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We demonstrate Doppler cooling of trapped magnesium ions using a frequency comb at 280 nm obtained from a frequency tripled Ti:sapphire laser. A comb line cools on the 3s_{1/2}-3p_{3/2} transition, while the nearest blue-detuned comb line contributes negligible heating. We observe the cooling-heating transition and long-term cooling of ion chains with several sympathetically cooled ions. Spatial thermometry shows that the ion is cooled to near the Doppler limit. Doppler cooling with frequency combs has the potential to open many additional atomic species to laser cooling by reaching further into the vacuum and extreme ultraviolet via high-harmonic generation and by providing a broad bandwidth from which multiple excitation sidebands can be obtained.

To compare the increasing number of optical frequency standards, highly stable optical signals have to be transferred over continental distances. We demonstrate optical-frequency transfer over a 1840-km underground optical fiber link using a single-span stabilization. The low inherent noise introduced by the fiber allows us to reach short term instabilities expressed as the modified Allan deviation of 2×10(-15) for a gate time τ of 1 s reaching 4×10(-19) in just 100 s. We find no systematic offset between the sent and transferred frequencies within the statistical uncertainty of about 3×10(-19). The spectral noise distribution of our fiber link at low Fourier frequencies leads to a τ(-2) slope in the modified Allan deviation, which is also derived theoretically.

We have measured the frequency of the extremely narrow 1S-2S two-photon transition in atomic hydrogen using a remote cesium fountain clock with the help of a 920 km stabilized optical fiber. With an improved detection method we obtain f(1S-2S)=2466 061 413 187 018 (11)  Hz with a relative uncertainty of 4.5×10(-15), confirming our previous measurement obtained with a local cesium clock [C. G. Parthey et al., Phys. Rev. Lett. 107, 203001 (2011)]. Combining these results with older measurements, we constrain the linear combinations of Lorentz boost symmetry violation parameters c((TX))=(3.1±1.9)×10(-11) and 0.92c((TY))+0.40c((TZ))=(2.6±5.3)×10(-11) in the standard model extension framework [D. Colladay, V. A. Kostelecký, Phys. Rev. D. 58, 116002 (1998)].

We have measured the 1S-2S transition frequency in atomic hydrogen via two-photon spectroscopy on a 5.8 K atomic beam. We obtain f(1S-2S) = 2,466,061,413,187,035 (10)  Hz for the hyperfine centroid, in agreement with, but 3.3 times better than the previous result [M. Fischer et al., Phys. Rev. Lett. 92, 230802 (2004)]. The improvement to a fractional frequency uncertainty of 4.2 × 10(-15) arises mainly from an improved stability of the spectroscopy laser, and a better determination of the main systematic uncertainties, namely, the second order Doppler and ac and dc Stark shifts. The probe laser frequency was phase coherently linked to the mobile cesium fountain clock FOM via a frequency comb.

We report on injection locking of optically excited mechanical oscillations of a single, trapped ion. The injection locking dynamics are studied by analyzing the oscillator spectrum with a spatially selective Fourier transform technique and the oscillator phase with stroboscopic imaging. In both cases we find excellent agreement with theory inside and outside the locking range. We attain injection locking with forces as low as 5(1)×10{-24}  N so this system appears promising for the detection of ultraweak oscillating forces.

Measuring the hydrogen-deuterium isotope shift via two-photon spectroscopy of the 1S-2S transition, we obtain 670,994,334,606(15) Hz. This is a 10-times improvement over the previous best measurement [A. Huber, Phys. Rev. Lett. 80, 468 (1998)] confirming its frequency value. A calculation of the difference of the mean square charge radii of deuterium and hydrogen results in d - p =3.82007(65)  fm2, a more than twofold improvement compared to the former value.

We demonstrate a method for precision spectroscopy on trapped ions in the limit of unresolved motional sidebands. By sympathetic cooling of a chain of crystallized ions, we suppress adverse temperature variations induced by the spectroscopy laser that usually lead to a distorted line profile and obtain a Voigt profile with negligible distortions. We applied the method to measure the absolute frequency of the astrophysically relevant D2 transition in single 24Mg+ ions and find 1 072 082 934.33(16) MHz, a nearly 400-fold improvement over previous results. Further, we find the excited state lifetime to be 3.84(10) ns.

We generated a series of harmonics in a xenon gas jet inside a cavity seeded by pulses from a Ti:sapphire mode-locked laser with a repetition rate of 10.8 MHz. Harmonics up to 19th order at 43 nm were observed with plateau harmonics at the microW power level. An elaborate dispersion compensation scheme and the use of a moderate repetition rate allowed for this significant improvement in output power of the plateau harmonics of 4 orders of magnitude over previous results. With this power level and repetition rate, high-resolution spectroscopy in the extreme ultraviolet region becomes conceivable. An interesting target would be the 1S-2S transition in hydrogenlike He+ at 60 nm.

A femtosecond frequency comb provides a vast number of equidistantly spaced narrow band laser modes that can be simultaneously tuned and frequency calibrated with 15 digit accuracy. Our Vernier spectrometer utilizes all of theses modes in a massively parallel manner to rapidly record both absorption and dispersion spectra with a sensitivity that is provided by a high finesse broadband optical resonator and a resolution that is only limited by the frequency comb line width while keeping the required setup simple.

We have remeasured the absolute 1S-2S transition frequency nu(H) in atomic hydrogen. A comparison with the result of the previous measurement performed in 1999 sets a limit of (-29+/-57) Hz for the drift of nu(H) with respect to the ground state hyperfine splitting nu(Cs) in 133Cs. Combining this result with the recently published optical transition frequency in 199Hg+ against nu(Cs) and a microwave 87Rb and 133Cs clock comparison, we deduce separate limits on alpha/alpha=(-0.9+/-2.9) x 10(-15) yr(-1) and the fractional time variation of the ratio of Rb and Cs nuclear magnetic moments mu(Rb)/mu(Cs) equal to (-0.5+/-1.7) x 10(-15) yr(-1). The latter provides information on the temporal behavior of the constant of strong interaction.

We demonstrate that multiphoton-induced photoelectron emission from a gold surface caused by low-energy (unamplified) 4-fs, 750-nm laser pulses is sensitive to the timing of electric field oscillations with respect to the pulse peak. This observation confirms recent theoretical predictions and opens the door to measuring the absolute value of the carrier-envelope phase difference of few-cycle light pulses with a solid-state detector.

The frequency comb created by a femtosecond mode-locked laser and a microstructured fiber is used to phase coherently measure the frequencies of both the Hg+ and Ca optical standards with respect to the SI second. We find the transition frequencies to be f(Hg) = 1 064 721 609 899 143(10) Hz and f(Ca) = 455 986 240 494 158(26) Hz, respectively. In addition to the unprecedented precision demonstrated here, this work is the precursor to all-optical atomic clocks based on the Hg+ and Ca standards. Furthermore, when combined with previous measurements, we find no time variations of these atomic frequencies within the uncertainties of the absolute value of( partial differential f(Ca)/ partial differential t)/f(Ca) < or =8 x 10(-14) yr(-1) and the absolute value of(partial differential f(Hg)/ partial differential t)/f(Hg) < or =30 x 10(-14) yr(-1).

We have used the frequency comb generated by a femtosecond mode-locked laser and broadened to more than an optical octave in a photonic crystal fiber to realize a frequency chain that links a 10 MHz radio frequency reference phase-coherently in one step to the optical region. By comparison with a similar frequency chain we set an upper limit for the uncertainty of this new approach to 5. 1x10(-16). This opens the door for measurement and synthesis of virtually any optical frequency and is ready to revolutionize frequency metrology.

Using a coherent nonlinear optical technique, slipping of the carrier through the envelope of 6-fs light wave packets emitted from a mode-locked-oscillator/pulse-compressor system has been measured, permitting the generation of intense, few-cycle light with precisely reproducible electric and magnetic fields. These pulses open the way to controlling the evolution of strong-field interactions on the time scale of the light oscillation cycle and are indispensable to reproducible attosecond x-ray pulse generation.

We report on an absolute frequency measurement of the hydrogen 1S-2S two-photon transition in a cold atomic beam with an accuracy of 1.8 parts in 10(14). Our experimental result of 2 466 061 413 187 103(46) Hz has been obtained by phase coherent comparison of the hydrogen transition frequency with an atomic cesium fountain clock. Both frequencies are linked with a comb of laser frequencies emitted by a mode locked laser.

We demonstrate a great simplification in the long-standing problem of measuring optical frequencies in terms of the cesium primary standard. An air-silica microstructure optical fiber broadens the frequency comb of a femtosecond laser to span the optical octave from 1064 to 532 nm, enabling us to measure the 282 THz frequency of an iodine-stabilized Nd:YAG laser directly in terms of the microwave frequency that controls the comb spacing. Additional measurements of established optical frequencies at 633 and 778 nm using the same femtosecond comb confirm the accepted uncertainties for these standards.

We demonstrate a versatile new technique that provides a phase coherent link between optical frequencies and the radio frequency domain. The regularly spaced comb of modes of a mode-locked femtosecond laser is used as a precise ruler to measure a large frequency gap between two different multiples (harmonics or subharmonics) of a laser frequency. In this way, we have determined a new value of the hydrogen 1S-2S two-photon resonance, f(1S-2S) = 2 466 061 413 187.29(37) kHz, representing now the most accurate measurement of an optical frequency.