arXiv subjects

Wenjie Dou

Publications and source records attributed to Wenjie Dou.

At least 55 records · Page 3Linked to original sources

arXiv2024

Enhancement of Chiral-Induced Spin Selectivity via Circularly Polarized Light

The notion of chiral-induced spin selectivity (CISS) has attracted intensive research interest recently. However, the practical applications of the CISS effects face challenges due to relatively low spin polarization. In this Letter, we propose a non-perturbative theory illustrating how circularly polarized (CP) light enhances CISS effects through strong light-matter interactions. We introduce a Floquet electronic friction model to study the nonadiabatic dynamics and spin transport through a chiral molecule in a molecule junction subjected to external driving. Our results show that the interplay of the nonadiabatic effects and light-matter interactions can significantly ($>90\%$) enhance electron spin polarization under CP light. Our predictions can be very useful in experiments for using CP light to control spin current in chiral molecular junctions.

cond-mat.mes-hall↗

arXiv2024

First-principles Nonadiabatic Dynamics of Molecules at Metal Surfaces with Vibrationally Coupled Electron Transfer

Accurate description of nonadiabatic dynamics of molecules at metal surfaces involving electron transfer has been a longstanding challenge for theory. Here, we tackle this problem by first constructing high-dimensional neural network diabatic potentials including state crossings determined by constrained density functional theory, then applying mixed quantum-classical surface hopping simulations to evolve coupled electron-nuclear motion. Our approach accurately describes the nonadiabatic effects in CO scattering from Au(111) without empirical parameters and yields results agreeing well with experiments under various conditions for this benchmark system. We find that both adiabatic and nonadiabatic energy loss channels have important contributions to the vibrational relaxation of highly vibrationally excited CO(vi = 17), whereas relaxation of low vibrationally excited states of CO(vi = 2) is weak and dominated by nonadiabatic energy loss. The presented approach paves the way for accurate first-principles simulations of electron transfer mediated nonadiabatic dynamics at metal surfaces.

cond-mat.mtrl-sci↗

arXiv2023

Electronic Friction Near Metal Surface: Incorporating Nuclear Quantum Effect with Ring Polymer Molecular Dynamics

Molecular dynamics with electronic friction (MDEF) approach can describe nonadiabatic effects accurately at metal surfaces in the weak nonadiabatic limit. That being said, MDEF treats nuclear motion classically, such that the nuclear quantum effects are missing completely in the approach. To address this limitation, we combine electronic friction with Ring Polymer Molecular Dynamics (RPMD). In particular, we apply the averaged electronic friction from the metal surface to the centroid mode of the ring polymer. We benchmark our approach against quantum dynamics to show that electronic friction with RPMD (EF-RPMD) can capture zero-point energy as well as transition dynamics accurately. In addition, we show EF-RPMD can correctly predict the electronic transfer rate near metal surfaces in the tunneling limit as well as the barrier crossing limit. We expect our approach will be very useful to study nonadiabatic dynamics near metal surface when nuclear quantum effects become essential.

physics.chem-ph↗

arXiv2023

Stochastic resolution of identity to CC2 for large systems: excited state properties

We apply a stochastic resolution of identity approximation (sRI) to the CC2 method for excitation energy calculations. A set of stochastic orbitals are employed to decouple the crucial 4-index electron repulsion integrals and optimize the contraction steps in CC2 response theory. The CC2 response for excitations builds upon sRI-CC2 ground-state calculations, which scales as O(N^3), where N is a measure for the system size. Overall, the current algorithm for excited states also allows a sharp scaling reduction from original O(N^5) to O(N^3). We test the sRI-CC2 for different molecular systems and basis sets, and we show our sRI-CC2 method can accurately reproduce the results of deterministic CC2 approach. Our sRI-CC2 exhibits an experimental scaling of O(N^2.88) for a hydrogen dimer chain, allowing us to calculate systems with nearly thousands of electrons.

physics.chem-ph↗

arXiv2023

Optical Regulation of Chiral-Induced Spin Selectivity

We present a non-perturbative theory that describes how light regulates chiral-induced spin selectivity (CISS) from the perspective of strong light-matter interactions. The research results indicate that 1) light can have opposite effects on the CISS, 2) the difference in CISS is caused by the steady states of nuclei coupled to spin electrons and 3) this steady state differences are caused by the different light-induced Lorentz forces felt by spin-up and spin-down electrons. The fundamental reason for these results is the impact of light on spin-orbital coupling (SOC), which is a complex process. This theoretical framework is verified by the calculations of Floquet SOC non-adiabatic nuclear dynamics.

quant-ph↗

arXiv2023

Nonadiabatic dynamics near metal surfaces with periodic drivings: A generalized surface hopping in Floquet representation

With light-matter interaction extending into strong regime, as well as rapid development of laser technology, systems subjecting to a time-periodic perturbation are attracted broad attention. Floquet theorem and Floquet time-independent Hamiltonian are powerful theoretical framework to investigate the systems subjecting to time-periodic drivings. In this study, we extend the previous generalized SH algorithm near metal surface (J. Chem. Theory Comput. 2017, 13, 6, 2430-2439) to the Floquet space, and hence, we develop a generalized Floquet representation based surface hopping (FR-SH) algorithm. Here, we consider open quantum system with fast drivings. We expect that the present algorithm will be useful for understanding the chemical processes of molecules under time-periodic drivings near the metal surface.

quant-ph↗

arXiv2023

Floquet Nonadiabatic Nuclear Dynamics with Photoinduced Lorenz-Like Force in Quantum Transport

In our recent paper [Mosallanejad et al., Phys. Rev. B 107(18), 184314, 2023], we have derived a Floquet electronic friction model to describe nonadiabatic molecular dynamics near metal surfaces in the presence of periodic driving. In this work, we demonstrate that Floquet driving can introduce an anti-symmetric electronic friction tensor in quantum transport, resulting in circular motion of the nuclei in the long time limit. Furthermore, we show that such a Lorentz-like force strongly affects nuclear motion: at lower voltage bias, Floquet driving can increase the temperature of nuclei; at larger voltage bias, Floquet driving can decrease the temperature of nuclei. In addition, Floquet driving can affect electron transport strenuously. Finally, we show that there is an optimal frequency that maximizes electron current. We expect that the Floquet electronic friction model is a powerful tool to study nonadiabatic molecular dynamics near metal surfaces under Floquet driving in complex systems.

quant-ph↗

arXiv2023

Periodically driven open quantum systems with vibronic interaction: Resonance effects and vibrationally mediated decoupling

Periodic driving and Floquet engineering have emerged as invaluable tools for controlling and uncovering novel phenomena in quantum systems. In this study, we adopt these methods to manipulate nonequilibrium processes within electronic-vibronic open quantum systems. Through resonance mechanisms and by focusing on the limit-cycle dynamics and quantum thermodynamic properties, we illustrate the intricate interplay between the driving field and vibronic states and its overall influence on the electronic system. Specifically, we observe an effective decoupling of the electronic system from the periodic driving at specific frequencies, a phenomenon that is mediated by the vibrational mode interaction. Additionally, we engineer the driving field to obtain a partial removal of the Franck-Condon blockade. These insights hold promise for efficient charge current control. Our results are obtained from numerically exact calculations of the hierarchical equations of motion and further analyzed by a time-periodic master equation approach.

quant-ph↗

arXiv2023

Predicting rate kernels via dynamic mode decomposition

Simulating dynamics of open quantum systems is sometimes a significant challenge, despite the availability of various exact or approximate methods. Particularly when dealing with complex systems, the huge computational cost will largely limit the applicability of these methods. We investigate the usage of dynamic mode decomposition (DMD) to evaluate the rate kernels in quantum rate processes. DMD is a data-driven model reduction technique that characterizes the rate kernels using snapshots collected from a small time window, allowing us to predict the long-term behaviors with only a limited number of samples. Our investigations show that whether the external field is involved or not, the DMD can give accurate prediction of the result compared with the traditional propagations, and simultaneously reduce the required computational cost.

quant-ph↗

arXiv2023

Electron transfer at molecule-metal interfaces under Floquet engineering: Rate constant and Floquet Marcus theory

Electron transfer (ET) at molecule-metal or molecule-semiconductor interfaces is a fundamental reaction that underlies all electro-chemical and molecular electronic processes as well as substrate-mediated surface photochemistry. In this study, we show that ET rates near a metal surface can be significantly manipulated by periodic modulations of an impurity level of the molecule near a metal surface. We employ the analytical Marcus theory and two numerical Floquet surface hopping algorithms that are developed previously, to calculate the ET rates near metal surface as a function of driving amplitudes and driving frequencies. We find that ET rates become faster with increasing the driving amplitude but no turnover effect, while have a turnover effect with increasing driving frequencies.

physics.chem-ph↗

arXiv2023

Nonadiabatic dynamics near metal surfaces under Floquet engineering: Floquet electronic friction vs. Floquet surface hopping

In the previous study (arXiv:2303.00479), we have derived a Floquet classical master equation (FCME) to treat nonadiabatic dynamics near metal surfaces under Floquet engineering. We have also proposed trajectory surface hopping algorithm to solve the FCME. In this study, we map the FCME into a Floquet Fokker-Planck equation in the limit of fast Floquet driving and fast electron motion as compared to nuclear motion. The Fokker-Planck equation is then being solved using Langevin dynamics with explicit friction and random force from the nonadiabatic effects of hybridized electron and Floquet states. We benchmark the Floquet electronic friction (FEF) dynamics against Floquet quantum master equation (FQME) and Floquet surface hopping (FSH). We find that Floquet driving results in violation of the second fluctuation-dissipation theorem, which further gives rise to heating effects.

cond-mat.mes-hall↗

arXiv2023

Floquet nonadiabatic dynamics in open quantum systems

The Born-Oppenheimer (BO) approximation has shaped our understanding on molecular dynamics microscopically in many physical and chemical systems. However, there are many cases that we must go beyond the BO approximation, particularly when strong light-matter interactions are considered. Floquet theory offers a powerful tool to treat time-periodic quantum systems. In this overview, we briefly review recent developments on Floquet nonadiabatic dynamics, with a special focus on open quantum systems. We first present the general Floquet Liouville von-Neumann (LvN) equation. We then show how to connect Floquet operators to real time observables. We proceed to outline the derivation of the Floquet quantum master equation in treating the dynamics under periodic driving in open quantum systems. We further present the Floquet mixed quantum classical Liouville equation (QCLE) to deal with coupled electron-nuclear dynamics. Finally, we embed FQCLE into a classical master equation (CME) to deal with Floquet nonadiabatic dynamics in open quantum systems. The formulations are general platforms for developing trajectory based dynamical approaches. As an example, we show how Floquet QCLE and Floquet CME can be implemented into a Langevin dynamics with Lorentz force and surface hopping algorithms.

quant-ph↗

arXiv2023

Nonadiabatic Dynamics Near Metal Surface With Periodic Drivings: A Floquet Surface Hopping Algorithm

We develop a Floquet surface hopping (FSH) approach to deal with nonadiabatic dynamics of molecules near metal surfaces subjected to time-periodic drivings from strong light-matter interactions. The method is based on a Floquet classical master equation (FCME) derived from a Floquet quantum master equation (FQME), followed by a Wigner transformation to treat nuclear motion classically. We then propose different trajectory surface hopping algorithms to solve the FCME. We find that a Floquet averaged surface hopping with electron density (FaSH-density) algorithm works the best as benchmarked with the FQME, capturing both the fast oscillations due to the driving as well as the correct steady state observables. This method will be very useful to study strong light-matter interactions with a manifold of electronic state.

quant-ph↗

arXiv2022

Stochastic resolution of identity to CC2 for large systems: ground-state properties

A stochastic resolution of identity approach (sRI) is applied to the second-order coupled cluster singles and doubles (CC2) model to calculate the ground-state energy. Utilizing a set of stochastic orbitals to optimize the expensive tensor contraction steps in CC2, we greatly reduce the overall computational cost. Compared with the RI-CC2 model, the sRI-CC2 achieves scaling reduction from O(N^5) to O(N^3), where N is a measure for the system size. When applying the sRI-CC2 to a series of hydrogen dimer chains, we demonstrate that the sRI-CC2 accurately reproduces RI-CC2 results for the correlation energies and exhibits a scaling of O(NH^2.71), with NH being the number of hydrogen atoms. Our calculations with different systems and basis sets show small changes in standard deviations, which indicates a broad applicability of our approach to various systems.

physics.chem-ph↗

arXiv2022

Active Spaces and Non-Orthogonal Configuration Interaction Approaches for Investigating Molecules on Metal Surfaces

We test a set of multiconfigurational wavefunction approaches for calculating the ground state electron population for a two-site Anderson model representing a molecule on a metal surface. In particular, we compare (i) a Hartree Fock like wavefunction where frontier orbitals are allowed to be nonorthogonal versus (ii) a fully non-orthogonal configuration interaction wavefunction based on constrained Hartree-Fock states. We test both the strong and weak metal-molecule hybridization ($Γ$) limits as well as the strong and weak electron-electron repulsion (U) limits. We obtain accurate results as compared with exact numerical renormalization group (NRG) theory, recovering charge transfer states where appropriate. The current framework should open a path to run molecular non-adiabatic dynamics on metal surfaces.

physics.chem-ph↗

arXiv2022

Floquet driven frictional effects

When the coupled electron-nuclear dynamics are subjected to strong Floquet driving, there is a strong breakdown of the Born-Oppenheimer approximation. In this article, we derive a Fokker-Planck equation to describe non-adiabatic molecular dynamics with electronic friction for Floquet driven systems. We first provide a new derivation of the Floquet quantum-classical Liouville equation (QCLE) for driven electron-nuclear dynamics. We then transform the Floquet QCLE into a Fokker-Planck equation with explicit forms of frictional force and random force. We recast the electronic friction in terms of Floquet Green's functions such that we can evaluate the electronic friction explicitly. We show that the Floquet electronic friction tensor exhibits antisymmetric terms even at equilibrium for real-valued Hamiltonian, suggesting that there is a Lorentz-like force in Floquet driven non-Born Oppenheimer dynamics even without any spin-orbit couplings.

quant-ph↗

arXiv2022

Chemical reactions in imperfect cavities: enhancement, suppression, and resonance

The use of optical cavities to control chemical reactions has been of great interest recently, following demonstrations of enhancement, suppression, and negligible effects on chemical reaction rates depending on the specific reaction and cavity frequency. In this work, we study the reaction rate inside imperfect cavities, where we introduce a broadening parameter in the spectral density to mimic Fabry-Pérot cavities. We investigate cavity modifications to reaction rates using non-Markovian Langevin dynamics with frictional and random forces to account for the presence of imperfect optical cavities. We demonstrate that in the regime of weak solvent and cavity friction, the cavity can enhance chemical reaction rates. On the other hand, in the high friction regime, cavities can suppress chemical reactions. Furthermore, we find that the broadening of the cavity spectral density gives rise to blue shifts of the resonance conditions and, surprisingly, increases the sharpness of the resonance effect.

physics.chem-ph↗

arXiv2022

Quantum thermodynamics of nonadiabatically driven systems: The effect of electron-phonon interaction

In this work we study the effects of nonadiabatic external driving on the thermodynamics of an electronic system coupled to two electronic leads and to a phonon mode, with and without damping. In the limit of slow driving, we establish nonadiabatic corrections to quantum thermodynamic quantities. In particular, we study the first-order correction to the electronic population, charge-current, and vibrational excitation using a perturbative expansion, and compare the results to the numerically exact hierarchical equations of motion (HEOM) approach. Furthermore, the HEOM analysis spans both the weak and strong system-bath coupling regime and the slow and fast driving limits. We show that the electronic friction and the nonadiabatic corrections to the charge-current provide a clear indicator for the Franck-Condon effect and for non-resonant tunneling processes. We also discuss the validity of the approximate quantum master equation approach and the benefits of using HEOM to study quantum thermodynamics out of equilibrium.

cond-mat.stat-mech↗