We describe a new technique for accurate measurement of absolute photoionization cross sections. By measuring the loss rateof atoms from a laser trap in the presence of ionizing light, we directly measure the photoionization rate. The only quantities requiring absolute calibration are the ionizing laser intensity and the fractional population in the relevant state. Our technique is capable of detecting extremely small ionization rates, which means that low-power cw sources can be used. We have applied this method to photoionization from the 5P(3/2) state of rubidium at wavelengths of 413 and 407 nm.The cross sections are 1.36(12) x 10(-17) and 1.25(11) x 10(-17) cm(2) , respectively.
We present and characterize a two-dimensional (2D) imaging spectrometer based on a virtually imaged phased array (VIPA) disperser for rapid, high-resolution molecular detection using mid-infrared (MIR) frequency combs at 3.1 and 3.8 μm. We demonstrate detection of CH4 at 3.1 μm with >3750 resolution elements spanning >80 nm with ~600 MHz resolution in a <10 μs acquisition time. In addition to broadband detection, we also demonstrate rapid, time-resolved single-image detection by capturing dynamic concentration changes of CH4 at a rate of ~375 frames per second. Changes in absorption above the noise floor of 5×10(-4) are readily detected on the millisecond time scale, leading to important future applications such as real-time monitoring of trace gas concentrations and detection of reactive intermediates.
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