From feb7e28acb00369cd878c7fecdaab97ecbe0dd2f Mon Sep 17 00:00:00 2001 From: Pierre-Francois Loos Date: Tue, 20 Oct 2020 11:56:31 +0200 Subject: [PATCH] saving work --- Response_Letter/Response_Letter.tex | 216 +- dynker.bib | 116 +- dynker.nb | 5119 ++++++++++++--------------- dynker.tex | 72 +- 4 files changed, 2595 insertions(+), 2928 deletions(-) diff --git a/Response_Letter/Response_Letter.tex b/Response_Letter/Response_Letter.tex index 57225fa..95b2c85 100644 --- a/Response_Letter/Response_Letter.tex +++ b/Response_Letter/Response_Letter.tex @@ -14,7 +14,7 @@ \justifying Please find attached a revised version of the manuscript entitled \begin{quote} -\textit{``Dynamical Kernels for Optical Excitations''}. + \textit{``Dynamical Kernels for Optical Excitations''}. \end{quote} We thank the reviewers for their constructive comments. Our detailed responses to their comments can be found below. @@ -30,36 +30,69 @@ We look forward to hearing from you. \begin{itemize} \item - {This paper presents a study of three different frequency-dependent kernels proposed in the literature that go beyond the static/adiabatic approximations of TDDFT and GW/BSE approaches to excitations. The presentation is very instructive and coherent, beginning by showing a universal aspect of these kernels (the context of Lowdin partitioning), before examining the performance of each on three simple molecular systems in a minimal basis. Although some of the main points discussed may not be new to experts in the field, the coherent placement of these issues together and clear explanations will be useful to the community. I am likely to recommend publication in JCP, once the following points are addressed. } + {This paper presents a study of three different frequency-dependent kernels proposed in the literature that go beyond the static/adiabatic approximations of TDDFT and GW/BSE approaches to excitations. + The presentation is very instructive and coherent, beginning by showing a universal aspect of these kernels (the context of Lowdin partitioning), before examining the performance of each on three simple molecular systems in a minimal basis. + Although some of the main points discussed may not be new to experts in the field, the coherent placement of these issues together and clear explanations will be useful to the community. + I am likely to recommend publication in JCP, once the following points are addressed. } + \\ + \alert{We would like to thank the reviewer for his/her positive comments.} + + \item + {The systems chosen are said to represent examples of valence, charge-transfer, and Rydberg excited states. + Some explanation is required for why they represent charge-transfer and Rydberg excited states.} \\ \alert{} \item - {(1) The systems chosen are said to represent examples of valence, charge-transfer, and Rydberg excited states. Some explanation is required for why they represent charge-transfer and Rydberg excited states. For HeH+ example, the internuclear separation is taken to be near equilibrium, if I understand it correctly. What then is the charge-transfer character of the excited states, i.e. how much of a significant change in the charge distribution do the excited states have compared to the ground state? For the He example, if I recall correctly, the lowest double-excitation of He lies in the continuum, i.e. is not a bound state but rather a resonance. So I am not sure whether it is really accurate to say it is a Rydberg excited state. Did the authors check if the excitation energies they are obtaining for this state lie below the ionization threshold? Perhaps the finite basis set makes this resonance appear bound. } + {For HeH+ example, the internuclear separation is taken to be near equilibrium, if I understand it correctly. + What then is the charge-transfer character of the excited states, i.e. how much of a significant change in the charge distribution do the excited states have compared to the ground state?} \\ - \alert{} + \alert{As now mentioned in the manuscript, a Mulliken or Lowdin population analysis reveal that 1.53 electrons are located on He and 0.47 electron on H in the ground state. + Thus, electronic excitations correspond to a charge transfer from He to H. + A paragraph has been added to discuss this point.} + + \item + {For the He example, if I recall correctly, the lowest double-excitation of He lies in the continuum, i.e. is not a bound state but rather a resonance. + So I am not sure whether it is really accurate to say it is a Rydberg excited state. + Did the authors check if the excitation energies they are obtaining for this state lie below the ionization threshold? + Perhaps the finite basis set makes this resonance appear bound.} + \\ + \alert{The reviewer is right. + In He, the lowest doubly-excited state is an auto-ionising resonance state, extremely high in energy and lies in the continuum. + Highly-accurate calculations estimate an excitation energy of $57.85$ hartree for this $1s^2 \rightarrow 2s^2$ transition. + In a minimal basis set though, it is of Rydberg nature as it corresponds to a transition from a relatively compact $s$-type function to a more diffuse one. + All of these information have been added to the revised version of the manuscript with additional references.} \item - {(2) In the introduction it is stated that only the correlation part of the kernel is frequency-dependent. However I believe this is only true for two-electron systems. For the N electron case the exact-exchange kernel defined within TDDFT is frequency-dependent (see e.g. Hellgren and Gross, PRA 88, 052507 (2013) and references therein, Hesselmann and Goerling JCP 134, 034120 (2011)) } + {In the introduction it is stated that only the correlation part of the kernel is frequency-dependent. + However I believe this is only true for two-electron systems. + For the $N$-electron case the exact-exchange kernel defined within TDDFT is frequency-dependent (see e.g. Hellgren and Gross, PRA 88, 052507 (2013) and references therein, Hesselmann and Goerling JCP 134, 034120 (2011)) } \\ - \alert{} + \alert{The reviewer is right. We have mentioned that, in a density-functional context, the exchange kernel can be frequency dependent if exact exchange is considered, and we have cited the two references provided by the reviewer.} \item - {(3) The authors comment that the D-TDDFT kernel (Eq 14) "is known to work best in the weak correlation regime where the true excitations have a clear single and double excitation character" (third last para end of sec IIIB). I found this a bit confusing. To me, weak correlation usually means that the ground-state is well-described by a single Slater determinant, so there are no very low-lying excitations. In this situation excitations of the system can have quite a mixed character, i.e. they need not be largely purely single excitations or largely purely double excitations, but could be, for example 50:50 mixtures of a single and double excitation. Perhaps the language just needs to be clarified in the sentence to reflect that what they mean is that one can define/quantify the single/double excitation character of the state? } + {The authors comment that the D-TDDFT kernel (Eq 14) ``is known to work best in the weak correlation regime where the true excitations have a clear single and double excitation character'' (third last para end of sec IIIB). + I found this a bit confusing. + To me, weak correlation usually means that the ground-state is well-described by a single Slater determinant, so there are no very low-lying excitations. + In this situation excitations of the system can have quite a mixed character, i.e. they need not be largely purely single excitations or largely purely double excitations, but could be, for example 50:50 mixtures of a single and double excitation. + Perhaps the language just needs to be clarified in the sentence to reflect that what they mean is that one can define/quantify the single/double excitation character of the state? } \\ - \alert{} + \alert{We agree with the reviewer that our original statement was unclear. + We have clarified our statement and we now state that the D-TDDFT kernel ``is known to work best in the weak correlation regime in the situation where one single and one double excitations are energetically close and well separated from the others''.} \item - {(4) In that same paragraph, when discussing the accuracy of the method for the excitations, it might be worth noting that in the cited reference 12 (Huix-Rotllant et al), it was observed that the best results seem to arise when using a hybrid kernel for the "static" part. } + {In that same paragraph, when discussing the accuracy of the method for the excitations, it might be worth noting that in the cited reference 12 (Huix-Rotllant et al), it was observed that the best results seem to arise when using a hybrid kernel for the ``static'' part. } \\ - \alert{} + \alert{Thank you for pointing that out. + The comment has been added in due place.} \item {Minor typos: -Sec IIIB: "...same idea was taking further..."- taking should be taken -Sec IV: "factitious" should be fictitious } + Sec IIIB: ``...same idea was taking further...''- taking should be taken. + Sec IV: "factitious" should be fictitious.} \\ - \alert{} + \alert{Thank you for spotting this unfortunate typos. + These have been corrected.} \end{itemize} @@ -70,138 +103,133 @@ Sec IV: "factitious" should be fictitious } \begin{itemize} \item - {The authors compare the performance of different ab initio methods to simulate the linear response -spectrum of systems of two interacting electrons, in particular their ability to describe double excitations -and accuracy to predict correct frequency of the single excitations. The three approaches under study use -a dynamical (frequency-dependent) kernel to compute the linear response, since as it is already known an -adiabatic exchange-correlation kernel can only reproduce single excitations. -The poles of the response function are computed using a matrix formulation within the 4-dimensional -vector space that describes a two-level system consisting of one valence and one conduction orbital -(HOMO and LUMO). Transition energies for H2, HeH+ and He using the dressed TDDFT as well as two -different dynamical kernels derived from BSE (including a perturbative treatment) are compared against -the exact solution. -The fact that dynamical(frequency-dependent) xc kernels are able to generate new poles in the linear -response was already observed in previous works which are cited in the manuscript. The authors revisit -this idea and test its effectiveness for different approximations to the dynamical kernel. The study is of -interest to the quantum chemistry community and the TDDFT community because it provides a careful -and useful comparison between different available dynamical kernels for systems for which the exact -spectrum can be computed numerically and used as reference. The manuscript provides a compact -introduction to each of the methods with references to relevant literature on the topic.} + {The authors compare the performance of different ab initio methods to simulate the linear response spectrum of systems of two interacting electrons, in particular their ability to describe double excitations and accuracy to predict correct frequency of the single excitations. + The three approaches under study use a dynamical (frequency-dependent) kernel to compute the linear response, since as it is already known an adiabatic exchange-correlation kernel can only reproduce single excitations. + The poles of the response function are computed using a matrix formulation within the 4-dimensional vector space that describes a two-level system consisting of one valence and one conduction orbital (HOMO and LUMO). + Transition energies for H2, HeH+ and He using the dressed TDDFT as well as two different dynamical kernels derived from BSE (including a perturbative treatment) are compared against the exact solution. + The fact that dynamical(frequency-dependent) xc kernels are able to generate new poles in the linear response was already observed in previous works which are cited in the manuscript. + The authors revisit this idea and test its effectiveness for different approximations to the dynamical kernel. + The study is of interest to the quantum chemistry community and the TDDFT community because it provides a careful and useful comparison between different available dynamical kernels for systems for which the exact spectrum can be computed numerically and used as reference. + The manuscript provides a compact introduction to each of the methods with references to relevant literature on the topic.} \\ - \alert{} + \alert{Again, we thank the second reviewer for his/her positive comments.} \item - {1. The particularities of the chosen model systems should be better discussed. Since the compared -methods are approximations their performance is likely to depend on the system under study as -well as on the basis set. -For example the dressed TDDFT method is suppose to work best in the case of doubles strongly -coupled to single excitations which from the tables seems not to be the case in these systems -(w1updown and w2updown are not very close in energy) so it's rather remarkable how well -dressed TDDFT predicts the energy of w2updown.} + {1. The particularities of the chosen model systems should be better discussed. + Since the compared methods are approximations their performance is likely to depend on the system under study as well as on the basis set. + For example the dressed TDDFT method is suppose to work best in the case of doubles strongly coupled to single excitations which from the tables seems not to be the case in these systems (w1updown and w2updown are not very close in energy) so it's rather remarkable how well dressed TDDFT predicts the energy of w2updown.} \\ - \alert{} + \alert{An entire paragraph explaining the pecularities of each system has been added. + As mentioned in the revised manuscript, the dressed TDDFT method works indeed best when the single and double excitations are close in energy. + However I believe that more importantly, it works best when these two excitations are well separated from the others which is the case here.} \item - {2. No explanation or reference is provided accompanying the statement that the model systems that -are chosen are prototypical of valence, charge-transfer and Rydberg excitations and weather these -different excitations can be well represented in the reduced (two-level) space used.} + {2. No explanation or reference is provided accompanying the statement that the model systems that are chosen are prototypical of valence, charge-transfer and Rydberg excitations and weather these different excitations can be well represented in the reduced (two-level) space used.} \\ - \alert{} + \alert{We have added a reference to the work of Senjean \textit{et al.}~where \ce{H2} and \ce{HeH+} are used as prototypical systems. The He atom is considered in the work of Romaniello \textit{et al.}~which is also cited. } \item - {3. The molecules H2 and HeH+ are studied at the equilibrium distance, right? It would be -interesting to assess the performance of the different dynamical kernel for stretched molecules. -If you claim the problem is an example of charge-transfer excitations then it would be good to -study the stretched molecules... -Would a larger basis set be needed in such case?} + {3. The molecules H2 and HeH+ are studied at the equilibrium distance, right? + It would be interesting to assess the performance of the different dynamical kernel for stretched molecules. + If you claim the problem is an example of charge-transfer excitations then it would be good to study the stretched molecules... + Would a larger basis set be needed in such case?} \\ - \alert{} + \alert{We have modified the manuscript to add stretched H2 and HeH+ (taken at five times the equilibrium distance).} \item - {4. The statement about the vanishing of the matrix element $=0$ in H2 could be discussed -better or a reference added.} + {4. The statement about the vanishing of the matrix element $\langle S|H|D \rangle=0$ in H2 could be discussed better or a reference added.} \\ - \alert{} + \alert{We have added a reference to the book of Szabo and Ostlund as well as an additional sentence explaining further why these elements vanish in this particular case. + In a nutshell, it is due to the symmetric nature of the \ce{H2} dimer and the lack of variational freedom in the minimal basis.} \item - {5. The results for He are not discussed at all. Why is the matrix element $=0$ vanishing for -H2 but not for He? Both systems share the same spatial symmetry (parity) ... -Can you really study Rydberg excitations using a minimal basis?} + {5. The results for He are not discussed at all. + Why is the matrix element $\langle S|H|D \rangle=0$ vanishing for H2 but not for He? + Both systems share the same spatial symmetry (parity) ... + Can you really study Rydberg excitations using a minimal basis?} \\ - \alert{} + \alert{For He, 6-31G is not a minimal basis. + Thus, there's some orbital relaxation in the excited states, and the matrix element $\langle S|H|D \rangle$ does not vanish.} \item - {6. It is also not discussed how the exact solution is computed. What is the exact Hamiltonian? Is the -eigensystem computed within the same minimal basis set? How are the excitation energies that -appear as 'exact' in the tables computed?} + {6. It is also not discussed how the exact solution is computed. + What is the exact Hamiltonian? + Is the eigensystem computed within the same minimal basis set? + How are the excitation energies that appear as ``exact'' in the tables computed?} \\ - \alert{} + \alert{The exact Hamiltonian (within this minimal basis) is provided by Eq.~(12).jwjehwyuiuuyylk + These are exact results within the one-electron space spanned by these basis functions. + The exact excitation energies are calculated as differences of these total energies. + This is now explicitly stated.} \item - {7. It would be illustrative to represent the ground state and the single and double excitations within a -single-particle picture for each system (H2, HeH+,He), maybe with a little figure. For example for -HeH+ is the HOMO consisting of 1 e up and 1 e down (one electron closer to H+ the other -closer to He?) and then a single exc would be promoting one of these electrons to the LUMO and -the double promoting both electrons to the LUMO? That means that within the minimal basis of 2 -orbitals both electrons have to do always the same, i.e. you can not describe the excitation of one -electron to the LUMO whereas the other one stays in the HOMO ? (of course this picture only -makes sense in the limit of weak interaction between particles)} + {7. It would be illustrative to represent the ground state and the single and double excitations within a single-particle picture for each system (H2, HeH+,He), maybe with a little figure. + For example for HeH+ is the HOMO consisting of 1 e up and 1 e down (one electron closer to H+ the other closer to He?) and then a single exc would be promoting one of these electrons to the LUMO and the double promoting both electrons to the LUMO? + That means that within the minimal basis of 2 orbitals both electrons have to do always the same, i.e. you can not describe the excitation of one electron to the LUMO whereas the other one stays in the HOMO ? (of course this picture only makes sense in the limit of weak interaction between particles)} \\ - \alert{} + \alert{We find this addition unnecessary as this kind of schemes are provided in standard textbook (like Szabo's and Ostlund's book) which are now cited in due place in our revised manuscript. + Therefore, we would prefer to eschew adding such figures.} \item {8. In order to address a larger community it would desirable to discuss briefly which orbitals are taking into account for each system when using the minimal basis. Maybe that helps understand the results. - What is the difference between using STO-3G and Pople's 6-31G and why is one or the -other chosen?} + What is the difference between using STO-3G and Pople's 6-31G and why is one or the other chosen?} \\ - \alert{} + \alert{Following the reviewer's advice, we have added a short description of the STO-3G and 6-31G basis for these three systems. + For a one-center system like He, a double-zeta basis must be considered in order to have two levels. + For two-center systems like H2 and HeH+, a minimal basis on each center must be considered to produce two-level systems.} \item {9. How does the dimension of the basis set affect the performance of the different dynamical kernel under study?} \\ - \alert{} + \alert{This is an open question that we hope to answer in the near future. + To do so, one must be able to solve the non-linear, frequency dependent eigensystem in a large basis, which is not straightforward from a tehcnical point of view. + Moreover, one must be able to characterized unambiguously the different excited states.} \item - {10. page 2, beginning of section A: -?two level quantum system made of 2 electrons in its singlet gs? is a bit misleading. The vector -space is 4-dimensional and if you place 2 electrons with opposite spin then the gs, which is a -singlet, consists of both electrons occupying the lowest orbital.} + {10. page 2, beginning of section A: ``two level quantum system made of 2 electrons in its singlet gs'' is a bit misleading. + The vector space is 4-dimensional and if you place 2 electrons with opposite spin then the gs, which is a singlet, consists of both electrons occupying the lowest orbital.} \\ - \alert{} + \alert{Following the reviewer's advice, we have replaced the sentence by \textit{``Let us consider a two-level quantum system where two opposite-spin electrons occupied the lowest-energy level. + In other words, the lowest orbital is doubly occupied and the system has a singlet ground state.''}} \item - {11. In page 2, end of second paragraph: when you say 'same numerical examples' do you mean the + {11. In page 2, end of second paragraph: when you say ``same numerical examples'' do you mean the same systems (H2, HeH+, He)?} \\ - \alert{} + \alert{Yes. We have substituted ``same numerical examples'' by ``same molecular systems'', which we believe is more explicit.} \item - {Beginning of section B, 'one single and one double excitation'} + {Beginning of section B, ``one single and one double excitation''} \\ - \alert{} + \alert{Thank you for spotting this. This has been fixed.} \item - {section B, by 'static problem' do you mean 'static kernel'?} + {section B, by ``static problem'' do you mean ``static kernel''?} \\ - \alert{} + \alert{By static problem, we mean the frequency-independent Hamiltonian. + This has been explicitly mentioned.} \item - {Table I has different unities than the rest of the tables, which is a bit confusing. Why didn't you -use the same unities everywhere? Is the column called 'exact' in tables 2,3,4 computed from the -values given in table I? It is not just $n*(ev-ec)$ ($n=1$ for single, $n=2$ for double) since the single and -doubles are not a multiple of each other and also that would be $E_{HF}$',right? so how are the exact -transition energies computed? Do they correspond to: omega1 up down= - <0|H|0> and -omega2 up down= - <0|H|0> ?} + {Table I has different unities than the rest of the tables, which is a bit confusing. + Why didn't you use the same unities everywhere? + Is the column called ``exact'' in tables 2,3,4 computed from the values given in table I? + It is not just $n*(ev-ec)$ ($n=1$ for single, $n=2$ for double) since the single and doubles are not a multiple of each other and also that would be $E_{HF}$',right? so how are the exact transition energies computed? Do they correspond to: omega1 up down= $\langle S|H|S \rangle - \langle 0|H|0 \rangle$ and +omega2 up down= $\langle D|H|D \rangle - \langle 0|H|0 \rangle$ ?} \\ - \alert{} + \alert{The reviewer is right, this is inconsistent. + The quantities gathered in Table I are now provided in eV, like the rest of the results. + The figures are now also plotted in eV. + Yes, the ``exact'' values in Tables II, III and IV are the same as in Table I. + These exact transition energies are computed as the difference of total energies (ie eigenvalues) provided by the Hamiltonian defined in Eq.~(12). + It does not correspond to the expressions provided by the reviewer as there is, in general, coupling between these terms.} \item - {15. page 5, second para: -Do you mean by 'static excitations' w1updown and w1upup?} + {15. page 5, second para: Do you mean by ``static excitations'' w1updown and w1upup?} \\ - \alert{} + \alert{Yes. This has been more clearly specified in the revised manuscript. + Thank you for mentioning that it wasn't clear enough.} \end{itemize} diff --git a/dynker.bib b/dynker.bib index 9765426..991763d 100644 --- a/dynker.bib +++ b/dynker.bib @@ -1,13 +1,98 @@ %% This BibTeX bibliography file was created using BibDesk. %% http://bibdesk.sourceforge.net/ -%% Created for Pierre-Francois Loos at 2020-09-08 20:27:46 +0200 +%% Created for Pierre-Francois Loos at 2020-10-20 11:56:13 +0200 %% Saved with string encoding Unicode (UTF-8) +@article{Marut_2020, + Author = {C. Marut and B. Senjean and E. Fromager and P. F. Loos}, + Date-Added = {2020-10-20 11:41:05 +0200}, + Date-Modified = {2020-10-20 11:42:39 +0200}, + Doi = {10.1039/d0fd00059k}, + Journal = {Faraday. Discuss.}, + Title = {Weight dependence of local exchange-correlation functionals in ensemble density-functional theory: double excitations in two-electron systems}, + Volume = {Advance article}, + Year = {2020}} + +@article{Bottcher_1974, + Author = {C. Bottcher and K. Docken}, + Date-Added = {2020-10-20 11:40:00 +0200}, + Date-Modified = {2020-10-20 11:40:00 +0200}, + Doi = {10.1088/0022-3700/7/1/002}, + Journal = {J. Phys. B: At. Mol. Phys.}, + Pages = {L5}, + Title = {Autoionizing States of the Hydrogen Molecule.}, + Volume = {7}, + Year = {1974}, + Bdsk-Url-1 = {https://doi.org/10.1088/0022-3700/7/1/002}} + +@article{Burges_1995, + Author = {A. Burgers and D. Wintgen and J.-M. Rost}, + Date-Added = {2020-10-20 11:39:21 +0200}, + Date-Modified = {2020-10-20 11:39:21 +0200}, + Doi = {10.1088/0953-4075/28/15/010}, + Journal = {J. Phys. B: At. Mol. Opt. Phys.}, + Pages = {3163--3183}, + Title = {Highly doubly excited S states of the helium atom}, + Volume = {28}, + Year = {1995}, + Bdsk-Url-1 = {https://doi.org/10.1088/0953-4075/28/15/010}} + +@article{Madden_1963, + Author = {R. P. Madden and K. Codling}, + Date-Added = {2020-10-20 11:38:50 +0200}, + Date-Modified = {2020-10-20 11:38:50 +0200}, + Doi = {10.1103/PhysRevLett.10.516}, + Journal = {Phys. Rev. Lett.}, + Pages = {516}, + Title = {New Autoionizing Atomic Energy Levels in He, Ne, and Ar}, + Volume = {10}, + Year = {1963}, + Bdsk-Url-1 = {https://doi.org/10.1103/PhysRevLett.10.516}} + +@article{Hesselmann_2011, + Author = {He{\ss}elmann,Andreas and G{\"o}rling,Andreas}, + Date-Added = {2020-10-16 09:43:08 +0200}, + Date-Modified = {2020-10-16 09:54:24 +0200}, + Doi = {10.1063/1.3517312}, + Journal = {The Journal of Chemical Physics}, + Number = {3}, + Pages = {034120}, + Title = {Efficient exact-exchange time-dependent density-functional theory methods and their relation to time-dependent Hartree--Fock}, + Volume = {134}, + Year = {2011}, + Bdsk-Url-1 = {https://doi.org/10.1063/1.3517312}} + +@article{Hellgren_2012, + Author = {Hellgren, Maria and Gross, E. K. U.}, + Date-Added = {2020-10-16 09:38:19 +0200}, + Date-Modified = {2020-10-16 09:54:49 +0200}, + Doi = {10.1103/PhysRevA.85.022514}, + Journal = {Phys. Rev. A}, + Pages = {022514}, + Title = {Discontinuities of the exchange-correlation kernel and charge-transfer excitations in time-dependent density-functional theory}, + Volume = {85}, + Year = {2012}, + Bdsk-Url-1 = {https://link.aps.org/doi/10.1103/PhysRevA.85.022514}, + Bdsk-Url-2 = {https://doi.org/10.1103/PhysRevA.85.022514}} + +@article{Hellgren_2013, + Author = {Hellgren, Maria and Gross, E. K. U.}, + Date-Added = {2020-10-16 09:37:50 +0200}, + Date-Modified = {2020-10-16 09:54:42 +0200}, + Doi = {10.1103/PhysRevA.88.052507}, + Journal = {Phys. Rev. A}, + Pages = {052507}, + Title = {Discontinuous functional for linear-response time-dependent density-functional theory: The exact-exchange kernel and approximate forms}, + Volume = {88}, + Year = {2013}, + Bdsk-Url-1 = {https://link.aps.org/doi/10.1103/PhysRevA.88.052507}, + Bdsk-Url-2 = {https://doi.org/10.1103/PhysRevA.88.052507}} + @article{Staroverov_1998, Abstract = {A technique for reducing computational effort in multireference second-order perturbation theory with very large complete active space {\v Z}CAS. SCF reference functions is proposed. This is achieved by construction of an effective Hamiltonian within the space of configurations dominating the reference function expansion. The method is tested on the standard problems of singlet\textendash{}triplet {\v Z}1A1\textendash{}3B1. separation in the CH 2 radical and vertical excitation energies in formaldehyde. Numerical results show that good accuracy can be obtained even with substantially reduced model spaces. q 1998 Elsevier Science B.V. All rights reserved.}, Author = {Staroverov, Viktor N. and Davidson, Ernest R.}, @@ -199,15 +284,16 @@ Year = {2019}, Bdsk-Url-1 = {https://doi.org/10.1021/acs.jpclett.9b00981}} -@misc{Loos_2020e, - Archiveprefix = {arXiv}, +@article{Loos_2020e, Author = {Pierre-Francois Loos and Xavier Blase}, - Date-Modified = {2020-09-08 20:27:45 +0200}, - Eprint = {2007.13501}, - Howpublished = {(J. Chem. Phys., in press)}, - Primaryclass = {physics.chem-ph}, + Date-Modified = {2020-10-15 22:26:21 +0200}, + Doi = {10.1063/5.0023168}, + Journal = {J. Chem. Phys.}, + Pages = {114120}, Title = {{{Dynamical Correction to the Bethe-Salpeter Equation Beyond the Plasmon-Pole Approximation}}}, - Year = {2020}} + Volume = {153}, + Year = {2020}, + Bdsk-Url-1 = {https://doi.org/10.1063/5.0023168}} @article{Lowdin_1963, Author = {P. L{\"o}wdin}, @@ -3552,14 +3638,9 @@ @article{Barca_2018a, Author = {Barca, Giuseppe M. J. and Gilbert, Andrew T. B. and Gill, Peter M. W.}, Date-Added = {2020-01-01 21:36:51 +0100}, - Date-Modified = {2020-01-01 21:36:51 +0100}, + Date-Modified = {2020-10-20 11:40:59 +0200}, Doi = {10.1021/acs.jctc.7b00994}, - File = {/Users/loos/Zotero/storage/TZI6VUVB/Barca et al. - 2018 - Simple Models for Difficult Electronic Excitations.pdf}, - Issn = {1549-9618, 1549-9626}, Journal = {J. Chem. Theory. Comput.}, - Language = {en}, - Month = mar, - Number = {3}, Pages = {1501-1509}, Title = {Simple {{Models}} for {{Difficult Electronic Excitations}}}, Volume = {14}, @@ -9964,14 +10045,9 @@ @article{Senjean_2015, Author = {Senjean, Bruno and Knecht, Stefan and Jensen, Hans J\o{}rgen Aa. and Fromager, Emmanuel}, Date-Added = {2020-01-01 21:36:51 +0100}, - Date-Modified = {2020-01-01 21:36:52 +0100}, + Date-Modified = {2020-10-19 22:09:10 +0200}, Doi = {10.1103/PhysRevA.92.012518}, - File = {/Users/loos/Zotero/storage/IC928IFM/Senjean et al. - 2015 - Linear interpolation method in ensemble Kohn-Sham .pdf}, - Issn = {1050-2947, 1094-1622}, Journal = {Phys. Rev. A}, - Language = {en}, - Month = jul, - Number = {1}, Pages = {012518}, Title = {Linear Interpolation Method in Ensemble {{Kohn}}-{{Sham}} and Range-Separated Density-Functional Approximations for Excited States}, Volume = {92}, diff --git a/dynker.nb b/dynker.nb index 5ca4676..c47899e 100644 --- a/dynker.nb +++ b/dynker.nb @@ -10,10 +10,10 @@ NotebookFileLineBreakTest NotebookFileLineBreakTest NotebookDataPosition[ 158, 7] -NotebookDataLength[ 1898504, 38397] -NotebookOptionsPosition[ 1867691, 37930] -NotebookOutlinePosition[ 1868138, 37948] -CellTagsIndexPosition[ 1868095, 37945] +NotebookDataLength[ 1872909, 37962] +NotebookOptionsPosition[ 1842223, 37498] +NotebookOutlinePosition[ 1842670, 37516] +CellTagsIndexPosition[ 1842627, 37513] WindowFrame->Normal*) (* Beginning of Notebook Content *) @@ -27174,6 +27174,71 @@ Cell[BoxData[ CellLabel-> "In[113]:=",ExpressionUUID->"5294030d-cd96-4dab-91fd-caa35839441f"], +Cell[BoxData[ + RowBox[{"(*", + RowBox[{"(*", " ", + 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Closed]] }, Open ]] diff --git a/dynker.tex b/dynker.tex index 67dbe4a..cb997ab 100644 --- a/dynker.tex +++ b/dynker.tex @@ -92,7 +92,9 @@ In Eq.~\eqref{eq:kernel}, \end{equation} is the (spin-resolved) Hartree-exchange-correlation (Hxc) dynamical kernel. In the case of a spin-independent kernel, we will drop the superscript $\sigma$. -As readily seen from Eq.~\eqref{eq:kernel-Hxc}, only the correlation (c) part of the kernel is frequency dependent and, in a wave function context, the static Hartree-exchange (Hx) matrix elements read +As readily seen from Eq.~\eqref{eq:kernel-Hxc}, only the correlation (c) part of the kernel is frequency dependent \alert{in a wave function context. +However, in a density-functional context, the exchange part of the kernel can be frequency dependent if exact exchange is considered. \cite{Hesselmann_2011,Hellgren_2013}} +In a wave function context, the static Hartree-exchange (Hx) matrix elements read \begin{equation} f_{ia,jb}^{\Hx,\sigma} = 2\sigma \ERI{ia}{jb} - \ERI{ib}{ja} \end{equation} @@ -190,7 +192,8 @@ In the next section, we illustrate these concepts and the various tricks that ca \label{sec:exact} %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% -Let us consider a two-level quantum system made of two electrons in its singlet ground state (\ie, the lowest orbital is doubly occupied). \cite{Romaniello_2009b} +\alert{Let us consider a two-level quantum system where two opposite-spin electrons occupied the lowest-energy level. \cite{Romaniello_2009b} +In other words, the lowest orbital is doubly occupied and the system has a singlet ground state.} We will label these two orbitals, $\MO{v}$ and $\MO{c}$, as valence ($v$) and conduction ($c$) orbitals with respective one-electron Hartree-Fock (HF) energies $\e{v}$ and $\e{c}$. In a more quantum chemical language, these correspond to the HOMO and LUMO orbitals (respectively). The ground state $\ket{0}$ has a one-electron configuration $\ket{v\bar{v}}$, while the doubly-excited state $\ket{D}$ has a configuration $\ket{c\bar{c}}$. @@ -229,47 +232,40 @@ with \end{subequations} and $\Delta\e{} = \e{c} - \e{v}$. The energy of the only triplet state is simply $\mel{T}{\hH}{T} = \EHF + \Delta\e{} - \ERI{vv}{cc}$. +\alert{Exact excitation energies are calculated as differences of these total energies. +Note that these energies are exact results within the one-electron space spanned by the basis functions.} -For the sake of illustration, we will use the same numerical examples throughout this study, and consider the singlet ground state of i) the \ce{H2} molecule ($R_{\ce{H-H}} = 1.4$ bohr) in the STO-3G basis, ii) the \ce{HeH+} molecule ($R_{\ce{He-H}} = 1.4632$ bohr) in the STO-3G basis, and iii) the \ce{He} atom in Pople's 6-31G basis set. -These three systems provide prototypical examples of valence, charge-transfer, and Rydberg excitations, respectively, and will be employed to quantity the performance of the various methods considered in the present study for each type of excited states. +For the sake of illustration, we will use the same \alert{molecular systems} throughout this study, and consider the singlet ground state of i) the \ce{H2} molecule ($R_{\ce{H-H}} = 1.4$ bohr) in the STO-3G basis, ii) the \ce{HeH+} molecule ($R_{\ce{He-H}} = 1.4632$ bohr) in the STO-3G basis, and iii) the \ce{He} atom in Pople's 6-31G basis set. \cite{SzaboBook} +\alert{The minimal basis (STO-3G) and double-zeta basis (6-31G) have been chosen to produce two-level systems. +The STO-3G basis for two-center systems (\ce{H2} and \ce{HeH+}) corresponds to one $s$-type gaussian basis function on each center, while the 6-31G basis for the helium atom corresponds to two (contracted) $s$-type gaussian functions with different exponents.} + +These three systems provide prototypical examples of valence, charge-transfer, and Rydberg excitations, respectively, and will be employed to quantity the performance of the various methods considered in the present study for each type of excited states. \cite{Senjean_2015,Romaniello_2009b} +\alert{ +In the case of \ce{H2}, the HOMO and LUMO orbitals have $\sigma_g$ and $\sigma_u$ symmetries, respectively. +The electronic configuration of the ground state is $\sigma_g^2$, and the doubly-excited state of configuration $\sigma_u^2$ has an auto-ionising resonance nature. \cite{Bottcher_1974,Barca_2018a,Marut_2020} +The singly-excited states correspond to $\sigma_g \sigma_u$ configurations. +In He, highly-accurate calculations reveal that the lowest doubly-excited state is an auto-ionising resonance state, extremely high in energy and lies in the continuum. \cite{Madden_1963,Burges_1995,Marut_2020} +However, in a minimal basis set such as STO-3G, it is of Rydberg nature as it corresponds to a transition from a relatively compact $s$-type function to a more diffuse one. +In the heteronuclear diatomic \ce{HeH+}, a Mulliken or Lowdin population analysis associates $1.53$ electrons on the \ce{He} center and $0.47$ electrons on \ce{H} for the ground state, \cite{SzaboBook} with an opposite trend for the excited states. Electronic excitation corresponds then to a charge transfer from the \ce{He} nucleus to the proton.} The numerical values of the various quantities defined above are gathered in Table \ref{tab:params} for each system. %%% TABLE I %%% \begin{table*} - \caption{Numerical values (in hartree) of the valence and conduction orbital energies, $\e{v}$ and $\e{c}$, and two-electron integrals in the orbital basis for various two-level systems. + \caption{Numerical values \alert{(in eV)} of the valence and conduction orbital energies, $\e{v}$ and $\e{c}$, and two-electron integrals in the orbital basis for various two-level systems. \label{tab:params} } \begin{ruledtabular} \begin{tabular}{llcccccccc} System & Method & $\e{v}$ & $\e{c}$ & $\ERI{vv}{vv}$ & $\ERI{cc}{cc}$ & $\ERI{vv}{cc}$ & $\ERI{vc}{cv}$ & $\ERI{vv}{vc}$ & $\ERI{vc}{cc}$ \\ \hline - \ce{H2} & HF/STO-3G & $-0.578\,203$ & $+0.670\,268$ & $+0.674\,594$ & $+0.697\,495$ & $+0.663\,564$ & $+0.181\,258$ & $0$ & $0$ \\ - \ce{HeH+} & HF/STO-3G & $-1.632\,802$ & $-0.172\,484$ & $+0.943\,099$ & $+0.752\,526$ & $+0.660\,254$ & $+0.145\,397$ & $-0.172\,968$ & $+0.037\,282$ \\ - \ce{He} & HF/6-31G & $-0.914\,127$ & $+1.399\,859$ & $+1.026\,907$ & $+0.766\,363$ & $+0.858\,133$ & $+0.227\,670$ & $+0.316\,490$ & $+0.255\,554$ \\ + \ce{H2} & HF/STO-3G & $-15.7282$ & $+18.2389$ & $+18.3566$ & $+18.9798$ & $+18.0565$ & $+4.9323$ & $0$ & $0$ \\ + \ce{HeH+} & HF/STO-3G & $-44.4308$ & $-4.6935$ & $+25.6630$ & $+20.4773$ & $+17.9664$ & $+3.9565$ & $-4.7067$ & $+1.0145$ \\ + \ce{He} & HF/6-31G & $-24.8747$ & $+38.0921$ & $+27.9436$ & $+20.8538$ & $+23.3510$ & $+6.1952$ & $+8.6121$ & $+6.9540$ \\ \end{tabular} \end{ruledtabular} \end{table*} %%% %%% %%% %%% -%%% TABLE I %%% -%\begin{table*} -% \caption{Numerical values (in hartree) of the energy of the valence and conduction orbitals, $\e{v}$ and $\e{c}$, and various two-electron integrals in the orbital basis for various two-level systems. -% \label{tab:gap} -% } -% \begin{ruledtabular} -% \begin{tabular}{llccccccccccccc} -% & \mc{3}{c}{Hartree-Fock} & \mc{3}{c}{$GW$} & \mc{3}{c}{GF2} & \mc{3}{c}{Exact} \\ -% \cline{2-4} \cline{5-7} \cline{8-10} \cline{11-13} -% System & $\Delta\e{}$& $-\e{v}$ & $-\e{c}$ & $\Delta\eGW{}$ & $-\eGW{v}$ & $-\eGW{c}$ & $\Delta\eGF{}$ & $-\eGF{v}$ & $-\eGF{c}$ & Gap & IP & EA \\ -% \hline -% \ce{H2} & $33.97$ & $15.73$ & $-18.24$ & $35.21$ & $16.35$ & $-18.86$ & $34.69$ & $16.09$ & $-18.60$ & & $16.29$ & \\ -% \ce{HeH+} & $39.74$ & $44.43$ & $+4.69$ & $39.49$ & $43.87$ & $+4.38$ & $39.55$ & $44.08$ & $+4.52$ & & $44.04$ & \\ -% \ce{He} & $62.97$ & $24.87$ & $-38.09$ & $60.88$ & $23.50$ & $-37.38$ & $61.66$ & $24.02$ & $-37.64$ & & $23.85$ \\ -% \end{tabular} -% \end{ruledtabular} -%\end{table*} -%%% %%% %%% %% - The exact values of the singlet single and double excitations, $\omega_{1}^{\updw}$ and $\omega_{2}^{\updw}$, and the triplet single excitation, $\omega_{1}^{\upup}$, are reported, for example, in Table \ref{tab:Maitra}. We are going to use these as reference for the remaining of this study. @@ -279,10 +275,10 @@ We are going to use these as reference for the remaining of this study. %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% The kernel proposed by Maitra and coworkers \cite{Maitra_2004,Cave_2004} in the context of dressed TDDFT (D-TDDFT) corresponds to an \textit{ad hoc} many-body theory correction to TDDFT. -More specifically, D-TDDFT adds to the static kernel a frequency-dependent part by reverse-engineering the exact Hamiltonian: a single and double excitations, assumed to be strongly coupled, are isolated from among the spectrum and added manually to the static kernel. -The very same idea was taking further by Huix-Rotllant, Casida and coworkers, \cite{Huix-Rotllant_2011} and tested on a large set of molecules. +More specifically, D-TDDFT adds to the static kernel a frequency-dependent part by reverse-engineering the exact Hamiltonian: \alert{one single and one double excitations}, assumed to be strongly coupled, are isolated from among the spectrum and added manually to the static kernel. +The very same idea was \alert{taken} further by Huix-Rotllant, Casida and coworkers, \cite{Huix-Rotllant_2011} and tested on a large set of molecules. Here, we start instead from a HF reference. -The static problem corresponds then to the time-dependent HF (TDHF) Hamiltonian, while in the TDA, it reduces to configuration interaction with singles (CIS). \cite{Dreuw_2005} +The static problem \alert{(\ie, the frequency-independent Hamiltonian)} corresponds then to the time-dependent HF (TDHF) Hamiltonian, while in the TDA, it reduces to configuration interaction with singles (CIS). \cite{Dreuw_2005} For the two-level model, the reverse-engineering process of the exact Hamiltonian \eqref{eq:H-exact} yields \begin{equation} \label{eq:f-Maitra} @@ -348,22 +344,24 @@ Because, there is nothing to dress for the triplet state, the TDHF and D-TDHF tr %%% %%% %%% %%% Although not particularly accurate for the single excitations, Maitra's dynamical kernel allows to access the double excitation with good accuracy and provides exactly the right number of solutions (two singlets and one triplet). -Note that this correlation kernel is known to work best in the weak correlation regime (which is the case here) where the true excitations have a clear single and double excitation character, \cite{Loos_2019,Loos_2020d} but it is not intended to explore strongly correlated systems. \cite{Carrascal_2018} +Note that this correlation kernel is known to work best in the weak correlation regime (which is the case here) \alert{in the situation where one single and one double excitations are energetically close and well separated from the others,} \cite{Maitra_2004,Loos_2019,Loos_2020d} but it is not intended to explore strongly correlated systems. \cite{Carrascal_2018} Its accuracy for the single excitations could be certainly improved in a density-functional theory context. However, this is not the point of the present investigation. +\alert{In Ref.~\onlinecite{Huix-Rotllant_2011}, the authors observed that the best results are obtained using a hybrid kernel for the static part.} Table \ref{tab:Maitra} also reports the slightly improved (thanks to error compensation) CIS and D-CIS excitation energies. In particular, single excitations are greatly improved without altering the accuracy of the double excitation. Graphically, the curves obtained for CIS and D-CIS are extremely similar to the ones of TDHF and D-TDHF depicted in Fig.~\ref{fig:Maitra}. -In the case of \ce{H2} in a minimal basis, because $\mel{S}{\hH}{D} = 0$, there is no dynamical correction for both singlets and triplets, and one cannot access the double excitation with Maitra's kernel. +In the case of \ce{H2} in a minimal basis, because $\mel{S}{\hH}{D} = 0$, \cite{SzaboBook} there is no dynamical correction for both singlets and triplets, and one cannot access the double excitation with Maitra's kernel. It would be, of course, a different story in a larger basis set where the coupling between singles and doubles would be non-zero. +\alert{The fact that $\mel{S}{\hH}{D} = 0$ for \ce{H2} in a minimal basis is the direct consequence of the lack of orbital relaxation in the excited states, which is itself due to the fact that the molecular orbitals in that case are unambiguously defined by symmetry.} %%% FIGURE 1 %%% \begin{figure} \includegraphics[width=\linewidth]{Maitra} \caption{ - $\det[\bH(\omega) - \omega \bI]$ as a function of $\omega$ (in hartree) for both the singlet (gray and black) and triplet (orange) manifolds of \ce{HeH+}. + $\det[\bH(\omega) - \omega \bI]$ as a function of $\omega$ (in \alert{eV}) for both the singlet (gray and black) and triplet (orange) manifolds of \ce{HeH+}. The static TDHF Hamiltonian (dashed) and dynamic D-TDHF Hamiltonian (solid) are considered. \label{fig:Maitra} } @@ -497,7 +495,7 @@ Let us highlight the fact that, unlike in Ref.~\onlinecite{Loos_2020e} where dyn \begin{figure} \includegraphics[width=\linewidth]{dBSE} \caption{ - $\det[\bH(\omega) - \omega \bI]$ as a function of $\omega$ (in hartree) for both the singlet (gray and black) and triplet (orange and red) manifolds of \ce{HeH+}. + $\det[\bH(\omega) - \omega \bI]$ as a function of $\omega$ \alert{(in eV)} for both the singlet (gray and black) and triplet (orange and red) manifolds of \ce{HeH+}. The static BSE Hamiltonian (dashed) and dynamic dBSE Hamiltonian (solid) are considered. \label{fig:dBSE} } @@ -688,14 +686,14 @@ In the case of BSE2, the perturbative partitioning (pBSE2) is simply \begin{figure} \includegraphics[width=\linewidth]{dBSE2} \caption{ - $\det[\bH(\omega) - \omega \bI]$ as a function of $\omega$ (in hartree) for both the singlet (gray and black) and triplet (orange and red) manifolds of \ce{HeH+}. + $\det[\bH(\omega) - \omega \bI]$ as a function of $\omega$ \alert{(in eV)} for both the singlet (gray and black) and triplet (orange and red) manifolds of \ce{HeH+}. The static BSE2 Hamiltonian (dashed) and dynamic dBSE2 Hamiltonian (solid) are considered. \label{fig:BSE2} } \end{figure} %%% %%% %%% %%% -As compared to dBSE, dBSE2 produces much larger dynamical corrections to the static excitation energies (see values in square brackets in Table \ref{tab:BSE2}) probably due to the poorer quality of its static reference (TDHF or CIS). +As compared to dBSE, dBSE2 produces much larger dynamical corrections to the static excitation energies, \alert{$\omega_1^{\updw}$ and $\omega_1^{\upup}$}, (see values in square brackets in Table \ref{tab:BSE2}) probably due to the poorer quality of its static reference (TDHF or CIS). Similarly to what has been observed in Sec.~\ref{sec:Maitra}, the TDA vertical excitations are slightly more accurate due to error compensations. Note also that the perturbative treatment is a remarkably good approximation to the dynamical scheme for single excitations (except for \ce{H2}, see below), especially in the TDA. This justifies the use of the perturbative treatment in Refs.~\onlinecite{Zhang_2013,Rebolini_2016}. @@ -712,7 +710,7 @@ However, one cannot access the double excitation. The take-home message of the present paper is that dynamical kernels have much more to give that one would think. In more scientific terms, dynamical kernels can provide, thanks to their frequency-dependent nature, additional excitations that can be associated to higher-order excitations (such as the infamous double excitations), an unappreciated feature of dynamical quantities. However, they sometimes give too much, and generate spurious excitations, \ie, excitation which does not correspond to any physical excited state. -The appearance of these factitious excitations is due to the approximate nature of the dynamical kernel. +The appearance of these \alert{fictitious} excitations is due to the approximate nature of the dynamical kernel. Moreover, because of the non-linear character of the linear response problem when one employs a dynamical kernel, it is computationally more involved to access these extra excitations. Using a simple two-model system, we have explored the physics of three dynamical kernels: i) a kernel based on the dressed TDDFT method introduced by Maitra and coworkers, \cite{Maitra_2004} ii) the dynamical kernel from the BSE formalism derived by Strinati in his hallmark 1988 paper, \cite{Strinati_1988} as well as the second-order BSE kernel derived by Zhang \textit{et al.}, \cite{Zhang_2013} and Rebolini and Toulouse. \cite{Rebolini_2016,Rebolini_PhD}