Real-Valued Path Integral as Green’s Functions of the Schrödinger Equation

Vassilis G. Papanicolaou

Kazuo Takatsuka

This paper elucidates the dual structure of the Schrödinger dynamics in two correlated stages: (1) We first derive the real-valued Schrödinger equation from scratch without referring to classical mechanics, wave mechanics, nor optics, and thereby attain a concrete and clear interpretation of the Schrödinger (wave) function. Beginning with a factorization of the density distribution function of the particles to two component vectors in configuration space, we impose very simple conditions on them such as translational invariance of space-time and the conservation of flux under a given potential function. A real-valued path-integral is formulated as a Green function for the real-valued Schrödinger equation. (2) We then study a quantum stochastic path dynamics in a manner compatible with the Schrödinger equation. The relation between them is like the Langevin dynamics with the diffusion equation. Each quantum path describes a \textquotedblleft trajectory\textquotedblright\ in configuration space representing, for instance, a singly launched electron in the double-slit experiment that leaves a spot one by one at the measurement board, while accumulated spots give rise to the fringe pattern as predicted by the absolute square of the Schrödinger function. We start from the relationship between the Ito stochastic differential equation, the Feynman-Kac formula, and the associated parabolic partial differential equations, to one of which\ the Schrödinger equation is transformed. The physical significance of the quantum intrinsic stochasticity and the indirect correlation among the quantum paths and so on are discussed. The self-referential nonlinear interrelationship between the Schrödinger functions (regarded as a whole) and the quantum paths (as its parts) is identified as the ultimate mystery in quantum dynamics.

Gin-yih Tsaur, Jyhpyng Wang

Abstract The Green function method is a powerful technique for solving the initial value problem in quantum mechanics. Once the Green function is solved the whole wavefunction evolution is represented in a concise form and can be evaluated conveniently by numerical integration. We present a method for constructing the Green functions systematically which is different from the conventional methods of eigenfunction expansion or path integration. By using variable changing, function substitution, and Fourier transforms, the time dependent Schrödinger equations can be simplified and the solutions for the simplified equations can be easily derived. We then obtain the Green functions for the original equations by the reverse transforms. The method is demonstrated for the linear potential, the harmonic oscillator, the centrifugal potential, and the centripetal barrier oscillator, where the Green function for the centripetal barrier oscillator has not been solved previously by conventional methods. The method and examples illustrated in this paper can be utilised to strengthen undergraduate courses on quantum mechanics and/or partial differential equation.

Ewan M. Wright