Choudhury Samrat, Aguiar Jeffery A, Fluss Michael J, Hsiung Luke L, Misra Amit, Uberuaga Blas P
Los Alamos National Laboratory, Los Alamos NM 87545.
Lawrence Livermore National Laboratory, Livermore, California 94551, USA.
Sci Rep. 2015 Aug 26;5:13086. doi: 10.1038/srep13086.
The properties and performance of metal/oxide nanocomposites are governed by the structure and chemistry of the metal/oxide interfaces. Here we report an integrated theoretical and experimental study examining the role of interfacial structure, particularly misfit dislocations, on solute segregation at a metal/oxide interface. We find that the local oxygen environment, which varies significantly between the misfit dislocations and the coherent terraces, dictates the segregation tendency of solutes to the interface. Depending on the nature of the solute and local oxygen content, segregation to misfit dislocations can change from attraction to repulsion, revealing the complex interplay between chemistry and structure at metal/oxide interfaces. These findings indicate that the solute chemistry at misfit dislocations is controlled by the dislocation density and oxygen content. Fundamental thermodynamic concepts – the Hume-Rothery rules and the Ellingham diagram – qualitatively predict the segregation behavior of solutes to such interfaces, providing design rules for novel interfacial chemistries.
金属/氧化物纳米复合材料的性质和性能由金属/氧化物界面的结构和化学性质决定。在此,我们报告一项综合理论与实验研究,考察界面结构,特别是失配位错,对金属/氧化物界面溶质偏聚的作用。我们发现,失配位错与共格平台之间的局部氧环境存在显著差异,它决定了溶质向界面的偏聚倾向。根据溶质的性质和局部氧含量,溶质向失配位错的偏聚可从吸引转变为排斥,揭示了金属/氧化物界面化学与结构之间的复杂相互作用。这些发现表明,失配位错处的溶质化学受位错密度和氧含量控制。基本的热力学概念——休姆-罗瑟里规则和埃林汉姆图——定性地预测了溶质向此类界面的偏聚行为,为新型界面化学提供了设计规则。