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 approximately 0.6 cm3 and holds molecules with a positive Stark shift. With deuterated ammonia from a quadrupole velocity filter, a trap density of approximately 10(8) cm(-3) is achieved with an average lifetime of 130 ms and a motional temperature of approximately 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.     

Resonator-enhanced optical dipole trap for fermionic lithium atoms

We demonstrate a novel optical dipole trap that is based on enhancement of the optical power density of a Nd:YAG laser beam in a resonator. The trap is particularly suited for experiments with ultracold gases, as it combines a potential depth of the order of 1 mK with storage times of several tens of seconds. We study the interactions in a gas of fermionic lithium atoms in our trap and observe the influence of spin-changing collisions and off-resonant photon scattering. A key element in reaching long storage times is the use of an ultralow-noise laser. The dependence of storage time on laser noise is investigated.     

Unconventional trapping of ultracold neutrons

In unconventional storage experiments we filled ultracold neutrons (UCN) into a Fomblin-grease coated trap and then immediately removed the UCN from the storage volume by an absorber, until their residual density in the trap was measured to be negligible. When subsequently the absorber was withdrawn a significant number of UCN of higher energies emerged from the trap. Their appearance cannot be attributed to heating or cooling of residual UCN. Further experiments were performed to investigate the origin of these UCN which we call `late UCN'. We noticed that application of a magnetic field gradient at the trap wall as well as a replacement of Fomblin grease on the surface by Fomblin oil gave rise to small but measurable alterations of storage behavior. These phenomena are consistent with the hypothesis of temporary adhesion of a few UCN to a rough wall.     

Prospects for sympathetic cooling of molecules in electrostatic, ac and microwave traps

We consider how trapped molecules can be sympathetically cooled by ultracold atoms. As a prototypical system, we study LiH molecules co-trapped with ultracold Li atoms. We calculate the elastic and inelastic collision cross sections of ⁷LiH + ⁷Li with the molecules initially in the ground state and in the first rotationally excited state. We then use these cross sections to simulate sympathetic cooling in a static electric trap, an ac electric trap, and a microwave trap. In the static trap we find that inelastic losses are too great for cooling to be feasible for this system. The ac and microwave traps confine ground-state molecules, and so inelastic losses are suppressed. However, collisions in the ac trap can take molecules from stable trajectories to unstable ones and so sympathetic cooling is accompanied by trap loss. In the microwave trap there are no such losses and sympathetic cooling should be possible.     

Bose-Einstein condensation of 87Rb in a levitated crossed dipole trap

We report an apparatus and method capable of producing Bose-Einstein condensates (BECs) of ～1 × 10^{6 87}Rb atoms, and ultimately designed for sympathetic cooling of ¹³³Cs and the creation of ultracold RbCs molecules. The method combines several elements: (i) the large recapture of a magnetic quadrupole trap from a magneto-optical trap; (ii) efficient forced RF evaporation in such a magnetic trap; (iii) the gain in phase-space density obtained when loading the magnetically trapped atoms into a far red-detuned optical dipole trap, and (iv) efficient evaporation to BEC within the dipole trap. We demonstrate that the system is capable of sympathetically cooling the |F = 1, m _F = ?1〉 and |1,0? sublevels with |1, +1〉 atoms. Finally we discuss the applicability of the method to sympathetic cooling of ¹³³Cs with ⁸⁷Rb.     

Microwave traps for cold polar molecules

We discuss the possibility of trapping polar molecules in the standing-wave electromagnetic field of a microwave resonant cavity. Such a trap has several novel features that make it very attractive for the development of ultracold molecule sources. Using commonly available technologies, microwave traps can be built with large depth (up to several Kelvin) and acceptance volume (up to several cm³), suitable for efficient loading with currently available sources of cold polar molecules. Unlike most previous traps for molecules, this technology can be used to confine the strong-field seeking absolute ground state of the molecule, in a free-space maximum of the microwave electric field. Such ground state molecules should be immune to inelastic collisional losses. We calculate elastic collision cross-sections for the trapped molecules, due to the electrical polarization of the molecules at the trap center, and find that they are extraordinarily large. Thus, molecules in a microwave trap should be very amenable to sympathetic and/or evaporative cooling. The combination of these properties seems to open a path to producing large samples of polar molecules at temperatures much lower than has been previously possible.Received: 30 June 2004, Published online: 23 November 2004PACS: 33.80.Ps Optical cooling of molecules; trapping - 34.50.-s Scattering of atoms and molecules - 33.80.-b Photon interactions with molecules - 33.55.Be Zeeman and Stark effects     

Controlling electronic spin relaxation of cold molecules with electric fields

We present a theoretical study of atom-molecule collisions in superimposed electric and magnetic fields and show that dynamics of electronic spin relaxation in molecules at temperatures below 0.5 K can be manipulated by varying the strength and the relative orientation of the applied fields. The mechanism of electric field control of Zeeman transitions is based on an intricate interplay between intramolecular spin-rotation couplings and molecule-field interactions. We suggest that electric fields may affect chemical reactions through inducing nonadiabatic spin transitions and facilitate evaporative cooling of molecules in a magnetic trap.     

Antimatter plasmas in a multipole trap for antihydrogen

We have demonstrated storage of plasmas of the charged constituents of the antihydrogen atom, antiprotons and positrons, in a Penning trap surrounded by a minimum-B magnetic trap designed for holding neutral antiatoms. The neutral trap comprises a superconducting octupole and two superconducting, solenoidal mirror coils. We have measured the storage lifetimes of antiproton and positron plasmas in the combined Penning-neutral trap, and compared these to lifetimes without the neutral trap fields. The magnetic well depth was 0.6 T, deep enough to trap ground state antihydrogen atoms of up to about 0.4 K in temperature. We have demonstrated that both particle species can be stored for times long enough to permit antihydrogen production and trapping studies.     

一种可控的Ioffe型冷分子表面微电阱

囚禁于阱中的粒子(原子或分子)可获得更长的相互作用时间,因而在精密测量中可获得更高的分辨率.阱中的粒子与外界隔离,从而可以被冷却到更低的温度.因此原子(或分子)阱已广泛应用到许多研究领域.然而中心电场强度为零的势阱会导致粒子发生非绝热跃迁,这是原子或分子损失的主要来源.该损失曾是制备原子玻色-爱因斯坦凝聚的最后一道障碍.本文提出了一种可控的Ioffe型表面微电阱,其电场强度处处不为零,可有效避免分子的非绝热损失.另外,通过调节电压等参数,势阱中心电场强度以及势阱中心距芯片表面的高度可以在较大范围内调节,例如在本文参数下,势阱中心电场强度可在0.15—5.5 kV/cm变化,势阱中心高度可在6.0—17.0μm变化.本文通过有限元软件计算了芯片表面微电阱的电场分布,并用Monte Carlo模拟验证了该方案的可行性.该表面微电阱不仅可用于分子芯片的集成,而且可用于表面量子简并气体的制备.为精密测量、量子计算、表面冷碰撞和冷化学等领域提供了一个平台.     

基于磁悬浮大体积交叉光学偶极阱的Dimple光阱装载研究

三维拉曼边带冷却后的铯原子样品装载于一个磁悬浮的大体积交叉光学偶极阱中, 继续加载一个小体积的光学偶极阱后, 实现了Dimple光学偶极阱对铯原子的高效装载. 对不同磁场下磁悬浮大体积光阱的有效装载势能进行理论分析与实验测量, 得出最优化的梯度磁场和均匀偏置磁场, 获得了基于磁悬浮大体积光阱的Dimple光学偶极阱的装载势能曲线, 实现了Dimple光学偶极阱对经拉曼边带冷却后俘获在磁悬浮的大体积光阱中的铯原子样品的有效装载. 比较了Dimple光学偶极阱分别从拉曼边带冷却、大体积的交叉光阱和消除反俘获势后的磁悬浮大体积光阱装载的结果, 将俘获在磁悬浮大体积光阱中的铯原子样品装载到Dimple光学偶极阱, 铯原子样品的密度提高了约15倍.     

Stark-potential evaporative cooling of polar molecules in a novel optical-access opened electrostatic trap

We propose a novel optical-access opened electrostatic trap to study the Stark-potential evaporative cooling of polar molecules by using two charged disk electrodes with a central hole of radius r0= 1.5 mm, and derive a set of new analytical equations to calculate the spatial distributions of the electrostatic field in the above charged-disk layout. Afterwards, we calculate the electric-field distributions of our electrostatic trap and the Stark potential for cold ND3 molecules, and analyze the dependences of both the electric field and the Stark potential on the geometric parameters of our charged-disk scheme,and find an optimal condition to form a desirable trap with the same trap depth in the x, y, and z directions. Also, we propose a desirable scheme to realize an efficient loading of cold polar molecules in the weak-field-seeking states, and investigate the dependences of the loading efficiency on both the initial forward velocity of the incident molecular beam and the loading time by Monte Carlo simulations. Our study shows that the maximal loading efficiency of our trap scheme can reach about 95%, and the corresponding temperature of the trapped cold molecules is about 28.8 m K. Finally, we study the Stark-potential evaporative cooling for cold polar molecules in our trap by the Monte Carlo method, and find that our simulated evaporative cooling results are consistent with our developed analytical model based on trapping-potential evaporative cooling.     

Theory and simulation of ion Coulomb crystal formation in a Penning trap

Ion Coulomb crystals (ICCs) are formed by laser-cooled ions in both radio-frequency and Penning traps. In radio-frequency traps, the crystals are generally stationary. In Penning traps, ICCs always rotate. The frequency of rotation is often set by an applied rotating wall drive that forces the crystal to rotate at the same frequency as the drive. In the absence of any applied rotating or oscillating fields, ICCs in a Penning trap can be in stable equilibrium with a range of rotation frequencies. The density and shape of the crystal adjust with the rotation frequency to ensure that equilibrium is reached. Here, we show that the parameters of the radial laser-cooling beam determine the rotation frequency of a small crystal in a Penning trap when no driving fields are present. We demonstrate, using an approximate theoretical treatment and realistic simulations, that the crystal rotation frequency is independent of the number of ions and the trap parameters, so long as the crystal radius remains smaller than the cooling laser beam waist. As the rotation frequency increases, the crystal eventually becomes a linear string, at which point it is no longer able to adjust its density. Instead, a small amplitude vibration in the zigzag mode of oscillation manifests itself as a rotation of the crystal at a fixed frequency that depends only on the applied trap potential.     

~(87)Rb玻色-爱因斯坦凝聚体的快速实验制备

采用二维磁光阱产生了-个快速~(87)Rb原子流,并在高真空的三维磁光阱中实现了~(87)Rb原子的快速俘获,进一步采用射频蒸发冷却技术实现了原子云的预冷却,然后将原子转移到远失谐的光学偶极阱中蒸发得到了玻色-爱因斯坦凝聚体.实验上可以在25 s内完成三维磁光阱的装载(约1.0×10~(10)个~(87)Rb原子),然后经过16 s的冷却过程最终在光学偶极阱中获得5.0×10~5个原子的玻色-爱因斯坦凝聚体.实验重点研究了二维磁光阱的优化设计和采用蓝失谐大功率光束对四极磁阱零点的堵塞,抑制四极磁阱中原子的马约拉纳损耗,更加有效地对原子云进行预冷却.     

Feedback-controlled electro-kinetic traps for single-molecule spectroscopy

A principal limitation of single-molecule spectroscopy in solution is the diffusion-limited residence time of a given molecule within the detection volume. A common solution to this problem is to immobilize molecules of interest on a passivated glass surface for extending the observation time to obtain reliable data statistics. However, surface tethering of molecules often introduces artifacts, particularly when studying the structural dynamics of biomolecules. To circumvent this limitation, we investigated alternative ways to extend single-molecule observation times in solution without surface immobilization. Among various possibilities, the so-called anti-Brownian electro-kinetic trap (or ABEL trap) seems best suited to achieve this goal. The essential part of that trap is a feedback-controlled electro-kinetic steering of a molecule’s position in reaction to its diffusive Brownian motion which is monitored by fluorescence, thus keeping the molecule within a sub-micron sized detection volume. Fluorescence trace recordings of over thousands of milliseconds duration on individual dye molecules within an ABEL trap have been reported. In this short review, we shall briefly discuss the principle and some results of ABEL trapping of individual molecules with possible extensions to future works.     

Observing a single hydrogen-like ion in a Penning trap at T = 4 K

We describe how a single hydrogen-like ion (C⁵⁺) is prepared, cooled with the method of resistive cooling and non-destructively detected with the image-current technique in a cryogenic Penning trap at T = 4 K. The storage time for C⁵⁺-ions in the cryogenically pumped vacuum chamber is longer than six months. The experimental techniques of preparing, cooling and detecting highly-charged ions in a Penning trap are relevant for precision experiments such as g-factor measurements, mass spectroscopy and laser spectroscopy. This revised version was published online in July 2006 with corrections to the Cover Date.     

Laser radiation pressure slowing of a molecular beam

We demonstrate deceleration of a beam of neutral strontium monofluoride molecules using radiative forces. Under certain conditions, the deceleration results in a substantial flux of detected molecules with velocities ?50 m/s. Simulations and other data indicate that the detection of molecules below this velocity is greatly diminished by transverse divergence from the beam. The observed slowing, from ～140 m/s, corresponds to scattering ?10(4) photons. We also observe longitudinal velocity compression under different conditions. Combined with molecular laser cooling techniques, this lays the groundwork to create slow and cold molecular beams suitable for trap loading.     

Two types of highly efficient electrostatic traps for single loading or multi-loading of polar molecules

Two novel electrostatic traps named octopole-based disk electrostatic trap(ODET)and tubular-based disk electrostatic trap(TDET)are proposed for trapping cold polar molecules in low-field-seeking states.Using MgF as the target molecule,single loading and multi-loading methods are numerically simulated with varied incident velocities of slow molecular beams in the two types of traps,respectively.In ODET,with an incident velocity of 10 m/s,a highest loading efficiency of 78.4% or 99.9% has been achieved under the single loading or multi-loading operation mode.In TDET,with an incident velocity of 11 m/s,a highest loading efficiency of 81.6% or 106.5% has been achieved using the two loading methods,respectively.With such high loading efficiencies,the trapped cold molecules can be applied in the researches of cold collisions,high precision spectroscopy,and precision measurements.Especially,together with a blue-detuned hollow beam,the new electrostatic traps proposed here offer a new platform for the following gradient-intensity cooling of MgF molecules,which may provide a new way to produce high density ultracold molecules.     

Light-induced evaporative cooling in a magneto-optical trap

This paper presents an experimental demonstration of light-induced evaporative cooling in a magneto-optical trap. An additional laser is used to interact with atoms at the edge of the atomic cloud in the trap. These atoms get an additional force and evaporated away from the trap by both the magnetic field and laser fields. The remaining atoms have lower kinetic energy and thus are cooled. It reports the measurements on the temperature and atomic number after the evaporative cooling with different parameters including the distance between the laser and the centre of the atomic cloud, the detuning, the intensity. The results show that the light-induced evaporative cooling is a way to generate an ultra-cold atom source.     

HITRAP: A Facility for Experiments with Trapped Highly Charged Ions

HITRAP is a planned ion trap facility for capturing and cooling of highly charged ions produced at GSI in the heavy-ion complex of the UNILAC-SIS accelerators and the ESR storage ring. In this facility heavy highly charged ions up to uranium will be available as bare nuclei, hydrogen-like ions or few-electron systems at low temperatures. The trap for receiving and studying these ions is designed for operation at extremely high vacuum by cooling to cryogenic temperatures. The stored highly charged ions can be investigated in the trap itself or can be extracted from the trap at energies up to about 10 keV/q. The proposed physics experiments are collision studies with highly charged ions at well-defined low energies (eV/u), high-accuracy measurements to determine the g-factor of the electron bound in a hydrogen-like heavy ion and the atomic binding energies of few-electron systems, laser spectroscopy of HFS transitions and X-ray spectroscopy. This revised version was published online in July 2006 with corrections to the Cover Date.     

The manipulation of charged particles into and out of electromagnetic traps

The manipulation of charged particles into and out of Paul and Penning ion traps is discussed in terms of the phase space volume of a particle collection and its manipulation. It is shown that such traps can have very large usable phase space volumes but that the shape of such volumes is severely mismatched to that of a typical ion beam from a separator or storage ring. Possible injection schemes are presented as well as some aspects of ion cooling within the trap and subsequent ion extraction. Possible applications to the manipulation of antiproton beams from LEAR and 10 MeV/A highly-stripped heavy ions at GSI are discussed.