No Arabic abstract
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.
The magnetic phase diagrams of RMnO3 (R = Er, Yb, Tm, Ho) are investigated up to 14 Tesla via magnetic and dielectric measurements. The stability range of the AFM order below the Neel temperature of the studied RMnO3 extends to far higher magnetic fields than previously assumed. Magnetic irreversibility indicating the presence of a spontaneous magnetic moment is found near 50 K for R=Er, Yb, and Tm. At very low temperatures and low magnetic fields the phase boundary defined by the ordering of the rare earth moments is resolved. The sizable dielectric anomalies observed along all phase boundaries are evidence for strong spin-lattice coupling in the hexagonal RMnO3. In HoMnO3 the strong magnetoelastic distortions are investigated in more detail via magnetostriction experiments up to 14 Tesla. The results are discussed based on existing data on magnetic symmetries and the interactions between the Mn-spins, the rare earth moments, and the lattice.
We study several new magneto-optical trapping configurations in $^{87}$Rb. These unconventional MOTs all use type-II transitions, where the angular momentum of the ground state is greater than or equal to that of the excited state, and they may use either red-detuned or blue-detuned light. We describe the conditions under which each new MOT forms. The various MOTs exhibit an enormous range of lifetimes, temperatures and density distributions. At the detunings where they are maximized, the lifetimes of the various MOTs vary from 0.1 to 15 s. One MOT forms large ring-like structures with no density at the centre. The temperature in the red-detuned MOTs can be three orders of magnitude higher than in the blue-detuned MOTs. We present measurements of the capture velocity of a blue-detuned MOT, and we study how the loss rate due to ultracold collisions depends on laser intensity and detuning.
We present a theoretical model describing recently observed collective effects in large magneto-optically trapped atomic ensembles. Based on a kinetic description we develop an efficient test particle method, which in addition to the single atom light pressure accounts for other relevant effects such as laser attenuation and forces due to multiply scattered light with position dependent absorption cross sections. Our calculations confirm the existence of a dynamical instability and provide deeper insights into the observed system dynamics.
We have used diffraction gratings to simplify the fabrication, and dramatically increase the atomic collection efficiency, of magneto-optical traps using micro-fabricated optics. The atom number enhancement was mainly due to the increased beam capture volume, afforded by the large area (4cm^2) shallow etch (200nm) binary grating chips. Here we provide a detailed theoretical and experimental investigation of the on-chip magneto-optical trap temperature and density in four different chip geometries using 87Rb, whilst studying effects due to MOT radiation pressure imbalance. With optimal initial MOTs on two of the chips we obtain both large atom number (2x10^7) _and_ sub-Doppler temperatures (50uK) after optical molasses.
The magnetoelectric effect in the system $RAl_3(BO_3)_4$ ($R$ = Tb, Ho, Er, Tm) is investigated between 3 K and room temperature and at magnetic fields up to 70 kOe. We show a systematic increase of the magnetoelectric effect with decreasing magnetic anisotropy of the rare earth moment. A giant magnetoelectric polarization is found in the magnetically (nearly) isotropic $HoAl_3(BO_3)_4$. The polarization value in transverse field geometry at 70 kOe reaches 3600 $mu C/m^2$ which is significantly higher than reported values for the field-induced polarization of linear magnetoelectric or even multiferroic compounds. The results indicate a very strong coupling of the f-moments to the lattice. They further indicate the importance of the field-induced ionic displacements in the unit cell resulting in a polar distortion and a change in symmetry on a microscopic scale. The system $RAl_3(BO_3)_4$ could be interesting for the technological utilization of the high-field magnetoelectric effect.