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Landau–Zener formula : ウィキペディア英語版
Landau–Zener formula
The Landau–Zener formula is an analytic solution to the equations of motion governing the transition dynamics of a 2-level quantum mechanical system, with a time-dependent Hamiltonian varying such that the energy separation of the two states is a linear function of time. The formula, giving the probability of a diabatic (not adiabatic) transition between the two energy states, was published separately by Lev Landau, Clarence Zener, Ernst Stueckelberg, and Ettore Majorana, in 1932.
If the system starts, in the infinite past, in the lower energy eigenstate, we wish to calculate the probability of finding the system in the upper energy eigenstate in the infinite future (a so-called Landau–Zener transition). For infinitely slow variation of the energy difference (that is, a Landau–Zener velocity of zero), the adiabatic theorem tells us that no such transition will take place, as the system will always be in an instantaneous eigenstate of the Hamiltonian at that moment in time. At non-zero velocities, transitions occur with probability as described by the Landau–Zener formula.
== Landau–Zener approximation ==

Such transitions occur between states of the entire system, hence any description of the system must include all external influences, including collisions and external electric and magnetic fields. In order that the equations of motion for the system might be solved analytically, a set of simplifications are made, known collectively as the Landau–Zener approximation. The simplifications are as follows:
# The perturbation parameter in the Hamiltonian is a known, linear function of time
# The energy separation of the diabatic states varies linearly with time
# The coupling in the diabatic Hamiltonian matrix is independent of time
The first simplification makes this a semi-classical treatment. In the case of an atom in a magnetic field, the field strength becomes a classical variable which can be precisely measured during the transition. This requirement is quite restrictive as a linear change will not, in general, be the optimal profile to achieve the desired transition probability.
The second simplification allows us to make the substitution
:\Delta E = E_2(t) - E_1(t) \equiv \alpha t, \,
where \scriptstyle and \scriptstyle are the energies of the two states at time \scriptstyle, given by the diagonal elements of the Hamiltonian matrix, and \scriptstyle is a constant. For the case of an atom in a magnetic field this corresponds to a linear change in magnetic field. For a linear Zeeman shift this follows directly from point 1.
The final simplification requires that the time–dependent perturbation does not
couple the diabatic states; rather, the coupling must be due to a static deviation from
a \scriptstyle coulomb potential, commonly described by a quantum defect.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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