Phys. Rev. Lett. 95, 080401 (2005) [4 pages]

Simple and Surprisingly Accurate Approach to the Chemical Bond Obtained from Dimensional Scaling

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Anatoly A. Svidzinsky1,2, Marlan O. Scully1,2,3, and Dudley R. Herschbach4
1Departments of Chemistry, and Mechanical and Aerospace Engineering, Princeton University, Princeton, New Jersey 08544, USA
2Departments of Physics, Chemical and Electrical Engineering, Texas A&M University, Texas 77843-4242, USA
3Max-Planck-Institut für Quantenoptik, D-85748 Garching, Germany
4Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, USA

Received 7 July 2004; published 17 August 2005

We present a new dimensional scaling transformation of the Schrödinger equation for the two electron bond. This yields, for the first time, a good description of the bond via D scaling. There also emerges, in the large-D limit, an intuitively appealing semiclassical picture, akin to a molecular model proposed by Bohr in 1913. In this limit, the electrons are confined to specific orbits in the scaled space, yet the uncertainty principle is maintained. A first-order perturbation correction, proportional to 1/D, substantially improves the agreement with the exact ground state potential energy curve. The present treatment is very simple mathematically, yet provides a strikingly accurate description of the potential curves for the lowest singlet, triplet, and excited states of H2. We find the modified D-scaling method also gives good results for other molecules. It can be combined advantageously with Hartree-Fock and other conventional methods.


©2005 The American Physical Society

URL: http://link.aps.org/doi/10.1103/PhysRevLett.95.080401
DOI: 10.1103/PhysRevLett.95.080401
PACS: 03.65.Sq, 31.25.Nj, 31.50.Bc

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