Heisenberg operators

Author(s):  
G. L. Squires
Keyword(s):  
1954 ◽  
Vol 12 (3) ◽  
pp. 317-322 ◽  
Author(s):  
J. C. Polkinghorne
Keyword(s):  

1954 ◽  
Vol 50 (4) ◽  
pp. 592-603
Author(s):  
R. J. Eden

ABSTRACTSets of rules are obtained for writing down directly the exact integral equations which are satisfied by certain functions of Heisenberg operators in quantum field theory. Three kinds of function are considered: the direct product, the chronological product and the M-product. The matrix elements of the M-product are equal to the Feynman amplitudes studied by Matthews & Salam (1) and the corresponding integral equation is called here the Matthews-Salam (M.-S.) equation. These authors have given a symbolic form of the M.-S. equation and a method of repeated differentiation and integration which can be used to obtain the explicit form of the integral equation in any particular example. In practice their method involves an immense amount of calculation even in quite simple examples. The rules obtained in the present paper make it possible to write down directly the M.-S. equation without any of the tedious calculations implied by the M.-S. method.So long as the exact theory is used, the three sets of equations (for direct, chronological and M-products) are completely equivalent. When bound state theory is considered by an approximation based on a power series in the coupling constant different results are obtained. The approximation is inapplicable to the direct product equations, and leads to different approximate equations for the amplitudes obtained from the chronological and the M-products even when these amplitudes are identical. This paradox is explained and it is shown that the equation coming from the M-product corresponds to the Bethe-Salpeter equation.


1982 ◽  
Vol 116 (1) ◽  
pp. 49-52 ◽  
Author(s):  
I.A. Fedoseev ◽  
A.N. Leznov ◽  
M.V. Saveliev

With the aid of the Heisenberg operators for the electromagnetic field in the neighbourhood of several molecules, the many-body interaction potentials are calculated by finding the energy of a test molecule in this field. In the first instance the calculation is made for the case where the intermolecular separations are very large. In this far-zone range, the energies depend on the molecules through their static polarizabilities. The three-body non-additive dispersion energy is calculated for an arbitrary configuration and the dependence on the geometry is investigated. The four-body non-additive potential is found for the regular tetrahedral configuration. The theory is extended to cover all separations outside regions of overlap. It is shown that the interaction energy in this case depends on the dynamic polarizabilities. The full Casimir-Polder potential follows directly from the general expression. The near-zone limit of the complete formula tends to the form obtained by using electrostatic couplings only: as with, for example, the Axilrod-Teller potential for N = 3. The work described here presents an alternative viewpoint to the conventional perturbation theory and lends further insight into the nature of intermolecular forces.


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