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Journal of Mathematical Physics

Time-dependent rotated Hartree: Formal development

Hans‐Dieter Meyer, Jasna Kučar, L. S. Cederbaum

Published Jun 1, 1988• 43 citations
Publisher

Abstract

A new approximation for solving the time-dependent Schrödinger equation is proposed. It improves the time-dependent Hartree approximation by including time-dependent unitary operators acting on the Hartree product. This allows for the approximate description of the correlation between the various degrees of freedom. The mathematical structure of the new approach is analyzed and an alternative Lie algebraic derivation is presented. By adopting two different time-dependent variational principles two different sets of equations are obtained. Differences between the two resulting methods are discussed.

DOI
10.1063/1.527934

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A new approximation for solving the time-dependent Schrödinger equation is proposed. It improves the time-dependent Hartree approximation by including time-dependent unitary operators acting on the Hartree product. This allows for the approximate description of the correlation between the various degrees of freedom. The mathematical structure of the new approach is analyzed and an alternative Lie algebraic derivation is presented. By adopting two different time-dependent variational principles two different sets of equations are obtained. Differences between the two resulting methods are discussed.
The previous time-dependent variation-perturbation theory, which is derived from the conventional time-dependent perturbation equations, contains two inconvenient features. When the perturbation becomes static, the wave function so obtained does not satisfy the time-dependent Schr\"odinger equation, and the perturbation equations cannot be reduced to the ordinary time-independent perturbation equations. To remove these difficulties, we introduce a perturbed time-dependent phase factor in deriving a new set of perturbation equations. We then construct the variation-perturbation functionals as in the previous theory; the perturbed wave functions are solved by minimizing these functionals. The same method is also applied to many-electron systems, using the coupled and uncoupled Hartree-Fock scheme.
We derive a multiconfigurational time-dependent Hartree theory for systems with particle conversion. In such systems particles of one kind can convert to another kind and the total number of particles varies in time. The theory thus extends the scope of the available and successful multiconfigurational time-dependent Hartree methods---which were solely formulated for and applied to systems with a fixed number of particles---to a broader class of physical systems and problems. As a guiding example we treat explicitly a system where bosonic atoms can combine to form bosonic molecules and vice versa. In the theory for particle conversion, the time-dependent many-particle wave function is written as a sum of configurations made of a different number of particles, and assembled from sets of atomic and molecular orbitals. Both the expansion coefficients and the orbitals forming the configurations are time-dependent quantities that are fully determined according to the Dirac-Frenkel time-dependent variational principle. By employing the Lagrangian formulation of the Dirac-Frenkel variational principle we arrive at two sets of coupled equations of motion, one for the atomic and molecular orbitals and one for the expansion coefficients. The first set is comprised of first-order differential equations in time and nonlinear integrodifferential equations in position space, whereas the second set consists of first-order differential equations with coefficients forming a time-dependent Hermitian matrix. Particular attention is paid to the reduced density matrices of the many-particle wave function that appear in the theory and enter the equations of motion. There are two kinds of reduced density matrices: particle-conserving reduced density matrices which directly only couple configurations with the same number of atoms and molecules, and particle nonconserving reduced density matrices which couple configurations with a different number of atoms and molecules. Closed-form and compact equations of motion are derived for contact as well as general two-body interactions, and their properties are analyzed and discussed.
We investigate variational principles for the approximation of quantum dynamics that apply for approximation manifolds that do not have complex linear tangent spaces. The first one, dating back to McLachlan [Mol. Phys. 8, 39–44 (1964)], minimizes the residuum of the time-dependent Schrödinger equation, while the second one, originating from the lecture notes of Kramer and Saraceno [Geometry of the Time-Dependent Variational Principle in Quantum Mechanics, Lecture Notes in Physics Vol. 140 (Springer, Berlin, 1981)], imposes the stationarity of an action functional. We characterize both principles in terms of metric and symplectic orthogonality conditions, consider their conservation properties, and derive an elementary a posteriori error estimate. As an application, we revisit the time-dependent Hartree approximation and frozen Gaussian wave packets.
The time-dependent variational principle of the Schr\"odinger equation is applied to a formally exact solution of the Schr\"odinger equation whose variational elements are operators which define a collective subspace of the many-body system under study. This generalizes the procedure employed to derive time-dependent Hartree-Fock theory. Four distinct formally exact time-independent variational principles, including several familiar forms, are derived. Application to a class of exactly soluble models, studied in the vibrational regime, illustrates the different modes of implementation of two of the principles. The general theory of large amplitude collective motion is derived. It is shown that the principles can be applied equally well, using either boson or fermion pair degrees of freedom. Some aspects of the relation to the semiclassical limit are discussed.[NUCLEAR STRUCTURE Time-dependent variational principle for collective motion. Invariance principle of Schr\"odinger equation. Generalized coherent state trial function. Exact time-independent variational principles. Variational principle for intrinsic state. Cranking variational principle. Large amplitude collective motion. Semiclassical limit.]