Laser action has been detected in distyryl benzene thin films and single crystals. Whereas amplified spontaneous emission prevails in thin films, we found, however that superfluorescence dominates the stimulated emission in single crystals.
Experimental data are presented which demonstrate superfluorescent radiation due to stimulated transitions between the lowest-bound diatomic states of xenon and the repulsive ground state. In this context, superfluorescence describes a condition where, even in the absence of feedback, radiation from the fluorescent medium is dominated by stimulated transitions. The continuum emission spectrum was highly anisotropic and narrowing of the spectrum was observed. The optical gain was greatest at a wavelength of 1730 ± 10 Å, where the experimentally estimated effective gain cross section is 1 × 10−18 cm2.
Spontaneous decay is a phenomenon that has been described for the first time by Dirac, Wigner
and Weisskopf, at the early ages of the development of quantum electrodynamics. The theory is
applicable to a multi-body system only when atoms don’t interact during their decay. Dicke introduces
in his seminal paper the case where this assumption doesn’t hold.
The results he obtains not only tell that the system emits pulses, but the pulse duration now depends
on 1/N, where N is the number of participating atoms to the process. The pulses temporal profile
is described by a squared hyperbolic secant function. The resulting emission intensity scales as N^2.
The atomic system radiates more intensively than the ordinary fluorescent emission, this is the reason
why the process is called superradiance, or by a generalization to extended systems, superfluorescence.
The superradiant emission has preferential escape directions, depending on the atomic sample shape.
Superradiance is a collective process and it takes place when the group of excited atoms is left unper-
turbed during the formation of of the macroscopic dipole. A fundamental difference compared to the
spontaneous and stimulated emission processes is that all atoms act together as a single entity and it
isn’t possible to identify single atoms involved.
This remarkable behaviour is manifest when the atomic coherence of the system, while influenced by
environmental interactions that cause dephasing in atoms, persists for a sufficient interval of time.
Typical dephasing mechanisms, such as collisions in gases or lattice phonon interactions in crystals,
make its experimental observation difficult. A possible solution to this problem is the use of optical
crystals doped with rare-earths that are characterized by long and narrow levels lifetimes.
We have studied the nature of the emission from a laser-excited KCI : O 2 − crystal and have observed that the emission evolves continuously from superfluorescence (SF) to amplified spontaneous emission (ASE) as the temperature of the crystal and hence the dephasing rate of the optical transition are increased. The sample is excited by a 30-ps pulse from a frequency-quadrupled Nd:YAG laser, and the 629.1-nm emission is detected using a streak camera system. At a temperature of 10 K the emission is characterized as SF with an average delay time of 200 ps and an average pulse width of 60 ps. As the temperature is increased to ~20 K, the output pulse broadens and the time delay increases to its maximum value of ~2 ns. As the temperature is increased still further, the time delay is observed to decrease, and at a temperature of 30 K the emission is characterized as ASE with a very small delay time and with an exponentially decaying time evolution. We modeled our experiment using the Maxwell-Bloch formalism and find good agreement for our measured output pulse shapes and for the dependence of delay time and pulse width on the dephasing rate.