arXiv subjects

Jun Ye

Publications and source records attributed to Jun Ye.

At least 253 records · Page 14Linked to original sources

arXiv2006

$^{87}$Sr lattice clock with inaccuracy below 10$^{-15}$

Aided by ultra-high resolution spectroscopy, the overall systematic uncertainty of the $^{1}S_{0}$-$^{3}P_{0}$ clock resonance for lattice-confined $^{87}$Sr has been characterized to $9\times10^{-16}$. This uncertainty is at a level similar to the Cs-fountain primary standard, while the potential stability for the lattice clocks exceeds that of Cs. The absolute frequency of the clock transition has been measured to be 429,228,004,229,874.0(1.1) Hz, where the $2.5\times10^{-15}$ fractional uncertainty represents the most accurate measurement of a neutral-atom-based optical transition frequency to date.

physics.atom-ph↗

arXiv2006

Photoassociation adiabatic passage of ultracold Rb atoms to form ultracold Rb_2 molecules

We theoretically explore photoassociation by Adiabatic Passage of two colliding cold ^{85}Rb atoms in an atomic trap to form an ultracold Rb_2 molecule. We consider the incoherent thermal nature of the scattering process in a trap and show that coherent manipulations of the atomic ensemble, such as adiabatic passage, are feasible if performed within the coherence time window dictated by the temperature, which is relatively long for cold atoms. We show that a sequence of ~2*10^7 pulses of moderate intensities, each lasting ~750 ns, can photoassociate a large fraction of the atomic ensemble at temperature of 100 microkelvin and density of 10^{11} atoms/cm^3. Use of multiple pulse sequences makes it possible to populate the ground vibrational state. Employing spontaneous decay from a selected excited state, one can accumulate the molecules in a narrow distribution of vibrational states in the ground electronic potential. Alternatively, by removing the created molecules from the beam path between pulse sets, one can create a low-density ensemble of molecules in their ground ro-vibrational state.

quant-ph↗

arXiv2006

Optical atomic coherence at the one-second time scale

Highest resolution laser spectroscopy has generally been limited to single trapped ion systems due to rapid decoherence which plagues neutral atom ensembles. Here, precision spectroscopy of ultracold neutral atoms confined in a trapping potential shows superior optical coherence without any deleterious effects from motional degrees of freedom, revealing optical resonance linewidths at the hertz level with an excellent signal to noise ratio. The resonance quality factor of 2.4 x 10^{14} is the highest ever recovered in any form of coherent spectroscopy. The spectral resolution permits direct observation of the breaking of nuclear spin degeneracy for the 1S0 and 3P0 optical clock states of 87Sr under a small magnetic bias field. This optical NMR-like approach allows an accurate measurement of the differential Lande g-factor between the two states. The optical atomic coherence demonstrated for collective excitation of a large number of atoms will have a strong impact on quantum measurement and precision frequency metrology.

physics.atom-ph↗

arXiv2006

Precise Control of Molecular Dynamics with a Femtosecond Frequency Comb - A Weak Field Route to Strong Field Coherent Control

We present a general and highly efficient scheme for performing narrow-band Raman transitions between molecular vibrational levels using a coherent train of weak pump-dump pairs of shaped ultrashort pulses. The use of weak pulses permits an analytic description within the framework of coherent control in the perturbative regime, while coherent accumulation of many pulse pairs enables near unity transfer efficiency with a high spectral selectivity, thus forming a powerful combination of pump-dump control schemes and the precision of the frequency comb. The concept is presented analytically and its feasibility and robustness are verified by simulations of dynamics in Rb$_2$. We consider application of this concept to the formation of stable, deeply bound, ultracold molecules.

quant-ph↗

arXiv2006

OH hyperfine ground state: from precision measurement to molecular qubits

We perform precision microwave spectroscopy--aided by Stark deceleration--to reveal the low magnetic field behavior of OH in its ^2Π_{3/2} ro-vibronic ground state, identifying two field-insensitive hyperfine transitions suitable as qubits and determining a differential Lande g-factor of 1.267(5)\times10^{-3} between opposite parity components of the Λ-doublet. The data are successfully modeled with an effective hyperfine Zeeman Hamiltonian, which we use to make a tenfold improvement of the magnetically sensitive, astrophysically important ΔF=\pm1 satellite-line frequencies, yielding 1720529887(10) Hz and 1612230825(15) Hz.

physics.atom-ph↗

arXiv2006

Tapered semiconductor amplifiers for optical frequency combs in the near infrared

A tapered semiconductor amplifier is injection seeded by a femtosecond optical frequency comb at 780 nm from a mode-locked Ti:sapphire laser. Energy gains over 17 dB (12 dB) are obtained for 1 mW (20 mW) of average input power when the input pulses are stretched into the picosecond range. A spectral window of supercontinuum light generated in a photonic fiber has also been amplified. Interferometric measurements show sub-hertz linewidths for a heterodyne beat between the input and amplified comb components, yielding no detectable phase-noise degradation under amplification. These amplifiers can be used to boost the infrared power in f-to-2f interferometers used to determine the carrier-to-envelope offset frequency, with clear advantages for stabilization of octave-spanning femtosecond lasers and other supercontinuum light sources with very limited power in the infrared.

physics.optics↗

arXiv2006

High resolution atomic coherent control via spectral phase manipulation of an optical frequency comb

We demonstrate high resolution coherent control of cold atomic Rubidium utilizing spectral phase manipulation of a femtosecond optical frequency comb. Transient coherent accumulation is directly manifested by the enhancement of signal amplitude and spectral resolution via the pulse number. The combination of frequency comb technology and spectral phase manipulation enables coherent control techniques to enter a new regime with natural linewidth resolutions.

physics.atom-ph↗

arXiv2006

Cold Molecule Spectroscopy for Constraining the Evolution of the Fine Structure Constant

We report precise measurements of ground-state, $λ$-doublet microwave transitions in the hydroxyl radical molecule (OH). Utilizing slow, cold molecules produced by a Stark decelerator we have improved over the precision of the previous best measurement by twenty-five-fold for the F' = 2 $\to$ F = 2 transition, yielding (1 667 358 996 $\pm$ 4) Hz, and by ten-fold for the F' = 1 $\to$ F = 1 transition, yielding (1 665 401 803 $\pm$ 12) Hz. Comparing these laboratory frequencies to those from OH megamasers in interstellar space will allow a sensitivity of 1 ppm for $Δα/α$ over $\sim$$10^{10}$ years.

physics.atom-ph↗

arXiv2005

Production of cold formaldehyde molecules for study and control of chemical reaction dynamics with hydroxyl radicals

We propose a method for controlling a class of low temperature chemical reactions. Specifically, we show the hydrogen abstraction channel in the reaction of formaldehyde (H$_{2}$CO) and the hydroxyl radical (OH) can be controlled through either the molecular state or an external electric field. We also outline experiments for investigating and demonstrating control over this important reaction. To this end, we report the first Stark deceleration of the H$_{2}$CO molecule. We have decelerated a molecular beam of H$_{2}$CO essentially to rest, producing cold molecule packets at a temperature of 100 mK with a few million molecules in the packet at a density of $\sim10^{6}$ cm$^{-3}$.

physics.atom-ph↗

arXiv2005

Systematic study of the $^{87}$Sr clock transition in an optical lattice

With ultracold $^{87}$Sr confined in a magic wavelength optical lattice, we present the most precise study (2.8 Hz statistical uncertainty) to-date of the $^1S_0$ - $^3P_0$ optical clock transition with a detailed analysis of systematic shifts (20 Hz uncertainty) in the absolute frequency measurement of 429 228 004 229 867 Hz. The high resolution permits an investigation of the optical lattice motional sideband structure. The local oscillator for this optical atomic clock is a stable diode laser with its Hz-level linewidth characterized across the optical spectrum using a femtosecond frequency comb.

physics.atom-ph↗

arXiv2005

Direct frequency comb measurements of absolute optical frequencies and population transfer dynamics

A phase-stabilized femtosecond laser comb is directly used for high-resolution spectroscopy and absolute optical frequency measurements of one- and two-photon transitions in laser-cooled \rb atoms. Absolute atomic transition frequencies, such as the 5S$_{1/2}$ F=2 \ra 7S$_{1/2}$ F"=2 two-photon resonance measured at 788 794 768 921(44) kHz, are determined without \textit{a priori} knowledge about their values. Detailed dynamics of population transfer driven by a sequence of pulses are uncovered and taken into account for the measurement of the 5P states via resonantly enhanced two-photon transitions.

physics.atom-ph↗

arXiv2005

Precision spectroscopy and density-dependent frequency shifts in ultracold Sr

By varying the density of an ultracold $^{88}$Sr sample from $10^9$ cm$^{-3}$ to $> 10^{12}$ cm$^{-3}$, we make the first definitive measurement of the density-related frequency shift and linewidth broadening of the $^1S_0$ - $^3P_1$ optical clock transition in an alkaline earth system. In addition, we report the most accurate measurement to date of the $^{88}$Sr $^1S_0 - ^3P_1$ optical clock transition frequency. Including a detailed analysis of systematic errors, the frequency is ($434 829 121 312 334 \pm 20_{stat} \pm 33_{sys}$) Hz.

physics.atom-ph↗

arXiv2004

A high-accuracy optical clock via three-level coherence in neutral bosonic $^{88}$Sr

An optical atomic clock scheme is developed that utilizes two lasers to establish coherent coupling between the $5s^2 \phantom{}^1S_0$ ground state of $^{88}$Sr and the first excited state, $5s5p \phantom{}^3P_0$. The coupling is mediated by the broad $5s5p \phantom{}^1P_1$ state, exploiting the phenomenon of electromagnetically induced transparency. The effective linewidth of the clock transition can be chosen at will by adjusting the laser intensity. By trapping the $^{88}$Sr atoms in an optical lattice, long interaction times with the two lasers are ensured; Doppler and recoil effects are eliminated. Based on a careful analysis of systematic errors, a clock accuracy of better than $2\times 10^{-17}$ is expected.

physics.atom-ph↗

arXiv2004

Narrow Line Cooling: Finite Photon Recoil Dynamics

We present an extensive study of the unique thermal and mechanical dynamics for narrow-line cooling on the 1S0 - 3P1 88Sr transition. For negative detuning, trap dynamics reveal a transition from the semiclassical regime to the photon-recoil-dominated quantum regime, yielding an absolute minima in the equilibrium temperature below the single-photon recoil limit. For positive detuning, the cloud divides into discrete momentum packets whose alignment mimics lattice points on a face-centered-cubic crystal. This novel behavior arises from velocity selection and "positive feedback" acceleration due to a finite number of photon recoils. Cooling is achieved with blue-detuned light around a velocity where gravity balances the radiative force.

physics.atom-ph↗

arXiv2004

Narrow Line Cooling and Momentum-Space Crystals

Narrow line laser cooling is advancing the frontier for experiments ranging from studies of fundamental atomic physics to high precision optical frequency standards. In this paper, we present an extensive description of the systems and techniques necessary to realize 689 nm 1S0 - 3P1 narrow line cooling of atomic 88Sr. Narrow line cooling and trapping dynamics are also studied in detail. By controlling the relative size of the power broadened transition linewidth and the single-photon recoil frequency shift, we show that it is possible to continuously bridge the gap between semiclassical and quantum mechanical cooling. Novel semiclassical cooling process, some of which are intimately linked to gravity, are also explored. Moreover, for laser frequencies tuned above the atomic resonance, we demonstrate momentum-space crystals containing up to 26 well defined lattice points. Gravitationally assisted cooling is also achieved with blue-detuned light. Theoretically, we find the blue detuned dynamics are universal to Doppler limited systems. This paper offers the most comprehensive study of narrow line laser cooling to date.

physics.atom-ph↗

arXiv2004

Efficient Stark deceleration of cold polar molecules

Stark deceleration has been utilized for slowing and trapping several species of neutral, ground-state polar molecules generated in a supersonic beam expansion. Due to the finite physical dimension of the electrode array and practical limitations of the applicable electric fields, only molecules within a specific range of velocities and positions can be efficiently slowed and trapped. These constraints result in a restricted phase space acceptance of the decelerator in directions both transverse and parallel to the molecular beam axis; hence, careful modeling is required for understanding and achieving efficient Stark decelerator operation. We present work on slowing of the hydroxyl radical (OH) elucidating the physics controlling the evolution of the molecular phase space packets both with experimental results and model calculations. From these results we deduce experimental conditions necessary for efficient operation of a Stark decelerator.

physics.atom-ph↗

arXiv2004

A pulsed, low-temperature beam of supersonically cooled free radical OH molecules

An improved system for creating a pulsed, low-temperature molecular beam of OH radicals has been developed. We use a pulsed discharge to create OH from H$_2$O seeded in Xe during a supersonic expansion, where the high-voltage pulse duration is significantly shorter than the width of the gas pulse. The pulsed discharge allows for control of the mean speed of the molecular packet as well as maintains a low temperature supersonic expansion. A hot filament is placed in the source chamber to initiate the discharge for shorter durations and at lower voltages, resulting in a translationally and rotationally colder packet of OH molecules.

physics.atom-ph↗

arXiv2004

Cold free radical molecules in the laboratory frame

A special class of molecules that are important to many subfields in molecular dynamics and chemical physics, namely free radical molecules, now enjoy a significant degree of center-of-mass motion control in the laboratory frame. The example reported in this paper concerns hydroxyl radical (OH), which, after the internal degrees of freedom are cooled in a supersonic expansion, has been bunched, accelerated, and slowed using time-varying inhomogeneous electric fields. In situ observations of laser-induced fluorescence along the beam propagation path allows for detailed characterization of the longitudinal phase-space manipulation of OH molecules by the electric fields. The creation of a pulse containing 1e3 to 1e6 molecules possessing a longitudinal velocity spread from 2 to 80 m/s around a mean laboratory velocity variable from 550 m/s to rest with only a few mm spatial extent represents an exciting and useful new experimental capability for exploring free radical dynamics. This paper offers the most detailed study of the Stark deceleration dynamics to date.

physics.atom-ph↗