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Encyclopedia > Morse potential
The Morse potential (blue) and harmonic oscillator potential (green). Unlike the energy levels of the harmonic oscillator potential, which are evenly spaced by ħω, the Morse potential level spacing decreases as the energy approaches the dissociation energy. The dissociation energy De is larger than the true energy required for dissociation D0 due to the zero point energy of the lowest (v = 0) vibrational level.
The Morse potential (blue) and harmonic oscillator potential (green). Unlike the energy levels of the harmonic oscillator potential, which are evenly spaced by ħω, the Morse potential level spacing decreases as the energy approaches the dissociation energy. The dissociation energy De is larger than the true energy required for dissociation D0 due to the zero point energy of the lowest (v = 0) vibrational level.

The Morse potential, named after physicist Philip M. Morse, is a convenient model for the potential energy of a diatomic molecule. It is a better approximation for the vibrational fine structure of the molecule because it implicitly includes the effects of bond breaking. A feature of the Morse potential which is absent for the harmonic oscillator model is that it accounts for unbounded states. It works better than the quantum harmonic oscillator model, because it accounts for anharmonicity, overtone frequencies, and combination frequencies. An overtone frequency occurs when a transition is n +/- 2 or greater and a combination frequency results from the addition or subtraction of two or more modes. The Morse potential energy function is of the form Image File history File links Download high-resolution version (2828x2612, 171 KB) Graphical depiction of the Morse potential with a harmonic potential for comparison. ... Image File history File links Download high-resolution version (2828x2612, 171 KB) Graphical depiction of the Morse potential with a harmonic potential for comparison. ... Full name : Philip McCord Morse Founding ORSA President (1952) B.S. Physics, 1926, Case Institute; Ph. ... In the physical sciences, potential energy is energy which is captured within a physical system by virtue of the relative positions or configurations of objects, and which has the potential to be released when the system is allowed to attain a configuration with a lower energy state. ... Diatomic molecules are molecules formed of two atoms of the same element. ... Oscillation is the variation, typically in time, of some measure as seen, for example, in a swinging pendulum. ... The quantum harmonic oscillator is the quantum mechanical analogue of the classical harmonic oscillator. ... Anharmonicity is the deviation of a system from being a harmonic oscillator. ... Sine waves of various frequencies; the bottom waves have higher frequencies than those above. ...

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Here r is the distance between the atoms, re is the equilibrium bond distance, De is the 'depth' of the potential energy function (the limit of the function as the bond distance approaches infinity), To is the difference in energy from E=0 to E at re, and a controls the 'width' of the potential and is equal to the square root of half the force constant divided by the morse potential, . The exponential functions are used as a power series cannot describe the spacing of experimentally observed energy levels. The dissociation energy of the bond can be calculated by subtracting the zero point energy E(0) from the depth of the well. The force constant of the bond can be found by taking the second derivative of the potential energy function. In mathematics, a power series (in one variable) is an infinite series of the form where the coefficients an, the center c, and the argument x are usually real or complex numbers. ... In chemistry, bond dissociation energy, D0, is one measure of the bond strength in a chemical bond. ... In a quantum mechanical system such as the particle in a box or the quantum harmonic oscillator, the lowest possible energy is called the zero-point energy. ... In mathematics, a derivative is the rate of change of a quantity. ...


Vibrational Energy


n is the vibrational quantum number

E(n) = (n + 1 / 2)hv0 − (n + 1 / 2)2 * (hv0)2 / 4De.
E(n + 1) − E(n) = hv0 − (n + 1) * (hv0)2 / 2De.

With the quantum harmonic oscillator, the energy between adjacent levels is constant, hv0. With the Morse potential, the energy between adjacent levels decreases with increasing n as is seen in nature. It fails at the value of n where E(n + 1) − E(n) is calculated to be zero or negative. The Morse potential is a good approximation for the vibrational fine structure at n values below this limit. The quantum harmonic oscillator is the quantum mechanical analogue of the classical harmonic oscillator. ...


Quantization in the Morse potential

Like the quantum harmonic oscillator, the energies and eigenstates of the Morse potential can be found using operator methods. One approach involves generalized factorization of the Hamiltonian, of which a specific parameterization gives rise to the Morse potential oscillator functions. The quantum harmonic oscillator is the quantum mechanical analogue of the classical harmonic oscillator. ...


See also

Neutral atoms and molecules are subject to two distinct forces in the limit of large distance, and short distance: an attractive van der Waals force, or dispersion force, at long ranges, and a repulsion force, the result of overlapping electron orbitals, referred to as Pauli repulsion (from Pauli exclusion principle). ...

References

  • P. M. Morse, Diatomic molecules according to the wave mechanics. II. Vibrational levels. Phys. Rev. 1929, 34, 57.
  • I.G. Kaplan, in Handbook of Molecular Physics and Quantum Chemistry, Wiley, 2003, p207.

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