ON THE RE-ARRANGEMENT ENERGY OF THE NUCLEAR MANY-BODY PROBLEM
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1 IC/67/14 INTERNATIONAL ATOMIC ENERGY AGENCY INTERNATIONAL CENTRE FOR THEORETICAL PHYSICS ON THE RE-ARRANGEMENT ENERGY OF THE NUCLEAR MANY-BODY PROBLEM M. E. GRYPEOS 1967 PIAZZA OBERDAN TRIESTE
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3 Ic/67/14 IHTEENATIOHAL ATOMIC EHEROI AGENCY IHTERNATIONAL CENTRE FOR THEORETICAL PETSICS ON THE RE-AREANGEMBHT EMERGY OP THE HUCLEAR MANY-BOOT PROBLEM* KJl. Grypeos TRIESTE Apxil 1967 * To "be submitted for publication
4 ABSTRACT Mittelstaedt's definition of the re-arrangement energy, which is related to many-body calculations for the separation energy of a particle "by means of model wave functionsjis extended in a straightforward manner to the case in which a trial many-body wave function is used. The "trial re-arrangement energy" so defined is studied in the case of the separation of a particle s from a system of A + 1 particles in which the A particles (nucleons) are not identical to the s. In this treatment a Jastrow-like trial wave function is used. Some general properties of this trial re-arrangement energy are derived and the first term of its cluster expansion is given in the case in which the A nucleons form an infinite nuclear matter of density g. numerical estimates of this first order term are performed for a case of physical interest. -1-
5 Ott THE RE-ARRANGEMENT ENERCT OP THE HUCLEAR MAUY-BOEY PROBLEM 1. INTRODUCTION Tlie re-arrangement energy enters as a contribution, in addition to the kinetic and potential energy, to the corresponding energy expressions of various processes in nuclear phyaics as, for example, the separation of a particle from a system of particles. Other such processes are the excitation of a particle or the scattering of a particle by a system. The re-arrangement energy is usually discussed in connection with Brueckner's theory in which perturbation many-body techniques are used /J A comprehensive definition of the concept of re-arrangement energy has been given by Mittelstaedt (see ref. 3)). Mittelstaedt's definition is independent of perturbation theory and refers to calculations in which model nuclear many-body wave functions $ are used, in which case the energy quantities are not expressed as expectation values but by means of the model wave functions $ and the actual wave functions ^. In the next section we briefly review Mittelstaedt's definition, employing this approach, which is very suitable as a starting point for perturbation calculations. Perturbation techniques are not the only means of treating manybody problems. Variational techniques have proved quite useful in a variety of many-body problems. In particular, short-range correlations of the nuclear many-body problem have been treated in a promising way by applying cluster expansion-variational techniques. '. The basic quantity in these techniques is a trial many-body wave funotion. In Sec. 3 Mittelstaedt's definition of the re-arrangement energy (connected to the process of the separation of a particle from a system) is extended to the case in which a trial many-body wave function is employed. Using this definition and a JASTROff-1 ike^" ^many-body t r i a l wave function, we investigate the properties of the "trial re-arrangement energy" whioh corresponds to the separation of a particle s from a system of A + 1 particles, in whioh the rest A partioles (nuoleons) are not identical to the s. Namely, we show that this trial re-arrangement energy is -2-
6 2. THE MODEL RE-ARRANGEMENT ENERGY Let us consider a many-body system consisting of A partioles (nucleons). The Hamiltonian of this system is taken to be A A r >i (1) The aotual ground state wave funotion of the system satisfies the Sohrodinger equation In order to oalculate the energy E. it has been shown convenient in many cases to introduce a model wave function $> A of such a kind that ^ can be normalized by ^P* I "*F«V *! Then the energy can be written ' (3). Consider now the process of the separation of a particle from a system of A + 1 particles. We shall indicate by s that particle among the A + 1 partioles which is separated. In the present paper we shall concern ourselves with separation processes. positive (or zero, if there wore no correlations between the particle s and the nucleons) and also that it does not depend explicitly upon the interparticle potentials. Finally, in the last section, we consider the case in which the A nucleons form an infinite nuclear matter of density p and we give the first-order term of the cluster expansion of ^ [TlTi- This term, whioh is proportional to p, is estimated in the case where the separated particle is a A particle in its ground state in nuclear matter. A variation^calculation connected with this problem has been performed during the last few years '. -3- "" "S.:
7 The Haralltonian operator for partiole s isi its separation energy is - E(s)» where 17 ^ (5) E., and E. are the energies of the systems of A + 1 particles and A partioles, respectively. We can write eq.. (5) as followst where QL.-, and OG. are the corresponding normalization volumes For simplioity we shall omit these in the following. L(s) oan be written where The quantity A defined above, whioh depends on the model wave funotions ^ : A = Ar$l» ia tiie mod - e l re-arrangement energy. Mittelstaedt has separated A into a kinetic and potential re-arrangement energy part: " + A P (9) -4-
8 where and r In the speoial case of infinite nuolear matter (A > oc and o"ii >«O such that the density p = is constant) one can express as follows: A 3. THE TRIAL RE-ARRAHGEMENT EHERCFT As we have pointed out in the introduction, one can in many cases apply the variational principle in calculating energy quantities and,for this purpose, matrix elements with respect to a trial many-body wave function are used. Considering again the prooess of the separation of a particle s from a system of A + 1 particles, we can write* for the trial expression of the separation energy E? r t - or where the "trial re-arrangement energy" is defined "by * We have added the superscript tr to indioate that we are considering a trial many-body function in the calculation. -5-
9 _ E We must emphasize thatafti?**! depends on the particular trial wave function we consider. In calculating the trial re-arrangement energy, a trial manybody wave function of the Jastrow type, which allows for correlations between pairs of particles, may be used. In the following we shall consider the trial re-arrangement energy in the case in which the separated particle s is not identioal to the rest A particles (nuoleons). The trial wave function of the system of A + 1 particles, one of which is the s, will be taken to be d>($) is the single-particle wave function for the s. The functions j,. * si which allow for correlations between the s and the nucleons, must be suoh that they tend to unity if the distances between the s and each nucleon tend to infinity. Also they must be equal to eero inside and at the hard oore radius if a hard care exists in the potential between the s and each nucleon. In the following when we write A [^ir \ we shall mean the trial re-arrangement energy with respect to the trial wave function (16). With this wave function we can easily calculate the nominator in the first term of the r.h.b. of (15). The internucleon potential V A "does not couple" the particle B and the nucleons (we assume that Tf j( x,\ commutes with V A )i (17) On the other hand T does couple. If we put -6-
10 «" ; * we can write where EL. is the nuoleon mass From (17) and (19) we obtain «Jv (20) Taking into aooount that and introducing the funotion (22)
11 we can write expression (20) as follows: ^h^k)fw(^^^' j ' (23) Substituting this into expression (15) and- applying Green's theorem we find: {24) Using the identity we easily obtain the following expression for /i L^Jr ] ' <«> can therefore conclude the following: i) ^\ r^^l ^- O. The equality holds if there were no correlations between the particle s and the nucleons in the trial wave function. ii) The trial re-arrangement energy A [^^1 doe s» o-fc depend explicitly upon the interparticle potential. However, there is an implicit -8-
12 dependenoe since the form of the correlation functions depends upon the interpartiole potential. From these properties we see that ArU^**") is of correlation (5) due to the action of the kinetic energy operator of the A particle system on the correlation functions y\. In view of these remarks it would perhaps "be appropriate to characterize A^XjJ*^] as "additional kinetio correlation energy". The other kinetio energy contributing to E{s) comes from the kinetic energy operator of the separated particle. 4. INFINITE NUCLSAH MATTER Expression (26) for Ap]7 ] can "be expanded as a power series of the constant density p_ of the infinite nuclear matter in the case in which the A nucleons form such a medium. The first term of this expansion can be easily obtained, while the others are more complicated and additional approximations seem necessary. If we use the cluster expansion?> + F fe V (27) in the nominator and denominator of (26) and introduce the so-called (configxirational) "generic distribution functions" ' A.' (28) that is, in our oase< -9-
13 we obtain for the "first-order trial re-arrangement energy": (30) A numerical estimate of this can "be given in the case of a A particle in its ground state in nuclear matter, A variational calculation of the first-order term of U//A has been performed d, Using for the /\-nucleon interaction the DCOTS-tfAHE potential < C = fa K (31) and for the f (32) we find A (33) This value corresponds to g= 0,172 nucleon/(fermi) and <*t = 2,18 which minimizes the first-order term in the expression for / «of DOWHS and GHTPEOS 6 ) (34) If we use for the f -10-
14 >- o ico - (35) in whioh is determined by the condition (36) which is a possible way of aohieving reasonably rapid oonvergenoe of the cluster expansion, we find 0) A = 32.4 This corresponds to the same value of Q (34) with ejtprwte^ (35) for the f. and to XC , whioh minimizes In the variational calculation of the binding energy of a A~ particle in nuclear matter \ Af'^r^] enters as an additional contribution but it was not calculated separately. In particular, its first-order part A(jtyrtvj was combined with the corresponding first-order terms coming from the Hantiltonian operator of the A-particle in order to derive expression (34) whioh shows that L/^ depends on the relative motion of a A -nucleon pair. Investigations of the A-nuclear matter problem by methods different from the cluster expansion-variational one have been done and in the early version of these investigations, which were based on Brueckner's independent pair approximation, and in particular on a solution of the Bethe-Goldstone equation, the corresponding re-arrangement energy correction was neglected '* '. These were considered by DAJBRCWSKI and KOHLER K The re-arrangement energy which enters in this approach was studied by means of Brueckner f s reaction matrix K and was calculated separately as an additional correction. In particular, it was split into two terms, the "particle" and the "hole re-arrangement energy", of which the.last one contributes mostly» * This is appropriate to the central density in heavy nuclei' -11-
15 ACKNOWLEDGMENTS I should like to acknowledge useful discussions and suggestions by Professor B.W. Downs, who also suggested thib investigation, and by Drs. D JJ. Brink and R.K. Bhaduri. Thanks are also due to Professor RJS.Peierls for hospitality at the Department of Theoretical Physics, University of Oxford, and Professors Abdus Salam and P. Budini for hospitality at the International Centre for Theoretical PhyBics, Trieste, where this work was oompleted. A fellowship from the IAEA is also acknowledged. -12-
16 REFERENCES 1) H.S.Kohler, Biiol * Phys. 88, 529 (1966) 2) D.J. Thouless, The quantum mechanios of many-body systems (Academic press); J.S. Bell and E. J. Squires, Adv. in Phys. 10, 211 (196l) 3) P. Mittelstaedt, Nucl. Phys. JL7, 499 (i960) 4) R. Jastrov, Phys. Rev. 9, 1479 (1955) 5) J.B. Aviles, Ann. Phys. (NY)^, 251 (1958) 6) B.W. Downs and M.E. Orypeos, Nuovo Cimento f 306 (1966) 7) J. De Boer, Rep. on Pro#r. in Fhys. Vol. XII, 305 (1948) 8) B.W. Downs and W.E. Ware, Phye. Rev. 133, B133(1964) 9) R. Hofstadter, Rev. Mod. Phys. 28, 214 (1956) 10) JJ). Walecka, Nuovo Cimento _16, 342 (i960) 11) J. Dabrowski and H.S. Kbhler, Phys Rev. _136_, B162 (1964)
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