Electron–hole(e–h)recombination is a fundamental process that governs energy dissipation and device efficiency in semiconductors.In two-dimensional(2D)materials,the formation of tightly bound excitons makes exciton-...Electron–hole(e–h)recombination is a fundamental process that governs energy dissipation and device efficiency in semiconductors.In two-dimensional(2D)materials,the formation of tightly bound excitons makes exciton-mediated e–h recombination the dominant decay pathway.In this work,nonradiative e–h recombination within excitons in monolayer MoS2 is investigated using first-principles simulations that combine nonadiabatic molecular dynamics with𝐺𝑊and real-time Bethe–Salpeter equation(BSE)propagation.A two-step process is identified:rapid intervalley redistribution induced by exchange interaction,followed by slower phonon-assisted recombination facilitated by exciton binding.By selectively removing the screened Coulomb and exchange terms from the BSE Hamiltonian,their respective contributions are disentangled—exchange interaction is found to increase the number of accessible recombination pathways,while binding reduces the excitation energy and enhances nonradiative decay.A reduction in recombination lifetime by over an order of magnitude is observed due to the excitonic many-body effects.These findings provide microscopic insights for understanding and tuning exciton lifetimes in 2D transition-metal dichalcogenides.展开更多
Understanding the photoexcitation induced spin dynamics in ferromagnetic metals is important for the design of photo-controlled ultrafast spintronic device.In this work,by the ab initio nonadiabatic molecular dynamics...Understanding the photoexcitation induced spin dynamics in ferromagnetic metals is important for the design of photo-controlled ultrafast spintronic device.In this work,by the ab initio nonadiabatic molecular dynamics simulation,we have studied the spin dynamics induced by spin–orbit coupling(SOC)in Co and Fe using both spin-diabatic and spin-adiabatic representations.In Co system,it is found that the Fermi surface(E_(F))is predominantly contributed by the spin-minority states.The SOC induced spin flip will occur for the photo-excited spin-majority electrons as they relax to the E_(F),and the spin-minority electrons tend to relax to the EFwith the same spin through the electron–phonon coupling(EPC).The reduction of spin-majority electrons and the increase of spin-minority electrons lead to demagnetization of Co within100 fs.By contrast,in Fe system,the E_(F) is dominated by the spin-majority states.In this case,the SOC induced spin flip occurs for the photo-excited spin-minority electrons,which leads to a magnetization enhancement.If we move the E_(F) of Fe to higher energy by 0.6eV,the E_(F) will be contributed by the spin-minority states and the demagnetization will be observed again.This work provides a new perspective for understanding the SOC induced spin dynamics mechanism in magnetic metal systems.展开更多
Using ab initio nonadiabatic molecular dynamics simulation, we study the time-dependent charge transport dynamics in a single-molecule junction formed by gold(Au) electrodes and a single benzene-1,4-dithiol(BDT)molecu...Using ab initio nonadiabatic molecular dynamics simulation, we study the time-dependent charge transport dynamics in a single-molecule junction formed by gold(Au) electrodes and a single benzene-1,4-dithiol(BDT)molecule. Two different types of charge transport channels are found in the simulation. One is the routine nonresonant charge transfer path, which occurs in several picoseconds. The other is activated when the electronic state of the electrodes and that of the molecule get close in energy, which is referred to as the resonant charge transport. More strikingly, the resonant charge transfer occurs in an ultrafast manner within 100 fs, which notably increases the conductance of the device. Further analysis shows that the resonant charge transport is directly assisted by the B_(2) and A1 molecular vibration modes. Our study provides atomic insights into the time-dependent charge transport dynamics in single-molecule junctions, which is important for designing highly efficient single-molecule devices.展开更多
The covalent triazine framework CTF-1 as a member of the two-dimensional covalent organic frameworks(COFs)is a category of novel metal-free photocatalysts for water splitting.The large band gap severely restricts its ...The covalent triazine framework CTF-1 as a member of the two-dimensional covalent organic frameworks(COFs)is a category of novel metal-free photocatalysts for water splitting.The large band gap severely restricts its energy conversion efficiency.By means of the first-principles calculations,we proposed the decoration of CTF-1 by anchoring halogen atoms onto benzene moieties for improving the solar-to-hydrogen(STH)efficiency.The electronic structures reveal that the halogen substitution successfully decreases the band gap of CTF-1.Meanwhile,the calculated free energy changes along the reaction pathway indicate that all these COFs can spontaneously drive overall water splitting under light irradiation in a specific acid-base environment.The time-dependent ab initio non-adiabatic molecular dynamics simulations suggest that the electron-hole recombination periods of these COFs fall in a few to tens of nanoseconds.Excitingly,CTF-1 modified by linking six iodine atoms onto the benzene ring in the para-position(CTF-1-6I)shows a quite low band gap of 2.81 eV,indicating that it is a visible-light driven COF for overall photocatalytic water splitting.Correspondingly,CTF-1-6I also exhibits an extraordinarily promising STH efficiency of 3.70%,which is an order magnitude higher than that of the pristine CTF-1.展开更多
We perform an ab initio non-adiabatic molecular dynamics simulation to investigate the non-equilibrium spin and electron dynamics in a prototypical topological insulator(TI)Bi,Ses.Different from the ground state,we re...We perform an ab initio non-adiabatic molecular dynamics simulation to investigate the non-equilibrium spin and electron dynamics in a prototypical topological insulator(TI)Bi,Ses.Different from the ground state,we reveal that backscattering can happen in an oscillating manner between time-reversal pair topological surface states(TSSs)in the non-equilibrium dynamics.Analysis shows the phonon excitation induces orbital composition change by electron-phonon interaction,which further stimulates spin canting through spin-orbit coupling.The spin canting of time-reversal pair TSSs leads to the non-zero non-adiabatic coupling between them and then issues in backscattering.Both the spin canting and backscattering result in ultrafast spin relaxation with a timescale around 10o fs.This study provides critical insights into the non-equilibrium electron and spin dynamics in TI at the ab initio level and paves a way for the design of ultrafast spintronic materials.展开更多
Embedded data are used to retrieve phases quicker with high accuracy in phase-modulated holographic data storage(HDS).We propose a method to design an embedded data distribution using iterations to enhance the intensi...Embedded data are used to retrieve phases quicker with high accuracy in phase-modulated holographic data storage(HDS).We propose a method to design an embedded data distribution using iterations to enhance the intensity of the high-frequency signal in the Fourier spectrum.The proposed method increases the antinoise performance and signal-to-noise ratio(SNR)of the Fourier spectrum distribution,realizing a more efficient phase retrieval.Experiments indicate that the bit error rate(BER)of this method can be reduced by a factor of one after 10 iterations.展开更多
基金supported by the National Key Research and Development Program of China (Grant Nos.2024YFA1409800 for J.Z.and2024YFA1408603 for Q.Z.)the National Natural Science Foundation of China (Grant Nos.12125408,12334004for J.Z.,and 12174363 for Q.Z.)+1 种基金the Innovation Program for Quantum Science and Technology (Grant No.2021ZD0303306 for J.Z.)the Strategic Priority Research Program of the Chinese Academy of Sciences(Grant No.XDB0450101 for J.Z.)。
文摘Electron–hole(e–h)recombination is a fundamental process that governs energy dissipation and device efficiency in semiconductors.In two-dimensional(2D)materials,the formation of tightly bound excitons makes exciton-mediated e–h recombination the dominant decay pathway.In this work,nonradiative e–h recombination within excitons in monolayer MoS2 is investigated using first-principles simulations that combine nonadiabatic molecular dynamics with𝐺𝑊and real-time Bethe–Salpeter equation(BSE)propagation.A two-step process is identified:rapid intervalley redistribution induced by exchange interaction,followed by slower phonon-assisted recombination facilitated by exciton binding.By selectively removing the screened Coulomb and exchange terms from the BSE Hamiltonian,their respective contributions are disentangled—exchange interaction is found to increase the number of accessible recombination pathways,while binding reduces the excitation energy and enhances nonradiative decay.A reduction in recombination lifetime by over an order of magnitude is observed due to the excitonic many-body effects.These findings provide microscopic insights for understanding and tuning exciton lifetimes in 2D transition-metal dichalcogenides.
基金support of Strategic Priority Research Program of the Chinese Academy of Sciences(Grant No.XDB0450101)the National Natural Science Foundation of China(Grant Nos.12125408 and 11974322)+1 种基金the Informatization Plan of Chinese Academy of Sciences(Grant No.CAS-WX2021SF-0105)the support of the National Natural Science Foundation of China(Grant No.12174363)。
文摘Understanding the photoexcitation induced spin dynamics in ferromagnetic metals is important for the design of photo-controlled ultrafast spintronic device.In this work,by the ab initio nonadiabatic molecular dynamics simulation,we have studied the spin dynamics induced by spin–orbit coupling(SOC)in Co and Fe using both spin-diabatic and spin-adiabatic representations.In Co system,it is found that the Fermi surface(E_(F))is predominantly contributed by the spin-minority states.The SOC induced spin flip will occur for the photo-excited spin-majority electrons as they relax to the E_(F),and the spin-minority electrons tend to relax to the EFwith the same spin through the electron–phonon coupling(EPC).The reduction of spin-majority electrons and the increase of spin-minority electrons lead to demagnetization of Co within100 fs.By contrast,in Fe system,the E_(F) is dominated by the spin-majority states.In this case,the SOC induced spin flip occurs for the photo-excited spin-minority electrons,which leads to a magnetization enhancement.If we move the E_(F) of Fe to higher energy by 0.6eV,the E_(F) will be contributed by the spin-minority states and the demagnetization will be observed again.This work provides a new perspective for understanding the SOC induced spin dynamics mechanism in magnetic metal systems.
基金the support of the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDB0450101)the National Key R&D Program of China (Grant No. 2017YFA0204904)+3 种基金the National Natural Science Foundation of China (Grant Nos. 11974322 and 12125408)the Informatization Plan of Chinese Academy of Sciences (Grant No. CAS-WX2021SF-0105)the National Natural Science Foundation of China (Grant No. 12174363)support from the National Science Foundation (Grant No. CHE-2102601)。
文摘Using ab initio nonadiabatic molecular dynamics simulation, we study the time-dependent charge transport dynamics in a single-molecule junction formed by gold(Au) electrodes and a single benzene-1,4-dithiol(BDT)molecule. Two different types of charge transport channels are found in the simulation. One is the routine nonresonant charge transfer path, which occurs in several picoseconds. The other is activated when the electronic state of the electrodes and that of the molecule get close in energy, which is referred to as the resonant charge transport. More strikingly, the resonant charge transfer occurs in an ultrafast manner within 100 fs, which notably increases the conductance of the device. Further analysis shows that the resonant charge transport is directly assisted by the B_(2) and A1 molecular vibration modes. Our study provides atomic insights into the time-dependent charge transport dynamics in single-molecule junctions, which is important for designing highly efficient single-molecule devices.
基金supported by the National Natural Science Foundation of China(21688102)the National Key Research and Development Program of China(2016YFA0200604)Anhui Initiative in Quantum Information Technologies(AHY090400)。
文摘The covalent triazine framework CTF-1 as a member of the two-dimensional covalent organic frameworks(COFs)is a category of novel metal-free photocatalysts for water splitting.The large band gap severely restricts its energy conversion efficiency.By means of the first-principles calculations,we proposed the decoration of CTF-1 by anchoring halogen atoms onto benzene moieties for improving the solar-to-hydrogen(STH)efficiency.The electronic structures reveal that the halogen substitution successfully decreases the band gap of CTF-1.Meanwhile,the calculated free energy changes along the reaction pathway indicate that all these COFs can spontaneously drive overall water splitting under light irradiation in a specific acid-base environment.The time-dependent ab initio non-adiabatic molecular dynamics simulations suggest that the electron-hole recombination periods of these COFs fall in a few to tens of nanoseconds.Excitingly,CTF-1 modified by linking six iodine atoms onto the benzene ring in the para-position(CTF-1-6I)shows a quite low band gap of 2.81 eV,indicating that it is a visible-light driven COF for overall photocatalytic water splitting.Correspondingly,CTF-1-6I also exhibits an extraordinarily promising STH efficiency of 3.70%,which is an order magnitude higher than that of the pristine CTF-1.
基金the support of the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB0450101)the Innovation Program for Quantum Science and Technology (2021ZD0303306)+2 种基金the National Natural Science Foundation of China (12125408, 11974322 and 12334004)the Informatization Plan of the Chinese Academy of Sciences (CASWX2021SF-0105)the support of the National Natural Science Foundation of China (12174363)。
基金supported by National Key R&D Program of China(Grant No.2017YFA0204904)National Natural Science Foundation of China(Grants No.11620101003 and 11974322)Anhui Initiative in Quantum Information Technologies(Grant No.AHY090300).Calculations were performed at Environmental Molecular Sciences Laboratory at the Pacific Northwest National Laboratory,a user facility sponsored by the Us Department of Energy Office of Biological and Environmental Research.
文摘We perform an ab initio non-adiabatic molecular dynamics simulation to investigate the non-equilibrium spin and electron dynamics in a prototypical topological insulator(TI)Bi,Ses.Different from the ground state,we reveal that backscattering can happen in an oscillating manner between time-reversal pair topological surface states(TSSs)in the non-equilibrium dynamics.Analysis shows the phonon excitation induces orbital composition change by electron-phonon interaction,which further stimulates spin canting through spin-orbit coupling.The spin canting of time-reversal pair TSSs leads to the non-zero non-adiabatic coupling between them and then issues in backscattering.Both the spin canting and backscattering result in ultrafast spin relaxation with a timescale around 10o fs.This study provides critical insights into the non-equilibrium electron and spin dynamics in TI at the ab initio level and paves a way for the design of ultrafast spintronic materials.
基金the Open Project Program of Wuhan National Laboratory for Optoelectronics(No.2019WNLOKF007)the National Key R&D Program of China(No.2018YFA0701800).
文摘Embedded data are used to retrieve phases quicker with high accuracy in phase-modulated holographic data storage(HDS).We propose a method to design an embedded data distribution using iterations to enhance the intensity of the high-frequency signal in the Fourier spectrum.The proposed method increases the antinoise performance and signal-to-noise ratio(SNR)of the Fourier spectrum distribution,realizing a more efficient phase retrieval.Experiments indicate that the bit error rate(BER)of this method can be reduced by a factor of one after 10 iterations.
