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John M. Doyle

Publications and source records attributed to John M. Doyle.

At least 73 records · Page 4Linked to original sources

$Λ$-Enhanced Imaging of Molecules in an Optical Trap

We report non-destructive imaging of optically trapped calcium monofluoride (CaF) molecules using in-situ $Λ$-enhanced gray molasses cooling. $200$ times more fluorescence is obtained compared to destructive on-resonance imaging, and the trapped molecules remain at a temperature of $20\,μ\text{K}$. The achieved number of scattered photons makes possible non-destructive single-shot detection of single molecules with high fidelity.

physics.atom-ph↗

Laser Cooling of Optically Trapped Molecules

Calcium monofluoride (CaF) molecules are loaded into an optical dipole trap (ODT) and subsequently laser cooled within the trap. Starting with magneto-optical trapping, we sub-Doppler cool CaF and then load $150(30)$ CaF molecules into an ODT. Enhanced loading by a factor of five is obtained when sub-Doppler cooling light and trapping light are on simultaneously. For trapped molecules, we directly observe efficient sub-Doppler cooling to a temperature of $60(5)$ $μ\text{K}$. The trapped molecular density of $8(2)\times10^7$ cm$^{-3}$ is an order of magnitude greater than in the initial sub-Doppler cooled sample. The trap lifetime of 750(40) ms is dominated by background gas collisions.

physics.atom-ph↗

Coherent Bichromatic Force Deflection of Molecules

We demonstrate the coherent optical bichromatic force on a molecule, the polar free radical strontium monohydroxide (SrOH). A dual-frequency retro-reflected laser beam addressing the $\tilde{X}^2Σ^+\leftrightarrow\tilde{A}^2Π_{1/2}$ electronic transition coherently imparts momentum onto a cryogenic beam of SrOH. This directional photon exchange creates a bichromatic force that transversely deflects the molecules. By adjusting the relative phase between the forward and counter propagating laser beams we reverse the direction of the applied force. A momentum transfer of $70\hbar k$ is achieved with minimal loss of molecules to dark states. Modeling of the bichromatic force is performed via direct numerical solution of the time-dependent density matrix and is compared with experimental observations. Our results open the door to further coherent manipulation of molecular motion, including the efficient optical deceleration of diatomic and polyatomic molecules with complex level structures.

physics.atom-ph↗

One dimensional magneto-optical compression of a cold CaF molecular beam

We demonstrate with a RF-MOT the one dimensional, transverse magneto-optical compression of a cold beam of calcium monofluoride (CaF). By continually alternating the magnetic field direction and laser polarizations of the magneto-optical trap, a photon scattering rate of $2π\times$0.4 MHz is achieved. A 3D model for this RF-MOT, validated by agreement with data, predicts a 3D RF-MOT capture velocity for CaF of 5 m/s.

physics.atom-ph↗

Methods, Analysis, and the Treatment of Systematic Errors for the Electron Electric Dipole Moment Search in Thorium Monoxide

We recently set a new limit on the electric dipole moment of the electron (eEDM) (J. Baron et al., ACME collaboration, Science 343 (2014), 269-272), which represented an order-of-magnitude improvement on the previous limit and placed more stringent constraints on many CP-violating extensions to the Standard Model. In this paper we discuss the measurement in detail. The experimental method and associated apparatus are described, together with the techniques used to isolate the eEDM signal. In particular, we detail the way experimental switches were used to suppress effects that can mimic the signal of interest. The methods used to search for systematic errors, and models explaining observed systematic errors, are also described. We briefly discuss possible improvements to the experiment.

physics.atom-ph↗

Sisyphus Laser Cooling of a Polyatomic Molecule

We perform magnetically-assisted Sisyphus laser cooling of the triatomic free radical strontium monohydroxide (SrOH). This is achieved with principal optical cycling in the rotationally closed $P\left(N"=1\right)$ branch of either the $\tilde{X}^{2}Σ^{+}\left(000\right)\leftrightarrow\tilde{A}^{2}Π_{1/2}\left(000\right)$ or the $\tilde{X}^{2}Σ^{+}\left(000\right)\leftrightarrow\tilde{B}^{2}Σ^{+}\left(000\right)$ vibronic transitions. Molecules lost into the excited vibrational states during the cooling process are repumped back through the $\tilde{B}\left(000\right)$ state for both the $\left(100\right)$ level of the Sr-O stretching mode and the $\left(02^{0}0\right)$ level of the bending mode. The transverse temperature of a SrOH molecular beam is reduced in one dimension by two orders of magnitude to $\sim700\ {\rm μK}$. This approach opens a path towards creating a variety of ultracold polyatomic molecules, including much larger ones, by means of direct laser cooling.

physics.atom-ph↗

Radiation Pressure Force from Optical Cycling on a Polyatomic Molecule

We demonstrate multiple photon cycling and radiative force deflection on the triatomic free radical strontium monohydroxide (SrOH). Optical cycling is achieved on SrOH in a cryogenic buffer-gas beam by employing the rotationally closed $P\left(N''=1\right)$ branch of the vibronic transition $\tilde{X}^{2}Σ^{+}\left(000\right)\leftrightarrow\tilde{A}^{2}Π_{1/2}\left(000\right)$. A single repumping laser excites the Sr-O stretching vibrational mode, and photon cycling of the molecule deflects the SrOH beam by an angle of $0.2^{\circ}$ via scattering of $\sim100$ photons per molecule. This approach can be used for direct laser cooling of SrOH and more complex, isoelectronic species.

physics.atom-ph↗

Laser slowing of CaF molecules to near the capture velocity of a molecular MOT

Laser slowing of CaF molecules down to the capture velocity of a magneto-optical trap (MOT) for molecules is achieved. Starting from a two-stage buffer gas beam source, we apply frequency-broadened "white-light" slowing and observe approximately 6x10^4 CaF molecules with velocities near 10\,m/s. CaF is a candidate for collisional studies in the mK regime. This work represents a significant step towards magneto-optical trapping of CaF.

physics.atom-ph↗

Continuous probe of cold complex molecules with infrared frequency comb spectroscopy

Cavity-enhanced frequency comb spectroscopy for molecule detection in the mid-infrared powerfully combines high resolution, high sensitivity, and broad spectral coverage. However, this technique, and essentially all spectroscopic methods, is limited in application to relatively small, simple molecules. Here we integrate comb spectroscopy with continuous, cold samples of molecules produced via buffer gas cooling, thus enabling the study of significantly more complex molecules. We report simultaneous gains in resolution, sensitivity, and bandwidth and demonstrate this combined capability with the first rotationally resolved direct absorption spectra in the CH stretch region of several complex molecules. These include nitromethane (CH$_3$NO$_2$), a model system that presents challenging questions to the understanding of large amplitude vibrational motion, as well as several large organic molecules with fundamental spectroscopic and astrochemical relevance, including naphthalene (C$_{10}$H$_8$), adamantane (C$_{10}$H$_{16}$), and hexamethylenetetramine (C$_{6}$N$_4$H$_{12}$). This general spectroscopic tool has the potential to significantly impact the field of molecular spectroscopy, simultaneously improving efficiency, spectral resolution, and specificity by orders of magnitude. This realization could open up new molecular species and new kinetics for precise investigations, including the study of complex molecules, weakly bound clusters, and cold chemistry.

physics.chem-ph↗

Direct Time-domain Observation of Conformational Relaxation in Gas-phase Cold Collisions

Cooling molecules in the gas phase is important for precision spectroscopy, cold molecule physics, and physical chemistry. Measurements of conformational relaxation cross sections shed important light on potential energy surfaces and energy flow within a molecule. However, gas-phase conformational cooling has not been previously observed directly. In this work, we directly observe conformational dynamics of 1,2-propanediol in cold (6K) collisions with atomic helium using microwave spectroscopy and buffer-gas cooling. Precise knowledge and control of the collisional environment in the buffer-gas allows us to measure the absolute collision cross-section for conformational relaxation. Several conformers of 1,2-propanediol are investigated and found to have relaxation cross-sections with He ranging from $σ=4.7(3.0)\times10^{-18}\:\mathrm{cm}^{2}$ to $σ>5\times10^{-16}\:\mathrm{cm}^{2}$. Our method is applicable to a broad class of molecules and could be used to provide information about the potential energy surfaces of previously uninvestigated molecules.

physics.chem-ph↗

Rotational state microwave mixing for laser cooling of complex diatomic molecules

We demonstrate the mixing of rotational states in the ground electronic state using microwave radiation to enhance optical cycling in the molecule yttrium (II) monoxide (YO). This mixing technique is used in conjunction with a frequency modulated and chirped continuous wave laser to slow longitudinally a cryogenic buffer gas beam of YO. We generate a measurable flux of YO below 10~m/s, directly loadable into a three-dimensional magneto-optical trap. This technique opens the door for laser cooling of molecules with more complex structure.

physics.atom-ph↗

Slow, Continuous Beams of Large Gas Phase Molecules

Cold, continuous, high flux beams of benzonitrile, fluorobenzine, and anisole have been created. Buffer-gas cooling with a cryogenic gas provides the cooling and slow forward beam velocities. The beam of benzonitrile was measured to have a forward velocity peaked at 67 $\pm 5$ m s$^{-1}$, and a continuous flux of $10^{15}$ molecules s$^{-1}$. These beams provide a continuous source for high resolution spectroscopy, and provide an attractive starting point for further spatial manipulation of such molecules, including eventual trapping.

physics.chem-ph↗

Buffer gas loaded magneto-optical traps for Yb, Tm, Er and Ho

Direct loading of lanthanide atoms into magneto-optical traps (MOTs) from a very slow cryogenic buffer gas beam source is achieved, without the need for laser slowing. The beam source has an average forward velocity of 60-70\,m/s and a velocity half-width of ~35 m/s, which allows for direct MOT loading of Yb, Tm, Er and Ho. Residual helium background gas originating from the beam results in a maximum trap lifetime of about 80 ms (with Yb). The addition of a single-frequency slowing laser applied to the Yb in the buffer gas beam increases the number of trapped Yb atoms to 1.3(0.7) x 10^8 with a loading rate of 2.0(1.0) x 10^10 atoms/s. Decay to metastable states is observed for all trapped species and decay rates are measured. Extension of this approach to the loading of molecules into a MOT is discussed.

physics.atom-ph↗

Magnetic Trapping of Molecules via Optical Loading and Magnetic Slowing

Calcium monofluoride (CaF) is magnetically slowed and trapped using optical pumping. Starting from a collisionally cooled slow beam, CaF with an initial velocity of ~ 30 m/s is slowed via magnetic forces as it enters a 800 mK deep magnetic trap. Employing two-stage optical pumping, CaF is irreversibly loaded into the trap via two scattered photons. We observe a trap lifetime exceeding 500 ms, limited by background collisions. This method paves the way for cooling and magnetic trapping of chemically diverse molecules without closed cycling transitions.

physics.atom-ph↗

Order of Magnitude Smaller Limit on the Electric Dipole Moment of the Electron

The Standard Model (SM) of particle physics fails to explain dark matter and why matter survived annihilation with antimatter following the Big Bang. Extensions to the SM, such as weak-scale Supersymmetry, may explain one or both of these phenomena by positing the existence of new particles and interactions that are asymmetric under time-reversal (T). These theories nearly always predict a small, yet potentially measurable ($10^{-27}$-$10^{-30}$ $e$ cm) electron electric dipole moment (EDM, $d_e$), which is an asymmetric charge distribution along the spin ($\vec{S}$). The EDM is also asymmetric under T. Using the polar molecule thorium monoxide (ThO), we measure $d_e = (-2.1 \pm 3.7_\mathrm{stat} \pm 2.5_\mathrm{syst})\times 10^{-29}$ $e$ cm. This corresponds to an upper limit of $|d_e| < 8.7\times 10^{-29}$ $e$ cm with 90 percent confidence, an order of magnitude improvement in sensitivity compared to the previous best limits. Our result constrains T-violating physics at the TeV energy scale.

physics.atom-ph↗

Properties of the ground $^3$F$_2$ state and the excited $^3$P$_0$ state of atomic thorium in cold collisions with $^3$He

We measure inelastic collisional cross sections for the ground $^3$F$_2$ state and the excited $^3$P$_0$ state of atomic thorium in cold collisions with $^3$He. We determine for Th ($^3$F$_2$) at 800 mK the ratio $γ\approx 500$ of the momentum-transfer to Zeeman relaxation cross sections for collisions with $^3$He. For Th ($^3$P$_0$), we study electronic inelastic processes and find no quenching even after $10^6$ collisions. We also determine the radiative lifetime of Th ($^3$P$_0$) to be $τ> 130$ ms. This great stability of the metastable state opens up the possibility for further study, including trapping.

physics.atom-ph↗

Vibrational quenching of the electronic ground state in ThO in cold collisions with $^3$He

We measure the ratio $γ$ of the momentum-transfer to the vibrational quenching cross section for the X ($^1Σ^+$), $ν=1$, $\mathrm{J=0}$ state of molecular thorium monoxide (ThO) in collisions with atomic $^3$He between 800 mK and 2.4 K. We observe indirect evidence for ThO--He van der Waals' complex formation, which has been predicted by theory. We determine the 3-body recombination rate constant $Γ_3$ at 2.4 K, and establish that the binding energy E$_b >$ 4 K.

physics.atom-ph↗

Manipulation of Molecules with Electromagnetic Fields

The goal of the present article is to review the major developments that have led to the current understanding of molecule-field interactions and experimental methods for manipulating molecules with electromagnetic fields. Molecule-field interactions are at the core of several, seemingly distinct, areas of molecular physics. This is reflected in the organization of this article, which includes sections on Field control of molecular beams, External field traps for cold molecules, Control of molecular orientation and molecular alignment, Manipulation of molecules by non-conservative forces, Ultracold molecules and ultracold chemistry, Controlled many-body phenomena, Entanglement of molecules and dipole arrays, and Stability of molecular systems in high-frequency super-intense laser fields. The article contains 853 references.

physics.atom-ph↗