Thermally stimulated exoelectron emission from solid Xe

Thermally-stimulated emission of exoelectrons and photons from solid Xe pre-irradiated by low-energy electrons were studied. A high sensitivity of thermally-stimulated luminescence (TSL) and thermally-stimulated exoelectron emission (TSEE) to sample prehistory was demonstrated. It was shown that electron traps in unannealed samples are characterized by a much broader distribution of trap levels in comparison with annealed samples and their concentration exceeds in number that in annealed samples. Both phenomena, TSL and TSEE, were found to be triggered by release of electrons from the same kind of traps. The data obtained suggest a competition between two relaxation channels: charge recombination and electron transport terminated by TSL and TSEE. It was found that TSEE predominates at low temperatures while at higher temperatures TSL prevails. An additional relaxation channel, a photon-stimulated exoelectron emission from pre-irradiated solid Xe, was revealed

Relaxation channels and transfer of energy stored by pre-irradiated rare gas solids

The processes of energy relaxation in rare gas solids pre-irradiated with an electron beam are discussed. We studied the emission of exoelectrons and photons from RGS. Investigations were performed by a set of activation spectroscopy methods applied simultaneously to each sample. Photon-stimulated exoelectron emission from solid Ne was observed for the first time

Anomalous low-temperature “post-desorption” from solid nitrogen

Anomalous low-temperature post-desorption (ALTpD) from the surface of nominally pure solid nitrogen pre-liminary irradiated by an electron beam was detected for the first time. The study was performed using a combi-nation of activation spectroscopy methods — thermally stimulated exoelectron emission (TSEE) and spectrally resolved thermally stimulated luminescence (TSL) — with detection of the ALTpD yield. Charge recombination reactions are considered to be the stimulating factor for the desorption from pre-irradiated α-phase solid nitrogen

Formation of (Xe2H)* centers in solid Xe via recombination: nonstationary luminescence and «internal electron emission»

The formation of excimers (Xe2H)* in solid Xe doped with molecular hydrogen under electron beam is studied using the original two-stage technique of nonstationary (NS) cathodoluminescence (CL) in combination with the current activation spectroscopy method — thermally stimulated exoelectron emission (TSEE). Charged species were generated using a high-density electron beam. The species produced were then probed with a lowdensity beam on gradual sample heating. The near UV emission of the (Xe2H)* was used to monitor the neutralization process. It is found that the temperature behavior of the NS CL band of (Xe2H)* clearly correlates with the yield of TSEE measured after identical pre-irradiation of the sample. The fingerprints of the thermally stimulated detrapping of electrons — «internal electron emission» in the spectrum of NS CL point to the essential role of neutralization reaction in the stability of the proton solvated by rare-gas atoms

Electron traps in solid Xe

Correlated real-time measurements of thermally stimulated luminescence and exoelectron emission from solid Xe pre-irradiated with an electron beam were performed. The study enabled us to distinguish between surface and bulk traps in solid Xe and to identify a peak related to electronically induced defects. The activation energy corresponding to annihilation of these defects was estimated by the following methods: the method of different heating rates, the initial-rise method, and the curve cleaning technique with fitting of the thermally stimulated luminescence glow curve

Optically-stimulated desorption of 'hot' excimers from pre-irradiated Ar solids

Electronically-induced desorption from solid Ar pre-irradiated by a low-energy electron beam was investigated by activation spectroscopy methods - photon-stimulated exoelectron emission and photon-stimulated luminescence in combination with spectrally-resolved measurements in the VUV range of the spectrum. Desorption of vibrationally excited argon molecules Ar2^*(v) from the surface of pre-irradiated solid Ar was observed for the first time. It was shown that desorption of 'hot' Ar2^*(v) molecules is caused by recombination of self-trapped holes with electrons released from traps by visible range photons. The possibility of optical stimulation of the phenomenon is evidenced.Comment: The complete version of the paper will be published in Fiz. Nizk. Temp. (Low Temp. Phys.

Comparative study of thermostimulated luminescence and electron emission of nitrogen nanoclusters and films

We have studied thermostimulated luminenscence and electron emission of nitrogen films and nanoclusters containing atomic nitrogen free radicals. Thermostimulated electron emission from N₂ nanoclusters was ob-served for the first time. Thermostimulated luminescence spectra obtained during N₂–He sample destruction are similar to those detected from N₂ films pre-irradiated by an electron beam. This similarity reveals common mechanisms of energy transfer and relaxation. The correlation of the luminescence intensity and the electron cur-rent in both systems points to the important role of ionic species in relaxation cascades. A sublimation of solid helium shells isolating nitrogen nanoclusters is a trigger for the initiation of thermostimulated luminescence and electron emission in these nitrogen–helium condensates