We demonstrate coherent dual frequency-comb spectroscopy for detecting variations in greenhouse gases. High signal-to-noise spectra are acquired spanning 5990 to 6260 cm -1 (1600 to 1670 nm) covering ~700 absorption features from CO 2 , CH 4 , H 2 O, HDO, and 13 CO 2 , across a 2-km open-air path. The transmission of each frequency comb tooth is resolved, leading to spectra with <1 kHz frequency accuracy, no instrument lineshape, and a 0.0033-cm -1 point spacing. The fitted path-averaged concentrations and temperature yield dry-air mole fractions. These are compared with a point sensor under well-mixed conditions to evaluate current absorption models for real atmospheres. In heterogeneous conditions, timeresolved data demonstrate tracking of strong variations in mole fractions. A precision of <1 ppm for CO 2 and <3 ppb for CH 4 is achieved in 5 minutes in this initial demonstration. Future portable systems could support regional emissions monitoring and validation of the spectral databases critical to global satellitebased trace gas monitoring.

We demonstrate a high-accuracy dual-comb spectrometer centered at 3.4 μm. The amplitude and phase spectra of the P, Q, and partial R branches of the methane ν 3 band are measured at 25 to 100 MHz point spacing with resolution under 10 kHz and a signal-to-noise ratio of up to 3500. A fit of the absorbance and phase spectra yields the center frequency of 132 rovibrational lines. The systematic uncertainty is estimated to be 300 kHz, which is 10 −3 of the Doppler width and a 10-fold improvement over Fourier transform spectroscopy. These data quantify the accuracy and resolution achievable with direct comb spectroscopy in the midinfrared.

Small gas-phase clusters (ion pairs) of the ionic liquid [emim](+)[Tf2N](-) have been generated in a supersonic expansion. Clusters are investigated via UV photofragmentation and time-of-flight mass spectrometry. Spectra between 42,000 and 45,000 cm(-1) reveal dynamical branching between direct dissociation of the ion pair to the cation and anion and to radical species. The IR spectrum between 2800 and 3200 cm(-1) was measured by action spectroscopy. Multiple conformations of the ion pair are found to be present in the molecular beam, leading to broad spectral features, further complicated by hydrogen bonding and Fermi resonances. The measured and theoretical spectra compare well, and the jet-cooled ion pair structures present in the molecular beam are strongly hydrogen bonded "stacked" conformers.

We demonstrate a dual-comb spectrometer using stabilized frequency combs spanning 177 to 220 THz (1360 to 1690 nm) in the near infrared. Comb-tooth-resolved measurements of amplitude and phase generate over 4×10(5) individually resolved spectral elements at 100 MHz point spacing and kilohertz-level resolution and accuracy. The signal-to-noise ratio is 100 to 3000 per comb tooth. Doppler-broadened phase and amplitude spectra of CO(2), CH(4), C(2)H(2), and H(2)O in a 30 m multipass cell agree with established spectral parameters, achieving high-resolution measurements with optical bandwidth generally associated with blackbody sources.

Exothermic reactive scattering of F atoms at the gas-liquid interface of a liquid hydrocarbon (squalane) surface has been studied under single collision conditions by shot noise limited high-resolution infrared absorption on the nascent HF(v,J) product. The nascent HF(v,J) vibrational distributions are inverted, indicating insufficient time for complete vibrational energy transfer into the surface liquid. The HF(v=2,J) rotational distributions are well fit with a two temperature Boltzmann analysis, with a near room temperature component (T(TD) approximately equal to 290 K) and a second much hotter scattering component (T(HDS) approximately equal to 1040 K). These data provide quantum state level support for microscopic branching in the atom abstraction dynamics corresponding to escape of nascent HF from the liquid surface on time scales both slow and fast with respect to rotational relaxation.

State-to-state reaction dynamics of the reaction F+HCl→HF(v,J)+Cl have been studied under single-collision conditions using an intense discharge F atom source in crossed supersonic molecular beams at Ecom=4.3(1.3)kcal∕mol. Nascent HF product is monitored by shot-noise limited direct infrared laser absorption, providing quantum state distributions as well as additional information on kinetic energy release from high resolution Dopplerimetry. The vibrational distributions are highly inverted, with 34(4)%, 44(2)%, and 8(1)% of the total population in vHF=1, 2, and 3, respectively, consistent with predominant energy release into the newly formed bond. However, there is a small [14(1)%] but significant formation channel into the vHF=0 ground state, which is directly detectable for the first time via direct absorption methods. Of particular dynamical interest, both the HF(v=2,J) and HF(v=1,J) populations exhibit strongly bimodal J distributions. These results differ significantly from previous flow and arrested-relaxation studies and may signal the presence of microscopic branching in the reaction dynamics.

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Reactive scattering dynamics of F+H(2)O-->HF+OH have been investigated under single-collision, crossed, supersonic jet conditions at 5.4(1.3) kcalmol, and nascent HF(v,J) rovibrational populations (v