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DOI: 10.1039/C8CP05662E
(Paper)
Phys. Chem. Chem. Phys., 2019, Advance Article

Felix
Plasser
*^{ab},
Sandra
Gómez
^{b},
Maximilian F. S. J.
Menger
^{bc},
Sebastian
Mai
^{b} and
Leticia
González
*^{b}
^{a}Department of Chemistry, Loughborough University, Loughborough, LE11 3TU, UK. E-mail: F.Plasser@lboro.ac.uk
^{b}Institute for Theoretical Chemistry, Faculty of Chemistry, University of Vienna, Währingerstr. 17, 1090 Vienna, Austria. E-mail: leticia.gonzalez@univie.ac.at
^{c}Dipartimento di Chimica e Chimica Industriale, University of Pisa, Via G. Moruzzi 13, 56124 Pisa, Italy

Received
6th September 2018
, Accepted 3rd October 2018

First published on 3rd October 2018

We report an implementation of the linear vibronic coupling (LVC) model within the surface hopping dynamics approach and present utilities for parameterizing this model in a blackbox fashion. This results in an extremely efficient method to obtain qualitative and even semi-quantitative information about the photodynamical behavior of a molecule, and provides a new route toward benchmarking the results of surface hopping computations. The merits and applicability of the method are demonstrated in a number of applications. First, the method is applied to the SO_{2} molecule showing that it is possible to compute its absorption spectrum beyond the Condon approximation, and that all the main features and timescales of previous on-the-fly dynamics simulations of intersystem crossing are reproduced while reducing the computational effort by three orders of magnitude. The dynamics results are benchmarked against exact wavepacket propagations on the same LVC potentials and against a variation of the electronic structure level. Four additional test cases are presented to exemplify the broader applicability of the model. The photodynamics of the isomeric adenine and 2-aminopurine molecules are studied and it is shown that the LVC model correctly predicts ultrafast decay in the former and an extended excited-state lifetime in the latter. Futhermore, the method correctly predicts ultrafast intersystem crossing in the modified nucleobase 2-thiocytosine and its absence in 5-azacytosine while it fails to describe the ultrafast internal conversion to the ground state in the latter.

Different strategies have been developed for reducing the number of electronic structure computations in trajectory dynamics simulations. These include a parameterization of the surfaces through interpolated diabatic Hamiltonians,^{19,20} on-the-fly constructed databases,^{21,22} or artificial neural networks.^{23,24} However, none of these approaches is in routine use, which probably derives from the fact that they do require a significant amount of electronic structure computations and expert knowledge to be applied successfully. Here, we want to proceed in a different way and combine the surface hopping method with a very popular approach that is in routine use and has been well-tested and refined by numerous groups over the last 30 years, the vibronic coupling (VC) model.^{25} VC models provide a description of the main physics of interacting potential surfaces, including the conical shape of their intersections, using only a minimum number of parameters with clear physical meaning. They can be parameterized using standardized protocols^{25–29} and are commonly used in the context of quantum dynamics, in particular within the well-established multiconfigurational time-dependent Hartree (MCTDH) method,^{30} and have been shown to be powerful for describing ultrafast nonadiabatic processes in organic and inorganic molecules,^{31–34} in transition metal complexes^{27,35,36} and at interfaces.^{37} Despite the huge popularity of surface hopping and VC models individually, it is difficult to find any combined application of both methods in the literature,^{38} and certainly no generally applicable implementation is available. However, such a combination will be highly desirable as it allows speeding up surface hopping simulations by orders of magnitude when compared to on-the-fly dynamics and allows for including essentially an unlimited number of degrees of freedom as opposed to quantum dynamics. At the same time, it does not introduce any new approximation that is not already included in either one of the two well-tested constituent methods. If a particular photophysical problem can be described by both methods individually it should also be described correctly by the combined approach. Conversely, as we will discuss below, the method provides a convenient and versatile approach for evaluating the reliability of its different ingredients such as the electronic structure data, the surface hopping algorithm, and the parameterized potential energy surfaces. Finally, it offers a new route for evaluating the influence of different degrees of freedom in VC models used in quantum dynamics. For the above reasons, we deem a general implementation of LVC surface hopping highly desirable.

With this motivation in mind, we created a general interface for performing surface hopping dynamics using VC models within the SHARC (surface hopping with arbitrary couplings) molecular dynamics package.^{7,17,39,40} In this work, we investigate the simplest possible case, i.e., a VC model using only linear terms (LVC) parameterized using only a single excited-state computation, and study its usefulness for addressing various photophysical problems. First, sulfur dioxide (SO_{2}) is studied, a molecule that has recently attracted significant attention,^{34,41–46} due to its ultrafast ISC occurring on a subpicosecond time scale. Here, we investigate whether the employed LVC model can predict the occurrence of ultrafast ISC and whether it correctly describes the participation of the different electronic states, a question that has been open since decades^{47} and was clarified only a few years ago.^{41,44} Second, adenine and its structural isomer 2-aminopurine (2AP) are investigated. The remarkable feature of these two molecules is that despite their structural similarity, they exhibit a completely different photophysical behavior.^{48,49} Adenine undergoes non-radiative decay on a subpicosecond time scale,^{50–54} whereas the closely related 2AP system possesses an extended excited state lifetime (>100 ps) in gas phase^{55} and is even fluorescent in many solvents.^{48,56} We examine whether the presented SHARC/LVC approach allows discriminating between these qualitatively different behaviours. As a third test case, the modified nucleobase 2-thiocytosine (2TC) is investigated. 2TC belongs to the class of thio-nucleobases, which have been the target of much research^{57–60} due to their interesting photophysical properties based on their remarkably ultrafast ISC. In 2TC, ISC occurs on a 200–400 fs time scale,^{58} whereas virtually no decay to the S_{0} occurs. Finally, we investigate 5-azacytosine (5AC), which is the chromophore of the widespread anti-cancer drug azacytidine.^{61} As its mechanism of action involves incorporation into DNA, its photophysics is of interest regarding drug-induced light sensitivity and the crucial feature is that it undergoes decay to the ground state rather than ISC.^{62,63}

Per construction, the LVC model works in the diabatic basis. It is worth noting that MCTDH works entirely in the diabatic basis and can directly take the LVC model as input. In contrast, SHARC expects input in the MCH representation and propagates the wavefunction in the diagonal picture. It will be, thus, necessary to transform the input as described below (Section 2.5). The SHARC output can be given in any of the three pictures explained above, and it is, thus, possible to perform a one-to-one comparison with MCTDH despite the fact that different representations were used for the wavefunction propagation.

V = V_{0}1 + W | (1) |

(2) |

(3) |

Ω^{2} = diag(ω_{1}^{2}, ω_{2}^{2}, …,ω_{3N}^{2}), | (4) |

(5) |

(6) |

(7) |

Within the current work, an LVC model is considered, which contains the following state-specific terms in the W matrix.

(8) |

(9) |

In the “one-shot” LVC approach, the ω_{i} values are simply the ground state vibrational frequencies while the ε_{n} energies and diabatic SOC constants are the vertical excitation energies and SOCs at the equilibrium geometry, respectively. The intrastate vibronic coupling constants are computed as the derivative of the electronic energy E_{n} of state n with respect to a normal mode^{25,27} computed at the reference geometry, which using eqn (6) can be rearranged as

(10) |

(11) |

Commonly, the λ parameters are evaluated indirectly using energy-based information only, by considering either the excited state Hessian^{25,27,34} or by fitting the potential energy surfaces to model potentials.^{28,29} However, following arguments by Yarkony and coworkers,^{66} it is possible to evaluate eqn (11) directly and this approach is used here. In the case of configuration interaction (CI) computations, the 〈Ψ^{MCH}_{m}|∂Ĥ^{MCH}/∂r_{α}|Ψ^{MCH}_{n}〉 terms can be obtained from derivatives of the CI-matrix yielding a quantity termed f^{CI} that is closely related to the nonadiabatic coupling vector.^{66,67} Similar equations have also been incorporated within coupled cluster theory.^{68,69} In cases where nonadiabatic coupling vectors are not available, it is possible to compute the λ^{(mn)}_{i} values in the same spirit through a numerical differentiation using a recently described algorithm^{65} based on wavefunction overlaps.^{70}

An LVC model, even when constructed in this simple way, provides qualitatively correct potential energy surfaces in the vicinity of the expansion point and assures the proper conical topology of intersections between adiabatic states. However, the quality of the description is expected to deteriorate if the molecule undergoes large-amplitude structural changes, such that anharmonicities and higher-order vibronic coupling terms become important. As a consequence, it is not expected that the presented protocol is adequate in describing all photochemical reactions or other processes involving strong structural rearrangements. In these cases, it may be possible to resort to higher-order VC models and more sophisticated parameterization schemes^{26,28} or on-the-fly dynamics will have to be applied. On the other hand, we expect that the simple “one-shot” LVC approach can provide a qualitatively correct description of photophysical processes, like internal conversion and ISC, that are dominated by the electron dynamics and do not involve the breaking or creation of chemical bonds or the motion of flexible groups. In Section 3, we investigate the applicability of this method for the description of a number of realistic photophysical processes and find remarkably good agreement with experiment as well as with more expensive computational protocols.

(12) |

(13) |

(14) |

H^{diag} = U^{†}H^{MCH}U, | (15) |

Practically, with the above diagonalization carried out, the coefficients c_{m}(t) can be propagated according to the matrix equation

(16) |

(17) |

In this work, the gradient g^{diag}_{m} of the diagonal state, needed to propagate eqn (12), is approximated as a linear combination of the MCH gradients

(18) |

As in other surface hopping approaches, after a successful hop the nuclear momenta are adjusted to conserve total energy and by default the full velocity vector is rescaled. Furthermore, the electronic coefficients are adjusted after each time step to consider decoherence; here we use the well-established energy-based decoherence correction introduced by Granucci et al.^{72}

VT = Tdiag(E_{1}, …, E_{Nst}) | (19) |

S(t,t + Δt) = T(t)^{T}T(t + Δt). | (20) |

Fig. 2 Workflow of the SHARC/LVC method. Input quantities, intermediates and output are given in grey, blue, and red boxes, respectively. Equation numbers are shown in yellow. |

In summary, the new interface provides all quantities in the MCH basis and in Cartesian coordinates, so that for the SHARC dynamics driver the simulations do not differ from on-the-fly simulations. This also means that all analysis procedures implemented in SHARC, considering, for example, Cartesian coordinates and electronic populations, can automatically be applied to the LVC-based simulations.

Technically speaking, in our original implementation the time-determining step was not the evaluation of the matrix operations but the communication between the Fortran SHARC driver and the LVC program written in Python. Therefore, a new driver for SHARC – called PySHARC – was developed within the course of this project, utilizing Python's C API (application program interface), thus allowing for in-memory communication between the Python interface and SHARC's Fortran routines, replacing the file based communication used so far. Additionally, the new implementation makes it possible to read all parameters just once and store them in memory reducing the number of file operations to be performed and enhancing efficiency even further.

The optical absorption spectrum of SO_{2} was computed according to a Wigner distribution of the ground state zero-point vibrational wavefunction,^{87} using normal modes computed at MR-CIS level. The surface hopping dynamics simulations on SO_{2} were started according to the excitation windows indicated as grey rectangles in Fig. 3 (4.1–4.6 eV for MR-CIS and 3.9–4.4 eV for MR-CISD). 4 singlet and 3 triplets states were considered in the dynamics and 200 trajectories, each, were propagated on the MR-CIS and MR-CISD potentials. A time step length of 0.5 fs and a locally diabatic method for wavefunction propagation were used.^{71} An energy-based decoherence correction (C = 0.1 H) was used.^{72} For MCTDH,^{30} the vibrational ground state wavefunction was promoted to the diabatic ^{1}B_{1} state and the dynamics was propagated for 700 fs using 10 single particle functions per normal mode, each expressed through 32 Legendre polynomials. UV absorption spectra were computed as the Fourier transform of the autocorrelation function obtained from the MCTDH dynamics and shifted by the zero-point energy of 0.1915 eV.

In the case of adenine the excitation window was chosen as 6.1 ± 0.1 eV and 209 trajectories were propagated for 1000 fs considering 5 singlet states. For 2AP the excitation window was chosen as 5.0 ± 0.1 eV and 163 trajectories were propagated for 50 ps considering 5 singlet states. The other set-up parameters (e.g., time step, propagator, decoherence correction) were kept as in the previous case. The normal modes used to construct the LVC model and to create the Wigner distribution were obtained at the RI-MP2/aug-cc-pVDZ level of theory using TURBOMOLE.^{88} For adenine and 2AP, relaxation time constants for the S_{2} → S_{1} and S_{1} → S_{0} processes were obtained by fitting a sequential first-order kinetics model to the population data. Errors of the time constants were obtained with the bootstrapping method,^{89} using 1000 bootstrapping samples for each ensemble (see S5 in the ESI† for more details on the fitting procedure). Note that these errors only describe the uncertainty due to the finite size of the trajectory ensembles but they make no statement about errors due to the electronic structure and dynamics methods.

The excitation windows chosen for 2TC and 5AC were 4.0 ± 0.1 eV and 5.0 ± 0.2 eV, respectively, and in both cases 200 trajectories were computed. The normal modes were computed at the respective MR-CIS levels.

State | MR-CIS | MR-CISD | |
---|---|---|---|

S_{1} |
^{1}B_{1} |
4.463 (0.0029) | 4.227 (0.0055) |

S_{2} |
^{1}A_{2} |
4.848 | 4.595 |

S_{3} |
^{1}B_{2} |
6.805 (0.0931) | — |

T_{1} |
^{3}B_{1} |
3.650 | 3.350 |

T_{2} |
^{3}B_{2} |
4.478 | 4.211 |

T_{3} |
^{3}A_{2} |
4.627 | 4.356 |

Next, optical absorption spectra were computed for SO_{2}. The original spectrum, computed from 1000 individual MR-CIS computations and initially reported in ref. 43, is shown in Fig. 3(a). This spectrum is somewhat blue-shifted with respect to the experiment^{90} (green line) but the spectral width is approximately reproduced. Next, the spectrum was recomputed using the LVC model constructed at the MR-CIS level [Fig. 3(b)]. As explained above, all parameters for this model (see Tables S1–S4, ESI†) were extracted from one single-point calculation at the equilibrium geometry. Remarkably, the LVC spectrum reproduces the full ab initio result very well in terms of location of the peak, its width, and the amount of contribution of the S_{2} state, with a fraction of the computational effort. For comparison, the absorption spectrum was also computed using the MCTDH method. This spectrum, shown in Fig. 3(c), exhibits a fine structure that cannot be obtained with semiclassical methods, but otherwise it agrees on the position and overall broadening. Employing the LVC model allows us to compute the spectrum also at the computationally much more expensive MR-CISD level, as presented in Fig. 3(e). This spectrum is red-shifted with respect to MR-CIS by about 0.2 eV, in agreement with Table 1, but otherwise the spectral shape is very similar. The MCTDH spectrum computed at the LVC(MR-CISD) level is presented in Fig. 3(f) showing a somewhat altered fine structure when compared to the MCTDH/LVC(MR-CIS) spectrum.

An important observation regarding the spectra presented above is that the adiabatic S_{2} state gains some intensity and contributes to the spectrum at higher energies. This feature clearly violates the Condon approximation as the S_{2} state is dark at the equilibrium geometry and, therefore, illustrates that the present protocol is able to compute spectra going beyond the Condon approximation. Hence, it is interesting to compare the spectra shown above with an LVC model that ignores the interstate couplings λ^{(mn)}_{i}. This corresponds to an approximation termed “vertical gradient”,^{91} meaning that the ground and excited state frequencies are the same, the oscillator strengths are constant, and only gradient information is used to construct the spectrum. This spectrum is shown in Fig. 3(d) and resembles that obtained using the full LVC model [Fig. 3(b)] with the exception that the high-energy shoulder deriving from the adiabatic S_{2} state cannot be reproduced.

As a next step, nonadiabatic dynamics simulations considering 4 singlet and 3 triplet states were performed for five of the computational protocols introduced in Fig. 3. These correspond to SHARC dynamics at the on-the-fly MR-CIS, LVC(MR-CIS), and LVC(MR-CISD) levels, as well as MCTDH simulations at the LVC(MR-CIS) and LVC(MR-CISD) levels. Here, the difference in computational effort is noteworthy: while the 111 on-the-fly MR-CIS trajectories from ref. 43 propagated for 700 fs required about 15000 core hours on a modern CPU, the parameterization and all 200 trajectories at the LVC(MR-CIS) level were finished in about 6 core hours using the PySHARC implementation. To be able to compare results between SHARC and MCTDH we use the diabatic (spectroscopic) representation,^{39}i.e., we expand the time-dependent electronic wavefunctions in terms of the electronic states of the symmetric equilibrium geometry using a procedure described in more detail in ref. 43. The results of the on-the-fly SHARC simulations at the MR-CIS level, originally reported in ref. 43, are shown in Fig. 4(a). The initial excitation goes predominantly to the ^{1}B_{1} state, which is the S_{1} state at the Franck–Condon geometry and the only symmetry-allowed state in the employed excitation window. Subsequently, the excited molecule stays on the S_{1} surface but an ultrafast change in diabatic character to ^{1}A_{2} occurs making ^{1}A_{2} the dominant state character already after 10 fs. Population of the triplet states is also ultrafast and after 700 fs the total triplet population amounts to 55%. The LVC model [Fig. 4(b)] reproduces the main features of the on-the-fly simulations. The initial inversion between the ^{1}B_{1} and ^{1}A_{2} characters occurs at exactly 10 fs. Sub-picosecond triplet population is observed as well, where most population is received by the ^{3}B_{2} state, in agreement with ref. 43 and 44. However, ISC is somewhat slower than in the on-the-fly calculations, and after 700 fs only 38% triplet population is reached. The reduced population of the triplet states can be explained by the fact that ISC is most efficient during strong elongation of the SO bonds,^{43} which is difficult to describe using LVC potentials. Nonetheless, it is remarkable that the dynamics of SO_{2} including all the involved states and timescales can be qualitatively described by the LVC model, especially considering that the nature of the involved states was still under dispute until few years ago.^{41,44}

The LVC method also directly allows judging the impact of quantum effects that cannot be captured by the surface hopping method. For this purpose quantum dynamics using the MCTDH method have been carried out for the LVC(MR-CIS) model, see Fig. 4(c). The results are very similar to the corresponding SHARC simulations [Fig. 4(b)] with the exception that stronger and more persistent oscillations between the singlet states are observed for MCTDH and that the triplet yield is somewhat lowered (only 27% after 700 fs).

A further advantage of the SHARC/LVC method is that it is possible to directly investigate the effects of different parameters and algorithmic choices in the surface hopping method to see whether they affect the agreement between SHARC and MCTDH. To exemplify this, we changed one algorithmic detail in the SHARC dynamics. In many SHARC applications, to conserve energy after a surface hop, typically the full velocity vector is rescaled. If nonadiabatic coupling vectors are available, a more rigorous alternative^{1,16} is to rescale only the component of the velocity parallel to the nonadiabatic coupling vector that induced the hop. The results of dynamics using this procedure are presented in Fig. 4(d). The different mode of rescaling leaves the qualitative picture unchanged but does affect the quantitative outcomes quite strongly. In particular, the triplet population after 700 fs is raised to 61%, which is twice as high as the MCTDH reference for the LVC(MR-CIS) potentials shown in Fig. 4(c). In addition, the oscillations between the singlet states are somewhat enhanced. It is noteworthy that the surface hopping results are so strongly affected by a seemingly innocuous algorithmic choice such as the mode of velocity rescaling. In the future, it will be thus of significant interest to evaluate the influence of other similar choices such as the treatment of frustrated hops and different options for decoherence corrections. The SHARC/LVC protocol provides an ideal way to perform such an evaluation for realistic high-dimensional systems, and a more detailed comparison of SHARC and MCTDH results is currently in progress in our group.

The efficiency of the LVC method allows for a significant improvement of the computational level in terms of the excitation level, active space, and one-electron basis set to perform dynamics at the MR-CISD(12,9)/VTZP level [Fig. 4(e)], which is not feasible for on-the-fly dynamics. One can see that at this level of theory, the ^{1}B_{1}/^{1}A_{2} inversion happens somewhat slower and the populations are equal only after 15 fs owing to the fact that the magnitude of the λ value coupling these two states is reduced from 0.20 eV to 0.15 eV (cf. Tables S1 and S2, ESI†). Otherwise the dynamics is very similar, giving 38% triplet population after 700 fs. The MCTDH results computed using the LVC(MR-CISD) potentials are presented in Fig. 4(f). In this case, the ^{1}B_{1}/^{1}A_{2} inversion occurs after 11.5 fs and the triplet yield after 700 fs amounts to 31%.

The MCTDH results shown here also compare well with the results of Lévêque et al. who used a more extended model Hamiltonian.^{44} In ref. 44 a similar oscillatory behaviour and a triplet yield of about 30% after 700 fs is reported. The main difference is that more persistent oscillations are observed in the present MCTDH/LVC(MR-CIS) dynamics. In a more general sense, the similarity of panels (b), (c), (e), and (f) suggests that neither the electronic structure level nor quantum effects play a decisive role in terms of the timescales or the states involved. On the other hand, a comparison with panel (a) shows that the inclusion of realistic on-the-fly potentials does have a notable effect on the triplet yield.

State | Ade | State | 2AP | |
---|---|---|---|---|

S_{1} |
1^{1}nπ* |
5.677 (0.000) | 1^{1}nπ* |
4.782 (0.003) |

S_{2} |
1^{1}ππ* |
6.142 (0.329) | 1^{1}ππ* |
4.991 (0.112) |

S_{3} |
2^{1}ππ* |
6.422 (0.055) | 2^{1}nπ* |
5.956 (0.001) |

S_{4} |
2^{1}nπ* |
6.764 (0.006) | 2^{1}ππ* |
6.590 (0.231) |

In a next step, the ultrafast dynamics after UV absorption are investigated for adenine and 2AP using the LVC(MR-CIS) model. The results for adenine are shown in Fig. 5(a). First, there is an ultrafast rise of the S_{1} state population, reaching a maximum value of 93% after 74 fs followed by a somewhat slower decay to S_{0}. Both features, the initial rise of S_{1} and its subsequent decay agree remarkably well with on-the-fly MR-CIS dynamics, reported previously.^{52} A similar sub-100 fs process in the excited state manifold has also been observed with a quadratic coupling model in reduced dimensionality.^{96} The obtained relaxation time constants are 31 ± 2 fs and 1070 ± 100 fs for S_{2} → S_{1} and S_{1} → S_{0}, respectively. These time constants agree very well with the experimental values of <100 fs and 700–1030 fs.^{50,51} At this point it is worth mentioning that the ultrafast nonradiative decay of adenine cannot be reproduced by time-dependent density functional theory (TDDFT) using a range of different popular density functionals.^{92,97} This shows that it is clearly a challenging feat to describe the process correctly and shows that an LVC model can even outperform on-the-fly TDDFT dynamics. While we do not claim that the SHARC/LVC protocol will always perform perfectly, it is fair to say that often it may be preferable to use an LVC model parameterized against a high-level reference instead of using a lower level method on-the-fly.

It is especially interesting to study whether the LVC model can describe the geometrical displacements leading to the S_{1}/S_{0} decay, which are characterized by strong out-of-plane distortions of the aromatic rings.^{52,53,97} To this end, we show in Fig. 6 four exemplary S_{1}/S_{0} hopping geometries from the LVC(MR-CIS) simulations. Indeed, the LVC model can predict these strong out-of-plane deformations, even though the LVC model is expanded around the almost perfectly planar S_{0} minimum. This is primarily achieved through non-zero out-of-plane λ values between the diabatic 2^{1}nπ* and 2^{1}ππ* states. Consequently, at the hopping geometries the adiabatic S_{1} state is a linear combination of the 2^{1}nπ* and 2^{1}ππ* states, while the adiabatic S_{0} state is mostly of closed-shell character (with a weight >70%).

Fig. 6 Selected S_{1}/S_{0} hopping geometries as obtained during LVC(MR-CIS) surface hopping dynamics of adenine. |

The dynamics results for 2AP are presented in Fig. 5(b). Also in this case an ultrafast rise of S_{1} occurs, and an S_{1} population of 92% is reached after only 32 fs. When compared to adenine, the subsequent decay to the ground state is significantly slowed down and after 1 ps, a ground state population of only 10% is reached, highlighting the enhanced nonradiative lifetime of 2AP. From Fig. 5(b) alone, it is challenging to obtain an accurate estimate of the excited state lifetime. Therefore, the dynamics simulations were extended up to 50 ps. Such dynamics simulations, requiring over 16 million electronic structure computations for the whole ensemble, are far beyond the scope of ab initio on-the-fly dynamics but can be easily performed with the LVC model. The results, presented in Fig. 5(c), reveal that after 9.0 ps, 50% of the population has decayed to the ground state. The fitted time constants for 2AP are 17 ± 1 fs and 13000 ± 1000 fs for the S_{2} → S_{1} and S_{1} → S_{0} processes. The latter timescale is about one order of magnitude faster than the experimental value of 156 ps reported for jet-cooled 2AP.^{55} The main source for this error is probably the description of the low frequency out-of-plane modes. These are expected to experience non-negligible anharmonicities, which are not described in the LVC model. In order to definitely answer the question whether this problem is related to the LVC approximation, the level of theory MR-CIS, or the surface hopping protocol one would have to perform ab initio MR-CIS dynamics, which are unfortunately unfeasible for the required timescale. Nonetheless, the employed LVC model correctly predicts two important properties of gas phase 2AP: that its lifetime is significantly longer than the one of adenine, and that it nevertheless decays on a picosecond timescale.

Fig. 7 Time evolution of the adiabatic populations of 2-thiocytosine after photoexcitation computed at the (a) on-the-fly and (b) LVC levels in SHARC using MR-CIS(6,5)/cc-pVDZ. |

As a final example, we want to discuss the 5-azacytosine molecule. The on-the-fly results^{63} for 5AC are presented in Fig. 8(a). The initial excitation is distributed over the S_{2} and S_{1}. A very rapid rise of S_{1} follows and after about 100 fs almost all the population is in S_{1}. Around the same time, the rise of S_{0} starts and after 600 fs about half the population has transferred to S_{0}. Triplet population is negligible. The SHARC/LVC dynamics [Fig. 8(b)] reproduces the initial ultrafast transfer to S_{1} and the absence of ISC in this system, and generally provides a good reproduction of the first 100 fs. However, it was not possible to reproduce the ultrafast decay to the ground state for 5AC. A likely reason for this behaviour is the presence of a barrier in the reaction path leading to the minimum energy conical intersection between S_{1} and S_{0}.^{63} In order to reproduce this barrier correctly, it is probably necessary to move beyond the LVC model.

Fig. 8 Time evolution of the adiabatic populations of 5-azacytosine after photoexcitation computed at the (a) on-the-fly and (b) LVC levels in SHARC using MR-CIS(6,5)/cc-pVDZ. |

In the case of SO_{2}, it was shown that the LVC model could reproduce all the features of the on-the-fly MR-CIS dynamics simulations while reducing the computational cost by about three orders of magnitude. It was also illustrated that the LVC model could be applied to evaluate the effects of the significantly enhanced MR-CISD level of electronic structure theory. Finally, because of the fact that the LVC model could be employed identically in quantum dynamics and surface hopping simulations, it provided a rigorous route for benchmarking the latter for realistic Hamiltonians of high-dimensional systems. Conversely, the method could, in the future, be used in the context of quantum dynamics studies, as it allows to efficiently evaluate the effect of neglecting different degrees of freedom.

An investigation of the prototypical adenine and 2AP molecules showed that the SHARC/LVC method allows to correctly discriminate between the different qualitative behavior of these two molecules: subpicosecond decay was found in the former whereas a significantly enhanced nonradiative lifetime was found in the latter. These results suggest that in cases where the LVC approximation is expected to work the method can be used as a blackbox and computationally cheap approach to evaluate whether or not a molecule is expected to be fluorescent – a notoriously difficult task in computational photochemistry.

Further tests were performed in 2TC and 5AC. In the case of 2TC, ultrafast decay of S_{2} and ISC was found in agreement with on-the-fly dynamics. For 5AC some qualitative features of the on-the-fly dynamics were reproduced but the SHARC/LVC protocol failed to describe ultrafast decay to the ground state. The case of 5AC serves as a reminder that the “one shot” LVC approach investigated here is only the lowest level of a hierarchy of possibilities to approximate on-the-fly dynamics and will not always provide a definite answer. Nonetheless, it is impressive that the correct qualitative behaviour was found in four out of the five molecules studied considering the simplicity and computational efficiency of the approach.

It was shown that SHARC/LVC allows for a speed up of about three orders of magnitude compared to on-the-fly dynamics. This means that one can study one thousand molecules instead of one, a nanosecond instead of a picosecond, or an ensemble of 100000 trajectories instead of 100 allowing to study even very rare processes. Due to this low computational cost and its ease of use, we expect the presented protocol to be a powerful addition to the currently available computational photochemistry toolbox. We believe that it is a significant advancement towards black-box nonadiabatic dynamics methods, which could find applications in high-throughput screening for different purposes, e.g., fluorescent dyes or photostable drug molecules. At the same time caution is certainly in place. The presented protocol arises from the dire need of performing ab initio photodynamics simulations without incurring excessive computational costs. Whenever on-the-fly dynamics simulations are feasible at the same electronic structure level these are to be preferred over LVC dynamics and if quantum dynamics are possible, these are to be preferred over LVC surface hopping. Conversely, the protocol presents an attractive option for cases where ab initio on-the-fly dynamics is too expensive or the number of degrees of freedom is too large for quantum dynamics. We have used a “one shot” LVC approach, where all excited-state data is obtained from a single electronic structure computation, to show that even this simplest approximation provides reasonable results, at least in cases where no strong structural rearrangement occurs. To improve the description, it is possible to move to more sophisticated vibronic coupling models, which are readily created using established protocols.^{26,28}

For the purpose of advancing to larger, more complex systems it will be possible to use embedding methods, to proceed through interpolation of diabatic Hamiltonians^{19,20} or to incorporate exciton models in the dynamics.^{98–100}

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## Footnote |

† Electronic supplementary information (ESI) available: Employed LVC parameters for SO_{2} (S1–S4) and details on the fitting procedures for Ade and 2AP (S5) (pdf); SHARC input files containing all LVC parameters and data underlying the presented figures (zip). See DOI: 10.1039/c8cp05662e |

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