arXiv subjects

S. A. Rangwala

Publications and source records attributed to S. A. Rangwala.

At least 37 records · Page 2Linked to original sources

arXiv2016

All-optical switching in a continuously operated and strongly coupled atom-cavity system

We experimentally demonstrate collective strong coupling, optical bi-stability (OB) and all-optical switching in a system consisting of ultracold 85Rb atoms, trapped in a dark magneto-optical trap (DMOT), coupled to an optical Fabry-Perot cavity. The strong coupling is established by measuring the vacuum Rabi splitting (VRS) of a weak on-axis probe beam. The dependence of VRS on the probe beam power is measured and bi-stability in the cavity transmission is observed. We demonstrate control over the transmission of the probe beam through the atom-cavity system using a free-space off-axis control beam and show that the cavity transmission can be switched on and off in micro-second timescales using micro-Watt control powers. The utility of the system as a tool for sensitive, in-situ and rapid measurements is envisaged.

physics.atom-ph↗

arXiv2016

Non-destructive detection of ions using atom-cavity collective strong coupling

We present a technique, based on atoms coupled to an optical cavity, for non-destructive detection of trapped ions. We demonstrate the vacuum-Rabi splitting (VRS), arising due to the collective strong coupling of ultracold Rb atoms to a cavity, to change in presence of trapped Rb+ ions. The Rb+ ions are optically dark and the Rb atoms are prepared in a dark magneto-optical trap (MOT). The VRS is measured on an optically open transition of the initially dark Rb atoms. The measurement itself is fast, non-destructive and has sufficient fidelity to permit the measurement of atomic-state selective ion-atom collision rate. This demonstration illustrates a method based on atom-cavity coupling to measure two particle interactions generically and non-destructively.

physics.atom-ph↗

arXiv2016

Photodissociation of trapped Rb$^+_2$ : Implications for simultaneous trapping of atoms and molecular ions

The direct photodissociation of trapped $^{85}$Rb$_2^+$ (rubidium) molecular ions by the cooling light for the $^{85}$Rb magneto-optical trap (MOT) is studied, both experimentally and theoretically. Vibrationally excited Rb$_{2}^{+}$ ions are created by photoionization of Rb$_{2}$ molecules formed photoassociatively in the Rb MOT and are trapped in a modified spherical Paul trap. The decay rate of the trapped Rb$_{2}^{+}$ ion signal in the presence of the MOT cooling light is measured and agreement with our calculated rates for molecular ion photodissociation is observed. The photodissociation mechanism due to the MOT light is expected to be active and therefore universal for all homonuclear diatomic alkali metal molecular ions.

physics.atom-ph↗

arXiv2015

Optical bistability enabled control of resonant light transmission for an atom-cavity system

The control of light transmission through a Fabry-Perot cavity containing atoms is theoretically investigated, when the cavity mode beam and an intersecting control beam are both close to specific atomic resonances. A four-level atomic system is considered and its interaction with the cavity mode is studied by solving for the time dependent cavity field and atomic state populations. The conditions for optical bistability of the atom-cavity system are obtained in steady state limit. For an ensemble of atoms in the cavity mode, the response of the intra-cavity light intensity to the intersecting resonant beam is understood for stationary atoms (closed system) and non-static atoms (open system). The open system is modelled by adjusting the atomic state populations to represent the exchange of atoms in the cavity mode, with the thermal environment. The solutions to the model are used to qualitatively explain the observed steady state and transient behaviour of the light in the cavity mode, in Sharma et. al. [1]. The control behaviour with three- and two-level atomic systems is also studied, and the rich physics arising out of these systems, for closed and open atomic systems is discussed.

physics.optics↗

arXiv2015

Optical control of resonant light transmission for an atom-cavity system

We demonstrate the manipulation of transmitted light through an optical Fabry-Perot cavity, built around a spectroscopy cell containing enriched rubidium vapor. Light resonant with the $^{87}$Rb D$_{2}$ ($F=2/F=1$) $\leftrightarrow F'$ manifold, is controlled by transverse intersection of the cavity mode by another resonant light beam. The cavity transmission can be suppressed or enhanced depending on the coupling of atomic states due to the intersecting beams. The extreme manifestation of cavity mode control is the precipitious destruction (negative logic switching) or buildup (positive logic switching) of the transmitted light intensity, on intersection of the transverse control beam with the cavity mode. Both the steady state and transient response are experimentally investigated. The mechanism behind the change in cavity transmission is discussed in brief.

physics.atom-ph↗

arXiv2013

Hybrid ion, atom and light trap

We present an unique experimental arrangement which permits the simultaneous trapping and cooling of ions and neutral atoms, within a Fabry-Perot (FP) cavity. The versatility of this hybrid trap experiment enables a variety of studies with trapped mixtures. The motivations behind the production of such a hybrid trap system are explained, followed by details of how the experiment is put together. Several experiments that have been performed with this system are presented and some opportunities with this system are discussed. However the primary emphasis is focussed on the aspects that pertain to the trapped ions, in this hybrid system.

physics.atom-ph↗

arXiv2013

Measurement of collisions between rubidium atoms and optically dark rubidium ions

We measure the collision rate coefficient between laser cooled Rubidium (Rb) atoms in a magneto-optical trap (MOT) and optically dark Rb+ ions in an overlapping Paul trap. In such a mixture, the ions are created from the MOT atoms and allowed to accumulate in the ion trap, which results in a significant reduction in the number of steady state MOT atoms. A theoretical rate equation model is developed to describe the evolution of the MOT atom number, due to ionization and ion-atom collision, and derive an expression for the ion-atom collision rate coefficient. The loss of MOT atoms is studied systematically, by sequentially switching on the various mechanisms in the experiment. Combining the measurements with the model allows the direct determination of the ion-atom collision rate coefficient. Finally the scope of the experimental technique developed here is discussed.

physics.atom-ph↗

arXiv2011

Sympathetic and swap cooling of trapped ions by cold atoms in a MOT

A mixed system of cooled and trapped, ions and atoms, paves the way for ion assisted cold chemistry and novel many body studies. Due to the different individual trapping mechanisms, trapped atoms are significantly colder than trapped ions, therefore in the combined system, the strong binary ion$-$atom interaction results in heat flow from ions to atoms. Conversely, trapped ions can also get collisionally heated by the cold atoms, making the resulting equilibrium between ions and atoms intriguing. Here we experimentally demonstrate, Rubidium ions (Rb$^+$) cool in contact with magneto-optically trapped (MOT) Rb atoms, contrary to the general expectation of ion heating for equal ion and atom masses. The cooling mechanism is explained theoretically and substantiated with numerical simulations. The importance of resonant charge exchange (RCx) collisions, which allows swap cooling of ions with atoms, wherein a single glancing collision event brings a fast ion to rest, is discussed.

physics.atom-ph↗

arXiv2011

Combined ion and atom trap for low temperature ion-atom physics

We report an experimental apparatus and technique which simultaneously traps ions and cold atoms with spatial overlap. Such an apparatus is motivated by the study of ion-atom processes at temperatures ranging from hot to ultra-cold. This area is a largely unexplored domain of physics with cold trapped atoms. In this article we discuss the general design considerations for combining these two traps and present our experimental setup. The ion trap and atom traps are characterized independently of each other. The simultaneous operation of both is then described and experimental signatures of the effect of the ions and cold-atoms on each other are presented. In conclusion the use of such an instrument for several problems in physics and chemistry is briefly discussed.

physics.atom-ph↗

arXiv2010

Investigation of Anti-Relaxation Coatings for Alkali-Metal Vapor Cells Using Surface Science Techniques

Many technologies based on cells containing alkali-metal atomic vapor benefit from the use of anti-relaxation surface coatings in order to preserve atomic spin polarization. In particular, paraffin has been used for this purpose for several decades and has been demonstrated to allow an atom to experience up to 10,000 collisions with the walls of its container without depolarizing, but the details of its operation remain poorly understood. We apply modern surface and bulk techniques to the study of paraffin coatings, in order to characterize the properties that enable the effective preservation of alkali spin polarization. These methods include Fourier transform infrared spectroscopy, differential scanning calorimetry, atomic force microscopy, near-edge X-ray absorption fine structure spectroscopy, and X-ray photoelectron spectroscopy. We also compare the light-induced atomic desorption yields of several different paraffin materials. Experimental results include the determination that crystallinity of the coating material is unnecessary, and the detection of C=C double bonds present within a particular class of effective paraffin coatings. Further study should lead to the development of more robust paraffin anti-relaxation coatings, as well as the design and synthesis of new classes of coating materials.

physics.chem-ph↗

arXiv2010

Rubidium dimers in paraffin-coated cells

Measurements were made to determine the density of rubidium dimer vapor in paraffin-coated cells. The number density of dimers and atoms in similar paraffin-coated and uncoated cells was measured by optical spectroscopy. Due to the relatively low melting point of paraffin, a limited temperature range of 43-80 deg C was explored, with the lower end corresponding to a dimer density of less than 10^7 cm^(-3). With one-minute integration time, a sensitivity to dimer number density of better than 10^6 cm^(-3) was achieved. No significant difference in dimer density was observed between the cells.

physics.atom-ph↗

arXiv2009

A Three Dimensional Lattice of Ion Traps

We propose an ion trap configuration such that individual traps can be stacked together in a three dimensional simple cubic arrangement. The isolated trap as well as the extended array of ion traps are characterized for different locations in the lattice, illustrating the robustness of the lattice of traps concept. Ease in the addressing of ions at each lattice site, individually or simultaneously, makes this system naturally suitable for a number of experiments. Application of this trap to precision spectroscopy, quantum information processing and the study of few particle interacting system are discussed.

physics.atom-ph↗

arXiv2008

Electric-field-induced change of alkali-metal vapor density in paraffin-coated cells

Alkali vapor cells with antirelaxation coating (especially paraffin-coated cells) have been a central tool in optical pumping and atomic spectroscopy experiments for 50 years. We have discovered a dramatic change of the alkali vapor density in a paraffin-coated cell upon application of an electric field to the cell. A systematic experimental characterization of the phenomenon is carried out for electric fields ranging in strength from 0-8 kV/cm for paraffin-coated cells containing rubidium and cells containing cesium. The typical response of the vapor density to a rapid (duration < 100 ms) change in electric field of sufficient magnitude includes (a) a rapid (duration of < 100 ms) and significant increase in alkali vapor density followed by (b) a less rapid (duration of ~ 1 s) and significant decrease in vapor density (below the equilibrium vapor density), and then (c) a slow (duration of ~ 100 s) recovery of the vapor density to its equilibrium value. Measurements conducted after the alkali vapor density has returned to its equilibrium value indicate minimal change (at the level of < 10%) in the relaxation rate of atomic polarization. Experiments suggest that the phenomenon is related to an electric-field-induced modification of the paraffin coating.

physics.atom-ph↗

arXiv2007

Trapping of Neutral Rubidium with a Macroscopic Three-Phase Electric Trap

We trap neutral ground-state rubidium atoms in a macroscopic trap based on purely electric fields. For this, three electrostatic field configurations are alternated in a periodic manner. The rubidium is precooled in a magneto-optical trap, transferred into a magnetic trap and then translated into the electric trap. The electric trap consists of six rod-shaped electrodes in cubic arrangement, giving ample optical access. Up to 10^5 atoms have been trapped with an initial temperature of around 20 microkelvin in the three-phase electric trap. The observations are in good agreement with detailed numerical simulations.

physics.atom-ph↗

arXiv2006

Water vapor at a translational temperature of one kelvin

We report the creation of a confined slow beam of heavy-water (D2O) molecules with a translational temperature around 1 kelvin. This is achieved by filtering slow D2O from a thermal ensemble with inhomogeneous static electric fields exploiting the quadratic Stark shift of D2O. All previous demonstrations of electric field manipulation of cold dipolar molecules rely on a predominantly linear Stark shift. Further, on the basis of elementary molecular properties and our filtering technique we argue that our D2O beam contains molecules in only a few ro-vibrational states.

physics.chem-ph↗

arXiv2005

Continuous loading of an electrostatic trap for polar molecules

A continuously operated electrostatic trap for polar molecules is demonstrated. The trap has a volume of ~0.6 cm^3 and holds molecules with a positive Stark shift. With deuterated ammonia from a quadrupole velocity filter, a trap density of ~10^8/cm^3 is achieved with an average lifetime of 130 ms and a motional temperature of ~300 mK. The trap offers good starting conditions for high-precision measurements, and can be used as a first stage in cooling schemes for molecules and as a "reaction vessel" in cold chemistry.

physics.chem-ph↗

arXiv2004

Two-dimensional trapping of dipolar molecules in time-varying electric fields

Simultaneous two-dimensional trapping of neutral dipolar molecules in low- and high-field seeking states is analyzed. A trapping potential of the order of 20 mK can be produced for molecules like ND3 with time-dependent electric fields. The analysis is in agreement with an experiment where slow molecules with longitudinal velocities of the order of 20 m/s are guided between four 50 cm long rods driven by an alternating electric potential at a frequency of a few kHz.

physics.chem-ph↗

arXiv2002

A continuous source of translationally cold dipolar molecules

The Stark interaction of polar molecules with an inhomogeneous electric field is exploited to select slow molecules from a room-temperature reservoir and guide them into an ultrahigh vacuum chamber. A linear electrostatic quadrupole with a curved section selects molecules with small transverse and longitudinal velocities. The source is tested with formaldehyde (H2CO) and deuterated ammonia (ND3). With H2CO a continuous flux is measured of approximately 10^9/s and a longitudinal temperature of a few K. The data are compared with the result of a Monte Carlo simulation.

physics.chem-ph↗