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We report measurements of the dynamics of isolated 8Li+ in single crystal rutile TiO2 using β-detected nuclear magnetic resonance. From spin-lattice relaxation and motional narrowing, we find two sets of thermally activated dynamics: one below 100 K and one at higher temperatures. At low temperature, the activation barrier is 26.8(6) meV with prefactor 1.23(5) × 1010 s-1. We suggest this is unrelated to Li+ motion and rather is a consequence of electron polarons in the vicinity of the implanted 8Li+ that are known to become mobile in this temperature range. Above 100 K, Li+ undergoes long-range diffusion as an isolated uncomplexed cation, characterized by an activation energy and prefactor of 0.32(2) eV and 1.0(5) × 1016 s-1, respectively, in agreement with macroscopic diffusion measurements. These results in the dilute limit from a microscopic probe indicate that Li+ concentration does not limit the diffusivity even up to high concentrations but that some key ingredient is missing in the calculations of the migration barrier. The anomalous prefactors provide further insight into both Li+ and polaron motion. [ABSTRACT FROM AUTHOR]

We report herein a means to modify the reactivity of alkenes, and particularly to modify their selectivity toward reactions with nonpolar reactants (e.g., nonpolar free radicals) in supercritical carbon dioxide near the critical point. Rate constants for free radical addition of the light hydrogen isotope muonium to ethylene, vinylidene fluoride, and vinylidene chloride in supercritical carbon dioxide are compared over a range of pressures and temperatures. Near carbon dioxide's critical point, the addition to ethylene exhibits critical speeding up, while the halogenated analogues display critical slowing. This suggests that supercritical carbon dioxide as a solvent may be used to tune alkene chemistry in near-critical conditions. [ABSTRACT FROM AUTHOR]