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arXiv:2001.08447 · Communications Physics

Cavity buildup dispersion spectroscopy

Agata Cygan, Adam J. Fleisher, R. Ciuryło, Keith A. Gillis, Joseph T. Hodges, Daniel Lisak

Published Jan 29, 2021• 17 citations
arXivHTMLPDF

Abstract

Abstract Measurements of ultrahigh-fidelity absorption spectra can help validate quantum theory, engineer ultracold chemistry, and remotely sense atmospheres. Recent achievements in cavity-enhanced spectroscopy using either frequency-based dispersion or time-based absorption approaches have set new records for accuracy with uncertainties at the sub-per-mil level. However, laser scanning or susceptibility to nonlinearities limits their ultimate performance. Here we present cavity buildup dispersion spectroscopy (CBDS), probing the CO molecule as an example, in which the dispersive frequency shift of a cavity resonance is encoded in the cavity’s transient response to a phase-locked non-resonant laser excitation. Beating between optical frequencies during buildup exactly localizes detuning from mode center, and thus enables single-shot dispersion measurements. CBDS can yield an accuracy limited by the chosen frequency standard and measurement duration and is currently 50 times less susceptible to detection nonlinearity compared to intensity-based methods. Moreover, CBDS is significantly faster than previous frequency-based cavity-enhanced methods. The generality of CBDS shows promise for improving fundamental research into a variety of light–matter interactions.

DOI
10.1038/s42005-021-00517-3

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Abstract Measurements of ultrahigh-fidelity absorption spectra can help validate quantum theory, engineer ultracold chemistry, and remotely sense atmospheres. Recent achievements in cavity-enhanced spectroscopy using either frequency-based dispersion or time-based absorption approaches have set new records for accuracy with uncertainties at the sub-per-mil level. However, laser scanning or susceptibility to nonlinearities limits their ultimate performance. Here we present cavity buildup dispersion spectroscopy (CBDS), probing the CO molecule as an example, in which the dispersive frequency shift of a cavity resonance is encoded in the cavity’s transient response to a phase-locked non-resonant laser excitation. Beating between optical frequencies during buildup exactly localizes detuning from mode center, and thus enables single-shot dispersion measurements. CBDS can yield an accuracy limited by the chosen frequency standard and measurement duration and is currently 50 times less susceptible to detection nonlinearity compared to intensity-based methods. Moreover, CBDS is significantly faster than previous frequency-based cavity-enhanced methods. The generality of CBDS shows promise for improving fundamental research into a variety of light–matter interactions.
We introduce cavity enhanced ultrafast transient absorption spectroscopy, which employs frequency combs and high-finesse optical cavities. % The schematic of apparatus is shown in Figure 1. Sub-100 fs pulses with a repetition rate of 90 MHz are generated by a home-built Ytterbium fiber laser. The amplified light has a power up to 10 W, which is used to pump an optical parametric oscillator, followed by second-harmonic generation(SHG) that converts the wavelength from near-IR to visible. A pump comb at 530 nm is separately generated by SHG. Both pump and probe combs are coupled into high-finesse cavities. Compared to the conventional transient absorption spectroscopy method, the detection sensitivity can be improved by a factor of (Fπ)2∼105\left(\frac{\mathcal{F}}{\pi} \right)^2 \sim 10^5(πF​)2∼105, where F\mathcal{F}F is the finesse of cavity. This ultrasensitive technology enables the direct all-optical dynamics study in molecular beams. We will apply the cavity enhanced ultrafast transient absorption spectroscopy to investigate the dynamics of visible chromophores and then extend the wavelength to mid-IR to study vibrational dynamics of small hydrogen-bonded clusters. %\begin{wrapfigure}{I}{1\textwidth} % \centering % \includegraphics[width = 0.7\textwidth]{CETAS_details.eps} %\caption{Schematic of cavity enhanced ultrafast transient absorption spectroscopy apparatus. An amplified fiber laser frequency comb is converted to visible light and pump and probe combs are coupled to high-finesse optical resonators. Transmission of the probe light is measured.} %\end{wrapfigure}
The goal of this work is to study and understand dynamics of atomic systems interacting with strong fields. To this end, a method referred to as strong-field spectroscopy is used, which measures the absorption spectrum of atoms interacting with such fields. In the scope of this work, a technique which allows the simultaneous measurement of absorption spectra of attosecond pulses and their reference signal is developed, which significantly increases the sensitivity to absorption changes. Additionally, a reconstruction method is introduced which retrieves the time-dependent evolution of the dipole response of an atomic system directly from a single absorption spectrum. Strong-field spectroscopy combines these techniques to examine the nonlinear strong-field dynamics in atomic and molecular systems and is applied to study the strongly correlated doubly excited states in helium. Furthermore, a measurement approach is introduced which uses the interaction with a high-intensity laser pulse to impose a time gate on the evolution of the coherent response of a system, which has previously been excited by an ultrashort laser pulse. With this approach the buildup of resonance phenomena in a wide range of physical systems can be studied. As a first application, the time-dependent buildup of a Fano resonance as well as the buildup of a whole Rydberg series are investigated.
Recently we have reported[1] on the measurements of electronic dephasing (T_2) and radiationless decay (T_1) in molecules using emission spectroscopy as a probe for the detection of the photon echo. This right-angle photon echo utilizes a single mode of a narrow-band (~MHz) cw dye laser and an intracavity electro-optical (EO) element that modulates the frequency of the laser.[2] Applying voltage pulses into the EO crystal switches the laser frequency from ω_0 (the peak frequency of the transition resonance) into another frequency ω. This switching procedure introduced by Brewer et al. for the observation of transients in the forward direction of the laser allows one to observe coherent transients in gases,[1,2] solids[3-5] and molecular beams.[6] Typically, the dispersion of the nonlinear EO crystal (e.g., AD*P) gives a 60 MHz frequency shift within the inhomogeneous resonance of the optical transition (width ~GHz or larger). Therefore, to switch the laser frequency further, one must use high-voltage signals that are usually hard to obtain especially for multiple-pulse experiments. Secondly, there is a limit on the frequency shift which is conditioned by the mode spacing of the cavity. Thirdly, because the laser is switched into a new group of molecules some complications may arise in interpreting the transient spectra especially in large molecules. This is because in large molecules the density of excited states is high and thus the buildup of transients of w molecules (which could be complex) will be superimposed on the decay of ω_0 molecules. Finally, off-resonance effects (e.g., beats) between the molecules at frequency ω and ω_0 cannot be avoided.
Optical cavities serve as powerful tools for sensing experiments, often relying on narrow-linewidth laser sources to minimize the impact of optical coherence on measurements. However, demands for affordable integrated and miniaturized sensing platforms in point-of-care diagnostics, environmental monitoring, and similar applications motivate switching to sources with broader linewidths suitable for both monolithic and heterogeneous integrations. Time-domain measurement techniques such as cavity ring-down spectroscopy (CRDS) are widely used in conjunction with optical cavities, but to date there has been no universal model that quantifies the impact of partial coherence on the cavity temporal transfer function. We apply a linear systems theory approach to develop a closed-form analytic model for cavity-based sensing that quantifies the influence of source bandwidth (i.e., temporal coherence) on spectroscopic measurements in the time domain. This approach can be applied to a variety of cavity-based spectroscopies. In this study, cavity-enhanced absorption spectroscopy (CEAS) and CRDS paradigms have been examined using standing- and traveling-wave resonator examples. Results show that although increased cavity loss is the primary factor reducing output power and photon lifetime in both CEAS and CRDS, broader source linewidths can also influence cavity buildup and transmission and must be accounted for when modeling the system response. The model is consistent with known results in the literature and provides a framework for evaluating source detuning and coherence effects on cavity dynamics.
A novel phase-modulation technique which permits subkilohertz-laser stability and new levels of precision in laser spectroscopy was reported recently. For spectroscopy, the basic arrangement consists of a combination of an optical pump and a probe field which is phase modulated. The pump prepares the atomic sample by burning a narrow hole within the atom's inhomogeneous line shape, and the probe beam samples the prepared hole when its modulation sidebands are swept into resonance. Off resonance, the probe is balanced as pairs of sidebands produce heterodyne beat signals of opposite phase which just cancel. On resonance, the balance is upset and yields a nonvanishing beat signal with a Lorentzian absorption or dispersion line shape and with residual noise approaching the shot noise limit. Here we investigate the theory of phase-modulation spectroscopy. We treat the nonlinear response of an atomic two-level quantum system subject to an intense pump and a weak copropagating or counterpropagating phase-modulated probe beam. The density-matrix equations of motion are solved by a Laplace-transform method and by the novel use of a translation operator which allows the infinite hierarchy of coupled equations to close. A solution equivalent to the rate-equation result is developed and coherence corrections are found which predict new resonances that have just been detected in this laboratory. The delayed pump-probe technique encountered in solid-state laser spectroscopy is analyzed in this context for two- and three-level quantum systems. The response of a Fabry-Perot cavity to a phase-modulated light wave is examined also and reveals an unexpected absorption feature.
Cavity Ring Down Spectroscopy has become an important method in gas phase spectroscopy and its uses promise to expand. While previous investigators have considered the decay of the stored energy in the cavity ring down cell following short pulsed excitation, this paper considers the effects of pulse reshaping during cavity ring down. It is found that in order to properly model these effects, one must consider not only the mode dependent loss of the ring down cavity, but also dispersion that shifts the resonant modes of the cavity. Only by considering the latter effect does one get a "causal" result where the free induction decay signal of the absorber occurs after the excitation pulse. It is demonstrated that in the limit that the cavity round trip time is long compared to both the T 2 time of the intracavity absorber and the temporal width of the excitation pulse, the reshaping of the n'th pulse out of the ring down cavity is the same as the reshaping produced by free space propagation over a distance of (2 n + 1) L where L is the separation of the mirrors in the cell. However, when the absorber T 2 becomes comparable to or longer than the cavity round trip time, then discrete modes of the ring down cavity become important. A general expression for the output is given for the important case of a weak absorber, and changes in the output are computed for a single absorption line as a function of the ratio of T 2 to the cavity round trip time for several values of the optical thickness of the sample. Lastly, it is suggested that monitoring changes in the pulse shape of the cavity ring down signal provides a way to characterize an absorption spectrum on a frequency scale of the laser bandwidth down to the cavity free spectral range.