 And the last speaker of the morning is Claudio, that is editing the Wiki page of the last minute, like always. Because people make comments. Yeah, yeah, yeah, yeah. I was telling the people here that in the first, one of the first schools of Jumbo, I spent the night before completely awake to do the release and this kind of stuff. I didn't sleep all the night before. I'm one of the second schools. So, I mean, editing of the Wiki pages, preferably okay. Okay, so now we have more Yambos centred overview on the electron phonon coupling in preparation of the Enson that we will do this afternoon. Yeah, okay. Thank you, Andrea. I'm Claudio Atacalite from X Marzai University. And let me start. I would like to thank Elena and Bartomeo for the previous talk that introduced all the ingredients, all the topics that I will speak about. So how to do electron phonon calculation with Yambos. So my point of reason will be mainly on the role of electron phonon coupling in the electronic structure. Now, until now, we have seen different things that you can calculate with the Yambos code, but in all the tutorial, we only speak about electrons. We never spoke about phonons or the coupling phonons. But as you have seen in this picture, unfortunately, atoms move. So we have to take an account, exactly. Even if because there are many physical phenomena that cannot be explained using only electrons. Many of them were mentioned before from superconductivity, joule heating, the electronic relaxation, and then the effect of phonon transport, the phonon motion that one can visualize in the experiment, the current phonons, the phonon stability, but also there are entire spectroscopy techniques that are related to the coupling of electron and phonons like Raman. So today, we will focus mainly on how phonons affect the electrons. And in particular, the electronic structure. The effect of phonons on electron is, they have a multiple effect. For example, they can create kink like in this figure here. So in this case, the Baerban structure was a straight line. And due to the presence of phonon, there is no information of this kink here, that is due to the real part of the self-energy in electron and phonon. Or they can enhance the effective mass of electrons. That's also one of the reasons why they change transport properties. The electron phonon coupling is also responsible for the closing of the gap of the materials. This is the example of silicon. In some particular case, a material can also change color due to the temperature of the electron phonon coupling. And this is visible in also in the spectrum. This is the spectrum of silicon at finite temperature. And as you can see, the temperature change the shape, the intensity, also the broadening of the peaks. So now, how we can describe this phenomenon. We have to, what we want to describe this, really, how the electronic levels change when we take into account the presence of phonon. So the coupling with the electron phonon that was shown before by Elena and Bartomeu. And to calculate this F, what we are interested in is the change of the electronic structure, the electronic levels with the temperature. And this change is due to the two different phenomena. One is really the electron phonon coupling that is this term here. So that is the change of the electronic bands with temperature. And there is also a second term, that is this thermal expansion term, that is due to the change of the bands, electronic bands, with volumes, and that change with the temperature. This is something that you can expect because you know that when you hit the material, the material can try to tend to expand, like in this figure here. If you think about iron, you just put on iron, on fire, and then iron expands to other materials. And the expansion of the unit cell of the material also will affect the bands of your system. This talk is mainly centered on the electron phonon interaction, but I will also explain you how one can calculate the thermal expansion. The thermal expansion is that if you simulate your system at different volumes, this is the example of silicon, the band structure will change. So this is the change of the band structure of silicon at different lattice vector. And this change here can be related to the derivatives of the phonon modes, that are these grune parameters, that can be easily calculated by finite difference in DFT, and so one can estimate the effect of the thermal expansion on the mass structure and can include in the calculation. This is something that will be out of YAMBO calculation, so we have to do it with DFT, and we will not consider anymore a part in this slide. Let me say that in general, the change of the electronic structure due to the thermal expansion for many materials is more compared to the phonon coupling. But anyway, it can be important. There are cases where they are comparable. So you have to keep in mind that during this talk, we will not consider anymore this term, but you can calculate it with DFT. So let's go back to the electron phonon coupling. I will follow an approach similar to the one of Bartomeo. Let's say that I want to show you how you really calculate these objects in the formula we are implementing in YAMBO. So we start from DFT, where you consider atoms at equilibrium, at capital R, these are the equilibrium proposition, and at the bottom it is the same notation of Bartomeo. And then for small u, we consider the displacement of atoms in respect to the equilibrium. So what we do, we expand, as you see in the previous slide also, we expanded this potential in the term of the small u up to the second order, because we are working on solids and so for the moment we are interested in an harmonic approximation. So we only do oscillation close to the minimum to make the ionic potential energy. So this gives us an additional terms in the Hamiltonian, that are these two terms here, that we can express in a second quantization way. For this, we will use the solution of the phonon set to a solution that we can calculate as a function of perturbation theory. So we know that it can state of the atomic system, so that they gain modes. And if we use this displacement, so the oscillation, the proper oscillation of the nuclei respect to their minimum position, this term here can be expressed in this way. That is the usual electron phonon coupling Hamiltonian that you can find in many books. Notice that for the moment, I just presented this term here and I didn't say nothing about the second term. I will come back in a moment to this second order correction. Now, all these ingredients that we need for the calculation of the electron phonon Hamiltonian as we see can be obtained from density functional perturbation theory. In this theory that was presented this morning, you have been a question for the variation of the wave function with respect to the phonon displacement and the variation of the potential. Solving this equation, you have access to the dynamical matrix element to give you the frequency and the gain modes of the atoms and to the electron phonon matrix element that is object G that will appear in the electron phonon Hamiltonian. With all these ingredients, we can construct a system of a question that couple electrons ions and describe all the coupling with these two words. And in particular, thanks to the ingredient we get from DFTP, we can construct the electron phonon coupling matrix element and the electron phonon coupling Hamiltonian that is this one. The phonon Hamiltonian that is this other Hamiltonian here where you can see the phonon like boson. And the electron Hamiltonian that is the connexium in this case, we will consider the electron as an independent particle. And if you want to represent this interaction in terms of a diagrammatic way, the electron phonon coupling is this diagram. It's an electron with the momentum K that scatter with the phonon a momentum Q and acquire a momentum and get a new moment that is K plus Q. That is exactly what describe this term here. Now, these are the ingredients that will be used today. How we can, how we will use this ingredient. That's in a simple way. Starting from this perturbation theory, we can, now that we have defined our perturbation the first and the second order, we can use a standard quantum mechanics approach that you can read in a standard quantum mechanics books to calculate the correction of the energy levels. And if you use perturbation theory in both the potential that generated by the atom and motion and also the perturbation theory in the wave function, the change of the wave function, you will see that the first correction the energy of an electron are made of these three terms. So the term that is the average of this first order term on the ground state wave function that will be zero because the ground state wave function the ground state wave function for a phonon mode is symmetric if you want is even why the potential is odd. So we can this term is zero. And then you have this term here that is the first correction of the wave function due to the atomic displacement coupled with the first correction of the potential and the second order that another second order term that is the ground state wave function coupled with the second order perturbation of the potential. And these are exactly the so-called fun and they by Waller term that are the term responsible for the change in the electronic levels. Notice that until now I didn't say how you calculate this second term here. I just say that from the density function perturbation to we get the first order term but I didn't say anything about the second order. And for the second order we will use an approximated version approximated by Waller that is based on this idea if we imagine that the derivative of the connection potential respect the mixed derivative of the connection potential with respect to the nuclei is and as prime are zero. So there's a called diagonal approximation that is a good approximation for solids but not so good for molecules. I will come back on this point. We can use the translation invariance of the correction to the electronic level to get the relation between these two terms determined that the second derivative of the self-consistent potential is the first derivative of the consistent potential. What we'll do at the end of this term here we will never calculate the density function perturbation theory but we will express it as a sum on some coefficient lambda that are function of the electron phonomatics element G. So at the end from our the FTP we will get to the G and with the G we will construct all the parts of the self-energy we need for the calculation. If you are interested on how much is good this approximation or when it fails I advise you to have a look to this paper by Samuel Ponce where they tested this approximation calculating exactly also this term here and they show that the fail is mainly it happens only mainly in molecules where this term cannot be disregarded. So if we put all together this correction to the band structure given by the first order the second order for the correction the potential held the first order from the fun and then we average on the ground state we function for electrons ions that means for the ion means average on the gaussians that are presented the phonon the ion motion the phonon coordinates we get our correction to the band structure that is this formula here in this formula that is derived from perturbation theory you can recognize that there is a factor here that is the both function of the phonon modes that depends on the temperature and here enter the dependence the temperature depends on the band structure so it means that due to the occupation of phonons the band structure will acquire a dependence on the temperature now how this approximation works let's see some example in compare with the experiment the classical a nice example that you can think is the band gap renormalization of diamon diamon is an indirect band gap material with a very large band gap of 7EB and with a very strong electron phonon copy and for this reason when you calculate the renormalization of the gap including electron phonon copy you get a renormalization of 600 mille-electron volt you can see here the red dots are the experiment also the blue two set of experiment and the calculation are the black line to give you the renormalization notice that you can also try to calculate the band gap renormalization using classical ions so it means like with molecular dynamics so you can image that you do a molecular dynamic simulation to make your atomos late every time you calculate the gap you have a rage and then you have the gap as function of the temperature but then if you do a calculation this way you notice that the gap go at this value here so the point is that the classical atoms one temperature go to zero they don't move anymore so you get really the bare gap that is this value here why quantum atoms even if the temperature go to zero they sometimes you can you can image the day way you can continue to oscillate or if you want they are delocalized they are described by way of function and that's the reason we have this curve that doesn't go the straight line but the curve will go at the final value and the difference between the the limit of the classical ions so the bare gap and the gap obtained with the electron form copy is exactly this correction here 600 milliliter volt then you may wonder how a gap closes I mean if conduction change or they change together this is a more difficult measurement but some group was able also to to measure the change independently of the valence and the conduction band using a smart idea that and I want to show you here is a X-ray spectroscopy in this kind of experiment you remove one electron from a core orbital and you promote it in the valence or opposite you fill the hole with the electron from the valence from the valence band that go to the core so in this two technique X-ray emission spectroscopy X-ray surface spectroscopy you can probe the position of the valence and the conduction band and you can probe the position of the valence and conduction band also at final temperature and if you suppose and it's not a bad approximation that the core orbitals are less affected by temperature because they are bounded to the nuclei and more bounded to nuclei you can try to plot the change of the valence and the conduction band as a function of the temperature compared with the theory so this is the change of the conduction and the valence band and the theory is the red line as you see that the both change in the case of C so there is also the possibility to measure the change in the isolated bands but ok we can go beyond the standard perturbation theory as we have done seen in this school and use also another point is that as you seen the electron phonon interaction correction to the gap can be quite large when you get your this is like a warning when you see the result like this is the old slide on 1997 you may wonder if really the result is good because you have to always consider that the electron phonon interaction reduce the gap so there is this effect to consider when you compare with the span so this perfect agreement in reality is not the perfect agreement and now we have seen all these results using standard perturbation theory but since this school we use the green function and the green function theory to do perturbation you may wonder if you can use this approach for the electron phonon coupling too and this is exactly the case electron phonon coupling can be reformulated in term of green function and diagram and in particular the fun part that you saw at the beginning that was due to the first order correction the self-consistent potential give rise to this diagram it is similar to the exchange and the dead by wall that this was a second order correction in the potential give rise to this diagram here that is in some sense similar to the art return if we look to the fun self-energy that is this formula here I will not derive it but I strongly advise you this review from justino where there is a very nice derivation and also nice reference you can see that this formula is similar to the one we obtained by perturbation theory with a difference than now in the denominator there are the phonon frequency if you eliminate this phonon frequency from the denominator you can see that you can sum up these two terms and you end up with the old formula obtained by static perturbation theory so these are the additional dynamical part that you get from the grid function now this dynamical part is important not only to get a better correction to the gap or to the electronic levels that for sure it will do it but also to get other phenomena because when you have a dynamical self-energy it gives you some electronic energy that are not real anymore so you have also an imaginary part a lifetime and this is exactly what you get if using the electron phonon self-energy you reconstruct your grid function in this way you can extract both the correction to the energy level and the lifetime and in particular you can plot also the imaginary part of the grid function that is the so-called spectra function that is the distribution of electrons that are not anymore a delta function but they acquire some broadening that are their lifetime so you have seen this for the electronic problem but also for the electron phonon covering problem is the same idea now how this apply to real material we can have a look on some particular case this for example is the top balance band that is the sodium fluoride from this paper of Gabriel Antonius and you can see that you have a quasi-particle peak that is this peak here that is due to the crossing of the self-energy with the straight line that is the bare energy and also an additional peak here that is like a satellite like peak that is due to the company with phonons so part of the spectra weight is this additional peak this activity is even stronger for bands that are not top balance on bottom conduction if I show you the band structure obtain it using this approach you can see that for particular bands like this zone here bands become completely diffused so you can also lose the concept of quasi-particle is really difficult to visualize the quasi-particle and zone and this is also visible in the experiment when they get these diffused bands in the measurement this effect of quasi-particle band structure are not visible only at the single particular level but it has been shown that they are also responsible for some for some properties also at the optical level and in particular if I consider I go back to the diamond and I consider the quasi-particle band structure of the the spectra function if you want the of the bottom conduction bands here and I use this two spectra functions to reconstruct my directness constant in independent particle approximations so it is a convolution of the grid function that is not bad approximation in this case the magnetic effects are weak in diamond so it is not a bad approximation if I use this the green pancreas this spectra function to reconstruct my optical properties and I compare it with the experiment I can see that there are oscillations these are the derivative of the directness constant that are not present in the bare calculation so using only the shifts of the levels that are the dot lines here so what it means that the the spectra weight that is lost from the main peak of the quasi-particle and there is a distributed around the main peak in this case is also visible in optical experiment as you can see in this experiment here so now you may wonder until now I show you only the effect of the electron phonon copy on the single particle level so you may wonder if you can combine the the electron phonon coupling with the phonons with the phonon coupling with excitons and this is possible also with Yambo if we start from our beta-salt-peter equation that you have seen in the previous talks in this equation you have a kernel that couple the different electrolyte excitation and that are at the beginning are just valence conduction differences and from this equation you get a spectra of your exciton that you can represent and from this spectra you can get also directly constant using this simple formula but you are obliged to every time to add like a smearing to get a spectra that repeat the experiment these are just the peaks of the experiment data so you may wonder if you can use the information from the electron phonon coupling to get the final temperature spectra from the beta-salt-peter and this is possible it is possible in a simplified way but it's implemented in Yambo you can use it the idea is to start from the beta-salt-peter equation and replace the bare energy of the your electron with the quasi-particle that you get from the electron phonon coupling calculation so with a shift due to the shift of the bands and the imaginary part if you do if you use this procedure what you get is an an H0 it is the one that the of the independent electron transition that contains also the a lifetime that is part here notice that now the final amyltonia is not there medium anymore but doesn't mean that you cannot solve the problem you can diagonalize your amyltonia and get your final temperature beta-salt-peter equation because you can repeat the equation a different temperature and with this final temperature beta-salt-peter you obtain both the dielectric constant where now the electronic levels the excitonic level depends on the temperature and also the dipoles and also the proton and also the excitonic radiative lifetime that are the imaginary part of this excitonic level if you put all together you can reproduce some experimental final temperature like here this is a silicon a different temperature from 0 to 600 Kelvin and you can also have the access to other information like how dipoles change with temperature how the lifetime change with temperature and so on but you have to be aware because this is an approximated approximated treatment of the axiom phonon problem so and moreover this is a more research topic that is an open research topic so there are different groups that are working on axiom phonon coupling the approximation that is implemented now in Yambo is in general valid for not too strong bound exciton and also as a physical problem that the lowest axiom should have 0 lifetime why now this approximation has not but ok anyway a good approximation for bulk semiconductor where they are not too strong bound axiom in general if you want to know more about axiom phonon coupling I advise you on the theory axiom phonon coupling by Antonio Senliui where there is in my opinion a clear derivation of the axiom phonon self-energy and this other paper by Bernardi Esangalli and moreover a new paper is coming out and I didn't know the title so I just put axiom phonon coupling revisited by Puglioparearia and Dramarini that are still working in the developing of the theory to go beyond the present approximation and axiom phonon problem today you will have two tutorials the first tutorial will be on the electron phonon coupling problem so the goal of this tutorial was to calculate is to calculate the renormalization of the bang up of a bulk semiconductor calculation will not be converged but it is just to give you an idea how it works in this tutorial there is a first part on the generation of the electron phonon matrix element because as you see in this presentation you need first of all the FTP to calculate phonon frequency and the electron phonon matrix element this part will not be shown in the tutorial everything in principle is explained there but it's a bit long so you can run it in a separate moment so the database are already present on the wiki web page and you can start from that one for the calculation of the electron phonon renormalization in this tutorial there will be also part on the acceleration of the convergence of the result because let me say that the calculation of the electron phonon self-energy can be quite demanding because we need a lot of k and q-point we recently implemented Yambou's approach to speed up this calculation this approach is present in the in the GPL version of the code the idea is to replace the self-energy that has a structure like this one with a part that is calculated on a coarse grid that are the matrix element that are calculated on this point here and the part that is averaged on a fine grid where we calculate additional phonon energy and electronic energy the addition of phonon energy are feigned by quantum espresso with simple code that interpolate a phonon bus structure in all the blue and zone and also the electronic energy are interpolated with some other technique this approach works very well and the speed up convergence you can see here the correction of the band gap of silicon versus the number of q-point with a without double grid you are converged very fast why without double grid you continue to oscillate this this approach will be published soon but it is available if you want to use it and there are some files as example even if we will not perform a full convergence study because it will require a lot of calculation of the electron phonon matrix element that is quite expensive but anyway we will provide some additional phonon grid to test how it works and in the second part of the tutorial you will use the result obtained on the by electron phonon cap so the quasi-particle bus structure to calculate optical properties at different level at the level of independent particle and beta-salt-peter so this will be the final idea was to have final temperature optics so I think that from my side this is more or less what I want to present on the Jambocode and implementation of the electron phonon coupling the paper that described the implementation are this three paper here there are a lot of my reference on the electron phonon coupling I advise you these two books for electron phonon and axion phonon the review of Feliciano Giustino that is really well done and the work on Cardona on the Allen-Cardona approach this this work of Samuel Ponsang Gabriel Antonius for the dynamical effect the non-diagonal approximation and all the approximations that are usually performed in the electron phonon energy and this paper for the electron phonon axion phonon coupling if you want to understand what are the limits of the present approach and that we will show you today that's my contribution thanks a lot Claudio really so we have already question here for the student thank you for a nice presentation I want to just ask you you mentioned that the exciton phonon coupling in Jambocode fails at the structure with strong exciton-binic energy but I know that there are some papers for example for boron nitride which has like two electron volts and more exciton-binic energy so what are the problems in it what we should like check if you can comment on it yeah, yeah, yeah the point is this that in a okay the point is this when you write your beta-salpeter equation what you should have done in principle you should include a new self-energy in the kernel that contain the electron phonon coupling and then solve this new beta-salpeter with this self-energy that should be the perfect approach with all the additional difficulty the energy is dynamic but this will be what and if you do like this you can realize that the lowest exciton in a system that has a direct bang up this was not the case of BN but in general the lowest exciton has to be a lifetime that is infinite because again when you create an exciton the lowest one has not the possibility to decay in any other way that is the reason that it has infinite lifetime instead if you introduce the imaginary part directly in the energy like we do you realize that also the lowest exciton has a lifetime so it will require a broadening that is not too large exaggerated even if in the case of BN direct so also the lowest exciton will have a broadening but it will probably be too large on the other hand the position of the peaks with the temperature can be correct because in this case we just have a shift of the electronic levels and that can be better described so in my opinion the broadening of the exciton so yes the lifetime of the lowest exciton is an open issue so we don't know so there is someone that tells that it's zero I mean it's interesting because it's a really active research at the moment even more papers say different things so there is a question from the audience online please if you want to unmute yourself yeah hi so my question is actually yeah for what I understood now we are only taking into account the optical limits so we are not taking into account the exciton dispersion in the exciton phonon coupling am I right so we are not taking into account the finite momentum of the exciton because as the speaker yesterday was telling us for the exciton phonon interaction is also important to take into account the finite momentum for the electron couple of the exciton in order to correctly describe the exciton phonon interaction okay let's say that this term of exciton let's say that the exciton phonon has different effects you can have additional peaks that are due to the scattering with the phonons so they are like if they were satellite of the exciton in some sense you can have the excitonic peak plus another peak that is an exciton plus a phonon plus an exciton plus a phonon and so on this kind of diagram in this case I'm not considered so we're not to consider the scattering with the phonons that create additional peaks in this approach we just consider the broadening of the of the annexion so we just like it if we give it a lifetime but not taking account the full scattering so that will be that's the way which we can think is approximated another question is there a way now in the current implementation of Yambo to extract also the exciton phonon coupling constant okay not yet okay thanks let's say that we are working on that and we hope it will be available in the future so there is another question from John Hingal can you unmute yourself yes, my question thank you for the very informative talk I would just like to ask as a Polyron can involve long range screening can Polyron make transport be computed without support of a long range hybrid functional such as HSE E06 how do you are you there I'm reading the question on the chat so I I know that for the Polyron I think you can calculate also without the need the longer range hybrid function because I remember this work about Justino that the reformulation of Polyrons in the unit cell and they were not based on a hybrid function so I guess you can get Polyrons also without hybrid functions you can check in the work of Justino they have done a very nice work on the calculation of Polyrons as far as I know for many materials they got a very good result in comparison with the experiment but for sure it will fail for others but I think you can do it thank you very much okay so another question so first of all thank you for your nice talk then if I properly understood if you want to add the electron phonon coupling in GW calculation you just have to add the proper self energy to the electronic one right yes but okay let's say that what this is exactly what we will do today we will add the electron phonon self energy to the band structure that means you can add it to the GW calculation in principle if you want there is an additional electron phonon coupling is that electron phonon coupling can change the screaming of the GW but this is not considered in Yambo now there are some work that consider also this other effect okay so can you please add some comments between the lifetime generated from the electron phonon coupling and the one that should be present due to the electron-electron interactions so maybe one is higher than the other or stuff like that yes as far as I know the one of the obtaining from the electron phonon coupling is in general much larger than the one due to the electron-electron scattering I don't know that's what I know in general then I think you can separate them using the temporal dependence that one of the using the electron-electron scattering is weak dependent from the temperature so I think you're going to extract both for them from the experiment that is when you see lifetime the electronic level there are many due to the electron phonon so on this question one comment is that the electron phonon lifetimes usually they are proportional to the density of states and instead the electron-electron lifetimes which we have in GW for example they have a barrier to be activated so which depends which is related to the gap so for example you show in the minimum of the conduction band they are very low and then they increase because you need enough energy to activate them maybe I can add something very I mean it's what I understood always maybe I can use the blackboard because if you're going to homogenize electron gas you consider a very simple case for a metal and then electron phonon with a simple the bi-model where actually just one phonon branch grows linearly so it's super simple then you can calculate the land width and you get very different behavior the electronic land widths are quadratic with the energy so this is the gamma as a function of the energy quadratic while the electron phonon land widths are like this so they rise in a energy step that is of the order of K B T so of the temperature and then they get constant so for low energy electrons the electron phonon is more important but quickly the electron becomes very much dominant so and indeed this is connected to homogenize electron gas the density of states is constant if you go to the real material this thing changes a little bit but the overall behavior is the same so one grows quadratically with the energy the other is pretty constant so phenomenologically they are really different it's not a question so you are showing us the double grid technique to compute the self-energy so if I'm not wrong you can do the same thing much accurately using for example vanier functions at every point you can compute the electron phonon coupling so what is the advantage of this double grid method or for example the EPW does exactly the same thing but much more accurately because you have electron phonon coupling at each and every point you take so what is the advantage of double grid I I agree that using a vanier function is better because you interpolate not only the energy of the electrons and the dispersion of the phonons but also the electron phonon matrix element so convergent it's usually faster let me say that so in general it's faster from a point of view of developers implemented double grid is much easier the advantage of double grid can be that you don't get a vanier function for higher conduction bands and in case you are interested in converging the real part of the self-energy maybe you need more conduction bands that you don't you cannot interpolate with vanier functions that can be the advantage of the double grid so one more question I don't know how to ask this but so if you consider the case of graphene DFPT is pretty bad describing the electron phonon interactions for example if you compute the phonons at K I mean there is normally where DFPT couldn't properly take into account that due to the bad description of screening so how could you improve the electron phonon coupling of the phonons in these cases I mean I don't know if there exists any no, no it doesn't mean different calculation for graphene especially for the K phonons the gamma phonons they get high symmetry phonons so you can use also supercell easily they show that the putting using a functional that can improve all correction from perturbation theory which is much easier to use you can get the better electron phonon coupling for the K phonons for the K point now include this effect in a theory like this one it's complicated you have to do some approximation or use a finite difference like complete a finite difference approach as shown before by Bartomeo in this case you can calculate the electron phonon coupling by finite difference using a more accurate function as a starting point this has been done for superconductors for other materials okay so I think we close the session now and at 2 we have to be back in the info lab for the afternoon and so thanks Claudio again yeah see you