Huang W J, Sun R, Tao J, Menard L D, Nuzzo R G, Zuo J M
Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Nat Mater. 2008 Apr;7(4):308-13. doi: 10.1038/nmat2132. Epub 2008 Mar 9.
Surface atoms have fewer interatomic bonds than those in the bulk that they often relax and reconstruct on extended two-dimensional surfaces. Far less is known about the surface structures of nanocrystals. Here, we show that coherent diffraction patterns recorded from individual nanocrystals are very sensitive to the atomic structure of nanocrystal surfaces. Nanocrystals of Au of 3-5 nm in diameter were studied by examining diffraction intensity oscillations around the Bragg peaks. Both results obtained from modelling the experimental data and molecular dynamics simulations strongly suggest inhomogeneous relaxations, involving large out-of-plane bond length contractions for the edge atoms (approximately 0.2 A); a significant contraction (approximately 0.13 A) for {100} surface atoms; and a much smaller contraction (approximately 0.05 A) for atoms in the middle of the {111} facets. These results denote a coordination/facet dependence that markedly differentiates the structural dynamics of nanocrystals from bulk crystalline surfaces.
表面原子的原子间键比体相中的原子间键少,因此它们常常在延展的二维表面上弛豫并重构。关于纳米晶体的表面结构,人们所知甚少。在此,我们表明从单个纳米晶体记录的相干衍射图案对纳米晶体表面的原子结构非常敏感。通过检查布拉格峰周围的衍射强度振荡,对直径为3 - 5纳米的金纳米晶体进行了研究。从对实验数据建模以及分子动力学模拟得到的结果都强烈表明存在不均匀弛豫,其中边缘原子的面外键长有大幅收缩(约0.2埃);{100}表面原子有显著收缩(约0.13埃);而{111}晶面中间的原子收缩要小得多(约0.05埃)。这些结果表明了一种配位/晶面依赖性,这显著地区分了纳米晶体与体相晶体表面的结构动力学。