Arthur Leonard Schawlow's 1981 lecture describes an external-cell arrangement: a beam splitter makes opposed beams, an optical chopper interrupts the pump, and a lock-in amplifier reads the probe detector with the chopper reference. Pump-on reduces absorption and raises the detector signal; scanning the laser finds the narrow resonance. Its first application used iodine; pressure and laser jitter limited the resolution.[ref]
Figure 1.
Counterpropagating pump and probe with synchronous transmission readout
. Original functional drawing of the cited external-cell principle. Beam separation is exaggerated; this is not a reconstruction of the pulsed sodium apparatus. Details.
For an original detector model, let be the probe power reaching a photodetector without sample attenuation and let be the sample's probe optical depths. After subtracting a stable detector background, the transmitted powers are
A positive synchronous change means less probe photon absorption, provided incident probe power is stable and scattered pump light is excluded. For small optical-depth changes the fractional signal is approximately . A lock-in amplifier's voltage also depends on gain, reference phase and chopping waveform; it is not automatically this dimensionless ratio.
Useful controls are blocking the pump, detuning far from the feature, reversing or adjusting beam alignment, and repeating the scan at several pump light intensities. Frequency calibration, sample pressure, transit through the beams and laser frequency fluctuations must be assessed separately. Nearly opposed beams leave a residual Doppler shift: for wave vectors , the simultaneous-resonance condition gives . Exact opposition removes this transverse sensitivity in the first-order model.