Reference approach in theory of pseudospin systems

For theoretical description of pseudospin systems with essential short-range and long-range interactions we use the method based on calculations of the free energy functional with taking into account the short-range interactions within the reference approach in cluster approximation. We propose a consistent formulation of the cluster expansion method for quantum pseudospin systems. We develop a method allowing one to obtain within the cluster approximation an Ornstein-Zernike type equation for reference cumulant Green function of an arbitrary order. In the two-particle cluster approximation we derived an explicit expression for pair temperature cumulant Green function of the reference system. In the cluster random phase approximation we calculated and studied thermodynamic characteristics, elementary excitation spectrum, and integral intensities of the Ising model in transverse field.


Introduction
Modern statistical theory of condensed media pays a great attention to studies of ferroelectric and magnetic materials, described by pseudospin models with essential short-range and long-range interactions, especially of hydrogen-bonded ferroelectrics [1][2][3][4][5][6][7][8][9][10][11][12] and low-dimensional magnets [13,14]. For an adequate description of these objects, such an approach is required that would allow to use different techniques for taking into account short-range and long-range interaction. This is a typical mathematical problem in theories of multiparticle systems. It has been successfully solved in studies of equilibrium properties of classical systems [15][16][17][18][19][20][21] and metals [21][22][23][24][25] with making use of the proposed in Refs. [15][16][17][18]22,24,25] approach. Within this approach, the long-range and short-range interactions are described in phase spaces of collective variables and individual coordinates, respectively. The system with short-range interaction is called then the reference system.
Using the idea of separating reference system [15][16][17][18], in Refs. [26][27][28][29][30] a method was proposed for description of pseudospin systems with essential short-range and long-range interactions. This method is based on calculation of the free energy functional with taking into account the short-range interactions within the reference approach. In Refs. [26,27,30] expansions of the free energy functional and functionals of the temperature cumulant Green functions (CGF) in the inverse long-range interaction radius were studied. For the first time there has been performed a total summation of the reducible in blocks diagrams in the free energy functional and of non-compact diagrams in functionals of CGFs for quantum pseudospin models. Expressions for the free energy and temperature CGFs of the considered systems were obtained. There was shown how to obtain consistent approximations for their thermodynamic and dynamic characteristics, using classification of the approximations for free energy functional according to loop diagrams.
It should be noted that obtained in Refs. [26][27][28][29][30] general expressions for thermodynamic and dynamic characteristics of pseudospin systems with short-range and long-range interactions contain thermodynamic and correlation functions of the reference system. Hence, to solve a general problem one needs to solve a reference one, that is, to calculate free energy and CGFs of the reference system. The maximal order of the reference CGFs depends on the order of the approximation for the long-range interactions. Depending on the reference Hamiltonian, the reference problem can be solved exactly (see, for instance, [14,[31][32][33][34][35][36]) or approximately, with taking into account peculiarities of the reference system. The best description of the reference system for a wide class of pseudospin models can be obtained on the basis of the cluster expansions method (see [1][2][3][4][5][6][7][8][9][10][11][12][37][38][39]). In some papers [40][41][42][43] this method was successfully used for studies of disordered magnetic and ferroelectric materials. Unfortunately, the cluster method was correctly developed only for Hamiltonians with commuting unary and interaction parts. Mostly it was used for calculations of thermodynamic characteristics of pseudospin models. In Refs. [44][45][46] a problem of calculation of distribution functions for Ising models within the cluster approach was considered but not solved completely. Equations for pair correlation functions of the reference system (Ornstein-Zernike type equation) in Refs. [44,45] were not derived consistently but constructed artificially. The problem of calculation of quasimomentum-dependent pair correlation functions was also considered in Ref. [46] within the cluster approach. The obtained there results are valid in paraphase only. Later, a method was proposed [47,48], which allows one to obtain Ornstein-Zernike type equations for an arbitrary order correlation functions of Ising models. These equations for pair and three-particle correlation functions were derived and solved within the two-particle cluster approximation (TPCA). It was shown that the proposed in Refs. [47,48] cluster approach to calculation of correlation functions of the reference Ising models yields known exact results [31,32] for pair and three-particle correlation functions of the one-dimensional Ising model.
In Refs. [48,49], using the four-particle cluster approximation, pair q-dependent correlation functions of deuterons were calculated for KD 2 PO 4 type ferroelectrics and ND 4 D 2 PO 4 type antiferroelectrics. Dynamics of hydrogen-bonded ferroelectrics with taking into account tunnelling effects was considered in Refs. [50][51][52] within the proposed in [50] original approach. For the first time it has been shown, that in the reference approach, with the short-range interactions and tunnelling taken into account in cluster approximation, the dynamic properties of the studied systems are to a great extent determined by an effective tunnelling parameter, renormalized by the short-range interactions. Later, this peculiarity of the dynamic properties of hydrogen-bonded compounds was noticed also in Ref. [53]. Unfortunately, expressions for dynamic (at q = 0 and E = 0) and static characteristics, calculated in Refs. [50][51][52], turned to be inconsistent. That results from the fact, that dynamic characteristics were obtained using the method of two-time temperature Green functions, equations for which were decoupled in the spirit of Tyablikov approximation. On this, the intracluster Green functions of the reference system were connected only via the long-range interactions, whereas the short-range correlations were not taken into account. Thus, there had not been developed a method, which would allow one to consistently describe thermodynamic and dynamic characteristics of reference quantum pseudospin models.
In the present paper, for theoretical description of pseudospin systems with essential short-range and long-range interactions we shall use the developed in Refs. [26][27][28][29][30] self-consistent reference approach. In Section 2 we shall briefly consider the main results obtained within this approach. Then, a consistent formulation of cluster expansion method for reference quantum pseudospin systems will be given for the first time. We shall propose a method, allowing to obtain Ornstein-Zernike type equations for reference temperature cumulant Green functions of an arbitrary order within a cluster approximation. An Ornstein-Zernike type equation for the pair correlator will be derived and solved in the two-particle cluster approximation. The last Section is devoted to investigation of the Ising model in transverse field (IMTF) within the cluster random phase approximation (CRPA) using the obtained earlier in this paper results.

Theory of pseudospin system with short-range interactions taken into account in reference approach
We consider pseudospin systems with short-range and long-range interactions, described by the Hamiltonian Here K ab and J ab νµ are the short-range and long-range parts of the pair interactions. S a ν (a = x, y, z or +, −, z) are components of a normalized (S z = −1, 1) spin S.
. Hereafter, the argument {Γ} will be frequently omitted. The factor β = 1/(k B T ), occurring in Γ, K, and J (in the presented above form of the Hamiltonian H), will be written explicitly only in some of final expressions.
After an identity transformation of the operators S a ν = S a ν + ∆S a ν in the last term of Hamiltonian (2.1), which describes the long-range interactions between pseudospins, we obtain 2) The first term in (2.2) describes the short-range interactions between pseudospins placed in a field created by the long-range interactions and by Γ a The Hamiltonian k H({κ}) is called the reference Hamiltonian [26]. The argument {κ} will be dropped often. Let us note that in the mean field approximation (MFA) over the long-range interactions, the last term in (2.2) is neglected. Our main task is to calculate the free energy and pair temperature cumulant Green functions for the models, described by Hamiltonian (2.1). Herẽ the averaging is performed with the density matrix For the sake of convenience, in our calculations we use not the free energy F ({Γ}) but the F ({Γ})-function (logarithm of the partition function). According to the theory proposed in Ref. [26], to solve the formulated problem, one should calculate the k F -function and CGFs (2.11) of the reference system (2.3). In the present paper the k F -function and pair CGFs will be calculated within the two-particle cluster approximation. Assuming that the reference problem is solved in Ref. [26] the expansion of the free energy functional in the inverse radius of the long-range interactions was studied, for the systems described by the Hamiltonian (2.1) and expressions for temperature Green functions were obtained. Here we present only some of their results for nonuniform fields (Γ a ν = Γ a ) up to r −d 0 in the long-range interactions. The F -function of the considered system reads where (2) ( q, ω n ) and J( q) are matrices 3 × 3 in the indices a, b; their elements are Fourier transforms k b (2) ( a b q,ωn ) and J ab ( q) of the pair CGFs of the reference system k b (2) ( a ν,τ 1 \ b µ,τ 2 \ ) and of the long-range interactions J ab νµ (for uniform fields (κ a ν = κ a )). For the pair CGFs b (2) ( a ν,τ 1 \ b µ,τ 2 \ ) in the frequency-momentum space, the following relation [26] holds Here we use the notation is the Fourier transform of the effective interaction in the considered system, whereas are Fourier transforms of the three and four-particle CGFs of the reference system, respectively.
We also present here an expression for the order parameter [26] S a = S a ρ = k S a k ρ + 1 2N a 1 ,a 2 q,ωn Hence, we have general expressions for the free energy (F = −k B T F ) and pair CGFs, and the equation for the order parameter in the r −d 0 approximation. These expressions contain the free energy and correlation functions of the reference system. 3. Two-particle cluster approximation for short-range interactions 3

.1. Problem formulation
Our task in this section is to obtain the k F ({κ})-function, parameters k S a ν k ρ and pair cumulant Green functions k b (2) ( a 1 ν,τ 1 \ a 2 µ,τ 2 \ ) of the reference pseudospin system, described by Hamiltonian k H({κ}) (2.3), in the two-particle cluster approximation in the short-range interactions.
Let us define the functional of the partition function logarithm (the k F ({ε})functional) of the reference model as [26] Dependence κ a ν,τ on τ here is necessary to perform functional differentiation with respect to κ a ν,τ [26]. It should be noted, that since spin operators at different sites commute, and κ a ν is a scalar, the quantity A τ (if A = S a ν or κ a ν ) can be written as Starting from (3.1), we introduce functionals of CGFs of the reference system They will be found using According to [26], the following relations between the k F ({κ})-function (2.9) and temperature CGFs (2.10) and their functionals hold .
That is, calculation of the k F ({κ})-function and temperature CGFs is reduced to calculation of the k F ({ε}, {κ})-functional.

Cluster approximation. Free energy
Let us calculate now the k F ({ε}, {κ})-functional in the two-particle cluster approximation. We perform a cluster expansion, with the lattice being divided into the two-particle clusters [47,54,55]. As a r ϕ a ν,τ S a ν,τ we denote an operator of the effective field created by the site r and acting on the site ν, provided that the site r is a nearest neighbour of the site ν (r ∈ π ν ). Obviously, the number of fields acting on an arbitrary site ν r∈π ν a r ϕ a ν,τ S a ν,τ is z (z is the nearest neighbours number). After an identity transformation, the reference Hamiltonian (3.2) takes the form Hereafter, the arguments {κ ν }, { r ϕ ν } will frequently omitted.
Let us present the k F ({ε})-functional (3.1) as Here and averaging is performed with the functional of the density matrix We restrict our consideration by the first order of the cluster expansion [47,54,55]; this corresponds to the two-particle cluster approximation. Then the k F ({ε})functional becomes a sum of the single-and two-particle intracluster F ({ε})-functionals Putting ε a ν = 0 (κ a ν,τ = κ a ν , r ϕ a ν,τ = r ϕ a ν , see also (3.6)), and going to the uniform fields case κ a ν = κ a ( r ϕ a ν = ϕ a ), from (3.16) we obtain the k F -function of the reference system in the TPCA for the uniform fields

System of equations for single-particle distribution functions and variational parameters
Let us find now equations for functionals k T τ S a ν,τ k ρ({ε}) and for cluster fields Starting from the fact that the k F ({ε})-functional (3.16) is a sum of the single-and two-particle F ({ε})-functionals, we get Here we introduce the notations From the explicit form of the intracluster F ({ε})-functionals (3.12), (3.17) it follows that where the averagings are performed with the density matrix functionals (3.15) and Hereafter, the functionals (3.31) and (3.32) will be called the single-particle and two-particle intracluster functionals of CGF, respectively. In analogy to (3.6), from (3.12) and (3.17) one can obtain expressions relating the intracluster F -functions with their functionals .
One can also derive expressions relating the single-particle and two-particle intracluster CGFs with their functionals ; we obtain the system of equations for the functionals k T τ S a ν,τ k ρ({ε}) and cluster fields r ϕ a ν,τ .
One can see that equation (3.42) for r ϕ a ν,τ , obtained from the k F ({ε})-functional extremum condition (3.40), is equivalent to equations That is, in the present approximation (see (3.36) -(3.39)) the relations between the density matrices are not violated: Putting ε a ν = 0 (κ a ν,τ = κ a ν , r ϕ a ν,τ = r ϕ a ν , see also (3.7), (3.36), (3.37)), taking into account the following relations and going to the uniform fields case κ a ν = κ a ( r ϕ a ν = ϕ a ,κ a ν =κ a , rκa ν =κ a ), from (3.41), (3.42) we obtain the system of equations for the single-particle distribution functions k S a k ρ and cluster fields ϕ a in the TPCA for the uniform fields case.
Here F 1 ({κ}) and F 12 ({κ}) are the single-particle and two-particle intracluster Ffunctions for the uniform fields case (3.22), (3.24). The factor 1 2 in the right hand side of equation (3.44) arose at going from the partial derivative of the F νr ({ rκ ν , νκ r })function with respect to rκa ν in the non-uniform fields case to the partial derivative of the F 12 ({κ})-function with respect toκ a in the uniform fields case.

Pair distribution functions
Let us briefly discuss the presented in [54] method of calculation of the pair CGFs functionals of the reference system, based on the technique developed in [47] for the Ising model. Starting from (3.5) and (3.41), we obtain an expression for the pair CGF functional.
Having in mind calculations of the pair CGFs (see (3.7)) for the uniform fields case, and since for specific systems single-particle intracluster pair CGFs T τS a 1 ν (τ 1 )S a 2 ν (τ 2 ) c ρν (see (3.31), (3.36)) in uniform fields case can be calculated directly, we need to obtain an equation for δκ a 3 ν,τ 3 /δ κ a 2 µ,τ 2 [47,54,56]. We introduce the notations Taking the functional derivative δ /δ κ a 2 µ,τ 2 from the both sides of equation (3.42), and taking into account the relation (see (3.20)), we obtain Going to a matrix form in (3.48) 1 and performing some transformations, we obtain: Introducing the notations We obtain an equation (3.51) with unknown r ϕ ′ νµ , ν ϕ ′ rµ . One more linearly independent equation still should be derived. After changing indices r ⇋ ν, we get One can easily see that (3.51) and (3.52) are a system of equations for r ϕ ′ νµ , ν ϕ ′ rµ . Summing up over r ∈ π ν in (3.51) and taking into account the fact that 1 + r∈π ν Here the matrices have a block structure; for instance in terms of (x, y, z): where the submatrices  Let us put ε a ν = 0 and go to the uniform fields case κ a ν = κ a in equation (3.54). Then it can be rewritten as where π νr = 1, r ∈ π ν 0, r / ∈ π ν . (3.57) It should be remembered, that with putting ε a ν = 0 we go from the single-particle and two-particle intracluster CGF functionals (see (3.31), (3.32)) to the corresponding CGFs (see (3.36), (3.37)).
Going to the frequency-momentum representation in (3.56) and solving the obtained equation, we get for κ ′ ( q, ω n ) 1 (ω n ) are 3 × 3 matrices in the indices a, b (a = x, y, z or +, −, z), their elements are Fourier transforms (F 1 ( a,b ωn )) of the pair intracluster CGFs T τS is the Fourier transform of the function π νr . For simple lattices with a hypercubic symmetry, π( q) reads d is the lattice dimensionality; α is the lattice constant. The obtained matrix expression (3.58) can be rewritten as where Θ( q) for simple lattices with a hypercubic symmetry is Putting ε a ν = 0, going to the uniform fields case in relation (3.45), and going to the frequency-momentum representation, we obtain expressions for pair CGFs, which are convenient to rewrite in a matrix form in the indices a, b: (3.63) Hence, in order to calculate the pair CGFs of the reference system in the uniform fields case from (3.63), we need to calculate (according to (3.61) and (3.59)) the single-and two-particle intracluster pair CGFs F

Thermodynamics. General results
We consider the Ising model in transverse field with a renormalized pseudospin operator (S z = (−1, 1)).
Here K and J νµ are the short-range and long-range pair interactions, respectively; Γ is the transverse field; the quantity h → 0 is introduced for the sake of convenience. Hereafter, the factor β = (k B T ) −1 is written explicitly. In the framework of MFA for the long-range interactions, the Hamiltonian (4.1) can be written as where and k H is the Hamiltonian of the reference IMTF According to the results of previous sections, the free energy of IMTF within the TPCA for the short-range interactions, with the long-range interactions taken into account within the MFA, is The k F -function of the reference IMTF is expressed via the single-particle and two-particle (4.10) intracluster F -functions. Let us show briefly how these functions can be obtained.
The Hamiltonian H 1 acts on the basis of two functions of state of a single particle 1 + 2 − (4.12) In the representation (4.12), the single-particle Hamiltonian reads Taking into account (4.8), one can easily obtain the single-particle partition function in an explicit form (4.14) The two particle Hamiltonian H 12 acts on the basis of four functions of state of a two-particle cluster.
In the representation (4.15), the Hamiltonian H 12 reads On the basis of (4.10) and (4.16) we obtain the two-particle partition function where (E 12 ) 4 = K , (4.18) whereas three other eigenvalues (E 12 ) 1 , (E 12 ) 2 , (E 12 ) 3 of the matrix (4.16) are roots of a cubic equation From (3.43) and (3.44), with taking into account the fact that in the framework of the MFA for the long-range interactions (this can be obtained from the explicit expression for the free energy (4.6)), we get equations for the parameters m = S z ρ , η = S x ρ and cluster fields ϕ a (a = z, x).
When the long-range interaction is absent (J 0 = 0), we have a system of two equations (4.21) and (4.22) for ϕ x , ϕ z in an implicit form ((E 12 ) i are roots of cubic equation (4.19)) and expressions (4.23) for m and (4.24) for η. When J 0 = 0, we have a system of three equations (4.21) -(4.23) for ϕ x , ϕ z , and m, and an expression for η.
Numerical analysis of the thermodynamic characteristics and longitudinal static susceptibility χ zz (which is too cumbersome to be presented here) obtained here within the TPCA in the short-range interactions, with the long-range interactions taken into account within the MFA, as well as study of the applicability bounds of these approach to the IMTF on different types of lattices at different values of the parameters Γ, J 0 will be given elsewhere. Here we shall only briefly consider the major results at K > 0, J 0 ≥ 0, Γ > 0. We shall use the terminology of ferroelectricity.
For the one-dimensional IMTF at J 0 = 0, the two-particle cluster approximation, unlike the MFA for the short-range interactions, does not predict existence of ferroelectric ordering (at T > 0 and arbitrary Γ the system is in the paraelectric phase). Comparison of the TPCA results for the free energy, entropy, and specific heat as functions of temperature (expressions for entropy and specific heat were obtained for the paraelectric phase only) at different values of Γ/K has shown, that this approximation yields fair results for these characteristics at all temperatures except for the low-temperature region. Thus, at high temperatures, the TPCA results accord with exact results not only qualitatively, but also well enough quantitatively. The lower temperature, the more results of TPCA differ from exact ones (too lower values of free energy, entropy, and specific heat), whereas in the low-temperature region T < T l (k B T l /K < th( 4 1 6 · Γ/K) + 1 6 · Γ/K) are qualitatively incorrect (for instance, the free energy is an increasing function of temperature).
For the one-dimensional model at J 0 > 0, as well as for two-dimensional and three-dimensional models at J 0 ≥ 0, the TPCA for the short-range interactions with, the long-range interactions taken into account within the MFA, predicts that a limiting value (Γ/K) k exists, which depends on J 0 and z, and above which a ferroelectric ordering is impossible (the latter is a qualitatively correct result). At (Γ/K) a < Γ/K < (Γ/K) k (where (Γ/K) a = c(z, Γ, J 0 , K)·zJ 0 /K, c(z, Γ, J 0 , K) ≈ 2) this approximation predicts a phase transition from the paraelectric phase to the ferroelectric phase on lowering temperature and the phase transition from the ferroelectric to the paraelectric phase -the so-called anti-Curie point. At small enough values of Γ/K ≤ (Γ/K) a the anti-Curie point is absent, but the temperature behavior of the thermodynamic characteristics remains qualitatively incorrect. The low-temperature region of T < T l , where the TPCA yields incorrect results for thermodynamic characteristics, is reduced when the values of Γ/K and J 0 /K decrease (see Table 1.). In the high-temperature region T > T l at J 0 = 0 and z > 2, the TPCA is much more correct than the mean field approximation for the short-range interactions.
We also performed a numerical analysis of the TPCA results at neglecting the variational parameter ϕ x (ϕ x = 0). This version of the approximation is not suitable for one-dimensional chains. Thus, at small enough values of J 0 /K < 0.09 and Γ/K, Curie temperature increases on increasing Γ/K. At J 0 = 0 and Γ/K ∈ ]0, 1.28] a ferroelectric ordering is predicted.
For two-dimensional and three-dimensional lattices, neglecting the variational parameter ϕ x leads to a slight quantitative worsening of the results in a hightemperature region and to a qualitatively correct description of temperature de- Table 1. Temperature of the anti-Curie point T a , temperature T l below which unphysical results for m(T ) and χ zz (T ) are obtained, and Curie temperature for a square lattice (z = 4) at different values of Γ and J 0 within the TPCA for the short-range interactions, calculated with the long-range interactions taken into account in the MFA. pendences of thermodynamic characteristics (m(T ), χ zz (T )) in a low-temperature region. This worsening is the smaller, the larger are the lattice dimensionality and the value of the long-range interaction, and the smaller is the transverse field.

Thermodynamics and intracluster pair distribution functions in paraelectric phase
In order to study the dynamic characterictics of the IMTF in the paraelectric phase, we write here certain relations for some thermodynamic quantities in the paraelectric phase (κ z =κ z =κ z = ϕ z = 0, m = 0). The eigenvalues (E 12 ) i of two-particle Hamiltonian (4.16) in the paraelectric phase are (see (4.19)): where From (4.25) we obtain the two-particle partition function in the paraelectric phase explicitly Z 12 = 2 ch(βL) + ch(βK) .  We also present here an expression for η = S x ρ : To calculate the pair CGFs of the reference model (4.4) within the TPCA (see (3.63)), we need to know the single-particle and two-particle intracluster pair CGFs 12 ( a,b ωn ) (a, b = x, y, z). Let us calculate now the two-particle incracluster CGFs. It is convenient to do so in the self-representation of the operator H 12 .
Since we have explicit expressions for the eigenvalues of the two-particle Hamiltonian (4.16) in the paraelectric phase (see (4.25)), it is easy to obtain the normalized unitary matrix, which diagonalizes the two-particle Hamiltonian Here we use the notations Going from the Pauli operators to their four-row analogs [50][51][52] σ a 1 = S a 1 ⊗ I ; σ a 2 = I ⊗ S a 2 ; a = x, y, z (4.32) (here I is the two-row unit matrix, ⊗ is the direct product symbol; matrices σ a ν obey Pauli commutation rules) and performing a unitary transformatioñ we obtain the pseudospin operators in a self-representation of the operator H 12 : Expanding operatorsσ a i (4.34) in finite series in the four-dimensional Hubbard operators [50][51][52], following [14,57], we easily calculate the two-particle cumulant pair intracluster Green functions: Here we use the notations A ± (ω n ) = 8K βLZ 12 Ksh(βL) The most convenient way to obtain the single-particle intracluster CGFs is, by performing a rotation in a spin space, to go to such a coordinate system, where Hamiltonian (4.13) is diagonal. We present here the final result (after the inverse transformation) in the paraelectric phase in terms of a = x, y, z: Here we use notations g ′ (ω n ) = ω n 2κ x · g(ω n ) . At obtaining (4.40) we used the fact that within TPCA for the short-range interactions, with taking into account the long-range interactions in the MFA, S x ρ 1 = S x ρ ≡ η.

Dynamics in paraelectric phase. Cluster random phase approximation
Our task is to investigate the dynamics characteristics of the IMTF in the paraelectric phase within the TPCA for the short-range interactions and within the (r −d 0 ) 0 approximation for the long-range interactions [54,58] -the cluster random phase approximation. The first step is then to calcualte the temperature CGFs.
It should be noted that from (4.44) one obtains the static longitudinal susceptibility (χ zz = βG zz (0, 0)) of the IMTF in the paraelectric phase (J 0 = J( q = 0)) which accords with the one calculated from thermodynamic relations in the TPCA for the short-range interactions, with the long-range interactions taken into account in the MFA.
To explore the dynamic properties of the IMTF we need to know not the temperature CGFs (4.44), but the retarded CGFs. We can calculate them [59] by performing analytical continuation of the temperature CGFs G ab ( q, ω n ) (iω n → E + iE ′ ) and going to the limit E ′ → 0. The final results for spectral densities J xx ( q, E) and J zz ( q, E), defined as and for the pair cumulant correlation function S z q S z − q c are the following. The spectral density J xx ( q, E) of the IMTF in the paraelectric phase within the CRPA reads Let us note, that an exact expression for J xx ( q, E) of the one-dimensional IMTF with the short-range interactions only [31] has not only the central peak (∼ δ(E)) but also two symmetrical resonance zones. Absence of the resonance zones within the CRPA for J xx ( q, E) results from neglecting fluctuations of cluster fields in this approximation. The spectral density J zz ( q, E) (in the paraelectric phase) can be presented as where E i ( q) (i = −, +, r) are the elementary excitation spectrum modes, determined from the equation (see (4.44), (4.46)) and k J i ( q) are the integral intensities of the elementary excitations spectrum modes . (4.52) Here we use the notations: , i 1 , i 2 , i 3 = (−, +, r) , It should be noted that at q = 0 (see (4.44), (4.46)) there are only two modes where The mode we obtain . (4.57) Let us briefly consider results of numerical analysis of the longitudinal characteristics of the IMTF at z = 2, J νµ = 0 (K = 1). As we have already mentioned, within CRPA the spectrum of the longitudinal characteristics of the model contains three nondamping modes E − (q), E + (q), E r (q) with the integral intensities k J − (q), k J + (q) and k J r (q) in the spectral density J zz (q, E). The calculated dependences of E i (q), k J i (q) at different transverse fields and temperatures are presented in fig. 1. On increasing Γ, temperature, and q, redistribution of the intensities from low frequencies to higher frequencies is observed. At large Γ and low temperatures the redistribution on increasing q takes place, first, mainly from E − (q) to E r (q), and then from E r (q) to E + (q). At large Γ and high temperatures the redistribution takes place mainly from E − (q) to E + (q). At small Γ the redistribution is practically absent.
In fig. 2 we present exact and approximate (CRPA) results for the static correlator S z ν S z ν+n at k B T = 0.6 and k B T = 1.0 at different Γ. The CRPA gives too low values of S z ν S z ν+n , especially at low temperatures. Thus, the autocorrelator S z ν S z ν at low temperatures is essentially less than unity. The higher temperature and smaller Γ, the better the CRPA results accord with exact ones.
Let us discuss also the redistribution of the modes intensities E − (0), E + (0) on changing Γ and temperature. At temperatures k B T > √ Γ, change of the modes positions and integral intensities (obtained within the CRPA) on changing Γ and T qualitatively describes change in the frequency dependences of the real part of the relaxation function Re Ψ zz (0, E), calculated numerically [35,36] or exactly. Thus, for instance, at Γ = 1 and k B T = 0.8 (see fig. 3) Re Ψ zz (0, E) has a prominent resonance zone at E close to zero. Smearing of this resonance zone on increasing T is qualitatively described by increasing k J + (0) and E − (0) and by decreasing k J − (0). On the other hand, for instance, at T → ∞ (see fig. 4), a shift of the resonance zone Re Ψ zz (0, E) to higher frequencies region on increasing Γ is described by increasing    E − (0) and k J + (0). The fact that the resonance zone at Γ = 0.5 is more prominent than at Γ = 1.0 is described by decreasing k J − (0) and increasing k J + (0) on increasing Γ. The fact that at Γ = 2.0 the resonance zone Re Ψ zz (0, E) is more prominent than at Γ = 1.5 is described by approaching of the modes positions E − (0), E + (0) on increasing Γ. In figs. 3, 4 we depicted also the results of the random phase approximation (RPA) for the short-range interactions. This approximation describes the frequency dependences of the real part of the relaxation function in the presented in figs. 3, 4 cases qualitatively well only at T → ∞ Γ = 1.5, 2.0.
We restricted the presented here numerical analysis of the longitudinal characteristics of the one-dimensional IMTF (at J νµ = 0) by the values of the transverse field 0.2 ≤ Γ ≤ 2. A more detailed analysis both at J νµ = 0 and at J νµ = 0 and with the values of the microparameters corresponding to the CsH 2 PO 4 crystal will be performed elsewhere.