module for the calculation of small and large polarons without supercells using the $\textit{ab initio}$ polaron equations; and a module for calculating electron-phonon couplings, band structure renormalization, and temperature-dependent optical spectra using the special displacement method. For each capability, we outline the methodology and implementation, and provide example calculations. We describe recent code refactoring to prepare EPW for exascale architectures, we discuss efficient parallelization strategies, and report on extreme parallel scaling tests.

cond-mat.mtrl-sci↗

arXiv2022

Data-Folding and Hyperspace Coding for Multi-Dimensonal Time-Series Data Imaging

Multi-Dimensional time series classification and prediction has been widely used in many fields, such as disease prevention, fault diagnosis and action recognition. However, the traditional method needs manual intervention and inference, and cannot realize the figurative expression of multi-Dimensional data, which lead to inadequate information mining. Inspired by the strong power of deep learning technology in image processing, we propose a unified time-series image fusion framework to transform multi-modal data into 2D-image, and then realize automatic feature extraction and classification based on a lightweight convolutional neural network. We present two basic image coding methods, Gray image coding, RGB image coding, and their step coding methods. Considering the universality of different application fields, we extended the coding method and propose two types transform coding, Transform-RGB coding and RGB-Transform coding, to improve the multi-domain representation ability. By applying to three typical scenes of Parkinson's disease diagnosis, bearing fault detection and gymnastics action recognition, we obtained the highest classification accuracy of 100%, 92.86% and 99.70% respectively, which were all higher than the classical processing methods. It proves the strong classification ability and universality of our coding framework to different multi-dimensional scenes. We expect that this method can be used and perform well in other scenarios, and be potential to facilitate the progress of related technology.

eess.SP↗

arXiv2022

Ab initio self-consistent many-body theory of polarons at all couplings

We present a theoretical framework to describe polarons from first principles within a many-body Green's function formalism. Starting from a general electron-phonon Hamiltonian, we derive a self-consistent Dyson equation in which the phonon-mediated self-energy is composed by two distinct terms. One term is the Fan-Migdal self-energy and describes dynamic electron-phonon processes, the other term is a new contribution to the self-energy originating from the static displacements of the atomic nuclei in the polaronic ground state. The lowest-order approximation to the present theory yields the standard many-body perturbation theory approach to electron-phonon interactions in the limit of large polarons, and the ab initio polaron equations introduced in [Sio et al., Phys. Rev. B 99, 235139 (2019); Phys. Rev. Lett. 122, 246403 (2019)] in the limit of small polarons. A practical recipe to implement the present unifying formalism in first-principles calculations is outlined. We apply our method to the Fröhlich model, and obtain remarkably accurate polaron energies at all couplings, in line with Feynman's polaron theory and diagrammatic Monte Carlo calculations. We also recover the well-known results of Fröhlich and Pekar at weak and strong coupling, respectively. The present approach enables predictive many-body calculations of polarons in real materials at all couplings.

cond-mat.mtrl-sci↗

arXiv2022

Unified approach to polarons and phonon-induced band structure renormalization

Ab initio calculations of the phonon-induced band structure renormalization are currently based on the perturbative Allen-Heine theory and its many-body generalizations. These approaches are unsuitable to describe materials where electrons form localized polarons. Here, we develop a self-consistent, many-body Green's function theory of band structure renormalization that incorporates localization and self-trapping. We show that the present approach reduces to the Allen-Heine theory in the weak-coupling limit, and to total energy calculations of self-trapped polarons in the strong-coupling limit. To demonstrate this methodology, we reproduce the path-integral results of Feynman and diagrammatic Monte Carlo calculations for the Fröhlich model at all couplings, and we calculate the zero point renormalization of the band gap of an ionic insulator including polaronic effects.

cond-mat.mtrl-sci↗

arXiv2020

Integrated Plasmonics: Broadband Dirac Plasmons in Borophene

The past decade has witnessed numerous discoveries of two-dimensional (2D) semimetals and insulators, whereas 2D metals are rarely identified. Borophene, a monolayer boron sheet, has recently emerged as a perfect 2D metal with unique structure and electronic properties. Here we study collective excitations in borophene, which exhibit two major plasmon modes with low damping rates extending from infrared to ultraviolet regime. The anisotropic 1D plasmon originates from electronic excitations of tilted Dirac cones in borophene, analogous to that in heavily doped Dirac semimetals. These features make borophene promising to realize directional polariton transportation and broadband optical communications for next-generation optoelectronic devices.

cond-mat.mtrl-sci↗

arXiv2020

Ultrafast Photoinduced Band Splitting and Carrier Dynamics in Chiral Tellurium Nanosheets

Trigonal tellurium (Te) is a chiral semiconductor that lacks both mirror and inversion symmetries, resulting in complex band structures with Weyl crossings and unique spin textures. Detailed time-resolved polarized reflectance spectroscopy is used to investigate its band structure and carrier dynamics. The polarized transient spectra reveal optical transitions between the uppermost spin-split H4 and H5 and the degenerate H6 valence bands (VB) and the lowest degenerate H6 conduction band (CB) as well as a higher energy transition at the L-point. Surprisingly, the degeneracy of the H6 CB (a proposed Weyl node) is lifted and the spin-split VB gap is reduced upon photoexcitation before relaxing to equilibrium as the carriers decay. Using ab initio density functional theory (DFT) calculations we conclude that the dynamic band structure is caused by a photoinduced shear strain in the Te film that breaks the screw symmetry of the crystal. The band-edge anisotropy is also reflected in the hot carrier decay rate, which is a factor of two slower along c-axis than perpendicular to it. The majority of photoexcited carriers near the band-edge are seen to recombine within 30 ps while higher lying transitions observed near 1.2 eV appear to have substantially longer lifetimes, potentially due to contributions of intervalley processes in the recombination rate. These new findings shed light on the strong correlation between photoinduced carriers and electronic structure in anisotropic crystals, which opens a potential pathway for designing novel Te-based devices that take advantage of the topological structures as well as strong spin-related properties.

cond-mat.mtrl-sci↗

arXiv2020

Ultrafast charge ordering by self-amplified exciton-phonon dynamics in TiSe$_2$

The origin of charge density waves (CDW) in TiSe$_2$ has long been debated, mainly due to the difficulties in identifying the timescales of how and when the excitonic pairing and electron-phonon coupling (EPC) come into play. Without a proper time resolution and microscopic mechanism, one has to assume simultaneous appearance of CDW and periodic lattice distortions (PLD). Here, we accomplish a complete separation of exciton and PLD dynamics and unravel their interplay in the ultrafast time domain in our real-time time-dependent density functional theory simulations. We find that laser pulses knock off the exciton order and induce a homogeneous bonding-antibonding transition in the initial 20 fs, then the weakened electronic order triggers ionic movements antiparallel to the original PLD. The EPC comes into play after the initial 20~fs, and the two processes mutually amplify each other leading to a complete inversion of CDW ordering. The self-amplified dynamics reproduces the evolution of band structures in excellent agreement with ultrafast photoemission experiment. Hence we resolve the key processes in the initial dynamics of CDW that help elucidate the mechanism underlying the long debated problem.

cond-mat.mes-hall↗

arXiv2019

Charge Density Wave Hampers Exciton Condensation in 1T-TiSe$_2$

The Bose-Einstein condensation of excitons continues to garner immense attention as a prototypical example for observing emergent properties from many-body quantum effects. In particular, Titanium Diselenide (TiSe$_2$) is a promising candidate for realizing exciton condensation and was experimentally observed only very recently. Surprisingly, the condensate was experimentally characterized by a soft plasmon mode that only exists near the transition temperature, $T_c$, of the charge density wave (CDW). Here, we characterize and analyze the experimental spectra using linear-response time-dependent density functional theory and find that the soft mode can be attributed to interband electronic transitions. At the CDW state below $T_c$, the periodic lattice distortions hamper the spontaneous formation of the exciton by introducing a CDW gap. The band gap raises the soft mode and merges it into the regular plasmon. Our surprising results contradict previous simplistic analytical models commonly used in the scientific literature. In addition, we find that a finite electronic temperature, $T_e$, introduces a dissipation channel and prevents the condensation above $T_c$. The combined effect of the CDW and $T_e$ explains the fragile temperature-dependence of the exciton condensation. Taken together, our work provides the first \textit{ab initio} atomic-level framework for rationalizing recent experiments and further manipulating exciton condensates in TiSe$_2$.

cond-mat.mtrl-sci↗

arXiv2019

Indirect but Efficient: Laser-Excited Electrons Can Drive Ultrafast Polarization Switching in Ferroelectric Materials

To enhance the efficiency of next-generation ferroelectric (FE) electronic devices, new techniques for controlling ferroelectric polarization switching are required. While most prior studies have attempted to induce polarization switching via the excitation of phonons, these experimental techniques required intricate and expensive terahertz sources and have not been completely successful. Here, we propose a new mechanism for rapidly and efficiently switching the FE polarization via laser-tuning of the underlying dynamical potential energy surface. Using time-dependent density functional calculations, we observe an ultrafast switching of the FE polarization in BaTiO3 within 200 fs. A laser pulse can induce a charge density redistribution that reduces the original FE charge order. This excitation results in both desirable and highly directional ionic forces that are always opposite to the original FE displacements. Our new mechanism enables the reversible switching of the FE polarization with optical pulses that can be produced from existing 800 nm experimental laser sources.

cond-mat.mtrl-sci↗

arXiv2019

Ultrafast carrier relaxation and its Pauli drag in photo-enhanced melting of solids

Ultrafast light-matter interaction is a powerful tool for the study of solids. Upon laser excitation, carrier multiplication and lattice acceleration beyond thermal velocity can occur, as a result of far-from-equilibrium carrier relaxation. The roles of electron-electron and electron-phonon scatterings are identified by first-principles dynamic simulations, from which a unified phase diagram emerges. It not only explains the experimentally-observed "inertial" melting but also predicts abnormal damping by Pauli Exclusion Principle with a new perspective on ultrahigh-intensity laser applications.

cond-mat.mtrl-sci↗

arXiv2019

Cooperative evolution of intraband and interband excitations for high harmonic generation in strained MoS2

Modulating electronic structure of two-dimensional (2D) materials represents an exciting avenue for tailoring their optoelectronic properties. Here, we identify a strain-induced, cooperative effect of intraband and interband excitations contributing to high harmonic generation (HHG) in prototype dichalcogenide MoS2 monolayer. We find that besides the dominant intraband contributions, interband current is also indispensable in modulating HHG. The HHG yields increase linearly with the compressive strain since flatter band dispersion and Berry curvature enhance both interband and intraband dynamics. Band structure can be retrieved with high reliability by monitoring the strain-induced evolution of HHG spectra, suggesting that strain not only provides an additional knob to control HHG in solids, but also marks a way towards a complete understanding of underlying microscopic mechanisms.

cond-mat.mes-hall↗