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We have developed an ab initio-based, fully quantum, numerically accurate methodology for the simulation of the exciton dynamics and time- and frequency-resolved fluorescence spectra of the cavity-controlled two-dimensional materials at finite temperatures and applied this methodology to the single-layer WSe2 system. Specifically, the multiple Davydov D2 Ansatz has been employed in combination with the method of thermofield dynamics for the finite-temperature extension of accurate time-dependent variation. This allowed us to establish dynamical and spectroscopic signatures of the polaronic and polaritonic effects as well as uncover their characteristic time scales in the relevant range of temperatures. Our study reveals the pivotal role of multidimensional conical intersections in controlling the many-body dynamics of highly intertwined excitonic, phononic, and photonic modes. Ministry of Education (MOE) Submitted/Accepted version The authors gratefully acknowledge the support of the Singapore Ministry of Education Academic Research Fund (Grant Nos. RG190/18 and RG87/20). K. Sun would also like to thank the Natural Science Foundation of Zhejiang Province (Grant No. LY18A040005) for partial Support. M. F. G. acknowledges the support of Hangzhou Dianzi University through startup funding.

We investigate dynamic signatures of the singlet fission (SF) process triggered by the excitation of a molecular system to an upper singlet state SN (N > 1) and develop a computational methodology for the simulation of nonlinear spectroscopic signals revealing the SN → TT1 SF in real time. We demonstrate that SF can proceed directly from the upper state SN, bypassing the lowest excited state, S1. We determine the main SN → TT1 reaction pathways and show by computer simulation and spectroscopic measurements that the SN-initiated SF can be faster and more efficient than the traditionally studied S1 → TT1 SF. We claim that the SN → TT1 SF offers novel promising opportunities for engineering SF systems and enhancing SF yields. Ministry of Education (MOE) Submitted/Accepted version L.C. was supported by the Key Research Project of Zhejiang Lab (2021PE0AC02). L.M. was supported by the National Natural Science Foundation of China (Grant 11874125). Y.Z. gratefully acknowledges the support of the Singapore Ministry of Education Academic Research Fund (Grants RG190/18 and RG87/20). G.G.G.’s research was funded by a DUT startup grant and by the National Natural Science Foundation of China (Grant 22088102). W.N. and M.F.G. acknowledge support of Hangzhou Dianzi University through startup funding

By employing the doorway-window (DW) on-the-fly simulation protocol, we performed ab initio simulations of peak evolutions and beating maps of electronic two-dimensional (2D) spectra of a polyatomic molecule in the gas phase. As the system under study, we chose pyrazine, which is a paradigmatic example of photodynamics dominated by conical intersections (CIs). From the technical perspective, we demonstrate that the DW protocol is a numerically efficient methodology suitable for simulations of 2D spectra for a wide range of excitation/detection frequencies and population times. From the information content perspective, we show that peak evolutions and beating maps not only reveal timescales of transitions through CIs but also pinpoint the most relevant coupling and tuning modes active at these CIs.

A numerically accurate, fully quantum methodology has been developed for the simulation of the dynamics and nonlinear spectroscopic signals of cavity-assisted, conical-intersection-controlled singlet fission systems. The methodology is capable of handling several molecular systems strongly coupled to the photonic mode of the cavity and treats the intrinsic conical intersection and cavity-induced polaritonic conical intersections in a numerically exact manner. Contributions of higher-lying molecular electronic states are accounted for comprehensively. The intriguing process of cavity-modified fission dynamics, including all of its electronic, vibrational, and photonic degrees of freedom, together with its two-dimensional spectroscopic manifestation, is simulated for two rubrene dimers strongly coupled to the cavity mode. Ministry of Education (MOE) Submitted/Accepted version The authors gratefully acknowledge the support of the Singapore Ministry of Education Academic Research Fund (Grants RG190/18 and RG87/20). K.S. thanks the Natural Science Foundation of Zhejiang Province (Grant LY18A040005) for partial support. M.F.G. acknowledges the support of Hangzhou Dianzi University through startup funding.

We investigate the dynamics of Landau-Zener transitions in an anisotropic, dissipative three-level model (3-LZM) using the numerically accurate multiple Davydov D2 Ansatz in the framework of time-dependent variation. It is demonstrated that a non-monotonic relationship exists between the Landau-Zener transition probability and the phonon coupling strength when the 3-LZM is driven by a linear external field. Under the influence of a periodic driving field, phonon coupling may induce peaks in contour plots of the transition probability when the magnitude of the system anisotropy matches the phonon frequency. Dynamics of the 3-LZM have also been probed in the presence of a super-ohmic phonon bath when driven by a periodic driving field. It is found that both the period and the amplitude of the Rabi cycle decay exponentially with the increasing bath coupling strength., 12 pages, 7 figures

The ultrafast nonadiabatic internal conversion in azomethane is explored by the on-the-fly trajectory surface-hopping simulations of photoinduced dynamics and femtosecond transient absorption (TA) pump-probe (PP) spectra at three electronic-structure theory levels, OM2/MRCI, SA-CASSCF, and XMS-CASPT2. All these dynamics simulations predict ultrafast internal conversion. On the one hand, the OM2/MRCI and SA-CASSCF methods yield similar excited-state dynamics, while the XMS-CASPT2 method predicts a much slower population decay. On the other hand, the TA PP signals simulated at the SA-CASSCF and XMS-CASPT2 levels show the similar spectral features, particularly for the similar stimulated emission contributions, while the OM2/MRCI signals are quite different. This demonstrates that the nonadiabatic population dynamics and time-resolved stimulated emission signals may reflect different aspects of photoinduced processes. The combination of the dynamical and spectral simulations definitely provides more accurate and detailed information which sheds light on the microscopic mechanisms of photophysical and photochemical processes.

Dynamics of the (sub-)Ohmic spin-boson model under various bath initial conditions is investigated by employing the Dirac-Frenkel time-dependent variational approach with the multiple Davydov $\mathrm{D_1}$ ansatz in the interaction picture. The validity of our approach is carefully checked by comparing results with those of the hierarchy equations of motion method. By analyzing the features of nonequilibrium dynamics, we identify the phase diagrams for different bath initial conditions. We find that for spectral exponent $s, Comment: 9 pages

The time-resolved polarization-sensitive transient-absorption (TA) pump-probe (PP) spectra are simulated using on-the-fly surface-hopping nonadiabatic dynamics and the doorway-window representation of nonlinear spectroscopy. A dendrimer model system composed of two linear phenylene ethynylene units (2-ring and 3-ring) is taken as an example. The ground-state bleach (GSB), stimulated emission (SE), and excited-state absorption (ESA) contributions as well as the total TA PP signals are obtained and carefully analyzed. It is shown that intramolecular excited-state energy transfer from the 2-ring unit to the 3-ring unit can be conveniently identified by employing pump and probe pulses with different polarizations. Our results demonstrate that time-resolved polarization-sensitive TA PP signals provide a powerful tool for the elucidation of excited-state energy-transfer pathways, notably in molecular systems possessing several optically bright nonadiabatically coupled electronic states with different orientations of transition dipole moments.

By employing the numerically exact multiple Davydov D2 ansatz, we study cavity-manipulated singlet fission that is mediated by polaritonic conical intersections for both one- and two-molecule systems. The population evolution of the TT state and the cavity photons is carefully examined in search for a high fission efficiency via cavity engineering. Several interesting mechanisms have been uncovered, such as photon-assisted singlet fission, system localization via a displaced photon state, and collective enhancement of the fission efficiency for the two-molecule system. It is also found that the system localization process in the two-molecule system differs substantially from that in the one-molecule system because of the appearance of a novel central polaritonic conical intersection in the two-molecule system. It has been demonstrated that the cavity-controlled singlet fission process can be switched on and off by controlling the average pumping photon number. Ministry of Education (MOE) Submitted/Accepted version The authors gratefully acknowledge the support of the Singapore Ministry of Education Academic Research Fund (Grant Nos. RG190/18 and RG87/20). K.S. thanks the Natural Science Foundation of Zhejiang Province (Grant No. LY18A040005) for partial support. M.F.G. acknowledges support of Hangzhou Dianzi University through startup funding.

Relaxation pathways of upper excited electronic states of malachite green (MG) in ethanol and in films are studied by steady-state and time-resolved spectroscopic techniques. In contrast to ethanol, where MG emits weak short-lived spectrally well separated S

Self assembled ordered structures, such as H- or J- type molecular aggregates of organic chromophores, are extremely interesting materials for different optoelectronic applications. In this work we present a novel characterization of light harvesting nanotubes formed by self-assembling of amphiphilic cyanine dyes in water, through a combined ultrafast spectroscopic and theoretical approach. In the condition of low inhomogeneous disorder at low temperature, broadband transient absorption spectroscopy revealed the presence of an unusual ultrafast behavior of the aggregate, manifested through intense and peculiar oscillations of the kinetic traces, lasting tens of picoseconds. Theoretical simulations were performed by adapting a model which grasps vibronically coherent effects in the double wall nanotube system experiencing inter-wall energy transfer. Good agreement between model predictions and experimental observations were obtained under the assumption of coupling between bright and dark electronic states. The model clarified the vibronic origin of the observed oscillations, evidencing new important pieces of information about transport mechanisms and excitonic interactions in these complex molecular systems.

By employing the time-dependent variational principle and the versatile multi-D2 Davydov trial states, in combination with the Green's function method, we study the dynamics of the Tavis-Cummings model and the Holstein-Tavis-Cummings model in the presence of diagonal disorder and cavity-qubit coupling disorder. For the Tavis-Cummings model, time evolution of the photon population, the optical absorption spectra, and the hetero-entanglement between the qubits and the cavity mode are calculated by using the Green's function method to corroborate numerically exact results of Davydov's Ansätze. For the Holstein-Tavis-Cummings model, only the latter is utilized to simulate effects of disorder on the photon population dynamics and the absorption spectra. We have demonstrated that the complementary employment of analytical and numerical methods permits uncovering a fairly comprehensive picture of a variety of complex behaviors in disordered multidimensional polaritonic cavity quantum electrodynamics systems. Ministry of Education (MOE) Submitted/Accepted version The authors acknowledge the support from the Singapore Ministry of Education Academic Research Fund (Grant Nos. RG190/18 and 2020-T1-002-075). K. Sun acknowledges the Natural Science Foundation of Zhejiang Province (Grant No. LY18A040005) for partial support. M.F.G. acknowledges Hangzhou Dianzi University for startup funding.

Two-dimensional (2D) electronic spectroscopy is a powerful nonlinear technique which provides spectroscopic information on two frequency axes as well as dynamical information as a function of the so-called waiting time. Herein, an ab initio theoretical framework for the simulation of electronic 2D spectra has been developed. The method is based on the classical approximation to the doorway-window representation of three-pulse photon-echo signals and the description of nuclear motion by classical trajectories. Nonadiabatic effects are taken into account by a trajectory surface-hopping algorithm. 2D electronic spectra were simulated with ab initio on-the-fly trajectory calculations using the ADC(2) electronic-structure method for the pyrazine molecule, which is a benchmark system for ultrafast radiationless decay through conical intersections. It is demonstrated that 2D spectroscopy with subfemtosecond UV pulses can provide unprecedented detailed information on the ultrafast photodynamics of polyatomic molecules.

A long 0.9 ps lifetime of the upper excited singlet state in perylene is resolved by femtosecond pump-probe measurements under ultraviolet (4.96 eV) excitation and further validated by theoretical simulations of transient absorption kinetics. This finding prompts exploration and development of novel perylene-based materials for upper excited state photochemistry applications.

The time-resolved polarization-sensitive transient-absorption (TA) pump-probe (PP) spectra are simulated using on-the-fly surface-hopping nonadiabatic dynamics and the doorway-window (DW) representation of nonlinear spectroscopy. A typical dendrimer model system composed of two linear phenylene ethynylene units (2-ring, 3-ring) is taken as an example. The fewest switches trajectory surface hopping algorithm along with the TDDFT method is adopted in the nonadiabatic dynamics simulations. The ground-state bleach (GSB), stimulated emission (SE), excited-state absorption (ESA) contributions as well as the total TA PP signals are obtained and carefully analyzed. The correlations between these signals and the coupled nuclear-electronic dynamics are established. It is shown that intramolecular excited-state energy transfer from the 2-ring unit to the 3-ring unit can be conveniently monitored and accurately identified by employing pump and probe pulses with different polarizations. Our on-the-fly nonadiabatic simulation results demonstrate that time-resolved polarization-sensitive TA PP signals provide a powerful tool for the elucidation of excited-state energy transfer pathways, notably in molecular systems possessing several optically-bright nonadiabatically-coupled electronic states with different orientations of transition dipole moments.

A computational protocol for simulating time-resolved photoelectron signals of medium-sized molecules is presented. The procedure is based on a trajectory surface-hopping description of the excited-state dynamics and a combined Dyson orbital and multicenter B-spline approach for the computation of cross sections and asymmetry parameters. The accuracy of the procedure has been illustrated for the case of ultrafast internal conversion of gas-phase pyrazine excited to the 1B2u(ππ*) state. The simulated spectra and the asymmetry map are compared to the experimental data, and a very good agreement was obtained without applying any energy-dependent rescaling or broadening. An interesting side result of this work is the finding that the signature of the 1Au(nπ*) state is indistinguishable from that of the 1B3u(nπ*) state in the time-resolved photoelectron spectrum. By locating four symmetrically equivalent minima on the lowest-excited (S1) adiabatic potential energy surface of pyrazine, we revealed the strong vibronic coupling of the 1Au(nπ*) and 1B3u(nπ*) states near the S1 ← S0 band origin.

Monitoring of wave packet dynamics at conical intersections by time- and frequency-resolved fluorescence spectroscopy has been investigated theoretically for a three-state two-mode model of a conical intersection coupled to a dissipative environment. The ideal and the actually measurable time- and frequency-gated fluorescence spectra are accurately and efficiently simulated by combining the hierarchy equations-of-motion method for dissipative quantum dynamics with the methodology of the equation-of-motion phase-matching approach for the calculation of spectroscopic signals. It is shown that time- and frequency-resolved fluorescence spectra reveal essential aspects of the wave packet dynamics at conical intersections and the effects of environment-induced dissipation. The results of the present work indicate that fluorescence up-conversion spectroscopy with femtosecond time resolution is an efficient tool for the characterization of ultrafast dynamics at conical intersections. Accepted version L.P.C. acknowledges support by a postdoctoral fellowship of the Alexander von Humboldt-Foundation. M.F.G. and W.D. acknowledge support from the Deutsche Forschungsgemeinschaft through a research grant and through the DFG Cluster of Excellence Munich-Centre for Advanced Photonics (http:// www.munich-photonics.de).

We study how the effects of finite pulse durations modify the fifth-order two-quantum two-dimensional (2Q-2D) and three-dimensional (3D) optical spectra. Instead of directly calculating the time domain polarization, the equivalent approach in frequency domain significantly simplifies the calculations and delivers exact expressions for the 2Q-2D and 3D spectra. Our results minimize the number of numerical integrations needed. We also derive simple analytical formulas for practically important situations when the laser pulses are short on the timescale of nuclear motion as well as short (or long) on the timescale of electronic dephasing. These formulas evaluate the measured spectra by multiplying the spectral response function by a factor depending on the spectral pulse envelopes.

Accuracies of three multiple Davydov Ansatze, namely, the multi- D 1 , the multi- D 1.5 , and the multi- D 2 Ansatz, in describing the population dynamics of the spin boson model, are carefully examined by a detailed comparison with numerically exact (multilayer) multiconfiguration time-dependent Hartree method. The comparison shows that these three Ansatze yield quantitatively accurate results in the adiabatic (slow bath), nonadiabatic (fast bath), as well as the intermediate regime. It is found that with an increase in the energy bias and/or spin-bath coupling, a much larger multiplicity is required for the three Ansatze to capture the correct population dynamics. The multi- D 1.5 Ansatz, which combines the accuracy of the multi- D 1 Ansatz and the simplicity of the multi- D 2 Ansatz, outperforms the multi- D 2 Ansatz. The multi- D 1.5 Ansatz thus provides a numerically promising alternative to the multi- D 1 Ansatz in the accurate simulation of spin-boson dynamics, especially for systems with a large number of vibrational degrees of freedom.

An ab initio theoretical framework for the simulation of femtosecond time-resolved transient absorption (TA) pump-probe (PP) spectra with quasi-classical trajectories is presented. The simulations are based on the classical approximation to the doorway-window (DW) representation of third-order four-wave-mixing signals. The DW formula accounts for the finite duration and spectral shape of the pump and probe pulses. In the classical DW formalism, classical trajectories are stochastically sampled from a positive definite doorway distribution, and the signals are evaluated by averaging over a positive definite window distribution. Nonadiabatic excited-state dynamics is described by a stochastic surface-hopping algorithm. The method has been implemented for the pyrazine molecule with the second-order algebraic-diagrammatic construction (ADC(2)) ab initio electronic-structure method. The methodology is illustrated by ab initio simulations of the ground-state bleach, stimulated emission, and excited-state absorption contributions to the TA PP spectrum of gas-phase pyrazine.

We have extended the multiconfigurational Ehrenfest approach to the simulation of four-wave-mixing signals of systems involving multiple electronic and vibrational degrees of freedom. As an illustration, we calculate signals of three widely used spectroscopic techniques, time- and frequency-resolved fluorescence spectroscopy, transient absorption spectroscopy, and two-dimensional (2D) electronic spectroscopy, for a two-electronic-state, twenty-four vibrational-mode conical intersection model. It has been shown that all these three spectroscopic signals characterize fast population transfer from the higher excited electronic state to the lower excited electronic state. While the time- and frequency-resolved spectrum maps the wave packet propagation exclusively on the electronically excited states, the transient absorption and 2D electronic spectra reflect the wave packet dynamics on both electronically excited states and the electronic ground state. Combining trajectory-guided Gaussian basis functions and the nonlinear response function formalism, the present approach provides a promising general technique for the applications of various Gaussian basis methods to the calculations of four-wave-mixing spectra of polyatomic molecules. Ministry of Education (MOE) Published version L. Chen acknowledges support from the Max-Planck Gesellschaft via the MPI-PKS visitors program. K. Sun would like to thank the Natural Science Foundation of Zhejiang Province (Grant No. LY18A040005) for support. M. F. Gelin acknowledges the support of Hangzhou Dianzi University through the startup funding. Y. Zhao would like to thank the support of the Singapore Ministry of Education Academic Research Fund Tier 1 (Grant Nos. 2018-T1- 002-175 and 2020-T1-002-075) and Tier 2 (Grant No. MOE2019- T2-1-085). D.V.S. acknowledges EPSRC (Grant No. EP/P021123/1).

Confined nanoscale spaces, electric fields, and tunneling currents make the molecular electronic junction an experimental device for the discovery of new out-of-equilibrium chemical reactions. Reaction-rate theory for current-activated chemical reactions is developed by combining the Keldysh nonequilibrium Green's function treatment of electrons, Fokker-Planck description of the reaction coordinate, and Kramers first-passage time calculations. The nonequilibrium Green's functions (NEGF) provide an adiabatic potential as well as a diffusion coefficient and temperature with local dependence on the reaction coordinate. Van Kampen's Fokker-Planck equation, which describes a Brownian particle moving in an external potential in an inhomogeneous medium with a position-dependent friction and diffusion coefficient, is used to obtain an analytic expression for the first-passage time. The theory is applied to several transport scenarios: a molecular junction with a single reaction coordinate dependent molecular orbital and a model diatomic molecular junction. We demonstrate the natural emergence of Landauer's blowtorch effect as a result of the interplay between the configuration dependent viscosity and diffusion coefficients. The resultant localized heating in conjunction with the bond-deformation due to current-induced forces is shown to be the determining factors when considering chemical reaction rates, each of which results from highly tunable parameters within the system.

For a broad class of quantum models of practical interest, we demonstrate that the Hamiltonian of the system nonlinearly coupled to a harmonic bath through the system and bath coordinates can be equivalently mapped into the Hamiltonian of the system bilinearly coupled to the bath through the system and bath momenta. We show that the Hamiltonian with bilinear system-bath momentum coupling can be treated by the hierarchical equations-of-motion (HEOM) method and present the corresponding proof-of-principle simulations. The developed methodology creates the opportunity to scrutinize a new family of nonlinear quantum systems by the numerically accurate HEOM method.

We propose a new approach to simulate four-wave-mixing signals of molecular systems at finite temperatures by combining the multiconfigurational Ehrenfest method with the thermo-field dynamics theory. In our approach, the four-time correlation functions at finite temperatures are mapped onto those at zero temperature in an enlarged Hilbert space with twice the vibrational degrees of freedom. As an illustration, we have simulated three multidimensional spectroscopic signals, time- and frequency-resolved fluorescence spectra, transient-absorption pump-probe spectra, and electronic two-dimensional (2D) spectra at finite temperatures, for a conical intersection-mediated singlet fission model of a rubrene crystal. It is shown that a detailed dynamical picture of the singlet fission process can be extracted from the three spectroscopic signals. An increasing temperature leads to lower intensities of the signals and broadened vibrational peaks, which can be attributed to faster singlet-triplet population transfer and stronger bath-induced electronic dephasing at higher temperatures. Ministry of Education (MOE) Submitted/Accepted version L.P.C. acknowledges support from the Max-Planck Gesellschaft via the MPI-PKS visitors program. D.V.S. acknowledges EPSRC (Grant No. EP/P021123/1). Y.Z. thanks the Singapore Ministry of Education Academic Research Fund Tier 1 (Grant Nos. 2018-T1-002-175 and 2020-T1-002-075) for support. M.F.G. acknowledges the support of Hangzhou Dianzi University through startup funding.

We present a unified and highly numerically efficient formalism for the simulation of quantum dynamics of complex molecular systems, which takes into account both temperature effects and static disorder. The methodology is based on the thermo-field dynamics formalism, and Gaussian static disorder is included into simulations via auxiliary bosonic operators. This approach, combined with the tensor-train/matrix-product state representation of the thermalized stochastic wave function, is applied to study the effect of dynamic and static disorders in charge-transfer processes in model organic semiconductor chains employing the Su-Schrieffer-Heeger (Holstein-Peierls) model Hamiltonian.

Experimental measurements of electron transport properties of molecular junctions are often performed in solvents. Solvent-molecule coupling and physical properties of the solvent can be used as the external stimulus to control the electric current through a molecule. In this paper, we propose a model that includes dynamical effects of solvent-molecule interaction in non-equilibrium Green's function calculations of the electric current. The solvent is considered as a macroscopic dipole moment that reorients stochastically and interacts with the electrons tunneling through the molecular junction. The Keldysh-Kadanoff-Baym equations for electronic Green's functions are solved in the time domain with subsequent averaging over random realizations of rotational variables using the Furutsu-Novikov method for the exact closure of infinite hierarchy of stochastic correlation functions. The developed theory requires the use of wideband approximation as well as classical treatment of solvent degrees of freedom. The theory is applied to a model molecular junction. It is demonstrated that not only electrostatic interaction between molecular junction and solvent but also solvent viscosity can be used to control electrical properties of the junction. Alignment of the rotating dipole moment breaks the particle-hole symmetry of the transmission favoring either hole or electron transport channels depending upon the aligning potential.

Volatile organic compounds (VOCs) present in human breath not only provide information about the internal chemistry of the body but can also be specific to diseases. Therefore, detection and analysis of specific VOCs can be used for medical diagnostics. However, up until today in spite of several existing VOC-based detection techniques and significant efforts, breath analysis is not a diagnostic method available for clinicians. Infrared absorption spectroscopy is a promising technique to fill this gap, with tens of identified VOCs in breath. Currently, a lack of digital spectral databases and several masking effects make difficult reliable molecular identification of observed absorption features. We demonstrate that calculations of rotational bands of vibrational spectra could serve as a basic method for molecular identification of spectral features observed in experiment. Results of comparison of several known VOCs spectra with the predictions of the theoretical model are presented.

We studied spectroscopic signatures of the nonadiabatic dynamics at conical intersections formed by the lowest excited singlet states in pyrazine. We considered two ab initio models of conical intersections in the excited states of pyrazine developed by Sala et al. [Phys. Chem. Chem. Phys. 16, 15957 (2014)]: a two-state (B2u and B3u), five-mode model and a three-state (B2u, B3u, and Au), nine-mode model. We simulated the signals of three widely used techniques: time- and frequency-resolved fluorescence spectroscopy, transient absorption pump–probe spectroscopy, and electronic two-dimensional spectroscopy. The signals were calculated through third-order response functions, which, in turn, were evaluated with the numerically accurate multiple Davydov ansatz. We establish spectroscopic signatures of the optically dark Au state and demonstrate that the key features of the photoinduced dynamics, such as electronic/nuclear populations, electronic/nuclear coherences, and electronic/nuclear energy transfer processes, are imprinted in the spectroscopic signals. We show that a fairly complete picture of the nonadiabatic dynamics at conical intersections can be obtained when several spectroscopic techniques are combined. Provided that the time resolution is sufficient, time- and frequency-resolved fluorescence may provide the best visualization of the nonadiabatic dynamics near conical intersections.

The effects of high pulse intensity and chirp on two-dimensional electronic spectroscopy signals are experimentally investigated in the highly non-perturbative regime using atomic rubidium vapor as clean model system. Data analysis is performed based on higher-order Feynman diagrams and non-perturbative numerical simulations of the system response. It is shown that higher-order contributions may lead to a fundamental change of the static appearance and beating-maps of the 2D spectra and that chirped pulses enhance or suppress distinct higher-order pathways. We further give an estimate of the threshold intensity beyond which the high-intensity effects become visible for the system under consideration.

We have extended the multiconfigurational Ehrenfest (MCE) approach to investigate the dynamics of a one-dimensional Holstein molecular crystal model. It has been shown that the extended MCE approach yields results in perfect agreement with benchmark calculations by the hierarchy equations of motion method. The accuracies of the MCE approach in describing the dynamical properties of the Holstein polaron over a wide range of exciton transfer integrals and exciton-phonon couplings are carefully examined by a detailed comparison with the fully variational multiple Davydov D2 ansatz. It is found that while the MCE approach and the multi-D2 ansatz produce almost exactly the same results for a small transfer integral, the results obtained by the multi-D2 ansatz start to deviate from those by the MCE approach at longer times for a large transfer integral. A large number of coherent state basis functions are required to characterize the delocalized features of the phonon wavefunction in the case of large transfer integral, which becomes computationally too demanding for the multi-D2 ansatz. The MCE approach, on the other hand, uses hundreds to thousands of trajectory guided basis functions and converges very well, thus providing an effective tool for accurate and efficient simulations of polaron dynamics.

Finite-temperature dynamics of singlet fission in crystalline rubrene is investigated by utilizing the Dirac-Frenkel time-dependent variational method in combination with multiple Davydov D2 trial states. To probe temperature effects on the singlet fission process mediated by a conical intersection, the variational method is extended to include number state propagation with thermally averaged Boltzmann distribution as initialization. This allows us to simulate two-dimensional electronic spectroscopic signals of two-mode and three-mode models of crystalline rubrene in the temperature range from 0 K to 300 K. It is demonstrated that an elevated temperature facilitates excitonic population transfer and accelerates the singlet fission process. In addition, increasing temperature leads to dramatic changes in two-dimensional spectra, thanks to temperature-dependent electronic dephasing and to an increased number of system eigenstates amenable to spectroscopic probing. Ministry of Education (MOE) Published version The authors thank Frank Grossmann for enlightening discussions. The authors gratefully acknowledge the support of the Singapore Ministry of Education Academic Research Fund Tier 1 (Grant No. RG190/18) and Tier 2 (Grant No. MOE2019-T2-1-085). M. F. Gelin acknowledges the support of Hangzhou Dianzi University through the startup funding. K. Sun would like to thank the Natural Science Foundation of Zhejiang Province (Grant No. LY18A040005) for support. Q. Xu acknowledges the support of the Graduate Scientific Research Foundation of Hangzhou Dianzi University.

The ultrafast transient dynamics of a free-base tetraphenylporphyrin (H2TPP) surface-mounted metal organic framework (SURMOF) is spectroscopically characterized and compared with that of H2TPP in e...

A long 0.9 ps lifetime of the upper excited singlet state in perylene is resolved by femtosecond pump–probe measurements under ultraviolet (4.96 eV) excitation and further validated by theoretical simulations of transient absorption kinetics. This finding prompts exploration and development of novel perylene-based materials for upper excited state photochemistry applications.

Ordered porphyrin-based metal organic frameworks (MOFs) may serve as a model for mimicking the natural photosynthesis with highly ordered chlorophylls, i.e., porphyrin-like chromophores. Study of light harvesting and energy transfer as the primary event of photosynthesis is of great importance leading to improvement of photovoltaics overall performance. Detailed characterization of ultrafast dynamics of zinc tetraphenylporphyrin (ZnTPP) surface mounted metal organic framework (SURMOF) is reported by using various steady-state and time-resolved laser spectroscopic techniques, i.e., time-correlated single photon counting, fluorescence up-conversion and transient absorption pump–probe with 20 fs resolution. Obtained results in these nanoporous materials were compared with corresponding results for ZnTPP in ethanol measured under the same conditions. Dramatic quenching of both upper excited singlet state S2 and first excited state S1 was observed. Subpicosecond and picosecond lifetimes were detected in transi...

We present a proof of concept that ultrafast dynamics combined with photochemical stability information of molecular photocatalysts can be acquired by electrospray ionization mass spectrometry combined with time-resolved femtosecond laser spectroscopy in an ion trap. This pump-probe "fragmentation action spectroscopy" gives straightforward access to information that usually requires high purity compounds and great experimental efforts. Results of gas-phase studies on the electronic dynamics of two supramolecular photocatalysts compare well to previous findings in solution and give further evidence for a directed electron transfer, a key process for photocatalytic hydrogen generation.

We present a theoretical description of double-pump femtosecond single-molecule signals with fluorescence detection. We simulate these signals in the weak-field regime for a model mimicking a chromophore with a Franck-Condon-active vibrational mode. We establish several signatures of these signals which are characteristic for the weak-field regime. The signatures include the quenching of vibrational beatings by electronic dephasing and a pronounced tilt of the phase-time profiles in the two-dimensional (2D) maps. We study how environment-induced slow modulations of the electronic dephasing and relevant chromophore parameters (electronic energy, orientation, vibrational frequency and relative shift of the potential energy surfaces) affect the signals.

A new ansatz for molecular vibronic wave functions based on a superposition of time-dependent Generalized Coherent States is developed and analysed. The methodology is specifically tailored to describe the time evolution of the wave function of a system in which several interacting electronic states are coupled to a bath of harmonic oscillators. The equations of motion for the wave packet parameters are obtained by using the Dirac–Frenkel time-dependent variational principle. The methodology is used to describe the quantum dynamical behavior of a model polaron system and its scaling and convergence properties are discussed and compared with numerically exact results.

Employing the Dirac-Frenkel time dependent variational method, the nonlinear spectra monitoring the singlet fission process mediated by a conical intersection (CI) of the two lowest excited electronic states are investigated for different optical dephasings. The simulated two-dimensional spectra at different population times follow ultrafast population transfer through the CI and exhibit spectral features related to the tuning mode. The anticorrelated oscillations of cross peaks located at symmetric positions with respect to the main diagonal are clearly identified after the stimulated-emission contribution quenches. The simulated transient absorption signals show a fast decay of the first excited singlet state and exhibit multiple peaks revealing the tuning mode. These findings could be regarded as signatures of the CI in the singlet fission process. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Published version

We study the effect of a dissipative environment on the orientational relaxation of a three-dimensional quantum linear rotor. We provide a derivation of the Hamiltonian of a linear rotor coupled to a harmonic bath from first principles, confirming earlier conjectures. The dynamics generated by this Hamiltonian is investigated by the hierarchical equations-of-motion method assuming a Drude spectral density of the bath. We perform numerically accurate simulations and analyze the behavior of orientational correlation functions and the rotational structures of infrared absorption and Raman scattering spectra. We explore the features of orientational correlation functions and their spectra for a wide range of system-bath couplings, bath memory times, and temperatures. We discuss the signatures of the orientational relaxation in the underdamped regime, the strongly damped regime, and the librational regime. We show that the behavior of orientational correlation functions and their spectra can conveniently be analyzed in terms of three characteristic times, which are explicitly expressed in terms of the parameters of the Hamiltonian.

We introduce and analyze the concept of the "ideal" time and frequency resolved transient-absorption pump-probe (PP) signal. The ideal signal provides the most direct link between the "real" (measurable) PP signal and the material system dynamics. The simulation of PP signals involves two steps. (i) The ideal signal, which exhibits perfect time and frequency resolution, is calculated. For this purpose, the probe pulse is replaced by an auxiliary continuous-wave pulse. (ii) The real signal is obtained by the convolution of the ideal signal with the appropriate time- and frequency-gate function, which depends on the envelope of the actual probe pulse. This concept has been used to simulate integral and dispersed PP signals for a model system exhibiting nonadiabatic and dissipative dynamics. The ideal signal is computed with the two-pulse equation-of-motion phase-matching approach which has been extended to take excited-state absorption into account. We demonstrate how the ideal signal, an object exhibiting the features of moving wave packets as well as stationary spectra, is related to real signals detected with short (good temporal resolution) or long (good frequency resolution) probe pulses.

The ultrafast nonadiabatic dynamics of a two-electronic-state four-vibrational-mode conical intersection coupled to a finite bath with up to 20 harmonic oscillators has been investigated by employing the multiple Davydov D

Unraveling the many facets of coherent and incoherent exciton motion in an ensemble of chromophores is an inherently complex quantum mechanical problem that has triggered a vivid debate on the role of quantum effects in molecular materials and biophysical systems. Here the dynamics of a statistical ensemble of molecular aggregates consisting of identical chromophores is investigated within a new theoretical framework. Taking account of intrinsic properties of the system, the Hamiltonian of the aggregate is partitioned into two mutually commuting vibrational and vibronic operators. This representation paves the way for an analysis that reveals the role of static disorder in ensembles of aggregates. Using analytical methods, it is demonstrated that after a critical time τD ≃ 2π/σ (σ being the dispersion of the disorder) any dynamic variable of the aggregate exhibits purely vibrational dynamics. This result is confirmed by exact numerical calculations of the time-dependent site populations of the aggregate. These findings may be useful for the interpretation of recent femtosecond spectroscopic experiments on molecular aggregates.

We consider a classical particle bilinearly coupled to a harmonic bath. Assuming that the evolution of the particle is monitored on a timescale which is longer than the characteristic bath correlation time, we derive a Markovian master equation for the probability density of the particle. The master equation is fully specified by the time correlation function of the momenta of the particle. We find the functional form of the momentum correlation function which yields the Keilson–Storer master equation (Keilson and Storer, 1952). We show that the parameters of this master equation can directly be related to the characteristic memory time of the bath.