William C. Swann

Frequency Ratio of Al+ and Hg+ Single-Ion Optical Clocks; Metrology at the 17th Decimal Place

Time has always had a special status in physics because of its fundamental role in specifying the regularities of nature and because of the extraordinary precision with which it can be measured. This precision enables tests of fundamental physics and cosmology, as well as practical applications such as satellite navigation. Recently, a regime of operation for atomic clocks based on optical transitions has become possible, promising even higher performance. We report the frequency ratio of two optical atomic clocks with a fractional uncertainty of 5.2 × 10–17. The ratio of aluminum and mercury single-ion optical clock frequencies νAl+/νHg+ is 1.052871833148990438(55), where the uncertainty comprises a statistical measurement uncertainty of 4.3 × 10–17, and systematic uncertainties of 1.9 × 10–17 and 2.3 × 10–17 in the mercury and aluminum frequency standards, respectively. Repeated measurements during the past year yield a preliminary constraint on the temporal variation of the fine-structure constant α of \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \({\dot{{\alpha}}}{/}{\alpha}=(-1.6{\pm}2.3){\times}10^{-17}{/}\mathrm{year}\) \end{document}.

Coherent multiheterodyne spectroscopy using stabilized optical frequency combs.

The broadband, coherent nature of narrow-linewidth fiber frequency combs is exploited to measure the full complex spectrum of a molecular gas through multiheterodyne spectroscopy. We measure the absorption and phase shift experienced by each of 155 000 individual frequency-comb lines, spaced by 100 MHz and spanning from 1495 to 1620 nm, after passing through hydrogen cyanide gas. The measured phase spectrum agrees with the Kramers-Kronig transformation of the absorption spectrum. This technique can provide a full complex spectrum rapidly, over wide bandwidths, and with hertz-level accuracy.

Dual-comb spectroscopy

Dual-comb spectroscopy is an emerging new spectroscopic tool that exploits the frequency resolution, frequency accuracy, broad bandwidth, and brightness of frequency combs for ultrahigh-resolution, high-sensitivity broadband spectroscopy. By using two coherent frequency combs, dual-comb spectroscopy allows a sample’s spectral response to be measured on a comb tooth-by-tooth basis rapidly and without the size constraints or instrument response limitations of conventional spectrometers. This review describes dual-comb spectroscopy and summarizes the current state of the art. As frequency comb technology progresses, dual-comb spectroscopy will continue to mature and could surpass conventional broadband spectroscopy for a wide range of laboratory and field applications.

Coherent transfer of an optical carrier over 251 km

We transfer an optical frequency over 251 km of optical fiber with a residual instability of 6x10(-19) at 100 s. This instability and the associated timing jitter are limited fundamentally by the noise on the optical fiber and the link length. We give a simple expression for calculating the achievable instability and jitter over a fiber link. Transfer of optical stability over this long distance requires a highly coherent optical source, provided here by a cw fiber laser locked to a high finesse optical cavity. A sufficient optical carrier signal is delivered to the remote fiber end by incorporating two-way, in-line erbium-doped fiber amplifiers to balance the 62 dB link loss.

Spectroscopy of the Methane {\nu}3 Band with an Accurate Mid-Infrared Coherent Dual- Comb Spectrometer

We demonstrate a high-accuracy dual-comb spectrometer centered at 3.4 {mu}m. The amplitude and phase spectra of the P, Q, and partial R branches of the methane {nu}{sub 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{sup -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.

Fiber-laser frequency combs with subhertz relative linewidths

We investigate the comb linewidths of self-referenced, fiber-laser-based frequency combs by measuring the heterodyne beat signal between two independent frequency combs that are phase locked to a common cw optical reference. We demonstrate that the optical comb lines can exhibit instrument-limited, subhertz relative linewidths across the comb spectra from 1200 to 1720 nm with a residual integrated optical phase jitter of approximately 1 rad in a 60 mHz to 500 kHz bandwidth. The projected relative pulse timing jitter is approximately 1 fs. This performance approaches that of Ti:sapphire frequency combs.

Optical two-way time and frequency transfer over free space

Using two-way exchange between coherent frequency combs, each phase-locked to the local optical oscillator, optical time–frequency transfer is demonstrated in free space across a 2-km-long link, with a timing deviation of 1 fs, a residual instability below 10−18 at 1,000 s and systematic offsets below 4 × 10−19.

Sensitivity of coherent dual-comb spectroscopy.

Coherent dual comb spectroscopy can provide high-resolution, high-accuracy measurements of a sample response in both magnitude and phase. We discuss the achievable signal-to-noise ratio (SNR) due to both additive white noise and multiplicative noise, and the corresponding sensitivity limit for trace gas detection. We show that sequential acquisition of the overall spectrum through a tunable filter, or parallel acquisition of the overall spectrum through a detector array, can significantly improve the SNR under some circumstances. We identify a useful figure of merit as the quality factor, equal to the product of the SNR, normalized by the square root of the acquisition time, and the number of resolved frequency elements. For a single detector and fiber-laser based system, this quality factor is 10(6) - 10(7) Hz(1/2).

Operation of an optically coherent frequency comb outside the metrology lab

We demonstrate a self-referenced fiber frequency comb that can operate outside the well-controlled optical laboratory. The frequency comb has residual optical linewidths of < 1 Hz, sub-radian residual optical phase noise, and residual pulse-to-pulse timing jitter of 2.4 - 5 fs, when locked to an optical reference. This fully phase-locked frequency comb has been successfully operated in a moving vehicle with 0.5 g peak accelerations and on a shaker table with a sustained 0.5 g rms integrated acceleration, while retaining its optical coherence and 5-fs-level timing jitter. This frequency comb should enable metrological measurements outside the laboratory with the precision and accuracy that are the hallmarks of comb-based systems.

Response dynamics of the frequency comb output from a femtosecond fiber laser

The frequency comb from a mode-locked fiber laser can be stabilized through feedback to the pump power. An understanding of the mechanisms and bandwidth governing this feedback is of practical importance for frequency comb design and of basic interest since it provides insight into the rich nonlinear laser dynamics. We compare experimental measurements of the response of a fiber-laser frequency comb to theory. The laser response to a pump-power change follows that of a simple low-pass filter with a time constant set by the gain relaxation time and the system-dependent nonlinear loss. Five different effects contribute to the magnitude of the response of the frequency comb spacing and offset frequency but the dominant effects are from the resonant contribution to the group velocity and intensity-dependent spectral shifts. The origins of the intensity-dependent spectral shifts are explained in terms of the laser parameters.