Depth profiling of positron annihilation characteristics has been used to investigate the pore size distribution in macroporous PMMA latex-templated SiO 2 films deposited on glass or Si and prepared with 11-70% porosity. The correlation between the annihilation characteristics shows that ortho-positronium (o-Ps) escape (re-emission) into vacuum occurs in all films with a porosity threshold that is pore size dependent. For 60 ± 2% porosity, the o-Ps re-emission yield decreases from ∼0.25 to ∼0.11 as the pore size increases from 32 to 75 nm. The o-Ps re-emission yield is shown to vary linearly with the specific surface area per mass unit and the slope is independent of pore size, 9.1 ± 0.4 g cm −2 . For 32 nm pores, the o-Ps annihilation lifetimes in the films, 17(2) ns and 106(5) ns, show that o-Ps annihilates from micropores with small effective size (1.4 ± 4 nm) and from macropores with large effective size (∼32 nm). Above the porosity threshold, the o-Ps-escape model predicts the annihilation lifetime in the films to 7 2 be 19 ± 2 ns. Our results imply that o-Ps efficiently detects the microporosity present in the silica walls. At low porosity, its capture into the micropores competes with its capture into the macropores. At higher porosity (when the distance between micropores and macropores becomes small), this capture into the micropores assists the capture into the macropores.
This study aims at identifying the release mechanisms of helium in uranium dioxide. Two sets of polycrystalline UO2 sintered samples presenting different microstructures were implanted with 3He ions at concentrations in the region of 0.1 at.%. Changes in helium concentrations were monitored using two Nuclear Reaction Analysis (NRA) techniques based on the 3He(d,α)1H reaction. 3He release is measured in-situ during sample annealing at temperatures ranging between 700°C and 1000°C. Accurate helium depth profiles are generated after each annealing stage. Results that provide data for further understanding helium release mechanisms are discussed. It is found that helium diffusion appears to be enhanced above 900°C in the vicinity of grain boundaries possibly as a result of the presence of defects.
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