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We have measured the kinetic energy of positronium (Ps) atoms emitted into a vacuum from a porous silica film subsequent to positron bombardment, via the Doppler spread of the linewidth of the Ps 1 3 S-2 3 P transition. We find that the deeper in the target film that positrons are implanted the colder is the emitted Ps, an effect we attribute to cooling via collisions in the pores as the atoms diffuse back to the film surface. We observed a lower limit to the mean Ps kinetic energy associated with motion in the direction of the laser, E x = 42 ± 3 meV, that is consistent with conversion of the confinement energy of Ps in the 2.7-nm-diameter pores to kinetic energy in vacuum. An implication is that a porous sample would need to be composed of pores greater than around 10 nm in diameter in order to produce thermal Ps in vacuum with temperatures of less than 100 K. By performing Doppler spectroscopy on intense pulses of Ps we have experimentally demonstrated the production of many excited-state Ps atoms simultaneously, which could have numerous applications, including laser cooling and fundamental spectroscopic studies of Ps and the production of antihydrogen.

We demonstrate experimentally the production of Rydberg positronium (Ps) atoms in a two-step process, comprising incoherent laser excitation, first to the 2(3)P state and then to states with principal quantum numbers ranging from 10 to 25. We find that excitation of 2(3)P atoms to Rydberg levels occurs very efficiently (~90%) and that the ~25% overall efficiency of the production of Rydberg atoms is determined almost entirely by the spectral overlap of the primary excitation laser and the Doppler broadened width of the 1 (3)S-2(3)P transition. The observed efficiency of Rydberg Ps production can be explained if stimulated emission back to the 2P states is suppressed, for example, by intermixing of the Rydberg state Stark sublevels. The efficient production of long-lived Rydberg Ps in a high magnetic field may make it possible to perform direct measurements of the gravitational free fall of Ps.

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We report optical spectroscopic measurements of molecular positronium (Ps(2)), performed via a previously unobserved L=1 excited state. Ps(2) molecules created in a porous silica film, and also in vacuum from an Al(111) crystal, were resonantly excited and then photoionized by pulsed lasers, providing conclusive evidence for the production of this molecular matter-antimatter system and its excited state. Future experiments making use of the photoionized vacuum L=1 Ps(2) could provide a source of Ps(+) ions, as well as other multipositronic systems, such as Ps(2)H(-) or Ps(2)O.