Optical frequency combs have revolutionized the measurement of optical frequencies and improved the precision of spectroscopic experiments. Besides their importance as a frequency-measuring ruler, the frequency combs themselves can excite target transitions (direct frequency comb spectroscopy). The direct frequency comb spectroscopy may extend the optical frequency metrology into spectral regions unreachable by continuous wave lasers. In high precision spectroscopy, atoms/ions/molecules trapped in place have been often used as a target to minimize systematic effects. Here, we demonstrate direct frequency comb spectroscopy of single 25Mg ions confined in a Paul trap, at deep-UV wavelengths. Only one mode out of about 20,000 can be resonant at a time. Even then we can detect the induced fluorescence with a spatially resolving single photon camera, allowing us to determine the absolute transition frequency. The demonstration shows that the direct frequency comb spectroscopy is an important tool for frequency metrology for shorter wavelengths where continuous wave lasers are unavailable.
For almost 20 years, optical frequency combs have enabled significant progress in high precision optical frequency metrology. A prominent example is the frequency of the 1S-2S two-photon transition in atomic hydrogen, which has been measured with a fractional uncertainty of 4.1 × 10−15 1, 2. Another milestone are the atomic clocks that have been improved by orders of magnitude by using optical transitions3. Many other fields such as astronomy4, low-noise frequency synthesis5, and trace gas analysis6 have benefited enormously from frequency combs. Frequency combs have also allowed control of the carrier-envelope phase of short pulses7 and by that enabled experiments with single attosecond pulses8. Thanks to the short pulse nature of the generating pulse train non-linear interactions are efficient so that frequency combs can be converted to much shorter wavelengths where continuous wave (cw) lasers are not available. While commercially available crystals are limited by transparency and phase matching requirements to about λ > 190 nm and not yet commercially available KBBF crystals improve this limit to approximately λ > 150 nm9, 10, high harmonic generation (HHG) can reach well into the X-ray regime11. Even though there is very low power with very low repetition rate generated at these most extreme wavelengths, frequency combs with a discernable mode spacing and μW power level can now be produced at least in the extreme ultra violet (EUV)12. The HHG process allows for a coherence time of 1 s provided that a suitable driving laser is used13. This compares well with the state-of-the-art cw lasers in the visible.
A coherent pulse train from a mode locked laser corresponds to a frequency comb in the spectral domain. The frequencies of the modes of the comb, either at the fundamental or upconverted wavelength, are given by f n = nf r + f o with the repetition frequency (=mode spacing) f r, which lies in the radio frequency domain. Knowing f r and the radio frequency offset f o, the optical frequencies of the modes f n may be computed after the large integer n has been determined14. While this property has been used for optical frequency metrology, it is possible to employ the modes for direct frequency comb spectroscopy (DFCS). Using a single mode of a frequency comb on the dipole allowed Cs D lines, V. Gerginov and co-workers could perform DFCS on an atomic beam15. While this is a beautiful demonstration, it also revealed some problems: large ac Stark shifts and high levels of stray light are expected due to the large number of spectator modes. These disadvantages are absent when driving a pure two-photon transition with a frequency comb, i.e. without near-resonant intermediate levels. In that case the modes contribute pairwise to the excitation, which leads to a transition rate that is given by the total power of all modes, while retaining the line width of an individual mode16, 17. In fact the first application of DFCS in 1978 was of this kind18. The original idea of Ye.V. Baklanov and V.P. Chebotayev for two-photon DFCS was to enter a new region of shorter wavelength not accessible with cw lasers19. However, in this case perfect cancellations of the first order Doppler effect is more difficult than with cw lasers. Due to their large band width, counter propagating photons may not have exactly opposite Doppler shifts leading to a type of time of flight broadening20, 21. Other problems emerge when a diverging atomic beam is used in conjunction with chirped pulses22. Trapping and holding the atoms or ions in place for interrogation is the solution to these issues that all modern optical clocks employ.
T.M. Fortier and coworkers were the first to demonstrate DFCS on cold calcium atoms in a magneto optical trap using the narrow intercombination line at 657 nm23. Later A.L. Wolf et al. were exciting clouds of calcium ions in a trap24 with a frequency comb. Recently we could show how to keep a trapped ion refrigerated by the cooling action of an individual mode of an UV comb25. However, in the previous work25, the systematic effects were not studied and the suitability of the method for precision spectroscopy was not ascertained.
Here we utilize a single mode from an ultraviolet frequency comb at 280 nm to excite the 3s 1/2−3p 3/2 transition in a single trapped 25Mg ion. Individual trapped Mg+ ions are used because large clouds of ions are subject to strong systematic shifts. The excitation is detected by observing the induced fluorescence with a spatially resolving single photon camera. Although the expected amount of fluorescence is extremely small since only one mode of the comb can contribute to a signal, we determine the absolute frequency of this transition with improved uncertainty over previous measurements using a cw laser. The technique can be extended straightforwardly to other transitions in different ions. It holds particular interest for future experiments with high harmonic frequency combs in the EUV regions, where no cw lasers are available. In this way, a vast spectral territory will become accessible to precision laser spectroscopy for the first time. This possibility would be for the benefit of fundamental physics as all hydrogen-like ions, like He+ have their metrologically relevant transitions26 there and beyond. DFCS in the EUV has only been performed with fast atoms on strong broadband transitions27,28,29 that have a short excited lifetime and are of limited metrological interest. In our demonstration, it is shown that high precision DFCS using single trapped ions is indeed possible without introducing significant distortions at deep-UV wavelengths. This is a prerequisite for future precision measurements including EUV shelving30.
Ion trapping and UV frequency comb generation
Our experimental apparatus is schematically shown in Fig. 1. Here we briefly describe the setup, while further details can be found in our previous publications25, 26. Ions are trapped in a linear radiofrequency (rf) quadrupole trap driven at 22 MHz, with radial and axial secular frequencies of ω r≈2π × 1 MHz and ω ax≈2π × 45 kHz, respectively. To minimize the micromotion and compensate for stray fields in the trapping region, suitably chosen voltages are applied to additional rods surrounding the rf-electrodes. The ion loading process starts with neutral Mg vapor from an atomic oven which is resonantly photo-ionized using a pulsed and frequency doubled dye laser at 285 nm that is pumped with the second harmonic of a Q-switched Nd:YAG laser. Typically we load one or two ions by cooling on the 280 nm 3s 1/2−3p 3/2 transition. The cooling radiation is obtained by frequency doubling a single-frequency dye (Rhodamine-19) laser at 560 nm. When an isotopically pure ion chain is desired, the loading is repeated until a pure sample of, for example, 25Mg+ is loaded. The probability of loading a particular isotope can be increased by tuning the photo-ionization laser to the optimum frequency. The frequency comb is obtained from a ~840 nm Ti:sapphire mode-locked ring laser that operates at a repetition rate of 373 MHz with a spectral bandwidth (FWHM) of ~20 nm and an average output power ~400 mW. The repetition rate is detected with a high-speed photodiode and stabilized via feedback to an intra-cavity piezoelectric transducer-mounted mirror. Approximately 40% of the output power is sent into an f−2f interferometer to detect the offset frequency f o 14. The offset frequency is stabilized to a radio frequency reference by feeding back to the rf-drive of an acousto-optic modulator (AOM) that drains power from the pump beam of the Ti:sapphire mode-locked laser. Both comb parameters (f r and f o) are locked to oscillators which are phase-locked to a GPS-calibrated hydrogen-maser, ensuring traceability of the frequency of each comb-line. The remaining ~240 mW of the comb power at 840 nm from the oscillator is first focused into a 1-mm thick beta barium borate (BBO) crystal to generate the second harmonic at 420 nm. The unconverted fundamental light is temporally overlapped with the 420 nm pulse train and focused in a second BBO crystal to generate the sum-frequency at 280 nm (see also25). The 280 nm pulse-train is sent through an AOM and focused into the trap. We typically deliver 40–80 μW at the ions. We estimate the power-per-comb-line at the few nW level, which provides an intensity on the order of 0.5 mW cm−2, which corresponds to 0.2% of the saturation intensity. The fluorescence from the ions is collected by a four-lens condenser (B. Halle Nachfl., N.A. ≈ 0.25). An iris limits the aperture of the condenser to obtain nearly diffraction limited images. A ×13 microscope objective images the intermediate focus onto a single photon camera (Quantar Technology, Mepsicron II) with a total magnification of about 100. To suppress the background light level a solar blind color filter is placed in front of the detector. In a conventional spectroscopy experiment with a cw laser and ions in the weak-binding regime, detuning-dependent heating and cooling gives rise to strong lineshape asymmetries that rule out any precision experiment. The same is true for DFCS of a single photon transition as shown in our previous work25. In order to keep the ions cold during the spectroscopy, sympathetic cooling can be employed. Such sympathetic cooling will be necessary for the envisioned EUV experiments26, 31, 32. Sympathetic cooling requires that the cooling and spectroscopy beams be focused on different ions and is thus less appropriate for Coulomb crystals composed of a very small number of ions. Since a cw cooling laser is available in the present experiments, we rapidly switch cooling and spectroscopy laser as demonstrated before33. The fixed frequency cooling laser and the frequency comb are alternatingly applied to the same ions. AOMs are used for switching the beams with a rise/fall time of <1 μs. The cooling and spectroscopy periods are both 2 ms. The lasers are both focused to w 0 ~ 20 μm. Due to the small angle between the lasers and the trap axis all ions in the chain are illuminated to some extent. For the center ion we estimate the Rabi frequency to be 2π × 29 MHz for the cooling laser and 2π × 1.4 MHz for one mode of the spectroscopy laser. The arrival times of the fluorescence counts are time-tagged and only those events registered within the spectroscopy periods are evaluated as the spectroscopy signal. The pulse sequence and data acquisition are controlled by a real-time I/O system (ADwin Pro-II). Examples of fluorescence images of the ion chain recorded during cooling and spectroscopy periods are shown in Fig. 2a, b respectively.
DFCS by fluorescence detection
The comb modes are scanned over the resonance by changing the repetition rate of the frequency comb while recording frames with images of the ions. For data analysis a region of interest (ROI) is defined around each ion and total fluorescence counts are extracted as a function of the absolute frequency. The latter is determined with the help of the frequency comb which is referenced to the hydrogen maser. The mode number is determined to be consistent with previous measurements performed with a cw laser26, 31. A typical spectroscopy signal is shown in Fig. 3. Assuming Poissonian statistics, the error bars in Fig. 3 are taken as the square root of the signal counts.
The repeating peaks of the signal shown in Fig. 3 reflect the comb-mode structure of the excitation laser. The signal contrast defined as a ratio between fluorescence counts at the peak and the base-line is ~3.6. This contrast deteriorates to ~0.01 without a properly defined ROI., i.e., with the full frame fluorescence signal. Exciting the transition with a multiple of comb lines, on and off resonant, does produce beatings in the fluorescence signal at f r and harmonics. Since we detect the signal for several seconds, any coherent line distortion due to that beating is averaged out. Therefore the data are fitted with a series of Lorentzians, where we assume that the noise of the fluorescence counts is given by shot noise only. Quantum interference with the off-resonant D1-line can be neglected as the line separation measured in units of the line width is large enough34. However, the spectrum of our frequency comb is broad enough to also address the D1-line. In that case it folds in between the repeated D2-lines shown in Fig. 3 and distorts the simple periodic Lorentzian shape. We avoid this by employing the cycling transitions with either σ + or σ − polarization as sketched in Fig. 4. There is no cycling transition connecting the ground state and the 3p 1/2 state.
The absolute frequency measurement is subject to several other systematic effects. Without the interleaving cooling laser, fluorescence would be seen only for red detuning because the large orbits of the heated ions essentially eliminates the fluorescence for blue detuning. Even with the cooling laser the ion motion is either amplified or damped during the spectroscopy periods causing a small asymmetry of the line shape. To estimate this effect we numerically simulate the detuning dependent ion trajectories and compute the florescence signal. We then determine the line center by fitting a Lorentzian to these data. This operational quantification of the line shift is adapted to a real data analysis. The result as a function of spectroscopy laser intensity is shown Fig. 5. It is interesting to note that this systematic error has a threshold behavior. With the above given laser parameters we estimate the saturation parameter to be less than 0.002 so that the line shift is less than 14 kHz. To compensate the Zeeman shift, we use Helmholtz coils to first cancel the residual magnetic fields at the trapping region. A small magnetic field is then applied along the spectroscopy laser beam to define a quantization axis. Microwave spectroscopy on the 3s 1/2(F = 3) → 3s 1/2(F = 2) transition reveals the applied magnetic field strength to be ~ 1.8 Gauss. The polarization of the cooling laser is set to be σ + using the 3s 1/2(F, m) = (3,3) → 3p 3/2(F,m) = (4,4) cycling transition (see Fig. 4). Frequency modulation sidebands are imposed on the cooling laser with an electro–optic modulator to prevent population trapping into the F = 2 ground state. Hence, during the cooling periods, the ions are prepared into 3s 1/2(F, m) = (3, 3) ground state35, 36. During the spectroscopy period, the 3s 1/2(F, m) = (3,3) → 3p 3/2(F,m) = (4,4) transition is then probed with the σ + polarized frequency comb. The Zeeman shift is equal in magnitude but opposite in sign for the (F,m) = (3,−3) → (F,m) = (4,−4) component driven (and cooled) with σ − polarization. We cancel the residual Zeeman shift by averaging the results for the two polarizations. A total of 48 line scans leaves us with a statistical uncertainty of 0.45 MHz. Imperfect circular polarization contributes 0.3 MHz to the uncertainty, determined by performing measurements with intentionally misaligned polarization. The ac-Stark shift of the ground and 3p 3/2 states induced by off-resonant comb-modes is estimated to be less than 7 kHz. The comb spectrum also covers the 3p 3/2 → 3d 5/2 transition and therefore gives rise to an ac-Stark shift of the 3p 3/2 state. In addition, the fluorescence from the 3d 5/2 states may distort the line-shape of the 3s 1/2 → 3p 3/2 spectroscopy signal. We used the appropriate three-level optical Bloch equations to model these effects and found them to contribute with less than 0.1 MHz. Considering all of these effects, the total uncertainty is estimated to 0.7 MHz. Other systematic shifts like the dc-Stark shift from the trapping fields and 2nd order Doppler shift are negligible. We obtain 1072085233.5(0.7) MHz for the 3s 1/2(F = 3)→3p 3/2(F = 4) transition. This is the smallest reported uncertainty on this transition, showcasing the ability of the frequency comb to perform precision spectroscopy31, 37. Using the hyperfine constants from the literature38, 39, the centroid frequency of the 25Mg+ D2 line is found to be 1072084553.3(0.7) MHz, where we assume that the hyperfine constants39 are as accurate as the number of digits shown. It should be noted that Table 239 gives the magnitude of A and B factors only such that the sign of the A factors has to be flipped (C. Sur, personal communication). This value is in good agreement with a recent measurement that uses the new method of quantum decoherence spectroscopy37. The uncertainty of the latter measurement is not intrinsic in the method, but was limited by the wavelength measurement. Our value also compares well with a previous determination from the 24Mg+ D2 transition frequency using a theoretical value for the isotope shift31. Table 1 summarizes our result in comparison with previous determinations of this transition.
In summary, DFCS using an individual mode and individual ions is demonstrated with the 3s 1/2−3p 3/2 transition of 25Mg+. Spatially resolved detection suppresses the contribution of the scattering background and enhances the contrast of the fluorescence signal by more than two orders of magnitude. The obtained transition frequency is confirmed to be consistent with conventional measurements using cw lasers. The method is simple and versatile and can be applied to a wide range of transitions and significantly shorter wavelengths. It does not require a special level structure that would be required for other sensitive detection methods such as shelving and quantum decoherence detection.
The data that support the findings of this study are available from the corresponding author upon reasonable request.
Parthey, C. G. et al. Improved measurement of the hydrogen 1S-2S transition frequency. Phys. Rev. Lett. 107, 203001 (2011).
Matveev, A. et al. Precision measurement of the hydrogen 1S-2S frequency via a 920-km fiber link. Phys. Rev. Lett. 110, 230801 (2013).
Ludlow, A. D. et al. Optical atomic clocks. Rev. Mod. Phys. 87, 637 (2015).
Wilken, T. et al. A spectrograph for exoplanet observations calibrated at the centimetre-per-second level. Nature 485, 611–614 (2012).
Fortier, T. et al. Generation of ultrastable microwaves via optical frequency division. Nat. Photnics 5, 425–429 (2011).
Bernhardt, B. et al. Cavity-enhanced dual-comb spectroscopy. Nat. Photonics 4, 55–57 (2010).
Jones, D. J. et al. Carrier-envelope phase control of femtosecond mode-locked lasers and direct optical frequency synthesis. Science 288, 635–639 (2000).
Corkum, P. B. & Krausz, F. Attosecond science. Nat. Phys. 3, 381–387 (2007).
Dai, S.-B. et al. 2.14 mW deep-ultraviolet laser at 165 nm by eighth-harmonic generation of a 1319 nm Nd:YAG laser in KBBF. Laser Phys. Lett. 13, 035401 (2016).
Nomura, Y. et al. Coherent quasi-cw 153 nm light source at 33 MHz repetition rate. Opt. Lett. 36, 1758–1760 (2011).
Popmintchev, T. et al. Bright coherent ultrahigh harmonics in the keV X-ray regime from mid-infrared Femtosecond lasers. Science 336, 1287–1291 (2012).
Pupeza, I. et al. Compact high-repetition-rate source of coherent 100 eV radiation. Nat. Photonics 7, 608–612 (2013).
Benko, C. et al. Extreme ultraviolet radiation with coherence time greater than 1 s. Nat. Photonics 8, 530–536 (2014).
Th. Udem, R., Holzwarth & Hänsch, T. W. Optical frequency metrology. Nature 416, 233–237 (2002).
Gerginov, V., Tanner, C. E., Diddams, S. A., Bartels, A. & Hollberg, L. High-resolution spectroscopy with a femtosecond laser frequency comb. Opt. Lett. 30, 1734–1736 (2005).
Snadden, M. J., Bell, A. S., Riis, E. & Ferguson, A. I. Two-photon spectroscopy of laser-cooled Rb using a mode-locked laser. Opt. Commun. 125, 70–76 (1996).
Fendel, P., Bergeson, S. D., Udem, Th & Hänsch, T. W. Two-photon frequency comb spectroscopy of the 6s-8s transition in cesium. Opt. Lett. 32, 701–703 (2007).
Eckstein, J. N., Ferguson, A. I. & Hänsch, T. W. High-resolution two-photon spectroscopy with picosecond light pulses. Phys. Rev. Lett. 40, 847 (1978).
Ye. V., Baklanov & Chebotayev, V. P. Narrow resonances of two-photon absorption of super-narrow pulses in a gas. Appl. Phys. B 12, 97 (1977).
Reinhardt, S., Peters, E., Hänsch, T. W. & Udem, Th. Two-photon direct frequency comb spectroscopy with chirped pulses. Phys. Rev. A 81, 033427 (2010).
Ozawa, A. & Kobayashi, Y. Chirped-pulse direct frequency-comb spectroscopy of two-photon transitions. Phys. Rev. A 86, 022514 (2012).
Yost, D. C. et al. Spectroscopy of the hydrogen 1S-3S transition with chirped laser pulses. Phys. Rev. A 93, 042509 (2016).
Fortier, T. M. et al. Kilohertz-resolution spectroscopy of cold atoms with an optical frequency comb. Phys. Rev. Lett. 97, 163905 (2006).
Wolf, A. L., van den Berg, S. A., Ubachs, W. & Eikema, K. S. E. Direct frequency comb spectroscopy of trapped ions. Phys. Rev. Lett. 102, 223901 (2009).
Davila-Rodriguez, J., Ozawa, A., Hänsch, T. W. & Udem, T. Doppler cooling trapped ions with a UV frequency comb. Phys. Rev. Lett. 116, 043002 (2016).
Herrmann, M., Batteiger, V., Knünz, S., Saathoff, G., Udem, Th & Hänsch, T. W. Frequency Metrology on single trapped ions in the weak binding limit: the 3 s1/2-3 s3/2 transition in 24Mg+. Phys. Rev. Lett. 102, 013006 (2009).
Zinkstok, R. T. et al. Frequency comb laser spectroscopy in the vacuum-ultraviolet region. Phys. Rev. A. 73, 061801 (2006).
Cingöz, A. et al. Direct frequency comb spectroscopy in the extreme ultraviolet. Nature 482, 68–71 (2012).
Ozawa, A. & Kobayashi, Y. vuv frequency-comb spectroscopy of atomic xenon. Phys. Rev. A 87, 022507 (2013).
Nagourney, W., Sandberg, J. & Dehmelt, H. Shelved optical electron amplifier: observation of quantum jumps. Phys. Rev. Lett. 56, 2797 (1986).
Batteiger, V. et al. Precision spectroscopy of the 3s-3p fine-structure doublet in Mg+. Phys. Rev. A 80, 022503 (2009).
Schmoeger, L. et al. Coulomb crystallization of highly charged ions. Science 347, 1233–1236 (2015).
Gardner, A., Sheridan, K., Groom, W., Seymour-Smith, N. & Keller, M. Precision spectroscopy technique for dipole-allowed transitions in laser-cooled ions. Appl. Phys. B 117, 755 (2014).
Horbatsch, M. & Hessels, E. A. Shifts from a distant neighboring resonance. Phys. Rev. A 82, 052519 (2010).
Hemmerling, B. et al. A single laser system for ground-state cooling of 25Mg+. Appl. Phys. B 104, 583 (2011).
Deslauriers, L. et al. Zero-point cooling and low heating of trapped 111Cd+ ions. Phys. Rev. A 70, 043408 (2004).
Clos, G., Enderlein, M., Warring, U. & Schaetz, T. Decoherence-assisted spectroscopy of a single Mg+ Ion. Phys. Rev. Lett. 112, 113003 (2014).
Itano, W. M. & Wineland, D. J. Precision measurement of the ground-state hyperfine constant of 25Mg+. Phys. Rev. A 24, 1364 (1981).
Sur, C., Sahoo, B. K., Chaudhuri, R. K., Das, B. & Mukherjee, D. Comparative studies of the magnetic dipole and electric quadrupole hyperfine constants for the ground and low lying excited states of 25Mg+. Eur. Phys. J. D 32, 25 (2005).
Ansbacher, W., Li, Y. & Pinnington, E. H. Precision lifetime measurement for the 3p levels of Mg II using frequency-doubled laser radiation to excite a fast ion beam. Phys. Lett. A 139, 165 (1989).
T.W.H. acknowledges support from the Max Planck Foundation. H.A.S and J.R.B. were supported by the Robert A. Welch Foundation, grant No. A 1546.
The authors declare no competing financial interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Ozawa, A., Davila-Rodriguez, J., Bounds, J.R. et al. Single ion fluorescence excited with a single mode of an UV frequency comb. Nat Commun 8, 44 (2017). https://doi.org/10.1038/s41467-017-00067-9
A Perspective on New Opportunities in Atom-by-Atom Synthesis of Heterogeneous Catalysts Using Atomic Layer Deposition
Catalysis Letters (2021)
Nature Photonics (2019)
Ultrastable Laser System for Spectroscopy of the 1.14 μm Inner-Shell Clock Transition in Tm and Its Absolute Frequency Measurement
Journal of Russian Laser Research (2019)
Scientific Reports (2018)