No Arabic abstract
We present measurements and calculations of the trap loss rate for laser cooled Rb atoms confined in either a magneto-optic or a magnetic quadrupole trap when exposed to a room temperature background gas of Ar. We study the loss rate as a function of trap depth and find that copious glancing elastic collisions, which occur in the so-called quantum-diffractive regime and impart very little energy to the trapped atoms, result in significant differences in the loss rate for the MOT compared to a pure magnetic trap due solely to the difference in potential depth. This finding highlights the importance of knowing the trap depth when attempting to infer the total collision cross section from measurements of trap loss rates. Moreover, this variation of trap loss rate with trap depth can be used to extract information about the differential cross section.
This work demonstrates that quantum diffractive collisions, those that result in very small momentum and energy transfer, are universal. Specifically, the cumulative energy distribution transferred to an initially stationary sensor particle by a quantum diffractive collision follows a universal function that depends only on the sensor particle mass and the thermally-averaged, total collision cross section. The characteristic energy scale corresponds to the localization length associated with the collision-induced quantum measurement, and the shape of the universal function is determined {it only} by the analytic form of the interaction potential at long range. Using cold $^{87}$Rb sensor atoms confined in a magnetic trap, we observe experimentally the universal function specific to van der Waals collisions, and realize a emph{self-defining} particle pressure sensor that can be used for any ambient gas. This provides the first primary and quantum definition of the Pascal, applicable to any species and therefore represents a key advance for vacuum and pressure metrology. The quantum pressure standard realized here was compared with a state-of-the-art orifice flow standard transferred by an ionization gauge calibrated for N$_2$. The pressure measurements agreed at the 0.5% level.
We show that micro-machined non-evaporable getter pumps (NEGs) can extend the time over which laser cooled atoms canbe produced in a magneto-optical trap (MOT), in the absence of other vacuum pumping mechanisms. In a first study, weincorporate a silicon-glass microfabricated ultra-high vacuum (UHV) cell with silicon etched NEG cavities and alumino-silicateglass (ASG) windows and demonstrate the observation of a repeatedly-loading MOT over a 10 minute period with a single laser-activated NEG. In a second study, the capacity of passive pumping with laser activated NEG materials is further investigated ina borosilicate glass-blown cuvette cell containing five NEG tablets. In this cell, the MOT remained visible for over 4 days withoutany external active pumping system. This MOT observation time exceeds the one obtained in the no-NEG scenario by almostfive orders of magnitude. The cell scalability and potential vacuum longevity made possible with NEG materials may enable inthe future the development of miniaturized cold-atom instruments.
Quantum coherence and interference effects in atomic and molecular physics has been extensively studied due to intriguing counterintuitive physics and potential important applications. Here we present one such application of using quantum coherence to generate and enhance gain in extreme ultra-violet(XUV)(@58.4nm in Helium) and infra-red(@794.76nm in Rubidium) regime of electromagnetic radiation. We show that using moderate external coherent drive, a substantial enhancement in the energy of the lasing pulse can be achieved under optimal conditions. We also discuss the role of coherence. The present paper is intended to be pedagogical on this subject of coherence-enhanced lasing.
We give a detailed account of the theoretical analysis and the experimental results of an x-ray-diffraction experiment on quantum-state selected and strongly laser-aligned gas-phase ensembles of the prototypical large asymmetric rotor molecule 2,5-diiodobenzonitrile, performed at the Linac Coherent Light Source [Phys. Rev. Lett. 112, 083002 (2014)]. This experiment is the first step toward coherent diffractive imaging of structures and structural dynamics of isolated molecules at atomic resolution, i. e., picometers and femtoseconds, using x-ray free-electron lasers.
We study a method for mass-selective removal of ions from a Paul trap by parametric excitation. This can be achieved by applying an oscillating electric quadrupole field at twice the secular frequency $omega_{text{sec}}$ using pairs of opposing electrodes. While excitation near the resonance with the frequency $omega_{text{sec}}$ only leads to a linear increase of the amplitude with excitation duration, parametric excitation near $2, omega_{text{sec}}$ results in an exponential increase of the amplitude. This enables efficient removal of ions from the trap with modest excitation voltages and narrow bandwidth, therefore substantially reducing the disturbance of ions with other charge-to-mass ratios. We numerically study and compare the mass selectivity of the two methods. In addition, we experimentally show that the barium isotopes with 136 and 137 nucleons can be removed from small ion crystals and ejected out of the trap while keeping $^{138}text{Ba}^{+}$ ions Doppler cooled, corresponding to a mass selectivity of better than $Delta m / m = 1/138$. This method can be widely applied to ion trapping experiments without major modifications, since it only requires modulating the potential of the ion trap.