The sensitivity of molecular fingerprinting is dramatically improved when placing the absorbing sample in a high-finesse optical cavity, thanks to the large increase of the effective path-length. As demonstrated recently, when the equidistant lines from a laser frequency comb are simultaneously injected into the cavity over a large spectral range, multiple trace-gases may be identified within a few milliseconds. Analyzing efficiently the light transmitted through the cavity however still remains challenging. Here, a novel approach, cavity-enhanced frequency comb Fourier transform spectroscopy, fully overcomes this difficulty and measures ultrasensitive, broad-bandwidth, high-resolution spectra within a few tens of $\mu$s. It could be implemented from the Terahertz to the ultraviolet regions without any need for detector arrays. We recorded, within 18 $\mu$s, spectra of the 1.0 $\mu$m overtone bands of ammonia spanning 20 nm with 4.5 GHz resolution and a noise-equivalent-absorption at one-second-averaging per spectral element of 3 10^-12 cm^-1Hz^-1/2, thus opening a route to time-resolved spectroscopy of rapidly-evolving single-events

Abstract:The mid-infrared part of the electromagnetic spectrum is the so-called molecular fingerprint region because gases have tell-tale absorption features associated with molecular rovibrations. This region can be for instance exploited to detect small traces of environmental and toxic vapours in atmospheric and industrial applications. Novel Fourier transform spectroscopy without moving parts, based on time-domain interferences between two comb sources, can in particular benefit optical diagnostics and precision spectroscopy.