Materials Science and Engineering Department, Idaho National Laboratory, Idaho Falls, ID, 83415, USA.
Fuel Design and Development Department, Idaho National Laboratory, Idaho Falls, ID, 83415, USA.
Sci Rep. 2018 Jan 8;8(1):98. doi: 10.1038/s41598-017-18548-8.
Innovations in nanostructuring of inorganic crystalline solids are often limited by prerequisite critical nucleation energy and solute supersaturation for formation of a phase. This research provides direct evidence supporting the viability of an unconventional irradiation-induced nanostructuring process, via transmission electron microscopy, that circumvents these preconditions. Using polymorphic silicon carbide (SiC) as a prototype, a surprising two-step nucleation route is demonstrated through which nanoscale distribution of the second phase is achieved by reaction of solutes with neutron irradiation-induced precursors. In the first step, nanoscale α-SiC precipitates in a β-SiC matrix unexpectedly nucleate heterogeneously at structural defects. This occurs at significantly lower temperatures compared with the usual β→α transition temperature. Subsequently, α-SiC precipitate acts as a surrogate template for its structural and compositional transition into a fission product precipitate, palladium silicide. These discoveries provide a modern view of irradiation engineering in polymorphic ceramics for advanced applications.
无机晶态固体的纳米结构化创新通常受到形成相所需的关键成核能和溶质过饱和度的限制。这项研究通过透射电子显微镜提供了直接证据,支持了一种规避这些前提条件的非常规辐照诱导纳米结构化过程的可行性。使用多晶碳化硅(SiC)作为原型,通过溶质与中子辐照诱导前体的反应,展示了令人惊讶的两步成核途径,从而实现了第二相的纳米级分布。在第一步中,β-SiC 基体中的纳米级 α-SiC 沉淀物出乎意料地在结构缺陷处异相形核。与通常的β→α转变温度相比,这发生在温度显著降低的情况下。随后,α-SiC 沉淀物作为其结构和组成向裂变产物沉淀物钯硅化物转变的替代模板。这些发现为先进应用中多晶陶瓷的辐照工程提供了现代观点。