Published online by Cambridge University Press: 15 February 2011
The temperature dependence of the critical amorphization dose,Dc, of four A2BO4 compositions, forsterite (Mg2SiO4), fayalite(Fe2SiO4), synthetic Mg2GeO4,and phenakite (Be2SiO4) was investigated by in situ TEM during 1.5 MeV Kr+ion beam irradiation attemperatures between 15 to 700 K. For the Mg- and Fe-compositions, theA-site is in octahedral coordination, and the structure is a derivative hep (Pbnm); for the Be-composition, the A- and B-sitesare in tetrahedral coordination, forming corner-sharing hexagonal rings(R3). Although the Dc's were quite close at 15 K for all the fourcompositions (0.2–0.5 dpa), Dc increased with increasingirradiation temperature at different rates. The Dc-temperaturecurve is the result of competition between amorphization and dynamicrecovery processes. The Dc rate of increase (highest to lowest)is: Be2SiO4, Mg2SiO4, Mg2GeO4, Fe2SiO4. At roomtemperature, Be2SiO4 amorphized at 1.55 dpa; Fe2SiO4, at only 0.22 dpa. Based on the Dc-temperature curves, the activation energy, Ea,of the dynamic recovery process and the critical temperature, Tc,above which complete amorphization does not occur are: 0.029, 0.047, 0.055and 0.079 eV and 390, 550, 650 and 995 K for Be2SiO4, Mg2SiO4, Mg2GeO4 and Fe2SiO4, respectively. These results are explainedin terms of the materials properties (e.g., bonding and thermodynamicstability) and cascade size which is a function of the density of thephases. Finally, we note the importance of increased amorphizationcross-section, as a function of temperature (e.g., the low rate of increaseof Dc with temperature for Fe2SiO4).