Zero-phonon line and phonon sideband

Figure 2. Energy diagram of an electronic transition with phonon coupling along the configurational coordinate ${\displaystyle q_{i}}$, a normal mode of the lattice. The upwards arrows represent absorption without phonons and with three phonons. The downwards arrows represent the symmetric process in emission.

Figure 3. Representation of three lattice normal modes (i, j, k) and how their intensities combine at the zero-phonon frequency, but are distributed within the phonon side band due to their different characteristic harmonic oscillator frequencies Ω.

The transition between the ground and the excited state is based on the Franck–Condon principle, that the electronic transition is very fast compared with the motion in the lattice. The energy transitions can then be symbolized by vertical arrows between the ground and excited state, that is, there is no motion along the configurational coordinates during the transition. Figure 2 is an energy diagram for interpreting absorption and emission with and without phonons in terms of the configurational coordinate ${\displaystyle q_{i}}$. The energy transitions originate at the lowest phonon energy level of the electronic states. As represented in the figure, the largest wavefunction overlap (and therefore largest transition probability) occurs when the photon energy is equal to the energy difference between the two electronic states (${\displaystyle E_{1}-E_{0}}$) plus three quanta of lattice mode ${\displaystyle i}$ vibrational energy (${\displaystyle \hbar \Omega _{i}}$). This three-phonon transition is mirrored in emission when the excited state quickly decays to its zero-point lattice vibration level by means of a radiationless process, and from there to the ground state via photon emission. The zero-phonon transition is depicted as having a lower wavefunction overlap and therefore a lower transition probability.

In addition to the Franck-Condon assumption, three other approximations are commonly assumed and are implicit in the figures. The first is that each lattice vibrational mode is well described by a quantum harmonic oscillator. This approximation is implied in the parabolic shape of the potential wells of Figure 2, and in the equal energy spacing between phonon energy levels. The second approximation is that only the lowest (zero-point) lattice vibration is excited. This is called the low temperature approximation and means that electronic transitions do not originate from any of the higher phonon levels. The third approximation is that the interaction between the chromophore and the lattice is the same in both the ground and the excited state. Specifically, the harmonic oscillator potential is equal in both states. This approximation, called linear coupling, is represented in Figure 2 by two equally shaped parabolic potentials and by equally spaced phonon energy levels in both the ground and excited states.

The strength of the zero-phonon transition arises in the superposition of all of the lattice modes. Each lattice mode ${\displaystyle m}$ has a characteristic vibrational frequency ${\displaystyle {\Omega }_{m}}$ which leads to an energy difference between phonons ${\displaystyle \hbar {\Omega }_{m}}$. When the transition probabilities for all the modes are summed, the zero-phonon transitions always add at the electronic origin (${\displaystyle E_{1}-E_{0}}$), while the transitions with phonons contribute at a distribution of energies. Figure 3 illustrates the superposition of transition probabilities of several lattice modes. The phonon transition contributions from all lattice modes constitute the phonon sideband.

The frequency separation between the maxima of the absorption and fluorescence phonon sidebands is the phonon contribution to the Stokes’ shift.

The shape of the zero-phonon line is Lorentzian with a width determined by the excited state lifetime T₁₀ according to the Heisenberg uncertainty principle. Without the influence of the lattice, the natural line width (full width at half maximum) of the chromophore is γ₀ = 1/T₁₀ . The lattice reduces the lifetime of the excited state by introducing radiationless decay mechanisms. At absolute zero the lifetime of the excited state influenced by the lattice is T₁. Above absolute zero, thermal motions will introduce random perturbations to the chromophores local environment. These perturbations shift the energy of the electronic transition, introducing a temperature dependent broadening of the line width. The measured width of a single chromophore's zero phonon line, the homogeneous line width, is then γ_h(T) ≥ 1/T₁ .

The line shape of the phonon side band is that of a Poisson distribution as it expresses a discrete number of events, electronic transitions with phonons, during a period of time. At higher temperatures, or when the chromophore interacts strongly with the matrix, the probability of multiphonon is high and the phonon side band approximates a Gaussian distribution.

The distribution of intensity between the zero-phonon line and the phonon sideband is characterized by the Debye-Waller factor α.

The zero-phonon line is an optical analogy to the Mössbauer lines, which originate in the recoil-free emission or absorption of gamma rays from the nuclei of atoms bound in a solid matrix. In the case of the optical zero-phonon line, the position of the chromophore is the physical parameter that may be perturbed, whereas in the gamma transition, the momenta of the atoms may be changed. More technically, the key to the analogy is the symmetry between position and momentum in the Hamiltonian of the quantum harmonic oscillator. Both position and momentum contribute in the same way (quadratically) to the total energy.

• Phonon
• Mössbauer effect
• Shpolskii matrix

• Friedrich, J. J.; D. Haarer (1984). "Photochemical Hole Burning: A Spectroscopic Study of Relaxation Processes in Polymers and Glasses". Angewandte Chemie International Edition in English. 23 (2): 113–140. doi:10.1002/anie.198401131.
• Silʹd, O. (1988). Zero-phonon lines and spectral hole burning in spectroscopy and photochemistry. Berlin: Springer-Verlag. ISBN 978-3-540-19214-5.

• Aleksander Rebane's site at Montana State University, Bozeman
• Hyperphysics: Molecular Spectra