Ion beam irradiation of ABO4 compounds with the fergusonite, monazite, scheelite, and zircon structures

The effects of irradiation on CaWO4, SrWO4, BaWO4, YVO4, LaVO4, YNbO4, and LaNbO4 were investigated on thin crystals using 1.0 MeV Kr ions at 50-1000 K. All of the ABO4 compounds can be amorphized with calculated damage cross sections (σa = 1/Fc0) in the range of ~ 0.30-1.09 × 10-14 cm2 ion-1 at zero Kelvin. Analysis of fluence-temperature data returned critical temperatures for amorphization (Tc) of 311 ± 1, 358 ± 90, 325 ± 19, 415 ± 17, 541 ± 6, 636 ± 26, and 1012 ± 1 K, respectively for the compounds listed above. Compared with previous in situ irradiation of ABO4 orthophosphate samples using 0.8 MeV Kr ions, the Tc values of LaVO4 and YVO4 are higher than those of LaPO4 and YPO4 by 82 K and 124 K, respectively. The Tc values of the three scheelite structures, CaWO4, SrWO4, and BaWO4, indicate that they are the most radiation tolerant compounds under these conditions. The A-B cation anti-site energies, EfAB, determined by DFT range from 2.48 to 10.58 eV and are highly correlated with the A-B cation ionic radius ratio, rA/rB, but are not correlated with Tc across the different structure types, suggesting that the formation and migration energies of Frenkel defects play a more important role in damage recovery in these compounds. We also discuss the role of cation and anion charge/iconicity as determined by DFT. ABO4 compounds with the zircon structure and B = P or V have a distinct advantage over those with B = Si as the damaged regions do not appear to be significantly affected by polymerization of (PO4)3- or (VO4)3- groups which might stabilize the amorphous fraction and ultimately lead to phase separation as observed in zircon (ZrSiO4)

Ion irradiation effects in nonmetals: formation of nanocrystals and novel microstructures

Ion implantation is a versatile and powerful technique for producing nanocrystal precipitates embedded in the near-surface region of materials. Radiation effects that occur during the implantation process can lead to complex microstructures and particle size distributions, and in the present work, we focus on the application of these effects to produce novel microstructural properties for insulating or semiconducting nanocrystals formed in optical host materials. Nanocrystal precipitates can be produced in two ways: by irradiation of pure ( i.e. , non-implanted) crystalline or amorphous materials, or by ion implantation followed by either thermal annealing or subsequent additional irradiation. Different methods for the formation of novel structural relationships between embedded nanocrystals and their hosts have been developed, and the results presented here demonstrate the general flexibility of ion implantation and irradiation techniques for producing unique near-surface nanocomposite microstructures in irradiated host materials.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/42336/1/10019-3-4-190_00030190.pd

A transient liquid-like phase in the displacement cascades of zircon, hafnon and thorite

The study of radiation effects in solids is important for the development of 'radiation-resistant' materials for fission-reactor applications'. The effects of heavy-ion irradiation in the isostructural orthosilicates zircon (ZrSiO4), hafnon (HfSiO4) and thorite (ThSiO4) are particularly important because these minerals are under active investigation for use as a waste form for plutonium-239 resulting from the dismantling of nuclear weapons(2-4). During ion irradiation, localized 'cascades' of displaced atoms can form as a result of ballistic collisions in the target material, and the temperature inside these regions may for a short time exceed the bulk melting temperature. Whether these cascades do indeed generate a localized liquid state(5-8) has, however, remained unclear. Here we investigate the irradiation-induced decomposition of zircon and hafnon, and find evidence for formation of a liquidlike state in the displacement cascades. Our results explain the frequent occurrence of ZrO2 in natural amorphous zircong(9-12) Moreover, we conclude that zircon-based nuclear waste forms should be maintained within strict temperature Limits, to avoid potentially detrimental irradiation-induced amorphization or phase decomposition of the zircon.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/62853/1/395056a0.pd

Surface alteration of borosilicate and phosphate nuclear waste glasses by hydration and irradiation

We examined the degradation of nuclear waste borosilicate and phosphate glasses containing strong alpha-emitter 238Pu at a specific activity of 6.33 × 105 MBq/g in comparison with similar non-radioactive, non-radioactive irradiated and radioactive samples containing beta- and gamma-emitters, namely radionuclides 134Cs and 137Cs. For irradiation and leaching experiments, we used borosilicate and phosphate glasses, which are well-known and currently used to immobilize high-level radioactive waste. The main focus was the observation of the surface of altered glasses. Comparative analysis of hydrolytic surface alteration of borosilicate and phosphate nuclear waste glasses reveals that the behavior of radioactive samples differs significantly from that of non-radioactive glasses