Abstract

In this study, we use Monte Carlo track chemistry simulations to show that “dry” secondary electrons, precursors of the “hydrated” electron (e−aq), can be scavenged on the sub-picosecond time scale prior to hydration, by a high concentration (>0.1–1 M) of azide ions (N3−) in water irradiated with 60Co γ-rays and tritium β-electrons at 25 °C. This is a striking result, as N3− is known to react very slowly with e−aq. These processes tend to significantly reduce the yields of H2 as observed experimentally. For both energetic Compton electrons (“linear energy transfer”, LET ∼ 0.3 keV/µm), which are generated by the cobalt-60 γ-rays, and 3H β-electrons (LET ∼ 6 keV/µm), our H2 yield results confirm previous Monte Carlo simulations, which indicated the necessity of including the capture of the precursors to e−aq. Interestingly, our calculations show no significant changes in the scavenging of “dry” electrons at high azide concentrations in passing from γ-radiolysis to tritium β-radiolysis (i.e., with LET). This led us to the conclusion that the higher H2 yield observed experimentally for 3H β-electrons compared with 60Co γ-rays is mainly explained by the difference in the radiation track structures during the chemical stage (>1 ps). The higher LET of tritium β-electrons leads to more molecular products (H2 in this case) in tritium radiolysis than in γ-radiolysis. Finally, a value of ∼0.5 nm was derived for the reaction distance between N3− and the “dry” electron from the H2 yields observed in 60Co γ-radiolysis at high N3− concentrations.

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