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FUNCTIONAL INTEGRAL APPROACH AND THE EIKONAL APPROXIMATION TO THE POLARON ENERGY AND MASS

Nhu Xuan Nguyen, Toan Thang Vu

Published Apr 30, 2024• 0 citations
Publisher

Abstract

This article uses the functional integral method and eikonal approximation to calculate the first-order correction for the energy and (effective) mass of the Polaron. The obtained results have demonstrated the effectiveness of the functional integral method compared to conventional perturbation theory when considering the Polaron problem in solid crystal.

DOI
10.56651/lqdtu.jst.v2.n01.762.pce

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This article uses the functional integral method and eikonal approximation to calculate the first-order correction for the energy and (effective) mass of the Polaron. The obtained results have demonstrated the effectiveness of the functional integral method compared to conventional perturbation theory when considering the Polaron problem in solid crystal.
Direct evaluation of Feynman's functional integral for the polaron maps it into a standard type of many-body theory. The perturbation expansion is shown to be well controlled and does not require any renormalization. This perturbation expansion has the pleasing feature that nthn\mathrm{th}nth-order terms in the polaron coupling constant are obtained from nthn\mathrm{th}nth-order perturbation theory, whereas the traditional perturbation formulation in terms of creation and annihilation operators requires a 2nth2n\mathrm{th}2nth-order perturbation calculation to generate the same results. In contrast to previous beliefs, the method is shown to enable the calculation of the polaron effective mass and relaxation time directly from the functional-integral expression. The ground-state energy is computed to second order in the polaron coupling constant to illustrate the use of the method and to establish agreement with previous perturbation treatments. In addition, we provide the first perturbation calculation of the polaron effective mass through second order in the coupling constant. Pad\'e approximants are shown to provide a vehicle for analytically extending the perturbation results into the region of intermediate and strong couplings, and the procedure yields reasonable agreement with variational calculations for values of the polaron coupling constant up to about $\ensuremath{\alpha}=10$. In addition, conditions are derived under which the original polaron action, used in the functional integral, reduces to some of the best variational trial actions utilized in the literature.
It is well known that two qualitatively different pictures arise in the description of the motion of an electron in an ionic crystal. In the first case, when the electron interacts weakly with the ionic lattice of the crystal, its motion is the same as the motion of a free band electron whose energy is shifted downward with respect to the bottom of the conduction band, and the effective mass is replaced by the renormalized mass (weak-coupling polaron). In the other limiting case, when the electron interacts strongly with the ionic crystal, an entire series of different self-consistent states of the electron and lattice, each of which has its own effective mass and radius (strong-coupling polaron), arises. Although the motion of an electron in an ionic crystal is described in both limiting cases with the help of the Pekar-Frohlich Hamiltonian, each case requires its own special methods of analysis. Thus, for example, in the strong-coupling theory a special form of adiabatic perturbation theory has been developed in which the trans-lational degeneracy is removed before the perturbation expansion is made. It has been possible to relate both descriptions within the framework of Feynman's varia-tional approach, in which a smooth upper bound was obtained for the energy of the ground state of the polaron for all values of the electron-phonon coupling constant a (see Fig. 1). We call attention in this connection to Ref. 6, where the thermodynamic properties are calculated with the help of a special method for performing the calculations and for finding averages of T-products. The approach developed there is more convenient for performing specific calculations than is the use of path integrals. It seems to us that it has definite advantages in the construction of general proofs concerning the choice of the approximating Hamiltonians (this is illustrated in Ref. 6 for the example of the linear Bogolyubov model), in the investigation of the characteristics of the behavior of a polaron in external fields, etc.
The effective mass of the Fröhlich polaron model in d spatial dimensions is obtained within the Gaussian-equivalent representation, that is, within a suitably rearranged perturbative path-integral approach, whose leading order already takes care of all Gaussian fluctuations. In doing so, the authors extend their earlier investigations ( Phys. Rev. B 50 3733 (1994)) of the polaron ground-state energy. Analytical expressions for the effective mass are derived in the weak- and strong-coupling limit. In the intermediate-coupling regime, the effective mass is calculated numerically for the cases of two and three dimensions. The new results are compared with previously known data.
In the expansion of the ground-state energy of a polaron in a weak magnetic field, the zeroth-order term is the polaron self-energy, while the first-order term is inversely proportional to the polaron effective mass. The effective mass so obtained is exactly equivalent to the freepolaron effective mass as defined by Fr\"ohlich. This equivalence principle is used to approximate the polaron effective mass by employing an approximate expression for the ground-state energy of a polaron in a weak magnetic field obtained by applying Feynman's path-integral variational method. The resultant polaron effective mass is found to be higher than Feynman's result by less than 1%.
The method of moments is employed to determine the ground state of the phonon-polaron system. The trial function employed in this calculation is a bare-electron wave function. It appears that the method is convergent for this problem. Although the energy is in general a complicated function of the parameter and must be determined numerically, it is possible to formally construct a power series expansion for the energy about the unperturbed energy in powers of the coupling constant. The first term in this series has been determined and agrees with the result of conventional perturbation theory. The second term has not yet been evaluated to all orders but it appears that it will have the opposite sign from the corresponding term in perturbation theory. The second and higher terms in some orders of approximation are singular for small values of the cutoff.