Cs-Ar optical amplifier with a saturation intensity of 10†kW-cm-2 and single-pass extraction efficiency of 28% at 852.2†nm.

Optical amplification by the stimulated emission of Cs(6p2P3/2)-Ar atomic pairs, observed in pump-probe experiments over a ∼290 GHz-wide spectral region lying to the red of the Cs D2 line (852.1 nm), has been realized by photoexciting thermalized, ground state Cs-Ar atoms in the 834-849 nm wavelength interval. When the gain medium is pumped at the peak of the CsAr B2Σ1/2+←X2Σ1/2+ transition at 836.7 nm, maximum gain occurs between 852.2 nm and 852.3 nm and >28% of the energy stored in the upper laser level is extracted with 8 ns (FWHM) probe pulses in a single pass. From the measured rate of saturation of the extracted pulse energy with increasing probe intensity, the product of γ0L and Esat, the saturation pulse energy, is measured directly to be 400 ± 20 µJ and the lower limit for the saturation intensity (Isat) of this amplifier is estimated to be 10 kW-cm-2 at 852.2 nm. Circularly polarizing the optical pump beam increases the optical-to-optical conversion efficiency by 20%, and the storage lifetime of the upper laser level is observed from temporally-resolved gain spectra to be 5 ± 1 ns. Pump excitation spectra also reveal a significant contribution from Ar-Cs-Ar (3-body) photoassociation and suprathermal Ar atoms generated by the dissociation of the CsAr B2Σ1/2+ complex. Multipass-amplifier geometries with broad-bandwidth probe signals are expected to yield upper state energy extraction efficiencies above 50%. This alkali-rare gas amplifier demonstrates the efficiencies available with the storage of energy in, and optical extraction from, excited atomic collision pairs.

Manipulating excited state hyperfine level populations in an atomic laser through electronic spin polarization: controlling upper laser level degeneracy and small Signal Gain.

Anisotropic coherent radiation has been generated from an isotropic medium, in the absence of an external magnetic field, by the spin polarization of an atomic excited state. Lasing on specific hyperfine lines of the 6p2P32→6s2S12 (D2) transition of Cs at 852.1 nm has been realized by photoexciting Cs-rare gas thermal collision pairs with a circularly-polarized (σ+) optical field. Subsequent dissociation of the transient Cs-rare gas B2Σ12+ diatomic molecule selectively populates the F = 4, 5 hyperfine levels of the Cs 6p2P32 state. Not only does electronic spin polarization of the upper laser level yield circularly-polarized coherent emission, but the effective degeneracy (g2) of the 6p2P32 state is altered by the non-statistical hyperfine state population distribution, thereby permitting control of the laser small signal gain with an elliptically-polarized pump optical field. The D2 laser efficiency and output power correlate directly with the molecular orbital structure of the Cs-rare gas B2Σ+ state in the region of internuclear separation at which the diatomic complex is born.

Mode suppression of 53 dB and pulse repetition rates of 2.87 and 36.4 GHz in a compact, mode-locked fiber laser comprising coupled Fabry-Perot cavities of low finesse (F = 2).

Multiplication of the pulse repetition frequency (PRF) of a compact, mode-locked fiber laser by a factor as large as 25 has been achieved with two coupled Fabry-Perot (FP) resonators of low finesse (F = 2). Reducing the FP finesse by at least two orders of magnitude, relative to previous pulse frequency multiplication architectures, has the effect of stabilizing the oscillator with respect to pulse-to-pulse amplitude, dropped pulses, and other effects of cavity detuning. Coupling two Fabry-Perot cavities, each encompassing a 3.3-3.6 cm length of fiber, in a hybrid geometry resembling that of the coupled-cavity laser interferometer has yielded side mode suppressions ≥ 50 dB while simultaneously doubling the laser PRF to 2.87 GHz. Pulses approximately 3.9 ps in duration (FWHM) are emitted at intervals of 27.5 ps, and in groups (bursts) of pulses separated by 350 ps. Thus, the PRF within the pulse bursts is 36 GHz, a factor of 25 greater than the free spectral range for a conventional mode-locked cavity having a length of 6.9 cm. Experimental data are in accord with simulations of the phase coherence and temporal behavior of the mode-locked pulses.

Spin Polarization of Rb and Cs np

We report the selective population of Rb or Cs np ^{2}P_{3/2} (n=5, 6; F=4, 5) hyperfine states by the photodissociation of a transient, alkali-rare gas diatomic molecule. Circularly polarized (σ^{-}), amplified spontaneous emission (ASE) on the D_{2} line of Rb or Cs (780.0 and 852.1 nm, respectively) is generated when Rb-Xe or Cs-Xe ground state collision pairs are photoexcited by a σ^{+}-polarized optical field having a wavelength within the D_{2} blue satellite continuum, associated with the B^{2}Σ_{1/2}^{+}←X^{2}Σ_{1/2}^{+} (free←free) transition of the diatomic molecule. The degree of spin polarization of Cs (6p ^{2}P_{3/2}), specifically, is found to be dependent on the interatomic distance (R) at which the excited complex is born, a result attributed to the structure of the B^{2}Σ_{1/2}^{+} state. For Cs-Xe atomic pairs, tuning the wavelength of the optical field from 843 to 848 nm varies the degree of circular polarization of the ASE from 63% to almost unity because of the perturbation, in the 5≤R≤6 Å interval, of the ^{2}Σ_{1/2}^{+} potential by a dσ molecular orbital associated with a higher ^{2}Λ electronic state. Monitoring only the Cs 6p ^{2}P_{3/2} spin polarization reveals a previously unobserved interaction of CsXe (B^{2}Σ_{1/2}^{+}) with the lowest vibrational levels of a ^{2}Λ state derived from Cs (5d)+Xe. By inserting a molecular intermediate into the alkali atom excitation mechanism, these experiments realize electronic spin polarization through populating no more than two np ^{2}P_{3/2} hyperfine states, and demonstrate a sensitive spectroscopic probe of R-dependent state-state interactions and their impact on interatomic potentials.