| Themes > Science > Physics > Molecular Physics > Molecular Spectra > Molecular Spectroscopy |
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The energy levels of each of these
vibrational modes are quantized. Because the potetial energy for these
vibrations is approximately parabolic (~r2) for low levels, the
vibrational levels can be approximated by the energy levels of the quantum
simple harmonic oscillator: |
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Individual molecules may vibrate and rotate simultaneously. Like the angular momentum of an electron, the angular momentum of a rotating molecule is quantized and must have specific spatial orientations depending on the quantum number "J". In fact, there can be only 2J+1 spacial orientations for each rotational levels. This 2J+1 is the "degeneracy." As a result of these restriction, rotational energy levels occur only at discreet values such that ,
where J= 0, 1, 2, 3, . . . . and "I" is the moment of inertia
of the molecule. We will see later that this formula is important
in determining the moment of inertia of the molecule. |
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So, depending on the temperature of the plasma, there will be molecules in a spread of rotational modes within each virational mode. This distribution of molecules in rotational levels will follow Maxwell-Boltzmann statistics according to the relation:
In this case, the degeneracy is G(J) = (2J+1)—since the angular momentum can have only certain spacial orientations. This is analogous to electronic angular momentum states having a degeneracy of (2l+1). The Boltzmann distribution curve for these rotational levels will look look like the graph at the right.
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Lasing occurs when a molecule transitions from a rotational level of one vibrational mode to a different rotational level of a different vibrational mode. Due to selection rules, the change in quantum number j must be +1 or –1. In transitions for which d j = +1, rotational energy is gained. These transitions will release less energy than transitions for which d j = -1, in which rotational energy is given up to the photon. If the difference in energy between the ground states of each mode is E0, transition energies will follow the formulas: d j = +1 : d j = -1 : where Transitions between rotational levels of differing vibrational energy levels emit photons with wavelengths in the infrared region, while transitions between rotational energy levels of the same vibrational level emit photons in the microwave region. |
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