Knowing when, why, and how materials evolve, degrade, or fail in radiation environments is pivotal to a wide range of fields from semiconductor processing to advanced nuclear reactor design. A variety of methods, including optical and electron microscopy, mechanical testing, and thermal techniques, have been used in the past to successfully monitor the microstructural and property evolution of materials exposed to extreme radiation environments.Acoustic techniques have also been used in the past for this purpose, although most methodologies have not achieved widespread adoption. However, with an increasing desire to understand microstructure and property evolution in situ, acoustic methods provide a promising pathway to uncover information not accessible to more traditional characterization techniques. This work highlights how two different classes of acoustic techniques may be used to monitor material evolution during in situ ion beam irradiation. The passive listening technique of acoustic emission is demonstrated on two model systems, quartz and palladium, and shown to be a useful tool in identifying the onset of damage events such as microcracking.An active acoustic technique in the form of transient grating spectroscopy is used to indirectly monitor the formation of small defect clusters in copper irradiated with self-ions at high temperature through the evolution of surface acoustic wave speeds.These studies together demonstrate the large potential for using acoustic techniques as in situ diagnostics. Such tools could be used to optimize ion beam processing techniques or identify modes and kinetics of materials degradation in extreme radiation environments.
Energy and cost efficient synthesis pathways are important for the production, processing, and recycling of rare earth metals necessary for a range of advanced energy and environmental applications. In this work, we present results of successful in situ liquid cell transmission electron microscopy production and imaging of rare earth element nanostructure synthesis, from aqueous salt solutions, via radiolysis due to exposure to a 200 keV electron beam. Nucleation, growth, and crystallization processes for nanostructures formed in yttrium(iii) nitrate hydrate (Y(NO3)3·4H2O), europium(iii) chloride hydrate (EuCl3·6H2O), and lanthanum(iii) chloride hydrate (LaCl3·7H2O) solutions are discussed. In situ electron diffraction analysis in a closed microfluidic configuration indicated that rare earth metal, salt, and metal oxide structures were synthesized. Real-time imaging of nanostructure formation was compared in closed cell and flow cell configurations. Notably, this work also includes the first known collection of automated crystal orientation mapping data through liquid using a microfluidic transmission electron microscope stage, which permits the deconvolution of amorphous and crystalline features (orientation and interfaces) inside the resulting nanostructures.
The National Nuclear Security Administration's Tritium Sustainment Program is responsible for the design, development, demonstration, testing, analysis, and characterization of tritium-producing burnable absorber rods (TPBARs) and their components, in addition to producing tritium for the nation's strategic stockpile. The FY18 call for proposals included the specific basic science research topic, "Demonstration and evaluation of advanced characterization methods, particularly for quantifying the concentration of light isotopes (1H, 2H, and 4He, 6Li, and 7Li) in metal or ceramic matrices". A project IWO-389859 was awarded to the Ion Beam Lab (IBL) at Sandia-NM in FY18. This reports the success we had in developing and demonstrating such a method: 42 MeV Si+ 7 from the IBL' s Tandem was used to recoil these light isotopes into special detectors that separated all these isotopes by simultaneously measuring the energy and stopping power of these reoils. This technique, called Heavy Ion - Elastic Recoil Detection or HI-ERD, accurately measured the enriched 6 Li/Li-total of 0.246 +- 0.016, compared to the known value of 0.239. The isotopes 1H, 2H, 4He, 6Li and 7Li were also measured. (page intentionally left blank)
Scott, Ethan A.; Hattar, Khalid M.; Taylor, Caitlin A.; Gaskins, John T.; Bai, Tingyu B.; Wang, Steven Y.; Gansky, Claire G.; Goorsky, Mark S.; Hopkins, Patrick E.
Scott, Ethan A.; Hattar, Khalid M.; Taylor, Caitlin A.; Gaskins, John T.; Bai, Tingyu B.; Wang, Steven Y.; Gansky, Claire G.; Goorsky, Mark S.; Hopkins, Patrick E.