We present a new method of comb-locked cavity ring-down spectroscopy for the Lamb-dip measurement of molecular ro-vibrational transitions. By locking both the probe laser frequency and a temperature-stabilized high-finesse cavity to an optical frequency comb, we realize saturation spectroscopy of molecules with kilohertz accuracy. The technique is demonstrated by recording the R(9) line in the υ = 3 - 0 overtone band of CO near 1567 nm. The Lamb-dip spectrum of such a weak line (transition rate 0.0075 s) is obtained using an input laser power of only 3 mW, and the position is determined to be 191 360 212 770 kHz with an uncertainty of 7 kHz (δν/ν∼3.5×10), which is currently limited by our rubidium clock.

Precision measurement of ro-vibrational transitions in the electronic ground state of the hydrogen molecule can be used to test quantum electrodynamics and also to determine the dimensionless proton-to-electron mass ratio. Saturation spectroscopy of the 2-0 overtone transitions of hydrogen deuterium (HD) were measured with three cavity-enhanced spectroscopy methods. With a sensitivity at the 10 − 13 c m − 1 level, we revealed a dispersion-like lineshape instead of a conventional Lamb “dip,” which explains the significant discrepancy among previous independent measurements. The spectra can be fit well by using the Fano profile. Centers of R(1) and R(3) lines were determined as 217 105 182 111 ( 19 ) s t a t ( 240 ) s y s k H z and 220 704 305 234 ( 20 ) s t a t ( 240 ) s y s k H z , respectively.

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Selective pumping and probing of highly excited states of molecules are essential in various studies but are also challenging because of high density of states, weak transition moments, and lack of precise spectroscopy data. We develop a comb-locked cavityassisted double-resonance spectroscopy (COCA-DR) method for precision measurements using low-power continuous-wave lasers. A high-finesse cavity locked with an optical frequency comb is used to enhance both the pumping power and the probing sensitivity. As a demonstration, Doppler-free stepwise two-photon absorption spectra of CO 2 were recorded by using two milliwatt diode lasers (1.60 and 1.67 μm), and the rotation energies in a highly excited state (CO-stretching quanta = 8) were determined with an unprecedented accuracy of a few kilohertz.

The (30012) ← (00001) band of 12C16O2 in the 1.6 μm region is used for satellite observation of carbon dioxide in the Earth’s atmosphere. Here, we report a Doppler-free spectroscopy study of this band with comb-locked wavelength-modulated cavity-enhanced absorption spectroscopy. Frequencies of 18 transitions with the rotational quantum numbers up to 42 were determined with sub-kHz accuracy, corresponding to a fractional uncertainty at the 10−12 level. With this precision, we revealed an anomalous decrease of the line shift and an increase of the line broadening for the Lamb dips of CO2 in the low-pressure regime compared to values obtained from Doppler-limited spectra at higher pressures.

Saturation spectroscopy is frequently used to obtain sub-Doppler measurement of atomic and molecular transitions. Optical resonant cavities can be used to enhance the effective absorption path length, and the laser power inside the cavity as well to saturate very weak ro-vibrational transitions of molecules. Three different cavity-enhanced methods, cavity enhanced absorption spectroscopy, cavity ring-down spectroscopy, and noise-immune cavity enhanced optical heterodyne molecular spectroscopy (NICE-OHMS), were compared by measuring the Lamb dip of a C 2 H 2 line at 1.4 µm using a cavity with a finesse of 120000. The center of the line was determined by different cavity-enhanced methods, each giving a sub-kHz (δν/ν≈10 −12) statistical uncertainty. The sensitivity and precision of different methods were analyzed and compared. As demonstrated in this study, the NICE-OHMS method is the most sensitive one, but more investigation on the systematic uncertainty is necessary before its application in metrology studies toward a sub-kHz accuracy.

Noise-immune cavity enhanced optical heterodyne molecular spectroscopy (NICE-OHMS) is extremely sensitive in detecting weak absorption. However, the use of NICE-OHMS for metrology study was also hindered by its sensitivity to influence from various experimental conditions such as the residual amplitude modulation. Here we demonstrate to use NICE-OHMS for precision measurements of Lamb-dip spectra of molecules. After a dedicated investigation of the systematic uncertainties in the NICE-OHMS measurement, the transition frequency of a ro-vibrational line of C 2 H 2 near 789 nm was determined to be 379 639 280 915.3±1.2 kHz (fractional uncertainty 3.2 × 10 −12), agreeing well with, but more accurate than, the value determined from previous cavity ring-down spectroscopy measurements. The study indicates the possibility to implement the very sensitive NICE-OHMS method for frequency metrology of molecules, or a molecular clock, in the near-infrared.