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Register a new userCross Section for Rydberg Antihydrogen Production via Charge Exchange Between Rydberg Positronium and Antiprotons in Magnetic Field
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The antihydrogen formation by charge exchange between cold antiprotons and Rydberg positronium Ps is studied by using the Classical Trajectory Monte Carlo (CTMC) method.
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We characterized the pulsed Rydberg-positronium production inside the AEgIS (Antimatter Experiment: Gravity, Interferometry, Spectroscopy) apparatus in view of antihydrogen formation by means of a charge exchange reaction between cold antiprotons and slow Rydberg-positronium atoms. Velocity measurements on positronium along two axes in a cryogenic environment (10K) and in 1T magnetic field were performed. The velocimetry was done by MCP-imaging of photoionized positronium previously excited to the $n=3$ state. One direction of velocity was measured via Doppler-scan of this $n=3$-line, another direction perpendicular to the former by delaying the exciting laser pulses in a time-of-flight measurement. Self-ionization in the magnetic field due to motional Stark effect was also quantified by using the same MCP-imaging technique for Rydberg positronium with an effective principal quantum number $n_{eff}$ ranging between 14 and 22. We conclude with a discussion about the optimization of our experimental parameters for creating Rydberg-positronium in preparation for an efficient pulsed production of antihydrogen.
Recently, antihydrogen atoms were trapped at CERN in a magnetic minimum (minimum-B) trap formed by superconducting octupole and mirror magnet coils. The trapped antiatoms were detected by rapidly turning off these magnets, thereby eliminating the magnetic minimum and releasing any antiatoms contained in the trap. Once released, these antiatoms quickly hit the trap wall, whereupon the positrons and antiprotons in the antiatoms annihilated. The antiproton annihilations produce easily detected signals; we used these signals to prove that we trapped antihydrogen. However, our technique could be confounded by mirror-trapped antiprotons, which would produce seemingly-identical annihilation signals upon hitting the trap wall. In this paper, we discuss possible sources of mirror-trapped antiprotons and show that antihydrogen and antiprotons can be readily distinguished, often with the aid of applied electric fields, by analyzing the annihilation locations and times. We further discuss the general properties of antiproton and antihydrogen trajectories in this magnetic geometry, and reconstruct the antihydrogen energy distribution from the measured annihilation time history.
We develop an effective field theory (EFT) to describe the few- and many-body propagation of one dimensional Rydberg polaritons. We show that the photonic transmission through the Rydberg medium can be found by mapping the propagation problem to a non-equilibrium quench, where the role of time and space are reversed. We include effective range corrections in the EFT and show that they dominate the dynamics near scattering resonances in the presence of deep bound states. Finally, we show how the long-range nature of the Rydberg-Rydberg interactions induces strong effective $N$-body interactions between Rydberg polaritons. These results pave the way towards studying non-perturbative effects in quantum field theories using Rydberg polaritons.
Long-range dipole-dipole and quadrupole-quadrupole interactions between pairs of Rydberg atoms are calculated perturbatively for calcium, strontium and ytterbium within the Coulomb approximation. Quantum defects, obtained by fitting existing laser spectroscopic data, are provided for all $S$, $P$, $D$ and $F$ series of strontium and for the $^3P_2$ series of calcium. The results show qualitative differences with the alkali metal atoms, including isotropically attractive interactions of the strontium $^1S_0$ states and a greater rarity of Forster resonances. Only two such resonances are identified, both in triplet series of strontium. The angular dependence of the long range interaction is briefly discussed.
We introduce the Rydberg Composite, a new class of Rydberg matter where a single Rydberg atom is interfaced with a dense environment of neutral ground state atoms. The properties of the Composite depend on both the Rydberg excitation, which provides the gross energetic and spatial scales, and on the distribution of ground state atoms within the volume of the Rydberg wave function, which sculpt the electronic states. The latter range from the trilobites, for small numbers of scatterers, to delocalized and chaotic eigenstates for disordered scatterer arrays, culminating in the dense scatterer limit in symmetry-dominated wave functions which promise good control in future experiments. We characterize these scenarios with different theoretical methods, enabling us to obtain scaling behavior for the regular spectrum and measures of chaos and delocalization in the disordered regime. Thus, we obtain a systematic description of the Composite states. The 2D monolayer Composite possesses the richest spectrum with an intricate band structure in the limit of homogeneous scatterers.
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