The radiative decay of (1)P(o) doubly excited states in helium has been investigated using a novel apparatus in which metastable atoms and vacuum ultraviolet photons are detected. The intensity ratio of the energetically narrow (sp,2n-)(1)P(o) and (2p,nd)(1)P(o) series to the broader (sp,2n+)(1)P(o) series is strikingly enhanced in comparison with conventional photoabsorption, photoion, or photoelectron measurements using synchrotron radiation. The experimental approach is a new way forward for the study of energetically narrow doubly excited states.

Long-lived, excited neutral particles, arising from the interaction of monochromatic synchrotron radiation with ground state He atoms, have been observed at photon energies close to the (N = 1,2,3 and 4) ionization thresholds. The measurements have been made using an unconventional experimental arrangement in which charged particles, responsible for the dominant signal in conventional photon impact studies, are prevented from reaching the detector. For , it appears that the formation, via photoexcitation, of relatively long-lived, doubly excited Rydberg states is a necessary step in the production of the observed signal. Four processes that might account for the production of the excited neutral particles are considered. The simplest, that atoms in the initial doubly excited Rydberg states are themselves directly observable, is considered unlikely. However, the lifetimes of the photoexcited double Rydberg states may be increased through the effects of electric fields present in the apparatus. Transitions from these double Rydberg states, occurring either as a result of collisions or by fluorescence, could result in metastable, singly excited neutral particles. The presence of signal related to the existence of long-lived doubly excited states could be significant in the interpretation of other photon impact measurements.

Two recent theoretical studies [C. Liu, Phys. Rev. A 64, 010501 (2001)]; M. Zitnik, ibid. 65, 032520 (2002)]] predict that the fluorescence lifetimes of helium doubly excited states converging to He+ N=2 should be longer than that of the He+ 2p ion state. This effect is caused by the electric field of the outer electron which, through Stark mixing, gives the inner fluorescing electron some series specific, stabilizing 2s character. We have obtained the first experimental evidence that confirms this effect by measuring the lifetime of the 2p3d(1P0) doubly excited state. This was determined to be 190+/-30 ps compared to 100 ps for the He+ 2p ion state. The measurements were performed using short pulses of synchrotron radiation to form doubly excited states and recording the arrival time of photons from fluorescence.

The creation and subsequent Auger decay of the 3d −1 core-hole state in HBr is studied using two-dimensional photoelectron spectroscopy. In this technique the yield of electrons is collected as a function of both photon and electron kinetic energy. The effects of post-collision interaction (PCI) observed in the energy shift of the HBr + (3d −1 ) photoelectron lines. The energy shifts are compared with previous experimental results on Kr. This comparison suggests that the molecular nature of HBr has little effect on the PCI energy exchange mechanism.