Giant oscillator strength

Interband optical transitions happen at the scale of the lattice constant which is small compared to the exciton radius. Therefore, for large excitons in direct-gap crystals the oscillator strength ${\displaystyle f_{\rm {ex}}}$ of exciton absorption is proportional to ${\displaystyle |\Phi _{\rm {ex}}(0)|^{2}}$ which is the value of the square of the wave function of the internal motion inside the exciton ${\displaystyle \Phi _{\rm {ex}}({\boldsymbol {r}}_{e}-{\boldsymbol {r}}_{h})}$ at coinciding values of the electron ${\displaystyle {\boldsymbol {r}}_{e}}$ and hole ${\displaystyle {\boldsymbol {r}}_{h}}$ coordinates. For large excitons ${\displaystyle |\Phi _{\rm {ex}}(0)|^{2}\approx 1/a_{\rm {ex}}^{3}}$ where ${\displaystyle a_{\rm {ex}}}$ is the exciton radius, hence, ${\displaystyle f_{\rm {ex}}\approx v/a_{\rm {ex}}^{3}\ll 1}$, here ${\displaystyle v}$ is the unit cell volume. The oscillator strength ${\displaystyle f_{i}}$ for producing a bound exciton can be expressed through its wave function ${\displaystyle \Psi _{i}({\boldsymbol {r}}_{e},{\boldsymbol {r}}_{h})}$ and ${\displaystyle f_{\rm {ex}}}$ as

${\displaystyle f_{i}={\frac {1}{v}}{\frac {(\int d{\boldsymbol {r}}_{e}\Psi _{i}({\boldsymbol {r}}_{e},{\boldsymbol {r}}_{e}))^{2}}{|\Phi _{\rm {ex}}(0)|^{2}}}f_{\rm {ex}}}$ .

Coinciding coordinates in the numerator, ${\displaystyle {\boldsymbol {r}}_{e}={\boldsymbol {r}}_{h}}$, reflect the fact the exciton is created at a spatial scale small compared with its radius. The integral in the numerator can only be performed for specific models of impurity excitons. However, if the exciton is weakly bound to impurity, hence, the radius of the bound exciton ${\displaystyle a_{i}}$ satisfies the condition ${\displaystyle a_{i}}$ ≥ ${\displaystyle a_{\rm {ex}}}$ and its wave function of the internal motion ${\displaystyle \Phi _{\rm {ex}}({\boldsymbol {r}}_{e}-{\boldsymbol {r}}_{h})}$ is only slightly distorted, then the integral in the numerator can be evaluated as ${\displaystyle (a_{i}/a_{\rm {ex}})^{3/2}}$. This immediately results in an estimate for ${\displaystyle f_{i}}$

${\displaystyle f_{i}\approx {\frac {a_{i}^{3}}{v}}f_{\rm {ex}}}$ .

This simple result reflects physics of the phenomenon of giant oscillator strength: coherent oscillation of electron polarization in the volume of about ${\displaystyle a_{i}^{3}>>v}$.

If the exciton is bound to a defect by a weak short-range potential, a more accurate estimate holds

${\displaystyle f_{i}=8\left({\frac {\mu }{m}}{\frac {E_{\rm {ex}}}{E_{i}}}\right)^{3/2}{\frac {\pi a_{\rm {ex}}^{3}}{v}}f_{\rm {ex}}}$.

Here ${\displaystyle m=m_{e}+m_{h}}$ is the exciton effective mass, ${\displaystyle \mu =(m_{e}^{-1}+m_{h}^{-1})^{-1}}$ is its reduced mass, ${\displaystyle E_{\rm {ex}}}$ is the exciton ionization energy, ${\displaystyle E_{i}}$ is the binding energy of the exciton to impurity, and ${\displaystyle m_{e}}$ and ${\displaystyle m_{h}}$ are the electron and hole effective masses.

Giant oscillator strength for shallow trapped excitons results in their short radiative lifetimes

${\displaystyle \tau _{i}\approx {\frac {3m_{0}c^{3}}{2e^{2}n\omega _{i}^{2}f_{i}}}.}$

Here ${\displaystyle m_{0}}$ is the electron mass in vacuum, ${\displaystyle c}$ is the speed of light, ${\displaystyle n}$ is the refraction index, and ${\displaystyle \omega _{i}}$ is the frequency of emitted light. Typical values of ${\displaystyle \tau _{i}}$ are about nanoseconds, and these short radiative lifetimes favor the radiative recombination of excitons over the non-radiative one.[5] When quantum yield of radiative emission is high, the process can be considered as resonance fluorescence.

Similar effects exist for optical transitions between exciton and biexciton states.

An alternative description of the same phenomenon is in terms of polaritons: giant cross-sections of the resonance scattering of electronic polaritons on impurities and lattice defects.

While specific values of ${\displaystyle f_{i}}$ and ${\displaystyle \tau _{i}}$ are not universal and change within collections of specimens, typical values confirm the above regularities. In CdS, with ${\displaystyle E_{i}\approx 6}$ meV, were observed impurity-exciton oscillator strengths ${\displaystyle f_{i}\approx 10}$.[6] The value ${\displaystyle f_{i}>1}$ per a single impurity center should not be surprising because the transition is a collective process including many electrons in the region of the volume of about ${\displaystyle a_{i}^{3}>>v}$. High oscillator strength results in low-power optical saturation and radiative life times ${\displaystyle \tau _{i}\approx 500}$ ps.[7][8] Similarly, radiative life times of about 1 ns were reported for impurity excitons in GaAs.[9] The same mechanism is responsible for short radiative times down to 100 ps for excitons confined in CuCl microcrystallites.[10]

Similarly, spectra of weakly trapped molecular excitons are also strongly influenced by adjacent exciton bands. It is an important property of typical molecular crystals with two or more symmetrically-equivalent molecules in the elementary cell, such as benzine and naphthalene, that their exciton absorption spectra consist of doublets (or multiplets) of bands strongly polarized along the crystal axes as was demonstrated by Antonina Prikhot'ko. This splitting of strongly polarized absorption bands that originated from the same molecular level and is known as the 'Davydov splitting' is the primary manifestation of molecular excitons. If the low-frequency component of the exciton multiplet is situated at the bottom of the exciton energy spectrum, then the absorption band of an impurity exciton approaching the bottom from below is enhanced in this component of the spectrum and reduced in two other components; in the spectroscopy of molecular excitons this phenomenon is sometimes referred to as the 'Rashba effect'.[11][12][13] As a result, the polarization ratio of an impurity exciton band depends on its spectral position and becomes indicative of the energy spectrum of free excitons.[14] In large organic molecules the energy of impurity excitons can be shifted gradually by changing the isotopic content of guest molecules. Building on this option, Vladimir Broude developed a method of studying the energy spectrum of excitons in the host crystal by changing the isotopic content of guest molecules.[15] Interchanging the host and the guest allows studying energy spectrum of excitons from the top. The isotopic technique has been more recently applied to study the energy transport in biological systems.[16]

• Exciton
• Polariton
• Oscillator strength
• Quantum yield
• Resonance fluorescence