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The first-order energy shift is not well defined, since there is no unique way to choose a basis of eigenstates for the unperturbed system. The various eigenstates for a given energy will perturb with different energies, or may well possess no continuous family of perturbations at all.
Using perturbation theory, the first-order energy shift can be calculated as = >, which requires the knowledge of accurate many-electron wave function. Due to the 1 / M N {\displaystyle 1/M_{N}} term in the expression, the specific mass shift also decrease as 1 / M N 2 {\displaystyle 1/M_{N}^{2}} as mass of nucleus increase, same as normal mass ...
If g = 1 (as is often the case for electronic states of molecules) the first-order energy becomes proportional to the expectation (average) value of the dipole operator , = | | = . Since the electric dipole moment is a vector ( tensor of the first rank), the diagonal elements of the perturbation matrix V int vanish between states that have a ...
For example, the three states (n x = 7, n y = 1), (n x = 1, n y = 7) and (n x = n y = 5) all have = and constitute a degenerate set. Degrees of degeneracy of different energy levels for a particle in a square box:
More precisely, if , each of these three components is actually a group of several transitions due to the residual spin–orbit coupling and relativistic corrections (which are of the same order, known as 'fine structure'). The first-order perturbation theory with these corrections yields the following formula for the hydrogen atom in the ...
For example, it gives the 2s orbital the same energy as the 2p orbital by raising the 2s state by 9.057 × 10 −5 eV. The Darwin term changes potential energy of the electron. It can be interpreted as a smearing out of the electrostatic interaction between the electron and nucleus due to zitterbewegung , or rapid quantum oscillations, of the ...
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Møller–Plesset perturbation theory (MP) is one of several quantum chemistry post-Hartree–Fock ab initio methods in the field of computational chemistry.It improves on the Hartree–Fock method by adding electron correlation effects by means of Rayleigh–Schrödinger perturbation theory (RS-PT), usually to second (MP2), third (MP3) or fourth (MP4) order.